It stands to reason that the chronically dehydrated human body cannot recover in one day, no matter how much water is imbibed. The cells will simply resist it, bereft of hydration for so long, unaccustomed to normal absorption. Think of a parched desert arroyo, suddenly flooded over from a deluge of stormy weather. What happens? Flash flood. The water simply can’t penetrate the long-dessicated surface right away, and rolls off like water off a duck’s back.

For someone beginning hydration as part of the 60 Day Program, the 2-litre goal may be difficult to achieve during the first week. The cells are simply not used to all this water. But whatever it takes, just keep drinking as much as you can, every day. After several days, intake will become gradually easier – less resistance, less that feeling of bloating.

Once it becomes comfortable to actually drink 2 litres each day, the challenge then becomes maintaining it day after day. Mainly a question of convenience: some planning will obviously be required, to accommodate travel schedules, etc.

After the second week, an odd thing happens: one experiences occasional dry mouth and thirst even though he’s taking in an unprecedented amount of water. What’s going on? This is still more evidence of the distinctness between thirst and hydration: two different things entirely.

Such a phenomenon can only be seen as the body’s confirmation of its true state of profound dehydration – years without meeting the body’s demands for intra and extracellular water content. Sensing a continued availability now for the first time, the water conservation systems can finally begin to relax as all the cells begin to receive the normal amount of water they have been denied for so long. Now the dramatic health changes can really begin to be come on line.

In his master work Water and Salt, Dr Batmanghelidj explains this phenomenon:

“If the body is once again conditioned to regular and adequate intake, the thirst sensation becomes sharp and the urge to drink water becomes strong… The re-hydration of cells takes place slowly.”

The extent of the chronic dehydration at this point truly becomes known to the individual, as this is the only way re-hydration can occur.

By the third or fourth week, it’s smooth sailing. This is when the potential for healing really becomes evident. Chronic problems with digestion, circulation, adrenal imbalance, nervousness, – on and on – what isn’t influenced by adequate hydration? The body is 75% water.

The most significant danger of dropping out of the program seems to occur during the first 2 weeks. Often it’s an unwillingness to schedule the water intake outside of commute times. An astonishing proportion of people either believe themselves or have been told by some physician that it is imprudent to “stress” the kidneys and bladder in this way, making so many trips to the bathroom, etc., or something equally ludicrous. Or the greatest delusion of all – the standard HCT myth of modern cardiology, correlating high blood pressure with “too much water in the blood.”

Most disconcerting the way that flagrant contradiction is commonly accepted without objection by generation after generation of heart meds patients. The old water content/viscosity index: standard hydraulics. Which is harder to pump, blood with more water content or less water content? Thicker or thinner blood?

Since its inception, the 60 Day Program has always made the general recommendation of adequate daily hydration, without going into much detail about it. But with the additional knowledge now of the alkalized, low molecular size water, coupled with specific directions on how to really discipline oneself to a 2 litre daily intake – these modifications have boosted the healing value of the 60 Day Program to new heights. Health changes that may have been good with the 60 Day Program alone may now manifest as truly dramatic quantum improvements. Life changing.

It’s a question of degree – common sense tells us that adherence to these simple principles of overall cell nutrition even slightly — of course it’s going to have a salubrious effect, usually a vast improvement over the previous life. But rigid and disciplined adherence to the hydrated 60 Day Program – well, who will put limits on what something like that can accomplish, no matter how immune suppressed, how diseased, how run down the individual is?

SPECIFIC APPLICATIONS OF THE 2 LITRE HYDRATION

Spinal Discs

Which appear thin and worn on X-ray are sometimes described as dessicated – dried out. For anyone undergoing flexion/distraction or spinal decompression therapy for disc problems, this simple type of hydration as described above can enhance the therapeutic efficacy exponentially. Particularly if collagen supplementation is also included. [See Collagen chapter]

Chronic Skin Disease

Eczema, acne, psoriasis, cracked, dry, loose skin – most patients have tried a variety of ointments, lotions, steroid creams, etc., usually with mediocre or no long term success. The reason is simple: true hydration is an inside-out job. Superficial topical applications cannot effectively hydrate the intra and extracellular spaces of skin cells. Period. Worse, the majority of skin care products contain waxes and sterols which give the illusion of smoothness but do so by actually sealing off the pores of the skin, thereby exacerbating the long term inflammatory problems by blocking the 2 most important requirements for healthy skin: air and water.

A few of the better skin products actually benefit the skin, but a much more effective approach is hydrating the skin cells from within by drinking 2 litres of water a day. After a few weeks of this daily flooding with the highest quality water, the skin cells become replete with their maximum water content. Couple with hydrolyzed Collagen, the skin will generally become noticeably thicker in a few weeks. Not rocket science here. Just not drug science.

Kidney and Bladder

Proper hydration may have a dramatic therapeutic effect on chronic kidney and bladder problems, especially if the patient has been on protracted medications for these conditions.

Kidney function diminishes after years of a diet loaded with refined sugars and hydrogenated snacks. In their constant struggle to maintain blood pH against a flood of acidifying food and drink, the kidneys cells – nephrons – experience rapid aging. As they weaken, their ability to clean the blood slows down. If imprudent diet choices persist, the work backs up. This happens slowly and subclinically: jaundice only comes much later.

Once they fall behind, the kidneys may never really catch up with the ongoing toxic load coming in every day. And a slow, downward spiral ensues. Couple this with the additional handicap of dehydration of the kidney cells themselves and the result is chronic kidney disease, leading to eventual failure. The ninth leading cause of death in the US, according to the CDC, 2009.

Another compounding factor will present if the patient is also on diuretics for high blood pressure. More and more demands are put on the already overworked kidneys, which are handicapped further by the increased blood viscosity – thicker blood.

In advanced cases, water intake must be increased very gradually because the kidney cells are so weak and overstressed. But if the trend is constant – daily increased hydration – and decreased intake of processed trash – kidney disease can begin to resolve, slowly and gradually.

The biggest obstacle of all actually seems to be finding out something like this is possible, especially if long term medications are involved. Pop quiz: do nephrologists ever say the drugs are going to cure you and you can stop taking them? Not likely. Remember, medical personnel are not trained to cure these types of problems. Their training is consistent across the board, with one common focus: sell as many drugs as possible. Most common sense solutions lie outside their ken.

Bladder Problems are much easier. Usually it’s an issue of muscle atrophy – disuse of the detrusor muscles of the bladder. Frequent tips to the bathroom at night are self-perpetuating. The slightest urge and up you get. With no opportunity to fill and thereby tone the bladder muscles, they become weak and thin. Coupled with a dehydration of the muscle cells, we see another downward spiral.

The introduction of high end water into this patient’s life is the most logical solution, for several reasons. Obviously more water will be available to hydrate the detrusor muscle cells, setting them up to strengthen. Waiting longer and longer to void the bladder, will slowly build muscle tone. Now we have an upward spiral – the stronger the detrusor muscles become, the more the bladder can hold and the less the feeling of urgency. Don’t worry, it’s not going to burst. Sleep improves – upward spiral – all things move toward equilibrium.

If the 2 litre goal can actually be attained in these chronic degenerative kidney and bladder cases, together with the clean diet, the patients may reclaim a normal drug-free life, for the first time in years. Easy-peasy. Again, the hard part is learning all this is possible, and then actually doing it. Chance of success will be significantly enhanced if one includes the 60 Day Program, and uses the best possible alkalized, low molecule size water. [The Three Attributes of Water]

Colon Disease

As the #3 type of cancer in the US, colon disease has reached epidemic proportions in this country. The primary excuse for these numbers is lack of knowledge about how this important organ works. The physiology of the colon is thoroughly covered in the Colon chapter, with simple instructions on clearing out years of layered sludge, and re-establishing normal probiotic vitality and immune function. Of course, a prerequisite is to stop loading up on the same unmetabolizable junk that brought on the problem in the first place.

Including the 2 litre hydration to the program will facilitate the elimination of the dislodged pieces of sludge, obviously. But an even more useful effect of new hydration may be the cleansing and re-vitalizing effect on the mucosal cells of the gut lining, as well as the muscles cells of the colon. The result will be a strengthening of overall peristalsis and providing a hospitable environment for the proliferation of normal flora throughout the tract.

Again, far and away the best results are seen with the use of the best water possible, which today is alkaline, low molecule sized water, as explained under The Three Attributes of Water under Chapters.

UPCOMING SEMINARS

The Nutrition Seminar:

• Long Beach CA – 7 Aug
• Sacramento CA – 21 Aug

Vaccine/Detox Seminar

• Phoenix AZ – 11 Sep
• Seattle WA – 18 Sep
• Palm Springs – 15 Oct (Gonstead Seminar)

In the Nutrition Seminar we deliver a complete discussion of the 60 day Detox Program, beginning with the no-brainer New West Diet. We begin with the distinction between natural and processed foods, going through the history of the natural diet, and the type of health picture it produced. The crucial topic of GMO is introduced, with some excellent resources being suggested: current books and DVDs. For the patient in survival mode, or one who simply wants to get back on track, these topics are vital:

• enzymes
• chelated minerals
• florabiotics
• collagen
• oral chelation
• megahydrate
• colon detox

For health care providers, the tools for a complete patient nutrition program are handed around.

If you have taken the seminar before, one big addition to the curriculum is the rise of GM foods, which has taken over world food production in the past 14 years. This shocking and monumentally important information is simply not available in mainstream media, with good reason. And so unless the doctors avail themselves of at least an introductory level of resources on the subject, they simply will not be aware why 80% of commercial foods today are Genetically Modified.

For those who cannot attend, both the full day seminars are available on recent DVD sets at the website

New cities are added all the time: See website under Seminar

Then in the Vaccine/Detox Seminar we will use the morning hours for highlights from the new text book Vaccination Is Not Immunization 2010.

A few of the morning topics:

• Why 68 vaccines before age 18
• Autism: an American epidemic
• Is mercury really gone?
• Do vaccines work?
• Why are American kids fatter, sicker and dumber than ever before?
• The Germ Theory vs. Bioterrain Theory of disease
• Doctor as caregiver or agent of the state?
• Exemptions laws: why more parents take the easy way out
• What is Prevnar?
• What is Human Papilloma Virus?
• When will the next false pandemic be created?

In the afternoon we will do as much as possible from the full day nutrition Seminar, focusing on the essentials of the 60 Day Program.

Most of the seminars above are 12 hour relicensing seminars, including technique for DCs.

Please call office to register for any event 408.298.1800 or email doc@thedoctorwithin.com

New Vaccine Book: Vaccination is Not Immunization – 2010

Dear Concerned Parent,

Do you have doubts whether vaccines can really protect your child from illness or disease? Do you worry that your child could become autistic, or develop asthma, allergies or even a fatal childhood disease?

Well then, what you’re about to read may come as a shock. It did for me when I first began to research vaccines and their effect on the body over a decade ago. Hundreds of hours of digging into the medical literature and checking the facts compelled me to speak out.

Much of what I discovered was in conflict with the way most of us are taught to care for our children. Let’s face it — most parents agree to have their newborn child vaccinated and believe it is the right thing to do. That child goes on to receive numerous vaccinations year after year up through their teens. All the while you, the parent, continue to think you’re doing the right thing.

Well. . .as it turns out, it can be a huge mistake. Read More…

Buy Now

Hydration & Dehydration: Two Litres a Day

Should the importance of hydration dawn on an individual to such an extent that he actually decides to attempt it – the 2 litres per day recommended in the 60 Day Program – here are some likely expectations:

It stands to reason that the chronically dehydrated human body cannot recover in one day, no matter how much water is imbibed. The cells will simply resist it, bereft of hydration for so long, unaccustomed to normal absorption. Think of a parched desert arroyo, suddenly flooded over from a deluge of stormy weather. What happens? Flash flood. The water simply can’t penetrate the long-dessicated surface right away, and rolls off like water off a duck’s back.

For someone beginning hydration as part of the 60 Day Program, the 2-litre goal may be difficult to achieve during the first week. The cells are simply not used to all this water. But whatever it takes, just keep drinking as much as you can, every day. After several days, intake will become gradually easier – less resistance, less that feeling of bloating.

Once it becomes comfortable to actually drink 2 litres each day, the challenge then becomes maintaining it day after day. Mainly a question of convenience: some planning will obviously be required, to accommodate travel schedules, etc.

After the second week, an odd thing happens: one experiences occasional dry mouth and thirst even though he’s taking in an unprecedented amount of water. What’s going on? This is still more evidence of the distinctness between thirst and hydration: two different things entirely.

Such a phenomenon can only be seen as the body’s confirmation of its true state of profound dehydration – years without meeting the body’s demands for intra and extracellular water content. Sensing a continued availability now for the first time, the water conservation systems can finally begin to relax as all the cells begin to receive the normal amount of water they have been denied for so long. Now the dramatic health changes can really begin to be come on line.

By the third or fourth week, it’s smooth sailing. This is when the potential for healing really becomes evident. Chronic problems with digestion, circulation, adrenal imbalance, nervousness, – on and on – what isn’t influenced by adequate hydration? The body is 75% water.

The most significant danger of dropping out of the program seems to occur during the first 2 weeks. Often it’s an unwillingness to schedule the water intake outside of commute times. An astonishing proportion of people either believe themselves or have been told by some physician that it is imprudent to “stress” the kidneys and bladder in this way, making so many trips to the bathroom, etc., or something equally ludicrous. Or the greatest delusion of all – the standard HCT myth of modern cardiology, correlating high blood pressure with “too much water in the blood.”

Most disconcerting the way that flagrant contradiction is commonly accepted without objection by generation after generation of heart meds patients. The old water content/viscosity index: standard hydraulics. Which is harder to pump, blood with more water content or less water content? Thicker or thinner blood?

Since its inception, the 60 Day Program has always made the general recommendation of adequate daily hydration, without going into much detail about it. But with the additional knowledge now of the alkalized, low molecular size water, coupled with specific directions on how to really discipline oneself to a 2 litre daily intake – these modifications have boosted the healing value of the 60 Day Program to new heights. Health changes that may have been good with the 60 Day Program alone may now manifest as truly dramatic quantum improvements. Life changing.

It’s a question of degree – common sense tells us that adherence to these simple principles of overall cell nutrition even slightly — of course it’s going to have a salubrious effect, usually a vast improvement over the previous life. But rigid and disciplined adherence to the hydrated 60 Day Program – well, who will put limits on what something like that can accomplish, no matter how immune suppressed, how diseased, how run down the individual is?

Spinal Discs

Which appear thin and worn on X-ray are sometimes described as dessicated – dried out. For anyone undergoing flexion/distraction or spinal decompression therapy for disc problems, this simple type of hydration as described above can enhance the therapeutic efficacy exponentially. Particularly if collagen supplementation is also included. [See Collagen chapter]

Chronic Skin Disease

Eczema, acne, psoriasis, cracked, dry, loose skin – most patients have tried a variety of ointments, lotions, steroid creams, etc., usually with mediocre or no long term success. The reason is simple: true hydration is an inside-out job. Superficial topical applications cannot effectively hydrate the intra and extracellular spaces of skin cells. Period. Worse, the majority of skin care products contain waxes and sterols which give the illusion of smoothness but do so by actually sealing off the pores of the skin, thereby exacerbating the long term inflammatory problems by blocking the 2 most important requirements for healthy skin: air and water.

A few of the better skin products actually benefit the skin, but a much more effective approach is hydrating the skin cells from within by drinking 2 litres of water a day. After a few weeks of this daily flooding with the highest quality water, the skin cells become replete with their maximum water content. Couple with hydrolyzed Collagen, the skin will generally become noticeably thicker in a few weeks. Not rocket science here. Just not drug science.

Kidney and Bladder

Proper hydration may have a dramatic therapeutic effect on chronic kidney and bladder problems, especially if the patient has been on protracted medications for these conditions.

Kidney function diminishes after years of a diet loaded with refined sugars and hydrogenated snacks. In their constant struggle to maintain blood pH against a flood of acidifying food and drink, the kidneys cells – nephrons – experience rapid aging. As they weaken, their ability to clean the blood slows down. If imprudent diet choices persist, the work backs up. This happens slowly and subclinically: jaundice only comes much later.

Once they fall behind, the kidneys may never really catch up with the ongoing toxic load coming in every day. And a slow, downward spiral ensues. Couple this with the additional handicap of dehydration of the kidney cells themselves and the result is chronic kidney disease, leading to eventual failure. The ninth leading cause of death in the US, according to the CDC, 2009.

Another compounding factor will present if the patient is also on diuretics for high blood pressure. More and more demands are put on the already overworked kidneys, which are handicapped further by the increased blood viscosity – thicker blood.

In advanced cases, water intake must be increased very gradually because the kidney cells are so weak and overstressed. But if the trend is constant – daily increased hydration – and decreased intake of processed trash – kidney disease can begin to resolve, slowly and gradually.

The biggest obstacle of all actually seems to be finding out something like this is possible, especially if long term medications are involved. Pop quiz: do nephrologists ever say the drugs are going to cure you and you can stop taking them? Not likely. Remember, medical personnel are not trained to cure these types of problems. Their training is consistent across the board, with one common focus: sell as many drugs as possible. Most common sense solutions lie outside their ken.

Bladder Problems

Are much easier. Usually it’s an issue of muscle atrophy – disuse of the detrusor muscles of the bladder. Frequent tips to the bathroom at night are self-perpetuating. The slightest urge and up you get. With no opportunity to fill and thereby tone the bladder muscles, they become weak and thin. Coupled with a dehydration of the muscle cells, we see another downward spiral.

The introduction of high end water into this patient’s life is the most logical solution, for several reasons. Obviously more water will be available to hydrate the detrusor muscle cells, setting them up to strengthen. Waiting longer and longer to void the bladder, will slowly build muscle tone. Now we have an upward spiral – the stronger the detrusor muscles become, the more the bladder can hold and the less the feeling of urgency. Don’t worry, it’s not going to burst. Sleep improves – upward spiral – all things move toward equilibrium.

If the 2 litre goal can actually be attained in these chronic degenerative kidney and bladder cases, together with the clean diet, the patients may reclaim a normal drug-free life, for the first time in years. Easy-peasy. Again, the hard part is learning all this is possible, and then actually doing it. Chance of success will be significantly enhanced if one includes the 60 Day Program, and uses the best possible alkalized, low molecule size water. [The 3 Attributes of Water]

Colon Disease

As the #3 type of cancer in the US, colon disease has reached epidemic proportions in this country. The primary excuse for these numbers is lack of knowledge about how this important organ works. The physiology of the colon is thoroughly covered in the Colon chapter, with simple instructions on clearing out years of layered sludge, and re-establishing normal probiotic vitality and immune function. Of course, a prerequisite is to stop loading up on the same unmetabolizable junk that brought on the problem in the first place.

Including the 2 litre hydration to the program will facilitate the elimination of the dislodged pieces of sludge, obviously. But an even more useful effect of new hydration may be the cleansing and re-vitalizing effect on the mucosal cells of the gut lining, as well as the muscles cells of the colon. The result will be a strengthening of overall peristalsis and providing a hospitable environment for the proliferation of normal flora throughout the tract.

Again, far and away the best results are seen with the use of the best water possible, which today is alkaline, low molecule sized water, as explained under The Three Attributes of Water under Chapters.

There is a machine for the home that can provide these 3 properties to your water supply at home that makes it far better than the unregulated bottled water you’re dragging in every week. For the few cases that are slow to respond to the 60 Day Program, provided they’re actually following it, of course, this alkalyzed water is the crowning touch, the missing piece of the puzzle. Anyone in San Jose can get this water for free from my office. Anyone who wants to learn about the machine should contact Dr George at 818 209 6817.

More Idiotic Things Doctors Have Told My Patients: Looking for horror stories – share your experiences!

I’ve finally decided to organize and keep track of some of the hundreds of scary stories I keep hearing in my practice, my travels, and in doing so many phone consults. The world needs to hear this stuff, and it’s definitely not going to be on Montel or Howard Stern!

I’m sure you all have some examples, maybe even wilder than these. So this is an open solicitation to share them with the world — just write them up and email them to me. Short version please.

I’ll start you out. Here’s a couple recent ones:

Incredibly Idiotic Things Doctors Have Told My Patients

Story #3312
I recently fell off my horse and sustained a Colles fracture of my R. wrist. Seeing the bone so obviously displaced, I grabbed it and forcefully set it myself, on the spot. Didn’t hurt then, but two hours later…oh boy! So, wanting to get a professional opinion, I consulted 3 orthopedic surgeons in the next few days. Their only difference was the length of the permanent scar their major reconstructive surgeries were going to leave– ranging from 7 inches to 15 inches! One wanted to do screws, another pins, and the third an entire plate! Now for the bad news: the cheapest one was gonna be $50 grand! My decision was to do nothing, except ice and palliative laser. Result: after 3 months I have complete range of motion, normal callus formation and no pain. If I had done it their way I probably would have had to give up my life work as a dressage instructor.
What do these guys study in school anyway? Hustling 101?
What happened to First Do No Harm?
— KF, Menlo Park

Story #3313
A patient came in with a simple case of right sided sciatica, caused by an obvious foraminal encroachment at L5, clearly visible on plain film. The reason he had come to me is that he had first visited Kaiser, who told him their first recommendation was rhizotomy! That’s right: severing and removing the nerve root because of radiating leg pain. This didn’t sound quite right to him and the patient wanted to get a second opinion. So he came here. After 2 weeks of chiropractic of course he was completely out of pain and was under care for full spinal correction.

Anything like this ever happen to any of you?? Submit stories to doc@thedoctorwithin.com

Recently I have learned how to take hydration to a whole new stratum. The technology is not even new — the Japanese have had it for 30 years. Now in the past 2 years it’s available here.

Just a word on the 3 attributes of water:

• molecular size
• pH
• oxidation

Water coming out of the taps in most houses is very harsh, to say the least. It is in huge molecules, probably closer to H200/O100 than it is to H2O. Molecules this large have difficulty being absorbed at the cellular level, even in the rare event the individual drinks adequate water.

Second is pH. Water we drink should be as close to normal blood pH as possible: 7.3 – 7.45. All the trashy foods and soft drinks we eat are constantly acidifying our body’s system: that means lowering the pH. Acidification promotes virtually every disease process known to man. So drinking high pH water will tip the scales in the opposite end: alkaline. Life functions soar.

Thirdly, the best water can act as a mild antioxidant, like Vitamin C or Vitamin E by neutralizing free radicals. See chapter on antioxidants.

Taken together, drinking 2 litres of this type of water per day can have a curative effect on almost any degenerative process, especially aging! What do we always say – old and dried up…? It’s literally true. When you can begin to hydrate again, for the first time in years, miraculous results occur. Was it really such a miracle though – to add the most vital nutrient human physiology is based on? These days common sense seems to be the real miracle.

There is a machine for the home that can provide these 3 properties to your water supply at home that makes it far better than the unregulated bottled water you’re dragging in every week. For the few cases that are slow to respond to the 60 Day Program, provided they’re actually following it, of course, this alkalized water is the crowning touch, the missing piece of the puzzle. Anyone in San Jose can get this water for free from my office. Anyone who wants to learn about the machine should contact
George Jogopulos DC at 818 209 6817 or email chirogeorge@gmail.com and ask for the DVD.

For more background science, see Dr Batmanghelidj’s last book: Water and Salt.

Vaccine for AIDS is now being tested. Considering the market value, with 40 million people in the world supposedly infected [1], and billions more who are not, the motivation is obvious.

Dr Leonard Horowitz in his book Emerging Viruses traces a history of AIDS not found in the popular press. [2]

In the early 1990s, Horowitz was sent by a large medical supplies company to investigate the bizarre case of Dr. David Acer, a Florida dentist. Acer, an AIDS victim, was said to have infected six of his patients with AIDS, perhaps intentionally, in the style of a serial killer. Horowitz was sent to check on the validity of these claims.

Acer was angry because he believed:

- US government medical researchers had created the AIDS virus because the Department of Defense wanted a biological weapon that could destroy an enemy’s immune system

- after the AIDS virus had been developed, it was intentionally deployed into test populations in Africa, New York, and San Francisco, both in humans and in monkeys

- huge economic interests were involved – in federal research grants, animal testing, virus engineering, vaccine development, vaccine production, as well as drugs to treat diseases caused by all this experimentation.

At first Horowitz wanted to prove that all this was some kind of conspiracy fantasy, but the more research he did, the more he found that corroborated Acer’s charges.

Horowitz found the 1988 videotape known as The Strecker Memorandum – a three-hour video by Robert Strecker, MD, PhD. [3] Strecker corroborated what Acer had claimed – that the AIDS virus had been requested, ordered, invented, and finally ‘deployed’ into the population, by government agencies together with big drug interests. Strecker’s reports were not only ignored, they were completely suppressed, by the very people who had hired him to find the truth, and then by all the media.

Strecker unearthed a 1970 document, later verified by Horowitz, wherein the Department of Defense provided $10 million to US government scientists to develop a “synthetic biological agent” from which there could be no natural immunity. (Horowitz, p.14) [2]

Strecker: “In 1972 the [World Health Organization] said, let’s make a T-cell destroyer… The same year, they said let’s test it, and then let’s inject it. And then they published their test sites which is a map of Africa…that corresponds exactly to the outbreak of AIDS.” (Horowitz, p.99)

“AIDS …was constructed”
- Strecker Memorandum [3]

The Strecker Memorandum offers evidence that:

- AIDS is not a homosexual disease
- AIDS is not a venereal disease
- AIDS did not come from African monkeys
- AIDS came out of a laboratory, not the
jungles of Africa

As Ayn Rand long ago pointed out, man will spend any amount of money to have the most modern, most efficient weapon for annihilating his enemies. Finding a virus that could disrupt the DNA of our immune cells, and which would run wild through the body, unchecked by the immune system – this was to be the Holy Grail of bioweapons research during the late 60s and early 70s.

In overwhelming detail, Horowitz proceeds to list the players in the research community, the World Health Organization, the drug empire, the Executive Office, the CDC, the CIA, the military, and the media who all played their parts in bringing AIDS to the world.

Yes, yes, at first the story seems like a premise for the next season of 24, and the reader is muttering things like ‘gimme a break’ or ‘preposterous’ or ‘I don’t want to hear this stuff.’ But soon you realize that Horowitz’s book is a solid enumeration of government documents and scientific references. The data is so conscientiously referenced that the reader will be hard-pressed to refute Horowitz’s basic discoveries:

- that monkey viruses are harmless to man unless they contaminate human vaccines, which were then injected into both monkeys and people. (p 450, 461, also Strecker Memo) Edward Jenner revisited

- that monkey viruses would have never crossed the species barrier without Gallo and others altering the viruses, then reinjecting them into humans via vaccines (p. 118, 130) [2]

- that in the late 1960s, National Cancer Institute’s senior researcher Robert Gallo and his colleagues created several AIDS-like viruses long before the discovery of HIV (p 75, 402 [2])

- that AIDS didn’t come from someone having sex with an African green monkey or from being bitten by one, or from one Patient Zero who spread it to the rest of the world (p.95) or from ‘bat guano’ on the floor of some cave in Kenya (Preston) [2]

- that the CIA stockpiled dozens of biological weapons, including smallpox, in storage facilities in Fort Detrick, Maryland, for decades after they were ordered to be destroyed (p.495)

- that Merck, the US Army, Litton Bionetics, and The National Cancer Institute were developing cancer-causing viruses for vaccines that were transported back and forth between the U.S. and Africa during the 1970s (p. 248) [2]

Once the reader is shown the amount of genetically altered blood samples and engineered viruses and experimental vaccines and infected animals that were shipped back and forth between the U.S. and Africa during the 1970s, it seems a wonder that it took so long for an epidemic to emerge.

Checking all this information out is a lot of work. Most people won’t do it. Most won’t even read the book. Easier to say – that’s ridiculous, because I never read anything like that in Time magazine or the Washington Post.
Exactly. And that’s just why most people’s attitudes toward vaccines don’t change – all their information comes from the monodimensional cookie-cutter “news” world of newspapers, magazines, and TV.

Whether the spread of AIDS was a scientific experiment that got out of control, or whether AIDS was intentionally deployed into the population, the obvious response of the drug companies must be to take advantage of the present situation and offer a vaccine, which will mean billion$ for them. That’s exactly what has been taking place.

WHERE’S MY EPIDEMIC?

Want a totally refreshing outlook on the whole AIDS thing? Most people missed the pivotal research article appearing in the Jun and Jul 00 issues of the Townsend Letter. Dr. Gary Null ties up a lot of loose ends in the confusion that has always surrounded HIV and AIDS. [4] Null is relentless in demanding proof for the programmed Conventional Wisdom that has been endlessly drummed into our digitized brains for the past 15 years:

- HIV is a virus that came from Africa which causes a distinct new disease called AIDS

- AIDS is a sexually-transmitted global epidemic for which there is no cure, a novel pathology never before seen in the human race, which threatens our survival, etc.

The HIV/AIDS mythology got started back on 23 Apr 84, when HHS secretary Heckler bumbled through her TV announcement that Robert Gallo had discovered a virus that was the “probable cause of AIDS.” [5] The media immediately dropped the word ‘probable,’ and never looked back. Even though it was soon proven that Luc Montagnier was actually the discoverer of HIV, and even though HIV itself has still never been definitively sequenced and photographed, the original story stuck. Even today, 99% of Americans over 5 years of age believe that there is a disease called AIDS and it’s caused by a distinct virus called HIV.

Null pulls together dozens of the world’s top researchers who disagree with the majority of the 300,000 studies that have been published on HIV/AIDS since 1984. These doctors are saying that HIV has never been isolated, and therefore cannot be the cause of AIDS. Null also wonders why AIDS is a different disease depending on where it is diagnosed. This fact raises serious doubts about whether AIDS is a disease at all. Not that people who manifest a similar group of symptoms aren’t dying in many countries. But that’s not enough to make AIDS a separate verifiable disease entity. Doesn’t a disease require a single isolated pathogen, causing AIDS the same way in Atlanta as it does in Zimbabwe or London?

Null explains that for every other viral disease that has ever been named, the causative virus has been isolated, identified, sequenced, distinguished from other viruses, and photographed. None of this has ever happened with HIV.

With HIV, no exact genetic duplicates of the virus have ever been identified from two different patients, or even within the SAME patient, for that matter! HIV virus has never been found in a human being!

SO THEN WHAT ARE ALL THESE PEOPLE DYING OF?

Many doctors feel that the symptoms of AIDS, which vary from
country to country, may simply be the result of “extreme oxidative stress” – that is to say, massive free radical damage to cells, which effects a dangerously depressed immune system. Remember, people can die of chronically lowered immune function, however that happens. No specific vector or disease is necessary.

Null explains that it is just as likely that AIDS causes HIV as vice versa. He cites many credible sources who show that what researchers are calling HIV is just a collection of some nonspecific cellular particles that are generally present in some form or other in the blood of AIDS patients. These particles are all that the original researchers – Montagnier and Robert Gallo – ever found. There is no distinct identifiable HIV virus! (Mullis [5]) In their original papers, there is no work that proves that HIV is the cause of AIDS.

Classical pathology shows that all other infectious diseases are dependent upon a certain number of isolated microbes being present. AIDS is the only disease for which the microbe has never been identified and the number never established. (Duesberg, [6] ) Science becomes religion.

Furthermore, AIDS testing varies widely from country to country. The numbers of people diagnosed with AIDS are greatly inflated because at least 25% of cases are diagnosed by symptoms only – no blood work at all. Taken like that, AIDS has the identical symptoms of at least seven other diseases, including TB, malaria, CMV, and traveler’s diarrhea! (Hodgkinson) [2]

This explains why the predicted spread of the AIDS epidemic into the general population has never occurred the way that the media was shrieking it would in 1987. [7] AIDS is still confined to the same risk groups as before: severe immune depression, including indiscriminate gay sex, IV drugs users, and starving people in overcrowded conditions.

There is also something fundamentally shaky about AIDS testing. AIDS is supposedly imminent if antibodies to some proteins created by Abbott Labs are present. (Maggiore [5]) For other diseases, the presence of antibodies means that the disease has been conquered and now the person has immunity. With AIDS, the presence of HIV antibodies is a test used to diagnose the disease. This is contrary to decades of scientific immunology. HIV is the only virus that supposedly causes a disease after the HIV has been neutralized by antibodies.

Kary Mullis PhD won the Nobel Prize in 1993 for inventing one of the principal diagnostic tests for AIDS: the polymerase chain reactor test. Dr. Mullis doubts that AIDS is an infectious disease at all. He notes that we made this mistake before, in the last century, with pellagra. This niacin deficiency disease was originally thought to be caused by a microbe. The difference with AIDS is we are no longer seeking the cause. That has been ruled upon with the force of a religious edict.

Mullis marvels that the arrival of AIDS on the scientific scene was unlike the advent of any other disorder in history, with the possible exception of possession by the devil. This whimsical remark is occasioned by the so-called ‘indicator diseases’ with which AIDS has been associated: pneumonia, tuberculosis, Epstein Barr, mono, etc. Suddenly we have this whole family of diseases which if they appear in an HIV positive person are automatically assumed to be caused by AIDS. [5]

Why go to all this trouble to create a disease complex? Could it be the huge AIDS industry?

“Everybody in the field of AIDS works for AIDS. Think of it as a big corporation.” (Mullis –Maggiore [7])

A really big corporation. Since 1985 the federal government has spent $90 billion on AIDS research. ([7]) According to the WHO, HIV is now found in 42 million people worldwide. That figure has not changed in 6 years. No need; imaginary numbers are tools of marketing, not science.

Null astutely predicted the forthcoming bait-and-switch that we will soon see with the advent of AIDS vaccines. Suddenly the presence of antibodies (HIV positive) will again be seen as a sign of cure, the way they have always been with other diseases. So which is it? Are antibodies a test for the presence of the disease or are they a sign that a cure has happened? Depends what they’re selling that particular week. [4]

Null debunks another media myth: the Centers for Disease Control have never proven the theory of transmission: they have never found one person who had passed AIDS from someone on to a third party. [4] This is the theory – the Conventional Wisdom that everybody supposedly knows, underlying the millions of media references to HIV/AIDS for the past 15 years, which has haunted the sexuality of Americans for the past two decades.

So if HIV doesn’t cause AIDS, then what does?

The conventional wisdom is that HIV causes AIDS which causes death. This notion is maintained in the public mind by incessant media and highly controlled publication of only those studies supporting this model. The problem is, scientifically it is insupportable.

First of all, what we refer to as AIDS may not be one specific disease. It may be that risk groups who destroy their immune systems by common lifestyle abuses just seem to die in a similar fashion.

As Laurie Garrett noted, many gay men in San Francisco and New York have had a lifestyle that has not significantly changed since AIDS was “discovered” in the early 80s. [8] Multiple sex partners, without protection, poor diet, mass intake of amyl nitrate and other party drugs, continuous antibiotic and prescription drug intake, dehydration, nutritional deficiency – any of these alone causes serious immune suppression. Taken together, they can annihilate the immune system – and this is what AIDS really is. The body is so confused and starved and toxic that it can no longer distinguish between a foreign invader and its own toxified cells. So it starts attacking itself.

Same story with other high risk groups. Poverty, IV drug users, toxifying lifestyle – pathologically depressed immune system. Sayonara.

In the 80s, AIDS was mainly caused by lifestyle. But in the 90s, Null shows that AIDS was caused just as often by drugs like AZT.

HIV itself could never cause the physical damage caused from AIDS drugs. But since AIDS is expected to be a progressive fatal disease, there is no attempt to distinguish the side effects of the drugs from the disease itself! [4] A marketing dream.

More people die from AZT than from AIDS itself. The largest cause of death among AIDS patients today is liver failure as a result of AIDS drugs like AZT. (World AIDS Conference, [5])

With continual pressure from the drug companies, and their agents in the FDA and the NIH, AZT is now enshrined in a position that is not permitted to be challenged. (Mullis–video) [5] But researchers who challenge the solemn dogma of AIDS/HIV/AZT soon find themselves with no funding and no avenues for publishing their findings. (Duesberg) [6]

AZT was originally a cancer chemo drug in the 60s that was abandoned because it was so toxic. It is a cytotoxic agent (cell-killer) which works by terminating DNA synthesis. When AIDS came along, AZT was brought out of storage, given a new PR package as the savior of AIDS, and that was it. It was never re-tested! Null points out that AZT is “highly poisonous” to anyone taking it long-term, so there must be some logical explanation for its exalted position in the AIDS religion. [4]

THE ROAD TO HELL

Peter Duesberg PhD of UC Berkeley, the first scientist to isolate the genetics of a retrovirus, was also one of the first to take a stand against the monstrous information steamroller that would level any opposition to the new AIDS/HIV religion. [6]

Duesberg is chagrined that the real crime is that immune-suppressed patients are distracted from courses of therapy that might actually cure them, because they buy into the idea that being HIV positive is a death sentence without AZT.
No one seemed to notice that AZT and its ilk never cured one patient of AIDS. [4] But now that fact is being acknowledged publicly, even by NIH director Dr Anthony Fauci. [9]

the AIDS vaccine

The AIDS vaccine has been in the developmental pipeline for many years. It has been tested in Uganda, Trinidad, Thailand, and the US. In 1999, a Silicon Valley biotech firm named VaxGen began testing an AIDS vaccine on 5000 high-risk volunteers. (www.jasmyn.org/vaxgen/ , Washington Post [10, 11] ) By Jan 2003, over 12 million doses of AIDS vaccine had been dispensed by the Thai FDA, licensed as a food supplement, and given to some 60,000 patients. (journal Vaccine [12])

GIVING US THE BIRD

An article in JAMA in Mar 2002 sort of ends the discussion on how scientific vaccine research really is. The article reported that the safety of “canarypox” as a culture medium for vaccines had now been established! (Vastag) [13] Infected canary tissue is now the preferred medium for growing AIDS vaccine.

At first reading, the above section will probably sound mad to the average reader, who has derived all his information about AIDS from years of the popular press. Again, don’t believe any of this – check the sources cited.

AIDS VACCINE CONFERENCE

There was a press conference held in Washington DC on 20 June 2001. Presentations were given by several researchers, including Barbara Loe Fisher and attorneys Walter Kyle and Jim Turner. The purpose of the conference was to draw attention to the millions that had been spent developing an AIDS vaccine. [14] At that time, four times as much money had been spent developing AIDS vaccine as for any other vaccine.

Much of the original money promoting the vaccine came from Bill Gates, who understands its global potential. Bush then proposed a 25% increase in AIDS vaccine research spending: to $367 million in 2002. (Garrett) [15]

The idea was to make an AIDS vaccine available to every 12 year old on the planet at some undisclosed time in the future. [14]

A few little wrinkles brought out in the 2001 conference:

- the new vaccine is for HIV, which has never been proven to be the cause of AIDS

- recipients of the vaccine become HIV positive [16]

- though scientifically untenable, the advance PR promotes the illusion that the vaccine will provide immunity to AIDS

- the vaccine is targeted for all 12 year olds

- the AIDS vaccine is likely being tested on US military personnel without their knowledge.

Luc Montagnier and Robert Gallo, the two scientists who ‘discovered’ HIV both maintain that HIV is not the cause of AIDS.

WHIPPED INTO HIGH GEAR

The global AIDS program went ballistic in July 2003 when

“President Bush named a former pharmaceutical executive as director of a new $15 billion program to battle the disease in Africa and the Caribbean.

The president said Randall Tobias would have the rank of ambassador. The former CEO for Eli Lilly & Co…” [17] Eli Lilly, the vaccine manufacturer.

$15 billion? That’s 100x more than has ever been spent bringing a vaccine to market. Again, it’s simple economics: the AIDS vaccine is for the global market.

A websearch on AIDS vaccine turns up hundreds of empty, illusory articles, which make no substantial sense, in light of the chimerical unsequenced never-isolated HIV virus.

NO BIG HURRY

Ever notice how the furor surrounding AIDS vaccine development has become much less urgent as time goes by? In 2007 Bill Gates predicted it will be another 10 years before the vaccine is out. [18] With a $90 billion dollar R&D industry happily rolling along, what’s the rush? As with most objectives in the world of vaccines, we have to keep reminding ourselves that the AIDS vaccine program has never been about saving the world from the ravages of a terrible disease, but rather marketing the saving of the world from the ravages of a terrible disease. That involves a huge annual global outlay, colossal funding for research which never has to produce an actual result, and the careers of tens of thousands of research scientists.

RUNNING OUT OF STEAM

It is becoming more and more difficult to sustain the momentum of the AIDS illusion in the face of recent failed human trials. At least 9 different AIDS vaccine trials were cancelled in 2008, not only because they couldn’t deliver the promised immunity, but worse – the subjects were getting increased susceptibility to AIDS from the vaccine. [11] After 25 years and billions in research every year, more of the leading scientists are admitting publicly that we still have no idea how to construct an AIDS vaccine.

Not surprising since no HIV virus has ever been identified.

In one of the 2008 African studies, the recipients of the test vaccine were actually more like to get AIDS because of the vaccine. Just like with smallpox, polio, and pertussis.

So although HIV has never been proven as a cause of AIDS, the AIDS vaccine has.

Scientifically on the same sinking ship with SARS, Avian flu, and anthrax, the AIDS vaccine program has been artificially shorn up all these years by its high global political profile, and the money that goes with all that. No industry in history has survived as long as the AIDS vaccine business without ever having to create an actual product. It’s 100% theoretical; and the theories were flawed from the outset. And now even the major proponents in the global scientific world are beginning to see that no matter how much money they pour into a false scientific premise, they simply can’t change the physical nature of nature. Many have suspected that truth for years, but what is different now is that they see they can’t keep up the pretense indefinitely.

The program is nowhere near over yet, but the faint tones of the AIDS vaccine’s death knell have been heard at the highest levels.

It will most likely die a very slow and very quiet death, as with smallpox vaccine. Perhaps after a decade or so, it’ll be like it never existed. So remember you read it here.

.

1. Lopes, G – Vaccine center issues warning THE WASHINGTON TIMES February 3, 2007

2. Horowitz, L – Emerging Viruses: AIDS and Ebola – Tetrahedron, Inc 1999.

3. Strecker, R MD – The Strecker Memorandum Eagle Rock 1-800-359-3177 1988.

4. Null, G, PhD – “What Ever Happened to the AIDS Epidemic?” Townsend Letter for Doctors #203, 204 Jun/Jul 2000.

5. Maggiore, C – videotape— The other side of AIDS 2002. www.questionAIDS.com

6. Duesberg, P PhD – Inventing the AIDS virus – Regency 1996.

7. Maggiore, C – What if everything you thought you knew about AIDS was wrong? www.questionAIDS.com 2001.

8. Garrett, L – The Coming Plague – Penguin 1994.

9. AZT: Death by Medicine – www.whale.to/a/azt_h.html

10. www.jasmyn.org/vaxgen/ – Ad for volunteers for AIDS Vaccine testing

11. Reuters – AIDS Vaccine Approved for Human Trials Washington Post 12 Jan 1998.

12. the journal Vaccine p 624, 20 Jan 2003.

13. Vastag, B – HIV Vaccine Study Nixed – Journal of the American Medical Association 287:11 20 Mar 2002.

14. Protect Medical Freedom website www.protectmedicalfreedom.com

15. Garrett, L – AIDS at 20 Newsday 3 June 2001.

16. http://www.iavi.org/

17. CBS News – Bush Names AIDS Czar –WASHINGTON, July 2, 2003. www.cbsnews.com/stories/2003/07/02/health/main561435.shtml

18. AIDS vaccine more than a decade away, Bill Gates says. Daily HIV / AIDS report kaisernetwork.org 3 Mar 2005.
kaisernetwork.org/daily_reports/rep_index.cfm?DR_ID=28443

UPCOMING SEMINARS

Over the years of delivering seminars and presentations. I would often have concerned parents come up to me and ask questions. Many had heard the horror stories, others were not sure whom they could trust, most had serious doubts about vaccinating.

Nearly all expressed the fear of having their child become autistic, defective or neurologically damaged. No one wants to put their child in harm’s way and the thought of seeing their child go from healthy to physically or mentally handicapped in a matter of months or years is too frightful to imagine. Which is precisely why we must imagine it now, before we vaccinate.

There is a very real potential of seeing your child have a delayed reaction as many as 20 years later. The injection of 68 vaccines, 36 of which are administered before your child is 2 years old, is altering the human genome in ways no one can predict

The new book for 2010 contains 290 references from medical studies, government reports and scientific research. All your questions and concerns are answered and addressed honestly and without hype.

You deserve to know all sides of the story and now you can. Make the decision to get informed and stay informed starting today!

The Nutrition Seminar:

• San Jose CA – 10 Jul
• Long Beach CA – 7 Aug
• Seattle WA – 21 Aug

Vaccine/Detox Seminar

• Ventura CA – 17 Jul
• Salt Lake City UT – 31 Jul

In the Nutrition Seminar we deliver a complete discussion of the 60 Day Detox Program, beginning with the no-brainer New West Diet. We begin with the distinction between natural and processed foods, going through the history of the natural diet, and the type of health picture is produced. The crucial topic of GMO is introduced, with some excellent resources being suggested: current books and DVDs. For the patient in survival mode, or one who simply wants to get back on track, these topics are vital:

• enzymes
• chelated minerals
• florabiotics
• collagen
• oral chelation
• megahydrate
• colon detox

For health care providers, the tools for a complete patient nutrition program are handed around.

If you have taken the seminar before, one big attention to the curriculum is the rise of GM foods, which has taken over world food production in the past 14 years. This shocking and monumentally important information is simply not available in mainstream media, with good reason. Unless the doctors avail themselves of at least an introductory level of resources on the subject, they simply will not be aware why 80% of commercial foods today are Genetically Modified.

For those who cannot attend, both the full day seminars are available on recent DVD sets at the website

New cities are added all the time: See website under Seminar

In the Vaccine/Detox Seminar we will use the morning hours for highlights from the new text book Vaccination Is Not Immunization 2010.

A few of the morning topics:

• Why 68 vaccines before age 18
• Autism: an American epidemic
• Is mercury really gone?
• Do vaccines work?
• Why are American kids fatter, sicker and dumber than ever before?
• The Germ Theory vs. Bioterrain Theory of Disease
• Doctor as caregiver or agent of the state?
• Exemptions laws: why more parents take the easy way out
• Vax facts Manufacturers vs. marketers
• What is Prevnar?
• What is Human Papilloma Virus?
• What is MCV4?
• Why don’t we know, since these are the vaccines kids are getting?

Then in the afternoon we will do as much as possible from the full day nutrition Seminar, focusing on the essentials of the 60 Day Program.

Most of the seminars above are 12 hour re-licensing seminars, including technique for DCs.

Please call office to register for any event 408.298.1800 or email doc@thedoctorwithin.com

I will also be doing a 3 hour vaccine lecture in Salt Lake City on Friday 30 July for a group called We Are Change.

The World of Collagen

First off, I want to apologize to all of you who have had to wait for your back-orders of collagen for the past 2 months. It will not be happening in the future: finally got it under control.

In Paris in early June I was fortunate to meet with some of the top people in the world in the collagen industry. I learned so much there that I completely re-wrote the collagen chapter on the site. So please re-read it now, if you read the earlier version. This information is simply not generally available, even online.

What is going on now is a worldwide surge in demand for collagen, really within the past 6 months. The few manufacturers of the high-end hydrolyzed collagen are struggling to keep up. What has happened is a sudden skyrocketing awareness of the dramatic improvements one see with the new low molecular weight collagen, taken consistently as a morning supplement.

In Japan it’s primarily cosmetic: women are learning the dramatic results with skin and hair thickness that come from supplementation of the new low molecular weight collagen, taken with juice in the morning. In China, demand is increasing at almost 100% per year. Like the US, China sees the significant results in rebuilding degenerated joints, far better than any glucosamine or steroid approach could ever hope for. In Europe, as in the US, people are becoming aware of hydrolyzed collagen as an anti-aging weapon, since collagen is the structural material for all our organs and tissues, not just the skin and joints. See chapter for a complete rundown.

I was very reluctant to add anything to the 60 Day Program because I want to keep it as simple and inexpensive as possible. Collagen however was a no-brainer since it acts as a virtual elixir for so many systems of the body which are dependent upon collagen based tissues. Collagen decreases as we age. If you don’t keep up, you shrivel. It’s that simple.

Read the chapter! You don’t have to wear out that fast!

The Three Attributes of Water

Hydration has always been a big part of the 60 Day Program. Going from almost no water, like many patients, to 2 litres a day can solve many health problems all by itself. I have always known hydration was a prime factor in many of the success stories that appear on the Feedback and Testimonials section of the site.

Recently I have learned how to take hydration to a whole new stratum. The technology is not even new — the Japanese have had it for 30 years. Now in the past 2 years it’s available here.

Just a word on the 3 attributes of water:

• molecular size
• pH
• oxidation

Water coming out of the taps in most houses is very harsh, to say the least. It is in huge molecules, probably closer to H200/O100 than it is to H2O. Molecules this large have difficulty being absorbed at the cellular level, even in the rare event the individual drinks adequate water.

Second is pH. Water we drink should be as close to normal blood pH as possible: 7.3 – 7.45. All the trashy foods and soft drinks we eat are constantly acidifying our body’s system: that means lowering the pH. Acidification promotes virtually every disease process known to man. So drinking high pH water will tip the scales in the opposite end: alkaline. Life functions soar.

Thirdly, the best water can act as a mild antioxidant, like Vitamin C or Vitamin E by neutralizing free radicals. See chapter on antioxidants.

Taken together, drinking 2 litres of this type of water per day can have a curative effect on almost any degenerative process, especially aging! What do we always say – old and dried up…? It’s literally true. When you can begin to hydrate again, for the first time in years, miraculous results occur. Was it really such a miracle though – to add the most vital nutrient human physiology is based on? These days common sense seems to be the real miracle.

There is a machine for the home that can provide these 3 properties to your water supply at home that makes it far better than the unregulated bottled water you’re dragging in every week. For the few cases that are slow to respond to the 60 Day Program, provided they’re actually following it, of course, this alkalized water is the crowning touch, the missing piece of the puzzle. Anyone in San Jose can get this water for free from my office. Anyone who wants to learn about the machine should contact
George Jogopulos DC at 818 209 6817 or email chirogeorge@gmail.com and ask for the DVD.

For more background science, see Dr Batmanghelidj’s last book: Water and Salt.

The Aim of Chiropractic

All classical science texts agree that the nervous system controls the function of all cells and tissues within the human body. One of the most epidemic breakdowns in that com system is the disruption of nerve messages within the spine. Stresses of birth, stresses of life, day to day micro-trauma – all these contribute to an increasingly inflexible spine, as we age.

Spinal nerves are the first casualty they are like fiber optic bundles that get partially squeezed, as a chronic situation. The result is well known and thoroughly documented: either overstimulation or understimulation of the affected nerve fibers. Either one is bad news for the organ or tissue that was supposed to get the message.

These simple facts of human biomechanics have become the center of controversy over the years, not because they aren’t true, but because of turf. If imbalanced organs or systems can be restored to balance simply by correcting the spine, then many of these ‘diseases’ that medical science is always diagnosing and prescribing drugs for really may not exist at all.

This is the elephant that cannot be talked about. That’s turf, my friends, when they’d rather guide you in the wrong direction than steer you in the right direction just because the competition has the answer.

Here we see a fundamental difference between holistic healing and organized medicine the goal. With any patient, is the goal of the doctor to get the sick person well, or is it merely to maneuver the patient into only those protocols which sell the most drugs and billable procedures?

A patient’s main complaint may be the simple result of nerve blockage – years and years of the same nerve being partly squeezed off. Let’s say sciatica is the painful symptom – years of sciatica. What is the mainstream recommendation? Advil, Motrin, Vicodin, etc. If that doesn’t work, disc surgery, rhizotomy, exploratory surgery, cut it open and have a look around, etc.

Noninvasive. That’s the word that means try the simple thing first, the harmless thing. Rule out subluxation the blocked nerve that may be the root cause of the chronic problem. No harm is done by trying this method – chiropractic – first, even in the rare case that it was not the cause.

That’s the underlying modern challenge of the suffering patient today: finding out the truth of the above few paragraphs.

After that the next big problem is to find the DC who understands it as well.

Referrals are good. A few things to look for when you’re chiro-shopping;

1. Nerve charts on the wall
2. An immediate and unhesitating explanation of the word subluxation, when you bring it up
3. Bone models
4. A very quick but thorough explanation of the whole chiropractic experience; what we’re will accomplish, how we will do it, how much it will cost — all up front and forthcoming
5. Analysis of your spinal X rays
6. Hands-on approach, easy on the shake-and-bake part
7. Smooth and confident delivery of the adjustment

When in doubt, walk out and keep shopping.

Taken together, with chiropractic, nutritional support, detox and hydration, there is virtually no ill condition that will not dramatically respond or resolve. After all we’re only flesh and blood.

The whole natural medicine concept reminds me of:

You’re born. You get no drugs and no vaccinations. During childhood you have the usual illnesses, but conservative treatment gets you through them without antibiotics or drugs, and you build your natural immune defenses. You don’t eat white sugar, white flour, hydrogenated oils, too much meat or cheese, or drink soft drinks or pasteurized milk. You concentrate on whole grains, fruits, vegetables, and a clean, natural diet. You never learn to drink coffee or to smoke cigarettes. The only pills you take are natural antioxidants and enzymes and minerals, which are part of your daily intake. You drink at least 1 liter of water every day.

Into adulthood, you never get sick: no colds, no flu, no headaches, no diabetes, no ADD, no thyroid problems, no panic attacks, growing pains, fatigue, or digestive disorders, no high blood pressure. The only pains you experience come from accidental injury. Perhaps you do moderate exercise or sports activity to maintain mobility and general fitness. You look to the care of your spine. Your entire adulthood is spent in this disease-free mode. As you age, your mind gets sharper, your body gets stronger, your immune system tougher. You experience no arthritis, cancer, or osteoporosis, no Parkinson’s or Alzheimer’s. Finally one day after 90 or 100 years, you flicker like a candle and go out.

The above paragraph may be useful in choosing a doctor. Some doctors will say all this is impossible; which for them is true. So don’t choose them. All this is possible; moreover, thousands and thousands of people are living it. So listen only to those who can help you achieve such a condition of living health. Because now we’ve arrived at the threshold of a time when good health and a powerful immune system are not only advisable; they are the very determinants of survival.

Sayonara Swine Flu: — I Hate Being Right

For those of you who followed the swine flu vaccine hoax on my website during the past year, you know that all my predictions came true. As soon as they created enough hysteria to sell vaccine contracts, the “pandemic” disappeared. Big surprise. By June 2010, all the states as well as all European countries were sending their shipments of swine flu back because nobody was getting the shots. People just never quite believed the threat was real. Which it certainly wasn’t.

Here’s the kicker Usually failed vaccines are put on the shelves and stockpiled for decades, even though they have expiration dates. Not the case for swine flu. Very suspiciously, the stockpiles are being burned just a few months after the “threat” has disappeared:

Which begs 2 questions:

1. What’s the hurry to burn them? If it was a real threat, why might it not come back? Wouldn’t we need the vaccines then? Are they covering up evidence here?
2. Were these “swine flu” vaccines really just some experimental Avian flu or some other kind of vaccine they had stockpiled that were completely untested? Seems likely, considering the research laid out in the Goodbye Swine Flu chapter approved after one month of testing!

The main point we must remember here is be ready for the next fake pandemic, which is almost certain to follow in the same tried and true pattern:

• Allege a new microbial disease in some exotic location
• Exaggerate the projected deaths and infection rate
• Offer drugs and vaccines as the only hope
• Spend the money
• Watch the “threat” vanish into thin air

I’m really not that smart — I just keep track of events.

The next pandemic’s coming, for certain sure. It has to be they need the money. Just don’t be so quick to fall for their same old lame story next time.

New Vaccine Book: Vaccination is Not Immunization – 2010

Vaccination Is Not Immunization is written for everyone concerned about the health and well-being of their children and of themselves. It’s all there: the history of vaccines; the ingredients of vaccines; the dangers of vaccines. It’s for parents, educators, those in the medical profession, midwives, nurses, those working in government and practitioners of alternative medicine as well.

Vaccination Is Not Immunization is 200 pages of fully documented information, along with some 290 references that will open your eyes. It is not an anti-vaccine text, but rather a detailed history of vaccines and how they came about. This latest edition has been updated to include the most recent vaccines released.

It’s written in an easy-to-understand language as well – not the “med-speak” found in medical journals. You’ll come away understanding the big picture as well as the actual science behind the most common vaccines.

You’ll have what you need to make an informed decision about how to best care for your child.

Over the years of delivering seminars and presentations I would often have concerned parents come up to me and ask questions. Many had seen the horror stories, others were not sure whom they could trust, most had serious doubts about vaccinating.

Nearly all expressed the fear of having their child become autistic, defective or neurologically damaged. No parents want to put their child in harm’s way; the thought of seeing their child go from healthy to physically or mentally handicapped in a matter of months or years is too frightful to imagine. Which is precisely why we must imagine it now, before we vaccinate.

There is a very real potential of seeing your child have a delayed reaction as many as 20 years later. The injection of 68 vaccines, 36 of which are administered before your child is 2 years old, is altering the human genome in ways no one can predict.

The new book for 2010 contains 290 references from medical studies, government reports and scientific research. All your questions and concerns are answered and addressed honestly and without hype.

You deserve to know all sides of the story and now you can. Make the decision to get informed and stay informed starting today!

Order Now

Click here to read the interview in Norwegian…

mat&helse | Medicine & physiology | matoghelse.no
Text: Iver Mysterud

The American chiropractor Tim O’Shea has studied the vaccine issue for nearly 17 years. He is highly critical of vaccination as a medical strategy!

Regarding the difference between vaccination and immunization, O’Shea refers to his book, Vaccination Is Not Immunization. There, he rejects that vaccination and immunization are synonyms, although many are led to believe that is the case. Immunization means that the body is immune to anything, and this happens when you have a disease or at least have been exposed to it. In contrast, O’Shea emphasizes that vaccination only means sticking a needle into a person’s arm and injecting a man-made substance called vaccine.

MH: Generally we hear from medical authorities that vaccines are safe, effective and necessary. How do you assess this statement?

TO: No vaccine has ever been shown to be safe or effective in studies that test risks against benefits. Clinical trials are carried out by producers who sell vaccines, and vaccines are then approved by the American Medical Products Agency (FDA), whose members are representatives of the pharmaceutical industry.

MH: Are vaccines important for our continued health and safety, or do they weaken and poison our children?

TO: I cannot give an exhaustive answer to such a question in a short interview, so here it is necessary to read my book. Each reader must answer the question for themselves, not because of some interview she has read, but only after thorough investigation. And this is the purpose of my book, Vaccination Is Not Immunization.

MH: Which vaccines are the most problematic, and what is the least problematic in terms of adverse effects?

TO: This is like asking what poison kills you the slowest. The worst is undoubtedly the triple vaccine, which is responsible for over 75 percent of the two billion U.S. dollars paid out in compensation for vaccine injuries in the U.S. since 1991. Triple vaccination is given against diphtheria, whooping cough and tetanus.

Civilization’s Future

MH: Can you explain the meaning of your claim “that the blood flow to our children are the future of our civilization”?

TO: This is a classic idea that dates back to the time doctors Claude Bernard and Antoine Béchamp lived. The statement refers to the old debate about the microbes from the outside or the state of the body’s internal environment is the cause of the disease. The standpoint we have in this debate will say something about how the disease can best be treated. The only solution is to stop the entry of allergy-causing substances and detoxify the body to substances that are already there. Remember that the blood represents the internal environment of any body cell bathed in every second. Blood condition determines whether the body’s cells are able to perform their two life functions: to transport oxygen and nutrients in and waste out. This is what really determines your health, not some temporary reactions to man-made molecules, which in reality is all vaccines offer.

MH: Are there any circumstances in which vaccines can be perceived as a health promotion strategy?

TO: Only for those who live by selling vaccines, directly or indirectly.

MH: In Norway we usually hear from medical authorities that there may be side effects of vaccines, but the benefits are far greater than the problems. How do you assess such a statement?

TO: These are just words. The statement is typical of any who have not studied the issue. The only training physicians get on drugs program about vaccines comes from the pharmaceutical industry. Everyone knows this. The American pediatrician Robert Mendelsohn was the first to point this out in the mid-1980s in his book, Confessions of a Medical Heretic. How could it have been different? Vaccination brings a child into a lifelong dependency relationship with organized medicine. To admit that one is aware of the toxicity of vaccines is career suicide for doctors, which many doctors themselves have pointed out. Vaccines are the sacred cow in the medical dogma.

Additives in Vaccines

MH: Many vaccines contain formaldehyde, mercury and other additives. What are the main problems with these ingredients?

TO: Mercury can cause permanent nerve damage and autoimmune disorders. Formaldehyde is a carcinogenic embalming fluid. Aluminum is highly toxic to the brain and can provide far more neurological problems than Alzheimer’s disease. It is strange that not many are scared of these additives. I cannot understand that it can be claimed so persistently that vaccines are safe, as long as there is no scientific evidence that this is the case.

MH: Is it possible to counteract the effects of these additives by taking the antidote vitamin C along with vaccines?

TO: It is interesting you use the word antidote, which is a term for a remedy that can abolish poisonous effects. Vaccines fit completely within the definition. So my counter question to you, since you brought this up is: Why in the world would you like to give a newborn child a toxic injection in the first place?

Advice for Parents

MH: If parents decide to let their children follow the official vaccination program, what kind of advice would you give them to minimize risks?

TO: None. They arrived at the decision without independent study and followed the path of least resistance, like most Americans. After that, Charles Darwin takes over, and I am out of the picture. I will not encourage reckless and irresponsible behavior in any way. But for people who have discovered too late that they have made a misjudgment by vaccination, the picture is different. They may have much to gain from following a detoxification program. My focus is not to allow people to fool themselves in the first place. It is a typically American tendency to apologize because they are too lazy to get information to make an informed decision before the incident.

MH: If parents decide not to follow the official vaccination program, what kind of advice can you give them to minimize the risk of getting sick?

TO: No advice is necessary. Unvaccinated children are much healthier than vaccinated children. They are rarely sick. Refer to the chapter “Parents of Unvaccinated Children” on the website (thedoctorwithin.com).

MH: When it comes to vaccination, is there one procedure that is suitable for every child, and if not, what criteria would you use to individualize disease prevention?

TO: There is no one procedure for all. The question assumes that the Germ Theory of Disease is a documented and properly scientific model, it is not.

Impact of Vaccines

MH: What short- and long-term effects of vaccinating children are found?

On this question O’Shea refers to the comprehensive review of his book (Vaccination Is Not Immunization), which there is no space to elaborate here. But he takes up the debate about autism, both the argument that this suffering can be caused by the meslingvirus MMR vaccine and mercury in other vaccines. He is highly critical of the way leading medical researchers and health authorities handle this matter.

TO: The main point of why vaccines are so harmful to the newborn is toxic effects on their vulnerable nerve tissue of additives in vaccines. Newborns are not born with a protective blood-brain barrier. It is not fully developed until they are at least five or six years old. A newborn’s brain releases ingredients such as mercury, aluminum and formaldehyde directly into the brain. This can have two possible consequences: The chemicals can kill existing brain cells, and they can prevent the formation of the protective layer around nerves (myelin) and relationships between the various brain parts. The effects of such impacts may not come until later in life.

An Emotional Issue

MH: Why are vaccines such a violently emotional theme?

TO: Vaccination takes place in the part of a person’s life when reliance on one-dimensional pharmaceutical medicine is impressed. Without vaccines, billions of U.S. dollars would be allocated away from organized medicine, and this can happen if people start to reflect on the forbidden idea that they can take greater responsibility for their own health. With the exception of trauma medicine, today’s a very bad history of most health themes. For this reason, the vaccine sacred cow cannot be attacked. Vaccines are the foundation for the entire pharmaceutical industry.

MH: How does one proceed to make a responsible decision in the child’s best interest?

TO: Offer parents responsible, underpinned, scientific, well-founded information on problems with vaccines from sources that do not make their living from selling them. Only then can parents make a truly informed choice.

Vaccines for Adults

MH: Are you as critical of the vaccinations for adults as you are vaccines for children?

TO: In the U.S., only two years ago, a recommended Vaccine Program for adults was launched. This is just marketing. Old people were originally excluded from vaccine recommendations, whereas now they are one of the primary targets. Has their physiology changed? Of course not! All that has changed are the marketing techniques. I will again point out the lack of studies on risk in relation to the utility. We see how even the original, controlled studies today have been replaced by their “poor” cousins, namely, population studies. These can be designed so that they provide any desired outcome from the same figures. As such, they are a good tool for marketing and political whim. Scientific relationship comes in a poor third in such a game.

Influenza Vaccine

MH: Is it a good idea for elderly people to take a flu vaccine every autumn to reduce the risk of the seasonal flu?

TO: Empirically, it seems that it is just those who take the flu vaccine who get the flu. Have you ever noticed that? There are a number of reasons it’s scientifically impossible that influenza vaccine can work, not least because the virus has a rapid mutation rate through the influenza season. Refer to my book (Vaccination Is Not Immunization) for further information. Flu vaccine contains mercury, formaldehyde and ethylene glycol, and formerly contained aluminum. With such a potentially toxic content, I do not think it is strange that no flu vaccine prevents influenza. In addition, the vaccine prevents the body from building up a natural immunity against influenza. An article from the leading medical journal, British Medical Journal, in a systematic review of literature shows that inactivated vaccines have little or no effect on influenza. Most studies are of poor methodological quality and results are affected by a number of factors not taken into account in the analysis. The article shows that there are few comparative studies about the safety of these vaccines.

Testing the Vaccines

MH: When vaccines are tested for efficacy and safety, how long are they studied? How long of test periods mean you have enough?

TO: Your first question assumes facts that do not exist. Are you a lawyer? It is not the time period that makes studies invalid. It’s who performed them. A really good study would be conducted only by independent researchers who do not have any financial ties to the outcome. In today’s world such a setup in practice is impossible, for who would afford to pay for such sophisticated test trials? Do you see the dilemma?

HPV Vaccination

MH: HPV vaccine against cervical cancer (Gardasil) has received much media attention in Norway. Should Norwegian school girls be vaccinated?

TO: Refer to the chapter “Human Papilloma Virus: The First Cancer Vaccine” on the website (thedoctorwithin.com), which is highly critical of HPV vaccine. The plan is to give the 12 year old girls the vaccine, although cervical cancer occurs most frequently in the age group about 50 years. The duration of the vaccine is five years. I believe therefore that such a vaccine logically should be given to women in a completely other age group, to women in late of 40-years. I believe, however, it is uncertain as to whether the vaccine is safe and its effect. There are a number of potential side effects, some of which are severe as paralysis and even death. It is also not considered whether the vaccine itself can cause cancer or impair fertility. I would definitely not give such a vaccine to my daughter … mh

Do you have doubts whether vaccines can really protect your child from illness or disease? Do you worry that your child could become autistic, or develop asthma, allergies or even a fatal childhood disease?

Well then, what you’re about to read may come as a shock. It did for me when I first began to research vaccines and their effect on the body over a decade ago. Hundreds of hours of digging into the medical literature and checking the facts compelled me to speak out.

Much of what I discovered was in conflict with the way most of us are taught to care for our children. Let’s face it — most parents agree to have their newborn child vaccinated and believe it is the right thing to do. That child goes on to receive numerous vaccinations year after year up through their teens. All the while you, the parent, continue to think you’re doing the right thing.

Well. . .as it turns out, it can be a huge mistake. Read More…

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• 12 Jun 2010 – LAX – The Nutrition Seminar
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• 31 July 2010 – Salt Lake City – The Vaccine/Detox seminar
• 7 August 2010 – Long Beach-The Nutrition Seminar

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Consultations

Many people read the chapters at the site, especially the Last Resort and the 60 Day Program and get new hope that their incurable conditions might not be quite as hopeless as they thought. For those in California, the in-office consult is available, in which a complete medical history and lifestyle analysis is coupled with a specifically detailed application of the 60 Day Program.

For those who can’t make it in, they can do almost as well with the one hour phone consult. Specializing in difficult, confusing, incurable and hopeless cases, these consults are for those who believe they’ve ‘tried everything.” News flash: they haven’t, because they’re still sick. When your doctor tells you there’s nothing more he can do for you, he’s telling the truth. Your misfortune is that he didn’t tell you sooner.

See website for details of both types of consult.

Interview with Dr. Andrew Wakefield 10 Apr 10

DW: Certainly, it’s very nice to be here. I’m a physician. I trained at Saint Mary’s Hospital in London, qualifying in 1981. I went into surgery, became a gastrointestinal surgeon with an interest in small bowel transplantation and experimental interest.

The residency is about eight, nine years.
Well in fact in the UK you go straight to medical schools. You do a five year medical school program whereas in this country, you go to college then you go on to medical school.

DW: ….part of the University of London which is the biggest medical school in Europe, yes. And then I went to Canada, I did a period on a travelling scholarship to look at small bowel transplantation. I went to the world’s leading center which was Toronto at the time. We made some discoveries, some observations there that led into a research career when I came back to the UK and started working initially on the liver transplant program at the Royal Free Hospital and then joined in with the gastroenterology team and continued from that point.

DW: …that was ’87, ’88. And my big interests at that time were Crohn’s disease, ulcerative colitis and we have made some interesting observations, published a great deal in those diseases. I have now published about a hundred thirty, one hundred forty peer-reviewed papers looking at the mechanism and cause of inflammatory bowel disease and then of course latterly, looking at how the brain and the bowel interact in the context of children with developmental disorders such as autism.

DW: I had an interest in measles virus and we’d published on the possible role of measles virus in Crohn’s disease, in a subset of patients with Crohn’s disease. We’ve been exposed to measles under unusual circumstances and this work came from our group, it came from the Mayo Clinic and it came from Sweden, from Dr. Eichbaum in Sweden showing that children who have been exposed to measles under unusual circumstances were at greater risk of Crohn’s. … kids who were exposed very early in life, in utero exposure. So they’ve been exposed in the womb to measles then went on to develop Crohn’s disease.

One unusual pattern of exposure to measles is clearly vaccination. You change the route, the dose, the age of exposure, and the strain of the virus. So it’s very unusual. Was that, part of the problem? So we published a paper in The Lancet suggesting a possible link between the measles vaccine in later inflammatory bowel disease and on the back of that, a paper came out in 1995 in The Lancet…

DW: Then we got a steady trickle of calls starting in May 1995 from parents saying my child was normal, they had their vaccine, the MMR, they regressed, they lost skills, they became autistic. I stopped them there, I said, I know nothing about autism at all, you must have got the wrong department and they said, but my child has got terrible bowel problems. They’ve got diarrhea 12 times a day. They’re failing to thrive. They’re falling off their growth charts. They got a bloated abdomen. I know they’re in pain but they’ve lost the ability to speak and so I have to infer that they’re in pain but they’re banging their head against the wall, there are screaming episodes, they’re waking at night.

DW: These kids were sick. And so we said, well, we need to look at this and we did and it turned out that the parents were right.

The way we went about this was, in a nutshell, we got a group of people, the best people in the world. In fact, Professor John Walker-Smith and his team, pediatric gastroenterologists who were then at the Royal Free group of child psychiatrists, neurologists, pathologists, and we got this team of people together and said, how should we investigate these very complex children? They’re clearly unwell.

Child psychiatry/psychology has been unable to unravel this mystery. They just label them with this behavioral disorder and yet these children are physically, medically unwell. How are we going to resolve that?

So we put this multi-disciplinary team together, we went through a process of determining which tests should be decided. The clinicians decided on the clinical tests. I was more involved in the research side to setting up the research test. We then went through a process of investigating a large number of children by the time I left the Royal Free in 2001; we looked at over 170 children. And what was remarkably consistent about them is they had a subtle but definite inflammatory bowel disease.

When the clinicians treated the inflammatory bowel disease, then the bowel symptoms got better. But also the behavioral symptoms got better and that was fascinating. Some children would start speaking. They would start speaking where they left off many years ago. They would smile. They would sleep at night. I think sleep was the first thing that came back. They started sleeping at night. When we first did this that didn’t happen, didn’t happen. We did it again, happened again. Did it again and happened again. It kept happening and so we thought there is really something in this.

Interviewer:…the treatment that you used to address the bowel disease?

DW: Well initially, it was just a simple sort of anti-inflammatory medication that we would use for Crohn’s or colitis. So a sulfasalazine-like drug or a 5-aminosalicylate.

So we became very, very interested in this whole process. And when we presented it to psychiatrists. They said, I just don’t get it. I don’t get this gut-brain thing. This is a brain problem; don’t talk to me about the intestine. But as gastroenterologists, we saw this all the time. I worked in a liver transplant program when patients became jaundiced, they became encephalopathic. Their brain stopped working. It started with the inability to join up dots on a page. Then they became more and more confused. Then they went into coma then they died.

And the way you treated that, the way you prevented that was to treat the gut. You treat it with antibiotics to get rid of the gut bacteria, or a special diet, or you put them on a regimen that cleans out the gut. And when you do that then the encephalopathy goes away. They wake up again.

So we’d seen this before in a different setting; jaundice. We had seen it in celiac disease, allergic sensitivity or an immunological intolerance of gluten. One of the presenting features of celiac disease can be dementia. It can be neuritis, inflammation of the nerves. It can be seizures. So these neurological complications of celiac or primary bowel disease were not new to us.

So, when we saw these children responding to a treatment for the gut in terms of getting better cognitively, then that was very, very interesting but not alien.

DW: So these children were being seen according to clinical need, they were being referred by their doctors and they were being treated according to the findings. So it was just a standard…there was nothing complicated about this. This is the thing – why are these kids been missed in the past? This isn’t rocket science. This is just the application of standard classical medicine.

Listen to the parent, examine the child, do the appropriate investigations and lo and behold, the answer is there. These children have an inflammatory bowel disease. Does it get to the root of their autism, no, not yet. Is it a start? Yes. Is it a good grounding in terms of understanding the biological basis of their complex disorder? Absolutely. And it all comes from listening to the parents’ story and not dismissing it by saying, “Well, your kid is autistic. They are bound to have to diarrhea 12 times a day.”

That doesn’t make sense at all but that’s what these parents were experiencing or one from America saying that they went to the doctor and the doctor said, “Don’t tell me about bowel symptoms, I trained at Harvard.” What does that mean? That is an absolute nonsense.

DW: … there tends to be a greater percentage of surgeons who have this arrogant attitude, who have got a God Syndrome. They tend to follow that path and avoid listening to the patients and sort of impose their views without applying this. It’s really delightful to see that wasn’t applied over on your side of the ocean — and refreshing.

You know, it’s pervasive. I’ve never met so many experts as I have in autism, experts about a disease about which we know nothing. We know nothing and yet we’re surrounded by experts and that paradox needs to be resolved.

Interviewer: The original study really highlighted you as one of the most prominent academic researchers in this area in the world. . Largely a result of your credentials and your training and working at one of the leading hospitals in the world and then publishing one of the leading respected journals. .. We strongly believe in the scientific method that there is value in doing a piece of research under very specific criteria and then having it reviewed by peers objectively and then analyzing to see if its true or not. I mean, that system works. And really forms the basis for much of what we apply and discuss. Unfortunately, it can be perverted.

But, ultimately, that process is designed to ferret out the truth which is one of the reasons why you rose to prominence because you had published in a peer-reviewed journal, Lancet, one of the leading medical journals in the world and they published your findings and then you did additional findings and you have 130 other papers that have been published in peer-reviewed journals. You’re one of the leading experts out there.

So, there are literally billions and billions of dollars involved here with the vaccine industry. That’s a lot of money. … it’s not surprising that we’re going to encounter evidence that there is something wrong with this system. That appears to be what’s happened here. So, recently, in the last few months, you have been criticized and bandied about in the media and you really haven’t shared your side of the story and this is the first time you’re really publicly doing that for reasons that you may discuss with us today.

DW: Well thanks for the opportunity to tell it. The reason I have not been able to tell it is because I’ve been going through legal proceedings at the General Medical Council (GMC)
which is our regulatory body for doctors in the UK and so I have been chomping it a bit but unable to say anything so it’s a great time now to have the opportunity to say something.

But in a nutshell, what we did was to publish a case series. Now, a case series is an observational study. It’s taking a look at a group of children or patients who have got a constellation of signs and symptoms and findings that bracket them together. There are similarities that mean they need publication. They are sufficiently novel and sufficiently interesting but they need publication in their own right. Its not a controlled study, it’s simply a case series. So it tells the story, the clinical story of those children. Part of that clinical story was the bowel symptoms and that lead to the discovery of a novel bowel disease. You would think that that would be cause for some small celebration but oh no. Why not?

You know, there was something that was treatable for the first time in this disorder. You had something tangible, treatable that you could really do something about as a doctor. It should have been a cause for celebration but no because part of the parents’ story in the majority of children was regression after a vaccine. Now, if those children had regressed after natural chickenpox, we would not be sitting here now, but they didn’t. They regressed after a vaccine. Their parents weren’t anti-vaccine. They took them to be vaccinated according to the schedule and they said to their doctor, well…

DW: Yeah, after my child was vaccinated, they weren’t well. They had a high fever for a week. They then became delirious. They then started losing their speech and language, those kinds of things. So it wasn’t just coincidence. It wasn’t just that the child, at around the time, children were diagnosed with autism had had their MMR, it wasn’t that. There were medical events associated with the exposure that then subsequently led to the child’s decline. And so we had to take that very seriously.

The parents were right about the bowel disease. Were they right about the vaccine? And when we published in The Lancet the story, we wonder about the sense of the story, we weren’t going to take out the bit about the vaccine. Then, things went very badly wrong.

The other thing, when I decided that I was going to get involved in this, now, I wasn’t going to back away from it.

DW: Sure, well I decided that I was going to review all of the safety studies about measles and measles-containing vaccines because if I was going to get into a fight, I needed to know what I was talking about. If I was going to challenge the status quo and say things that might have an adverse effect on vaccine uptake, I had to know what I was talking about.

So I read all the papers and I was appalled. I was absolutely appalled at the quality of the safety studies of the single and combined MMR vaccine in particular, and then I wrote to my colleagues in advance of the paper coming out and I said this is going attract a lot of attention in the media and I have to tell you, that I have now read all these studies. I have written a 250-page report which I’m very happy for you to read. I cannot support the continued use of the MMR vaccine. I will continue vigorously to support the use of the single vaccine but I cannot support the use of the MMR.

Now at that stage, the dean of the medical school Arie Zuckerman had decided that he was going to have a press briefing, a press conference. Get people together, tell them about the findings of the study. And, I wrote to him, I copied this letter to him so he had an opportunity at this stage to say no press briefing. We don’t want to get into the vaccine issue.

…The original plan was that Wakefield doesn’t attend the press briefing or if the question is raised at the press briefing, it doesn’t go to Wakefield. Dr Zuckerman had three opportunities to de-fuse this; he didn’t. As soon as the question came up at the press briefing which inevitably it was going to do, he directed it straight to me. And I responded in exactly the same way that I said I would respond in advance of that press briefing.

Now, it wasn’t based upon the observations in 12 children, it was based upon reading all of the safety studies and producing a 250-page safety report on those studies which I’d offered to my colleagues to read. And that was the basis for my recommendation that parents be allowed to use the option of the single vaccines.

…that press briefing was in February 1989. Now, what happened then is at that time, single vaccines were still available in the UK. Otherwise, I would not have made that recommendation.

In September of that year, the government withdrew the importation license for the single vaccines. So here was the demand that it’s maximum for the single vaccines, parents that still wanted to get their children were vaccinated. I was encouraging the use of the single vaccine but the government took away the option of single vaccines from parents.

Interviewer: You weren’t advocating not to vaccinate, you were encouraging people to vaccinate, you just said, lets get them singly because from your exhaustive review, there appeared to be some complications when you combined them all together.

DW: Yeah. We’ve got a problem here and until that problem is resolved, children need to be protected, but give parents the option of the single vaccine. And they, the government, at the height of the demand for the single vaccine, withdrew that option. In other words, to protect the policy, MMR, and not protect the children.

So here they are, the government or the Department of Health putting the concerns for the protection of the policy before concerns for the protection of children.

So, I’m afraid it’s my opinion that it is entirely their responsibility that there has been a declining vaccine uptake in the UK because they removed the option of the single vaccines and there have been outbreaks of infectious disease as a consequence.

We went on and saw more children, published more papers. We published a total of about 19 papers on this disorder in total.
All peer reviewed. Strangely, these have never been discussed when it comes down to the public relations exercise of the other side to discredit me The only paper that is discussed is that Lancet paper.

Interviewer: And which Lancet paper was that?

DW: That was the first. That was the 1989.

They don’t talk about the detailed characterization of the bowel disease that we went through. What happened to kids who had not one shot but two shots of MMR? Where they were worse than the kids who had one shot. All those sorts of things never get discussed.

And then they don’t talk about the replication of the studies elsewhere around the world.
… it’s replicated in Canada, in the U.S., in Venezuela, in Italy, but they never get mentioned. All you ever hear is that no one else has ever been able to replicate the findings. I’m afraid that is false.

Here we are as academic researchers doing this work thinking this is useful and yes, it’s contentious but nonetheless, it’s very important. And what had happened is that the Department of Health had contacted my medical school, the dean in particular, and had tried to close this research down; had tried to close down the clinical care of children with autism at the Royal Free, expressing concerns that it was unethical that all these children had autism.

Well, here you had the world’s leading pediatric gastroenterologist and his colleagues saying, yes, they are justified and here are the findings. We’re happy to show you the findings at any stage, in any venue that you like. But nonetheless, there was a concerted effort behind the scenes to stop the work. And it was particularly the concern of the Department of Heath that there was pending litigation that I had agreed to act as an expert in the litigation giving access to these children, to the process of justice. Not trying to prove that it was right or wrong but …doing my best as an expert to determine whether there is a case in law against the vaccine manufacturers.

DW: I hope I’m getting the dates right here but its in 1996-97.

So, I had agreed to do that and I wrote to my colleagues in ’97 saying that I felt there was a professional and moral obligation because these children, when their parents die or become infirm, they are on the street, no one cares, and no one is going to look after them. And if society does not fulfill its absolute moral and professional and social obligation to look after these children, they’re going to die on the street and that’s a fact and it’s already happened. So I felt very, very strongly that as a doctor looking at this, I had a duty to get involved in litigation.

Now what I thought at the time, what the lawyers thought is that it was the drug companies that were going to be sued. It wasn’t. What had happened when the MMR was introduced in the UK is that somehow the Department of Health or the government had done a deal with the manufacturers of one of the vaccines, SmithKline Beecham to indemnify them against litigation. Now, why would they do that? What was the purpose of that?

Well, it turns out, that the vaccine that they had at the time contained a strain of the mumps virus, Urabe AM9, which was dangerous. It caused meningitis. It was produced in Japan. It was introduced into Canada and very quickly in Canada, when it came into use as MMR; they found that it caused meningitis.

Rapidly after that, it was withdrawn, it was then withdrawn in Canada and it was still introduced in the UK and it’s my opinion that SmithKline Beecham did not want to introduce it because they knew of these problems. They had a potential liability, a real liability. And the government therefore, in order to give the contract to the home team, to a British company, indemnified them.

I think a lot of that process was circumvented. For example, the relied on safety studies of the Merck vaccine that is M-M-R II which does not contain this dangerous mumps strain. So it’s a much safer vaccine.

So there were two other options But they weren’t British.
One was French, one was American. They didn’t want to give it to that company for some reason.

So rather than introduce, what they did is take those safety studies from America using a different vaccine and say, oh it looks pretty good to us therefore we can introduce this vaccine in the UK. You can’t do that. You can’t take one antihypertensive brand from one company and one from another and say well, that’s fine, so we’re going to give that one a license, and that’s what happened.

..you’ve got a brand of the vaccine where there have already been problems. So the vaccine with this dangerous Urabe AM9 strain came in the UK and lo and behold, it had to be withdrawn four years later overnight because it was causing meningitis.

It was causing the complication that had been seen in Canada, that had been seen in Japan and had been seen in Australia. And the vaccine was withdrawn. Was it taken off the market? No.

What happened to it next? It was put into storage and then it was sent to Third World countries like Brazil to be used in mass vaccination campaigns. So here you have a vaccine that has been taken away from different countries, First World countries but has not been discarded and is then sold on to Brazil. What happens when they do a mass vaccination campaign in Brazil? They have an outbreak, an epidemic of meningitis.

DW: ..what really provoked me into getting more and more involved in this is that a member of the Scottish Department of Health, a whistleblower, met me on Newcastle station in the north of England, met with me and with the lawyers and exposed this process. He said, “I came from Canada to advise the UK government on the introduction of MMR. I said do not use this vaccine. They ignored me. You have to have active surveillance for adverse events. You got to go out and look for these adverse events because they are real in Canada and they may well be real in the UK. So you have to look for them. They ignored me.”

And they went ahead and they introduced this vaccine and lo and behold, it had to be withdrawn. And so he felt very bad about this and he knew that children have been damaged and he felt the need to expose this process.

….That was in 2004. So six years later, still nothing has resolved, no compensation or I guess reprimand or any other process that was directed at those responsible for making that decision.

DW: and it seems ludicrous to me and it’s now time for this to be exposed. It’s time to get this out there because I’m no longer under this legal stricture that prevents me from doing so, and so it’s coming out.

DW: Between then and 2004, between the publication of the paper in 2004, I lost my job at the Royal Free and there was a great deal of pressure to stop this work. The new professor of medicine sat down with me and the secretary of the medical school and he said, “You no longer form part of my plans for this department, the future of this department.” He said, “Your science is not good.”

I said, “It’s interesting you should say that. Have you ever read any of the papers that we have ever published?” And he paused and he said, “I don’t need to.” There was some natural wisdom that he had been given from God that he didn’t need to read the papers. So we got into a little discussion about who was the bad scientist and our relationship didn’t improve from that point on. So I left the Royal Free.

I left in 2001, November of 2001.

DW: I was in the UK at that time, travelling backwards and forwards to the States where the story was exactly the same as I had heard in the UK, as I heard in Canada, or as I have heard in Europe, exactly the same story. And I had been introduced to Bernie Rimland and realized how pervasive this problem was and how rapidly it was growing.

One of the pioneers in the medical field of autism in other words, taking autism from the psychological and behavioral and putting it firmly in the, this is a medical disorder camp was Bernie Rimland, the late Bernie Rimland. So he was a fine man and someone who had a big influence upon where I went and what I do with my career.

So, I initially looked at helping set up a center in Florida and then finally settled on Austin, Texas which has a tremendous community spirit. I started to live here in about 2005.

… that was the beginning of the media attention. In 2004, I suddenly got this contact from a freelance journalist Brian Deer working on behalf of the Sunday Times making a whole series of allegations against my colleagues and I. In his opinion, these children did not need investigation, in his opinion, these children did not need a colonoscopy or a lumbar puncture or these other investigations that my clinical colleagues had deemed they most certainly did need.

… he had no formal medical training.

He’s just a journalist.

but it was his opinion. He believed that I had got together with a lawyer, had rounded up these children for the purpose of creating a legal case against the manufacturers of the vaccine in order to bring about the downfall of the vaccine in order to launch my own vaccine onto the market. It was a great story.

If he had done his homework, he would have found that it was impossible because the manufacturers were indemnified.

it was just so fanciful. Where do you start to unpick a story like that?

But the bizarre thing is what mutated from that original story, none of which really made any sense. The children were not involved in litigation when they were referred to the Royal Free. They had nothing to do with litigation until afterwards. They were not herded, rounded up by lawyers. They didn’t come from lawyers. These were parents who heard about the work or read about the work or had been talking to friends at child groups who made spontaneous contact with me because in the newspapers they had seen the work on Crohn’s disease. That’s how they came.

So he made so many factual errors but he nonetheless managed to persuade the General Medical Council to initiate a process of investigation against us.

And we, that are my colleagues and I, had recently been found guilty of some of the most ludicrous charges. For example, experimenting on children in the absence of ethical approval. So they determined that the world’s leading pediatric gastroenterologist was not fit to determine whether these children needed a colonoscopy or not for clinical indications. They determined it was researched.

So what happened is, when the parents called me with this highly complex story, I couldn’t help them but I knew someone who could and that was John Walker-Smith. So I said, you need to get a referral from your doctor, your family doctor to Professor Walker-Smith.

He’s a physician. He is the professor of pediatric gastroenterology. In fact, he is probably the founding father of the discipline of pediatric gastroenterology worldwide.
a very eminent doctor who was a co-defendant at the GMC. So I recommended that the parents seek a referral to him.

That is my communication to them, sign posting them to a doctor who might help their child. I also offered because of the complexity of the whole story, to talk to their doctor, the family doctor if it would help to communicate what we were thinking in terms of how the gut and the brain might be linked and what we might be able to do in terms of professor Walker-Smith’s clinical input and my research input to help this child.

And that offer was on the table. So some doctors contacted me, some parents put me in contact with the doctors and I spoke to them. I communicated to them and the referrals were made accordingly or not.

At the GMC, I was found guilty of causing children to have, for example, lumbar punctures, spinal taps because of this communication.

Now, that’s got to be a completely new charge causing children to have these tests. I didn’t do the test. I wasn’t there when the tests were done. I didn’t prescribe the tests. But I caused the children to have them because the parents called me and I suggested getting a referral to Walker-Smith. That is how complex and how bizarre and tortuous this process has become.

Well the principal charge, the principal finding against us is that we had investigated these children without ethics committee approval. We had undertaken and a series of investigations had been undertaken on these children without ethics committee approval.

Now, firstly, let me make it absolutely clear that tests that are clinically indicated are not researched and they do not require the approval of a hospital ethics committee. They are just like you going to the doctor, the doctor saying, “Wow, you got a bad throat. I’m going to take a blood sample to see if you got strep titers.” That is a clinical test. And my clinical colleagues were perfectly capable of making the decision about those clinical tests but the GMC argued that those were research tests. They weren’t.

They also argued that the research tests were not covered under an ethical approval. That also was false. What they had failed to identify in their due diligence was that there was an existing ethical approval for the research elements that were undertaken in The Lancet paper and that was work that I did and that was related to a detailed microscopic examination of the tissues in the children.

So, they were wrong on both counts. They had called clinical tests research tests – wrong, and they had said there was no ethical approval for the research tests that formed part of The Lancet paper, wrong also.

So the major conviction against me, against my two colleagues was that there were tests being done that were researched that didn’t have ethical approval and they were wrong on both counts.

Interviewer: Do you have any theories or understanding as to why this conclusion was reached or this verdict?

DW: I think there are two possibilities,. They rarely get confronted with research issues and they were unable to distinguish between research and clinical. It was beyond their remit. They did not get it.

Alternatively, there was pressure on them to find us guilty. Now, I don’t like to believe that that’s the case. I don’t like to believe that they acquiesce to any kind of external pressure from the government to find us guilty. I really hope that that’s not the case. I like to believe that there is still justice and there is still fair mindedness. I will never know. I suspect.

DW: Well the paper was originally, underwent a partial retraction in 2004. What does that mean? It meant that the editor of The Lancet, Richard Horton asked that we issue a partial retraction of the interpretation that MMR vaccine causes autism. Well, we had never provided that interpretation. Is it a possibility? Yes. Can you retract the possibility? No. It’s totally illogical. So, many of my colleagues, who I think were quite frightened by this whole process decided to issue a partial retraction. Three of us said, no.

DW: There were 13 and 10 retracted and three said no. This doesn’t make any sense scientifically. You can’t retract the possibility.

We did not come to the conclusion that the vaccine causes autism but quite the opposite. So, no we’re not going to get involved in this. When the final decision came at the GMC, principally that there wasn’t ethical committee approval for this study then, Dr. Horton decided to completely retract the paper even though it was a clinical case series that did not need ethical approval for the test that were done clinically.

So, what we were left with then is a situation where this paper, these children, the reality of the bowel disease, the existence of these children, their demise after the MMR vaccine was effectively removed from the record. Does that make any difference? Absolutely not. That’s just political posturing. Does it actually mean these children didn’t exist, that their problem weren’t real, that they didn’t regress after the vaccine? No.

In fact, I think what has happened is it’s alienated a great number of the scientific and medical community because it’s just a case of Big Brother. It’s just censorship trying to deal with dissent against the possibility that vaccines are not as safe as they have been purported to be.

And so, it’s interesting therefore when you look at The Lancet, it’s owned by Elsevier, the publisher is Elsevier and there has been a very interesting article on autism which looks at the links between Elsevier, its chairman and his board position on Glaxo SmithKline.

Elsevier is a massive publisher. Perhaps the largest publisher of medical journals in the world. I mean, they have hundreds of hundreds of different journals that they publish, The Lancet being one of them.

Which brings us to the next point – we subsequently published a paper in another Elsevier journal that is Neurotoxicology. And this was part of a long, long study.

When you do vaccine safety studies, they are very often done in primates, non-human primates before they go into children. The rhesus macaque, an old world monkey is one of those primates, and so we decided some years ago, eight or so years ago, to do the study that had never been done.

To take the vaccine schedule, what happens in the real world if we expose these infant primates to what kids get between the age of day one and preschool boosters, the vaccine schedule in the 1990′s with thimerosal in it. What’s the outcome?

What’s the outcome in terms of their development, in terms of their cognition, in terms of their intestinal function, in terms of their immune function, brain imaging, all those kinds of things…. a very, very detailed study. It should have been done.

It was never done. It had never been done, extraordinary. Parents might expect that the total vaccine schedule that their children are going to get has been looked at for safety in total. It has not. The individual vaccines are looked at but the schedule is not.

So we decided we do the study. The first paper just looked at the effect of the thimerosal, the mercury containing hepatitis B vaccine on day one, and looking at the acquisition of essential reflexes like feeding reflexes.

And we compared with unvaccinated animals; animals that have been given saline as a control. And what we found is there was a significant delay in the acquisition of these basic life saving reflexes in the recipients of the vaccine.

As early as the first few days of life, very, very worrying. We published that paper, it went through rigorous peer review. It was published online in Neurotoxicolgy and then lo and behold, after the GMC decision, they decided not to proceed to publication in the paper itself. The paper was withdrawn. Not based upon its clinical and scientific merits, they have been through the process of peer review that you and I talked about, a process that we recognize as absolutely essential to the conduct of science. It had been through that. It had been published and then it was withdrawn.

This is extraordinary. Had it been withdrawn for a scientific reason, the editor would have been able to deal with it but it was not withdrawn for a scientific reason. Well, the publishing house shouldn’t be telling the journal what they should and shouldn’t publish.

It’s absolutely an extraordinary situation. So this was a decision that had come from the top, from the publishers. And as I’ve said before, we do not know that Elsevier and Glaxo SmithKline have this link with the chairman of Elsevier. So one can speculate. I don’t know.

Huge potential for conflict of interest. It should be disclosed. One hopes it didn’t influence the decision to withdraw that paper. But the important factor is that it was a decision taken by the publishing company and not by the editor, the scientific editor of the journal itself.

Interviewer: One of your biggest critics in the United States is Dr. Paul Offit who is recognized as one of the leading advocates for vaccine, actually not just vaccinations but mandatory vaccinations, compulsory vaccinations which essentially eliminates the freedom of choice of a parent to decide for themselves whether or not they chose to give their children this vaccine.

And this is actually the same physician, Dr. Offit who has huge potential for conflict of interest because he has generated millions of dollars from developing his own vaccine, a rotavirus vaccine.

And interestingly, one of the other rotavirus vaccines was just recently found to be contaminated with pig virus. That’s another side issue but this Dr. Offit has been noted to say that it is safe and to not expect any side effects from giving an innocent infant or child 10,000 vaccines on one day, vaccinations. It is just profoundly absurd to think that anyone could say this thing, let alone someone who is purported to be an expert in vaccines. So I’m wondering if you could comment on that; on his comment I guess. You want to think about it for a bit but…

DW: No, I’m very happy to talk about it. Something that has given me cause for concern. So let’s just put Dr. Offit in the frame, in saying what I’m going to say, I have offered on several occasions by recorded delivery and mail to debate Dr. Offit in public at any time in any place of his choosing and that he has never taken me up on. And I don’t suppose that he is going to.

Let’s just characterize Dr. Offit’s sense of proportion and due diligence in what he says. For example, in his book , Autism and False Prophets, he claimed that I had made the recommendation to use single vaccines in the UK in February 1998 when the single vaccines were not available. They were. I would not have made the recommendation had they not been. If you Google that. If you put in “withdrawal single vaccines UK’ into Google, the first website that comes up gives you the precise date on which they were withdrawn in the fall of that year; six months beyond what I had said. That is all Dr. Offit had to do to check his facts. That was all he had to do.

DW: He did not do it. Instead, he decided to go into his book, go into print and defame me by suggesting that I would make a recommendation which was in effect unethical. So that is a measure if you like of Dr. Offit’s application to the task at hand.

Now we come to your specific question about the use of 10,000 which I think he’s now revised to a hundred thousand vaccine antigens on one day. This is based upon a theoretical study that he did looking at the sort of genetic variability of the genes responsible for antibody production and saying, well, based upon
the number that we have available; we should be able to produce this number of antibodies.

That is an entirely theoretical mathematical piece of jiggery pokery. It has absolutely nothing whatsoever to do with the real world and it’s bizarre that he would go out there and say that. That really, really worries me from a safety standpoint.

If you just take for example, MMR and you add in the varicella vaccine, the chickenpox vaccine, MMRV as ProQuad what happens is you double the rate of convulsions as an adverse reaction.

So just adding one and not 999,000 but just one extra vaccine in, you double the rate of an adverse, a potentially serious adverse reaction.

To the extent that that ProQuad vaccine had to be withdrawn.

So the notion that you could give a child a hundred thousand vaccine antigens on one day is utter nonsense. And what is extraordinary, what is telling I suppose is that no other immunologist or vaccinologist or any other person with any credible standing has stood behind Dr. Offit and said yes, you can go for it.

The thing that really worries me is that there is a tendency – and it’s a public relations exercise – to separate this into pro and anti vaccine. It’s much easier for Paul Offit to call us anti-vaccine than it is to engage in the debate. I am not anti-vaccine at all.

In fact, ironically, it is people who are putting the safety first agenda, a safety first vaccine agenda, not profit or policy but safety first vaccine agenda who will ultimately be the saviors of vaccine policy in this country and around the world because vaccine policy, as you know, depends upon public confidence.

And if the public lose confidence in people like Dr. Offit which is a real risk, then they will withdraw from vaccines altogether across the board and that will lead to the resurgence of infectious disease and problems.

Now, vaccines are imperfect and there needs to be a safety first agenda that optimizes the safety of those vaccines above any other issue that puts the health of children first. And so, you have this situation where those who are driving the safety first agenda are in fact the ones who will preserve public confidence in the long run rather than destroy it by making extraordinary statements like you can give a child a hundred thousand vaccine antigens on the same day. That in the end will be the downfall of this program.

interviewer: , The Lancet just wrote an editorial or an article about the anti-vaccine people or movement and characterized her as one of the leading organizations in this movement. One of the arguments that they gave against this and essentially a proof that they are making some negative results of the public listening to them is that there has been an increase or relative increase in measles and mumps as a result of people listening to this message and choosing not to vaccinate.

So the results, the incidence of vaccinations has gone down, the incidence of these diseases have gone up. I’m wondering if you can…that seems to be their central argument as a justification that the organizations that are proponents of vaccine safety are having a negative public health impact and eventually, they’re going to use this as some type of justification to implement mandatory vaccinations. So I’m wondering if you can address that because that seems to be their main argument.

DW: It’s a very important issue. Let’s just break that argument down. Let’s take measles first. Has there been a resurgence of measles in the UK? Yes there have been some more cases. How might that have come about?

You’ll remember that I recommended the use of single vaccines. In February 1998, I recommended the urge the use of single vaccines. Six months, seven months later, the government withdrew the importation license therefore that option was taken away from parents. So parents who were not anti-vaccine were having a major option taken away from them for how to protect their children when they had genuine safety concerns about MMR; concerns which were engendered in the fact that a few years earlier one was withdrawn for safety reasons.

So they were perfectly justified in being concerned. So the government removes the option and lo and behold, what happens, measles comes back. So, who is to blame for the resurgence of measles? They’re putting protection of the policy before protection of children.

Let’s come to mumps now. Mumps is extremely interesting. Mumps in this country, in the U.S. the CDC did a study. When Maurice Hillerman went from Merck, the head of vaccines at Merck, to the CDC ….. I have a mumps vaccine; I would like you to use it. They did a study and they said there is no need. Mumps is a trivial disease in children; we do not need this vaccine.

Exactly the same happened in the UK. The Department of Health, the Medicines Control Agency, the regulators in the UK said, this is a trivial disease in children. We do not need a mumps vaccine. But it got in. It got in and there is a story behind this that will be published in a book by Patrick Tearney that will be coming out sometime later, hopefully this year.

What they did is they got the vaccine into the program. Now, the problem has been that the mumps vaccine does not work. It does not protect enough people in the first instance and those that it does protect, the protection does not last. Now, they foresaw this problem. They said one of the big problems with the mumps vaccine… This is Merck in this country and this was SmithKline in the UK.

The mumps vaccine, the antibody levels, the protection levels fall off very quickly and they had anticipated this. They said, here is the problem, if the vaccine does not work, its called secondary failure. The antibody levels falling off, the protection diminishing over time, then we are turning a trivial disease in children into a potentially more dangerous disease in adults because you and I know and people out there know that mumps in adult males can cause testicular inflammation and sterility — orchitis. It can cause other problems.

So there was the risk. If they introduced this vaccine, is there going to be a long term problem because they’re taking a trivial disease and turning it into a more dangerous disease? That is exactly what’s happened.

So we’re now seeing outbreaks of mumps in highly vaccinated populations; populations of people who have received not one but two doses and more because reboosting them with another vaccine doesn’t work.

Interviewer: So your suggestion is that if you have a population that is not vaccinated, their likelihood of getting mumps as an adult is much lower than a population that was.

DW: That’s right because if they caught it as children, if they caught it as infants, they’ve had a mild trivial dose of mumps, they developed lifelong immunity and therefore they are immune.

Interviewer: So the natural immunity that they would typically get in a community that hadn’t been vaccinated is going to be far superior and prevent – essentially eliminate – the only known dangerous complication of mumps which is this testicular inflammation and swelling which is going to lead to infertility.

DW: I mean there are other problems as well, we have pancreatitis… that’s the major one. So you have effectively taken a trivial disease and by vaccinating, you have turned it into a more dangerous disease. Now, they are in a real mess.

They are in a real mess because one dose of MMR doesn’t prevent it. Two doses of MMR don’t prevent it; three doses. You are creating a population that is dependent upon reboosting with vaccines for the rest of their lives to avoid this complication, a man-made complication.

Interviewer: And isn’t that convenient and isn’t that perhaps the model that they’re using to have this, create a problem with a very solution that they’re proposing that requires continuous use of that solution which massively and exponentially increases their profits because the demand for the solution goes to the roof. This is just one disease, mumps. This hasn’t even been studied for the other diseases and the all the ones that are in the pipeline.

DW: Was there a conspiracy to anticipate that? I don’t know. You never substitute conspiracy for incompetence. I think they made a huge error.

. DW: There was incompetence. They were incompetent. They were so zealous. So urgently needed to get this vaccine into the market that they ignored the potential problems and now we have a big, big problem. Mumps vaccine is a dangerous vaccine. It does not work.

DW: I think there is no doubt that if you create a population that’s dependent upon boosting and boosting and boosting on a regular basis with vaccines, your volume of sales is going go up dramatically. So there is benefit. My concern is that this madness has to be curtailed. It has to be stopped. There has to be an injection of common sense into the whole regulatory process. It’s not there at the moment. It’s not there. And we’re seeing mumps epidemics occurring all around the developed world as a consequence of this. So in blaming it on Barbara Loe Fisher and NVIC is utter nonsense.

Interviewer: Are there any other diseases that are similar to mumps that you can see or predict or project that maybe an issue coming down the road?

DW: I think the one that concerns me most is chickenpox. I have real concerns about a chickenpox vaccine that may produce the same effects because chickenpox, for the great majority of children, is a mild disease.

DW: Similar to mumps. Chickenpox in adults is not. Chickenpox in adults can be an extremely severe disease producing inflammation of the brain, a major problem. So if you are again displacing the age of susceptibility to an older age because you vaccinated and the vaccine does not work over a long period then you’ve got major problems.

And there are other issues with chickenpox vaccine that go beyond that. We’re now seeing shingles in children. We’re seeing shingles in adults because they’re not getting the natural re-exposure in the community to children who are infected with chickenpox, that natural boosting of immunity over time. So, if I were to single out a vaccine that I would be particularly concerned about and certainly deserves long term study, it would be the chickenpox vaccine.

Interviewer: So another concern certainly one of my significant concerns is the absolute ludicrous insanity of recommending that a child, a newborn, harmless, innocent child be given hepatitis B vaccine on the day they were born. This is a disease that is really only blood borne so it has to be by getting a transfusion or through having sexual intercourse.

There is no really other known route of exposure except from getting it from the mother which is easily, if they were that concerned about it, they could just do a blood test and find out if the mother has it and then if she does, then you can give the child a vaccine. But that’s not being done. Its being done… most of the newborns in this country, even unknown to the parents are…well the child is taken away in the nursery and is given a shot, they’re not even asked. So, to me this is insanity and actually, if you’re vigilant about it you can refuse it but you have to be very, very careful and know that before. So I’m wondering if you could comment on hepatitis B.

DW: This is a huge issue. I mean, quite apart from the fact you could make a very good case for hepatitis B immunization given the endemic nature of this disease and the high mortality and morbidity worldwide, coming down to the specific issue…

DW: Coming down to the issue of giving it on Day One of life, there are several issues that surround that.

The first is when we did this primate study giving that hepatitis B vaccine on day one. We looked for the safety studies of that policy. What had been done to establish the safety of giving it on day one? Not just giving it on day one but giving it on day one to every infant whether they were born at 24 weeks or 30 weeks or 36 weeks or 40 weeks, whatever their gestational…their birth weight was, whether they were 10 lbs or 3 lbs or 2 lbs, they were getting the same shot at day one as a matter of policy. Safety studies…

Interviewer: Nonexistent.

DW: We couldn’t find them. And that was really shocking, really shocking. How could this be? If you’re going to make a case for it, if you’re going to do it, you’re going to make it a matter of policy for every kid in the country then you’ve got to be absolutely certain that you got the safety set that is right because if not, you may produce insidious problems, minor degrees of damage which you don’t pick up straight away but are catastrophic later on. So you better make sure you’ve done the homework and they hadn’t.

DW: And so this is a real source of concern for me. Then you come to the other issues that you raised and that is it’s the hospital policy. So here is a mother who has just been through 24, 48 hours of labor, who is absolutely exhausted, is not in a position to give informed consent, is simply not in a position to do it. They’re not even asked in many cases. As you say, the child is just taken away because it’s policy. Now this has got to stop. That is criminal assault and that has got to stop.

There has got to be some degree of legal control over that process because that mother is not in a position to give fully informed consent and as often, as you point out, never asked. So there are separate issues here; one about the safety profiling of this whole process and the other is about the policy issue that surrounds how it’s done.

Interviewer: Informed consent really is a central right that we all have. That has been taken away from us. Not even told that we’ve lost it, we’re not even aware.

I appreciate your comments on informed consent and interestingly, but one of the benefits that had come out of World War II is that we have the Nuremberg trials where the atrocities in Germany were addressed and we developed the Nuremberg Code which really had this whole aspect on informed consent to give because that was one of the atrocities that occurred, they were performing these experiments on humans. And what the code essentially developed was that it’s unethical to perform these trials without informed voluntary consent.

Interestingly, Dr. Offit, as mentioned earlier, is really a very strong proponent of mandatory vaccinations for the benefit of the public health because the benefits outweigh the risk which is really preposterous in light of the information you’ve just shared because we just don’t even know what the risks are because the studies haven’t even been done. So I’m wondering if you can comment on that.

DW:
It’s particularly alarming to here talk about mandatory vaccination. Mandatory vaccination itself is a reflection of the failure of the process. If you have to mandate a vaccination, if you have not got the will of the people, if you have not got the confidence of the people in your vaccination policy and therefore you have to mandate it, you have to coerce people, you have to threaten them with not going to school or no social welfare. Then you have failed.

You have completely failed in your aim to gain the confidence of the public in your public health policy. So it’s a reflection ironically of the failure of the system, the need to mandate the process. I am completely and utterly against the idea that you can take the rights of the parent away for the care of their child, for the decisions made in the context of what their child should and shouldn’t have and hand them over to the State.

One of the most telling cases I ever came across was a mother at a meeting, a mother of an autistic child and her job had been as a nurse to take the children who had been made wards of court because their parents wouldn’t vaccinate them and vaccinate those children; to forcibly vaccinate those children. To take them from their parents and give them the shot because their parents had voluntarily decided not to and the government had intervened and determined that it had the right.

And what had happened to her in the cruelest of ironies is that her child had regressed after a vaccine and become profoundly autistic. She has to live with that knowledge for the rest of her life. That she did that. That she was part of the that system that encouraged, that endorsed that process which is more reminiscent of Stalinist Russia than it is of latter day America.

Interviewer: I think that also brings up the point of really the challenge we have in this country where you have probably one of the best disciplines, pediatricians and literally one of the lowest paid. Really incredibly motivated dedicated individuals. I mean, there is just no question but that is reflective of the majority of these pediatricians. And yet, they are so firmly committed to this process to the point where they almost become violent if someone opposes them. And yet, for them to seriously reflect on the possibility that they might be causing harm is so massively abhorring to them that they can’t even consider it.

It’s just not something they can objectively review. It’s the same issue. And really one of the challenges that we have is to have them overcome that because they would be admitting that the bulk of what they’re doing is actually potentially causing more harm than good.

DW: Yes, I feel extremely sorry and then concerned for pediatricians as a group in as much that they have been driven down a path largely by the insurance industry where they’ll be remunerated for five minutes, or 10 minutes or a brief consult and within that time, you’ve almost got your pen in your hand to write the script or to give the vaccine.

So, you are dependent in order to make an adequate living on getting information from the CDC, from the AAP, from all of these people and believing in that information and acting on that information but not being in a position to go away and assimilate it yourself.

Now, I don’t believe that. I think that if people were really concerned, they would actually go and read these papers and come to their own determination of what was right and what was wrong and what to believe and what not to believe.

An example of this was we wrote a paper recently in response to Dr. Ari Brown who is a proponent of vaccines and a spokesman for the Immunization Action Coalition which was utter nonsense. It was a written for the people. It was to explain why vaccines are safe but it was I’m afraid factually, totally inaccurate and scientifically bereft of any common sense at all. And when we wrote a response to this, does that get out to the pediatricians? Do they see that? Is that the leaflet the parents pick out when they go into the doctors? No. But it should be because that is truly the essence of informed consent is to look at the pros and cons.

DW: It doesn’t matter what happens to me. It’s irrelevant. You know I decided this. When you go down this path, you decide this a long time ago, is that this story was written before you and I were ever born. This is the history of medicine. If you look at thalidomide, the first doctor, an obstetrician in Australia, McBride who described thalidomide in The Lancet interestingly was
struck off. He was struck off. The drug companies went after him and his research was criticized and the details don’t matter but the process is there.

In Australia too when the Merck Vioxx trials were going on recently there was a disclosure of internal memos and how to deal with doctors who dissented from the safety of Vioxx and it was about isolating, discrediting and the last one said, we may have to seek them out and destroy them where they live.

So this what medicine has in store for it if it calls into question the safety of a company’s drugs. When I was interviewed on NBC, although this didn’t make it off the cutting room floor, I was asked if I was just into conspiracy theory and I said, this is not conspiracy theory this is more like corporate policy.

So, the other thing to say is this pro and anti-vaccine argument, it’s interesting there was a recall of Toyota cars recently because there were safety concerns about jamming of the gas pedal. Were the people who called for the withdrawal of those cars anti-car? I don’t think so. They weren’t anti-car at all. They were concerned about people crashing and dying on the freeway. So that doesn’t make them anti-car and so dichotomizing this argument into pro and anti-vaccine makes no sense at all, absolutely none.

DW: And finally, you would think that this community that’s been beaten up and impoverished and is surrounded by all these experts who are telling them that they are wrong would go away. They’re not going to go away. These parents aren’t going to go away. The children aren’t going to go away.

And there was a recent study, I think it was from the University of Michigan after everything that had happened all the millions that have been spent on public relations, all the kicking and brutalizing of physicians who get involved in this, all of the discrediting; one in four parents believe that vaccines cause autism.

In other words, they’ve lost. They’ve lost the public relations war. We’ve done nothing. From our side, this is the first time I’ve spoken about it. You and I are sitting here for the first time. We have done nothing. Our expenditure on public relation is zero. One in four parents in this country. Why? The answer is very simple, because it’s real.

That’s the truth and no amount of public relations, coercion, and vilification is going to change that.

DW: So I’m afraid that they either take notice of the fact that one in four parents believes vaccines cause autism. This isn’t a cross section of the population. Those one in four tend to be the intelligentsia, the educated, the professional, and the people who listen and talk and read. So this is not a reflection, this is a real problem for the system. And if the system does not acknowledge that and take notice of it then it is going to be in real trouble because now, the fight back begins. And what that’s one in four going to become?

Interviewer: Well that’s a challenge. I mean we are dealing with a progressively increasing epidemic. The future of our culture, of the children. You know, someone has got to stand up for these defenseless and innocent kids.

DW: Absolutely.

DM: we’re going to definitely spread this word out to as many people as we can. This is a story that needs to be heard. This story needs to be spread and ultimately, get that one in four up to two in four and three in four. At one in four, you are reaching a tipping point. At 50% that’s the majority of the people. So we’re making a difference. I don’t think we’re far away that we’ve got them running. They don’t have really a choice except to change.

Interviewer:
What’s your next step at this point?

DW: Well, I’ve got the opportunity now to get the story out there. So there is a book. I’ve written a book. At the GMC I was accused of callous disregard for children suffering which rather extraordinary even to me having experienced what I’ve experienced to be accused of callous disregard for children is a stretch. So the book is called Callous Disregard.

There is just tinge of irony in that. And it’s really about the circumstances that surrounded The Lancet paper and everything that flowed from it but also the whistle blower in the background and that behind the scenes action that I wasn’t aware of at the time but was forced into the open by the disclosures at the General Medical Council.

So it’s a story that hasn’t been told that needs to be told. The second part of it which I’m writing at the moment will focus largely on the American experience and my involvement with Congressional testimony and that kind of thing and all the behind the scenes jiggery pokery that went on there. So that book will be coming out hopefully in time for Autism One here in Chicago in late May.

It’s just to get the story out there and put the other side. If people want to involve themselves in this debate and to discuss this, then read that book, understand it .

Interviewer:
At this point, you’re still conducting research in Austin?

DW: Yes, I’ve just been offered a new position which allows me to integrate the research efforts of a variety of autism organizations around the world and to focus on those issues that the Interagency Coordinating Committee (IACC) with all its money and all its power seems to loathe to do and that is to look directly at environmental causes included within that of course is vaccines.

So, the IACC seems to be moving around that issue but the elephant in the room is clearly the vaccine. I don’t want to look at it now. My concern is to rule it in or rule it out. If they’re fine they’re fine, if they’re not, they’re not. We need to know. The public need to know. The medical profession needs to know. So that we can make informed choices and give informed consent.

.

Interviewer: Why have you been called to the General Medical Council?

Why is this hearing being held at all in front of the regulatory body of the UK, and who bought the case and what is the case? The case, it seems, was brought by a single complaint by a freelance journalist who had been working for the Sunday Times, and others, and had been trying to uncover some misdemeanour on our behalf at the Royal Free in the investigation of children with regressive autism, many of the parents of whom said their children regressed after the Measles, Mumps, Rubella vaccine.

When I began this work in 1995 parents approached me and said– my child developed perfectly normally, they had their MMR vaccine, I wasn’t anti-vaccine, I took them along, they had their vaccine according to the routine schedule and then the lights went out, eyes glazed over, they lost speech, they lost interaction, they stopped playing with their siblings, they never smiled, they were grizzly, and eventually having lost skills and became mute and self injurious. They were diagnosed with autism or atypical autism.

And I said, I am terribly sorry, I know nothing about autism, how can I possibly help, and they said, well, my child has terrible bowel problems, diarrhea, pain, I know they are in pain, they can’t tell me they are in pain because they have lost the ability to speak, but I know they are in pain, my instinct as a mother tells me my child is in pain, they are screaming, they are drawing their knees up to their chest, particularly bad when they have their bowel opened. Losing weight, failing to thrive, and the doctor says your child is autistic, that is just the way it is.

Well, that is not just the way it is, that is not what autism is, these are children who are sick, who are clearly unwell. So we put the autism to one side and we said how do we manage these children if they had these symptoms and they were developmentally normal and we would investigate? And so we decided we would, over the course of many months, we put together a protocol, a clinical protocol, for the investigation of these children. What investigations do these children need in order for us to unearth the origins of their problem, for example, do we do a colonoscopy to investigate their bowel problems, are the bowel problems linked to the behaviour?

Because the parents were reporting us–when my child’s bowel is bad, when they are in pain, their behaviour is terrible, they can’t concentrate, they are at their worst autistically, and their autistic mannerisms get worse when their intestine is bad and gets better when their intestine improves, and this was intriguing to us as gastroenterologists because we had seen this before in other gastrointestinal diseases.

Gastrointestinal inflammable diseases like Celiac disease, or bacterial overgrowth when you lose a lot of your small intestinal, where bowel bacteria overgrowth leads to deterioration in behaviour, what is called encephalopathy, and often even progressing to coma, and the way you treat that is to treat the bowel, get rid of the bugs in the bowel and the behaviour improves. So we had seen it before, this gut-brain link, something in the bowel affecting the brain, and treating the bowel helping the brain, so why was this different? Was this a similar process?

Was, for example, some form of intoxication, some bacterial by-product coming from the intestine and injuring the brain, rather like drinking alcohol, you drink alcohol, it gets to the brain, injures the brain, affects the brain, affects behaviour, and so this was no different, it is not difficult, it is not rocket science, very very straightforward. Something going on in the gut primarily, and injures the brain, so this was an entirely reasonable idea to look at.

The other thing is these children had regressed in the face of a viral insult, they had been given a live viral vaccine, they had been given viruses which were known to be able to infect the brain and cause inflammation in the brain, for example autism. So it was entirely appropriate that they would undergo a series of investigations, in other words could we find in a laboratory setting evidence of measles virus in the inflamed intestine. Research.

So combining as we should do in an academic institute like the Royal Free, clinical investigation with research. And we progressed through the process thereby refining the clinical investigation. This is necessary, that isn’t, this is telling us something, this isn’t, out that goes, and then refining the process, so we were getting the maximum amount of information from investigating these children for the minimum inconvenience and risk to the child, and that is just good medicine.

So during this process I was approached by some lawyers who were acting on behalf of these children, investigating the parental claim that their child had regressed, disappeared, become autistic after a vaccine. And they said to me, would you help us? You have an interest in Crohn’s disease and measles virus, measles vaccine. We are now seeing these in new children, what do you think, can you help us in this process?

And I thought about it long and hard, and I decided that I would. Vaccination is designed for the greater good, to protect the majority and it does so at the expense of a minority, and that minority of children are those that are damaged by the vaccine. We don’t know the size of the number because it has never been investigated properly, but nonetheless, even if you accept that is a permissible ethical approach, that we can protect the majority at the expense of the minority, then that minority are a group of children who have paid the price for protecting the rest of society, and therefore society has an absolute moral and ethical obligation to care for those children for the rest of their lives, period.

That is it, there is no escaping that moral imperative. Yet to acknowledge those children in a public health setting is to raise doubts about the safety of vaccines. Therefore it is much better to put them in a corner and forget about them, to pretend they simply don’t exist.

That is what had happened to these children. The studies that had been designed to look at safety had been designed in such a way as they would never capture these children, nor did anyone want to capture them, nor was anyone interested in the parents story when they said my child has regressed after a vaccine. They were just put in a corner, told it couldn’t happen and never investigated, and that was absolutely unacceptable.

Part 2 Access to Justice

So, the other thing that happened, around the same time, is a parent called me, she is the mother of two autistic children from the Midlands, and she was an older parent, and she had a husband who was older than she was. He was infirm and she herself had arthritis. And she called me one day and she said, doctor Wakefield please don’t be judgemental, don’t judge me harshly she said, but when I die, I am taking my children with me, and I thought long and hard about that, and I wasn’t in any way judgemental, in fact quite the opposite, I was struck.

She said to me, Dr Wakefield, no one else cares about my children, I am the only person who loves them and when I die or become infirm to the extent that I can no longer care for them, they are going to be lost, they are going to be on the street and they are going to die on the street because the world doesn’t care. And she was right, she was absolutely right, there was nothing for these children, and you will know that in the Thatcher era all the long stay institutions, the old asylums were closed down and turned into luxury apartments and there is nothing left. It is care in the community, what does that mean? It just means shoving people with long term mental disabilities out into the community where they can injure themselves or injure other people, or whatever. Who knows, who follows them, who cares? And that was the future for these children

So, I decided at that point that I would help the lawyers, because if nothing else I was in a position to look at this scientifically, objectively and provide an answer that would, or would not take this story forward, but would nonetheless give these children access to the due process of justice, and that is what they had been denied.

It was about access to justice and surely that cannot be denied anyone, you would think, in a civilised society.

So the lawyers asked me what we should do, how would you go about in a scientific context, taking this to the next step, determining whether this temporal association that the mother has made between a child’s exposure to this vaccine and regression, how would you then further link that if possible to the virus, and I said the bowel disease that we have seen in these children and the Crohn’s disease looks like an infectious disease and you would look for evidence of the virus in sites of infection or obvious swelling of the lymph glands, there is one site in the intestine, it is like swelling of the tonsils when you get a sore throat, you would look in the tonsil for the organism that was causing it.

So if you have got swelling of the lymph glands in the intestine, look in there for the evidence of the virus, and measles virus, and measles was a virus that was known to cause this kind of swelling of the intestinal lymph glands. So it made logical sense to look in those areas and so we set up a study.

I was asked to design a study that would take this to that level, and then we would look for evidence of the virus in the intestine, and after a series of exchanges, and a protocol was prepared. We received acknowledgement of funding from the LAB to conduct that study. If it was negative it was negative, if it was positive it was positive, either way it got published. It was not designed to produce a particular answer, it was just designed to produce an answer: is the virus there, or not? It didn’t make it causation but it was a piece, a crucial piece of the jigsaw that took it to the next level.

Part 5: The Whistle-blower

Dr Alistair Torres who was from the Scottish Dept of Health, had been brought in to advise on the introduction of MMR vaccine.

The experience in Canada was that they introduced a vaccine which contained a mumps component made up of a strain of the vaccine called Urabe, which was originally generated in Japan and they had run into problems with this vaccine. It produced meningitis in children (1:43). The mumps virus was identified in the brain of the children and the vaccine was pulled in Canada, it was pulled, it was stopped in 1997. (1:53) Nonetheless this was the vaccine that was intended to be introduced into the UK a year later in 1988.

They changed the name, but the vaccine was identical, so it had gone from Trivirix to Pluserix in the UK, an identical vaccine that had already been withdrawn for safety reasons, in Canada.

Now Torres advised the JCVI not to introduce this vaccine because it was not safe. He was overruled. He said if you are going to introduce it then you should have active surveillance. That is doctors or people going out and asking doctors–have you seen and cases of the following in the past month, not waiting for doctors to spontaneously report.

Spontaneous reporting picks up 1-2% of those adverse reactions…..It is totally inadequate but they were totally overruled – no active surveillance (3:02).

So they were going to intro a vaccine that has been withdrawn in other countries, known to be unsafe and they were going to have no active surveillance (3:08) for possible adverse events in this country. Now this was done, he said, for competitive pricing reasons.

The strain of the vaccine that contained the dangerous mumps component was approx. 1/4 the price of the American MMRII made by Merck.

There had been no reports of meningitis using the Merck vaccine which contained a strain of mumps called Jeryl Lynn….So what we had was a cheaper vaccine that was known to be dangerous (3:47).

So when the vaccines were licensed or the proposal to licence these vaccines, the JCVI or members of that committee (4:0) went to SmithKline Beecham and said we want your vaccine. SKB said we are not happy about it because this has already been withdrawn in Canada, it has got this mumps component in it which is dodgy.

They said if we are going to do it then we want an indemnity, we want indemnity from prosecution for damage to children on the basis (4:27) of the receipt of the vaccine. It appears that indemnity was granted, and Torres told us about this (4:33), and he said at the meeting, the girl there from SKB said we are immunising the children and the government is immunising us.

So the vaccine was produced, licensed, given, and cases of meningitis started to appear. They were recorded and documented in the minutes of the JCVI which are now available on line and have been obtained by us as part of our investigation.

More and more cases began to be reported, and the Scottish Dept. withdrew this vax. Certain health areas rejected the Urabe-containing vaccine but still the JCVI continued with it. There was no withdrawal of this vaccine until finally a study was grudgingly done in Nottingham where they found a much higher risk of meningitis with this vaccine (5:33) than had previously been predicted by passive surveillance, and the vaccine was withdrawn overnight, and it was only withdrawn overnight because it was leaked to the press.

It appeared in a newspaper and suddenly the vaccine was pulled. So a dangerous vaccine, a knowingly dangerous vaccine was introduced and ultimately proven to be dangerous and had to be withdrawn (6:00) in 1992.

Part 6 Government liability

You would think under those circumstances having withdrawn this vaccine (3:37) in Australia, Canada and Japan, and the UK that that would be it, they would get rid of it, because it is not safe, but no (3:46) they go on making it, and what do they do with it, they ship it out to the third world.

There was a mass vaccine campaign in Brazil in the 90′s where they gave the great majority of Brazilian children a revaccination with MMR, during a very short space of time, with the Urabe containing vaccine, which they knew to be dangerous, which produced an epidemic of meningitis (4:16), a huge peak in the numbers of cases, and there was a paper written about it after, and one of the points in the discussion in the paper was perhaps it was not a good idea, in effect, to do mass vaccination campaigns because it produced the true incidence of side effects to a vaccine.

Well, who wrote that, who in God’s name wrote that? So this is, if you like, the morality of the people we are dealing with. Why is that vax even on the shelf? Why is it being sold at cut rate price to third world countries? What is the thinking behind this? Because it is certainly not a moral imperative, it must be a commercial one. So that’s why we are here and that is why we will remain here, and continue to fight this (5:12) kind of thing, because you can’t treat people as expendable. You can’t damage them and put them to one side.

Adolph Hitler in Mein Kampf once wrote the greater truth excludes the lesser truth. In the mind of people like Adolph Hitler, that kind of thinking failed in the 1940s and it is going to fail now. You cannot treat people in a civilised society as expendable.

Yes, there may be an argument for a vaccine programme that protects the greater good but that does not mean that you can render those who are damaged, just consign them to the dustcart because they are an inconvenience, or their (6:08) mere presence undermines public confidence, better to keep them hidden out the way and there are too many of these children now, they won’t be hidden away, and parents are getting very very angry, and they have every right to be angry, and the truth is going to come out, and it is going to be a very very painful truth when it does come out.

The tragedy is, it is going to damage public confidence in vaccine policy across the board because people are going to say we don’t believe you any more, we don’t trust you, you lied to us and when that happens all vaccination policy is compromised, the whole pillar of public health comes tumbling down and a lot of trouble is going to ensue as you are going to deal with a population who are not protected from these infections and we are going to run into big problems, and that responsibility for that lays at the door of the public health figures and their commercial partners who have allowed this to happen.

smaller particle size

the 3 added amino acids

The clumping has no effect on solubility: the instant you spoon the collagen into any liquid it all dissolves immediately. That is one characteristic of high bioavailability of course: how fast it dissolves.

These peptide globules are one result from going to the new low molecular weight of 2000 daltons. In addition, the supplemental glycine, carnitine, and glucosamine you see on the label may attract the smaller particles of the collagen, sometimes resulting in small clumps throughout the sample. This didn’t happen in the earlier product because the extra aminos were about the same size as the larger particle collagen.

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The new particle size represents an unprecedented advance in the global collagen industry. Consequently, during the past few months the demand for the new low molecular weight blend has gone through the roof. Manufacturers are struggling to meet the demands and have told us that there may be some delays in production during the summer. This may result in backorders that may last a few weeks. The good news however is that once the production problems are smoothed out, we will be able to obtain all we need and there will be no further delays in delivery.

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Please read the new re-write of the Collagen chapter.