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‏إظهار الرسائل ذات التسميات squalenes. إظهار كافة الرسائل
‏إظهار الرسائل ذات التسميات squalenes. إظهار كافة الرسائل

An Open Letter to Dr. Steven Novella Concerning His Positions on Vaccines and Autism and Dr. Novella's Reply

UPDATE: See end of this comment for Dr. Novella's reply

Dear Dr. Novella

I am a parent of a 13 year old boy with Autistic Disorder. I also have a blog site on which I commented unfavorably on your response to the possibility that the IACC might recommend some vaccine autism research. I ask your response to a few questions if you have the time and are inclined to respond.

One is your apparent opposition to any further research exploring possible vaccine autism connections. I am not an "anti-vaxxer". I have never attributed my son's autism to vaccines. Until recently I accepted the official view that vaccines play no role in causing autism. More recently my views have moved toward an undecided position. This change began when reading Dr. Bernadine Healy's observations about the limitations of the epidemiological studies which are usually used to allegedly "debunk" any vaccine autism connection. In her comments she indicated that such studies are not specific enough to address the possible impact of vaccines or their ingredients on potentially vulnerable population subsets.To this layperson Dr. Healy's criticism seems reasonable as does her call, a call also made by Dr. Julie Gerberding, that an observational study comparing autism rates in existing vaccinated and non vaccinated populations could and should be done. Your opposition to further vaccine autism study does not, with respect, seem either reasonable OR science based. I ask if you could provide a clear rationale for opposing a study which has been called for by two prominent health authorities and which might provide useful information to what is a heated debate on all sides.

The second question I have for you concerns the increase in autism diagnoses which has really been quite startling by any measure. In my son's lifetime the figure has changed from 1 in 500 to 1 in 150 with the two recent studies indicating it might now be 1 in 91. Many authorities dispute though that the increases are real pointing to the autism definition changes in the DSM and ICD diagnostic manuals in the 1993-4 period and increased social awareness as the reasons for the increases in diagnoses. Is it your view that the increase in autism diagnoses does not reflect a real increase in autism disorders? If so what are the implications of that position for the argument that epidemiological studies have disproved any thimerosal vaccine link because autism rates increased after removal of thimerosal from MOST vaccines?

Also if you have the time and inclination do you think Dr. Healy's observations that thimerosal which continued to be found in flu vaccines, some of which historically were administered to pregnant mothers, was a matter worthy of investigation given that the thimerosal crosses the placenta is a legitimate concern worthy of further investigation? This is an important matter here in Canada where the squalene adjuvant was removed from the vaccines given to pregnant women but there has been no indication that thimerosal has been removed.

I would genuinely appreciate your responses to these questions which I am posting on my blog site. If you do me the courtesy of an informed reply I would be happy to post that reply as well.

Respectfully,


Harold L Doherty

cc. Facing Autism In New Brunswick

UPDATE:

Dr. Novella's Reply:

Harold,

Thanks for your thoughtful e-mail. I would be happy to address your questions.

Regarding further research - it is always possible, in the face of negative results, to call for still more research. And it is easy to make this seem like the default scientific position. ESP proponents, after a century of failed research, call for still more research, and accuses anyone who says further research is not worthwhile of being unscientific.

Also, to clarify my position, I am not categorically against further research into vaccines and autism. I think any such research is most likely to confirm the lack of a correlation. And if there is a susceptible sub-population, of course it would be good to know about it to make the vaccine program even safer. (But keep in mind - it is a common form of special pleading to argue that, when the effect you are looking for is absent, that is only exists is a subpopulation that existing data was not powerful enough to detect. This may be true, but it is just post-hoc speculation, and doesn't change the fact that the data is negative.)

My position is that ideological groups should not be dictating how scarce research funds are allocated. When we put money, people, and resources into chasing down an unlikely hypothesis those resources are not available for what might be more promising research. My position is that objective scientists, justifying their position with a careful analysis of the research, should decide how best to allocate scarce research funds. The anti-vax movement, however, is trying desperately to put their thumb on the scale - and that is what I oppose. They are trying to subvert autism activism to serve an anti-vaccine agenda - and they are hurting the autism community as a result, in my opinion.

I respect Healy and Gerberding, but I disagree with their approach in that they think more research will satisfy vaccine critics, but this is a naive position. The anti-vaccine movement has already demonstrated that they are impervious to facts and evidence, and spending time and money trying to placate them is a fool's errand. The CDC even went as far as to include them in designing a trial looking at vaccines and neurological disorders, and then only after the results came back negative, did they criticize the study.

You specifically mention an observational study comparing vaccinated and unvaccinated children - I do not oppose this. If it can be done with reasonable resources, there are scientists willing to carry out such a study and think it is worthwhile, and the results will be useful, then I fully support it and await the results. (And in fact I have never opposed such studies.) What I and others have written is that an experimental (not observation) comparison of vaccinated vs unvaccinated children is unethical, because it would randomize children to no get standard preventive care, and that directly violates human research ethical guidelines. Observational studies are fine, but they are never definitive, and they will not, in my opinion, change or end the debate. They will not move the anti-vaccinationists one bit

The increase in autism diagnoses has been studied from multiple angles - not just the expansion of the diagnosis.

You will find a summary of relevant research here: http://sciencebasedmedicine.org/reference/vaccines-and-autism/

So far, every way it has been looked at the hypothesis that the increase in diagnosis of ASD is due to increased surveillance and expanded diagnosis has been confirmed. There is evidence of diagnostic substitution (as ASD numbers increase, the numbers of other similar diagnoses decrease). There is evidence that different age groups have the same prevalence of ASD (rather than increasing with younger age, as would result from a true increase in ASD). And if you apply the same diagnostic and surveillance methods to a cohort over time, you get the same ASD prevalence. The data is actually quite convincing that true autism rates are not significantly increasing (you cannot rule out a small real increase, or decrease for that matter, that the data is not powerful enough to detect) but that there has been expanded diagnosis with diagnostic substitution and increased surveillance.

I discuss this further here ( http://www.sciencebasedmedicine.org/?p=95) and here ( http://www.sciencebasedmedicine.org/?p=340)

The implications of this position to the alleged thimerosal link is complex, but supports a lack of correlation. What the data shows is that in various countries ASD diagnoses began to rise around the same time (as diagnostic patterns changed), in the early 1990s, and have continued to rise through today. Meanwhile, vaccine policies have varied considerably with regard to total thimerosal dose, with several countries, at different times, removing most thimerosal from vaccines. Every study looking at the data shows no correlation between the steadily increasing ASD diagnostic rates with the rising and falling thimerosal doses at different times in different countries. This is powerful evidence for a lack of correlation. As you likely know, toxicity is always about dose, and seeing a proper dose-response is essential to proving toxicity causation. What we have with thimerosal is an absolute lack of any dose-response, in many studies and sets of data.

Also, please keep in mind that the anti-vaccine movement used the increase in ASD in the 1990s as their original justification for the claim that thimerosal causes autism. They predicted that autism rates would decline after thimerosal was removed from the childhood vaccine schedule, and we agreed that if that happened we would need to rethink the possibility of a connection. Well, rates continued to rise without a blip, effectively putting the final nail in the coffin of the thimerosal hypothesis.

Regarding thimerosal and pregnancy, to the extent that this has already been studied (again, you can find references in the vaccine-and-autism link above) there has been no correlation. I do not oppose further research, however, if the CDC or others think it is warranted and feasible.

Thanks again for the interesting questions, and I hope this adequately clarifies my position.

Regards,

Steve Novella

PS - You can publish my response on your blog, and I will do likewise.








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New Brunswick's H1N1 (Swine Flu) Vaccine Autism Experiment

New Brunswick is about to conduct its own H1N1 Vaccine Autism experiment. The H1N1 vaccines used here will contain both thimerosal AND unspecified adjuvants. As with most public health authorities the NB government information is not balanced concerning the possible risks associated with the vaccines generally and specifically with respect to possible vaccine autism connections. There is frequent mention of authorities like the WHO which called this H1N1 flu virus a pandemic in the first place, and the CDC, in supporting the safety of the vaccines generally.

There is also the usual one sided information concerning possible vaccine autism connections, information which fails to mention credible health authorities like Dr. Bernadine Healy, Dr. Julie Gerberding and Dr. Jon Poling who have said that more research needs to be done on vaccine autism issues. Nor does the information release mention the critique offered by those like Dr. Healy who points out that the "science" to date on vaccine autism issues, the epidemiological studies, are not specific enough to determine the impact of vaccines on vulnerable population subsets, on individual children with conditions that might render them vulnerable. Dr. Healy also points out that flu vaccines have contained thimerosal and thimerosal crosses the placenta. (Dr. Poling, a neurologist, was involved with the issue with his daughter on whose behalf it was successfully claimed that her autism resulted from vaccination. The US government settled on the basis that her "autism like symptoms" were caused by the vaccine aggravation of her pre-existing mitochondrial disorder).

The NB government communication release does not mention that no observational study has been done comparing autism rates of vaccinated populations with autism rates of unvaccinated populations. With the use of vaccines containing thimerosal and adjuvants, most likely squalene, with pregnant women and young children targeted for early receipt of the H1N1 vaccines, the NB government is essentially conducting such a study. Hopefully they will remember these events in assessing NB autism rates 2 to 5 years from now as the young children vaccinated with the thimerosal and adjuvant (squalene) and the new born children of vaccinated pregnant women mature.

I don't know if vaccines cause or trigger autism. I am no longer assured by overstated health authority pronouncements that vaccines do not cause autism, that the science is closed on these issues, when people of such credibility as Dr. Healy, Dr. Gerberding and Dr. Poling say more research is needed.

I do hope that our NB health authorities turn out to be right whether it is from a lucky guess or not. I hope that they save every child and adult from H1N1 flu death with no resulting cases of autism. But I am far from convinced that such will be the case. I absolutely hope that they remember this H1N1 flu vaccine and assess future autism rates with an eye to its ingredients - thimerosal, squalene and whatever other ingredients it contains. And it is probably hoping for too much for them to actually record and compare the autism rates of children who are vaccinated with the H1N1 vaccine and those whose parents refuse the vaccination for them. Time will tell.







H1N1 flu virus update (09/10/08)

NB 1521

Oct. 8, 2009

FREDERICTON (CNB) - The following update on the H1N1 flu virus was issued by the Office of the Chief Medical Officer of Health for New Brunswick on Thursday, Oct. 8:

  • We have moved forward with our seasonal vaccination program, according to plans. It started last week and will run for the month of October. The public awareness piece accompanying the campaign speaks to those most at risk of developing complications from seasonal influenza. They are: children six-to-23 months old, pregnant women, people with chronic health conditions, and the elderly. We encourage these groups to get the publicly funded vaccine. A list of clinics by region may be found at www.gnb.ca/flu.
  • There has been a frequently referred to, but as-yet unpublished, Canadian study that suggests an association between seasonal flu vaccine and acquiring a mild case of the H1N1 virus. This study is inconsistent with other international studies, and has failed to show a relationship that one causes the other. Both the Public Health Agency of Canada and the World Health Organization have responded to the study, saying that preliminary data show that there is no link between having a severe bout of pandemic flu and having had a seasonal flu shot last year. New Brunswick's position on this study has never changed.
  • We know that seasonal flu is fatal to 100-150 New Brunswickers each year, and that children are hospitalized by influenza more than any other age group.
  • In making decisions for the province, we balanced this known significant risk and a vast body of published research against the results of one unpublished study, and determined that the best way to protect all New Brunswickers from both diseases was to move ahead with our plans to run a seasonal flu immunization campaign in October, and an H1N1 immunization campaign through November.
  • We are running both campaigns because it is the best decision for New Brunswick. We made operational decisions early on that will allow us to have the capacity to offer both vaccines.
  • There has never been a one-size-fits-all approach to seasonal vaccines in Canada, and this year is no different. Provinces and territories have not previously had to administer two separate flu immunization programs in a single season, and some of the decisions taken on seasonal and H1N1 vaccine timing reflect concerns over logistics, capacity and likely vaccine uptake.
  • The seasonal flu vaccine is safe, and those in the high-risk groups, in particular, should take the steps to receive it as soon as possible.
  • There have also been reports and public speculation about the safety of the H1N1 vaccine. The contents of the H1N1 vaccine will protect against contracting H1N1. The included additives and preservatives are there to help the vaccine work, and are not cause for alarm.
  • As a multi-dose vaccine, the H1N1 influenza vaccine will contain a mercury-based preservative called thimerosal to prevent contamination of the vaccine by serious infectious agents from the growth of bacteria. Thimerosal also has a stabilizing effect on the vaccine, ensuring its effectiveness.
  • The seasonal flu vaccine and most hepatitis B vaccines are also multi-dose vaccines, and thimerosal is added during the manufacturing process to maintain sterility of the vaccine.
  • There is no safety reason to avoid using vaccines containing thimerosal. The best available scientific evidence to date shows no link between vaccines containing thimerosal and any adverse health condition, including neurodevelopmental disorders such as autism.
  • The National Advisory Committee on Immunization (NACI) has reviewed the safety of thimerosal and concluded that, "There is no legitimate safety reason to avoid the use of thimerosal-containing products for children or older individuals, including pregnant women." International bodies, such as the World Health Organization (WHO) and the U.S. Food and Drug Administration, share this opinion.
  • Most of the H1N1 vaccine available in New Brunswick will also contain an adjuvant. An adjuvant is a substance that is added to a vaccine in order to boost an individual's immune response. It also means that less of the virus, or antigen, is needed to make a dose of the vaccine. Unadjuvanted vaccine has no booster element, and more antigen is needed to create this kind of vaccine.
  • By developing an adjuvanted vaccine, Canada has used less of the virus material (antigen), allowing us to immunize more people in a timely manner.
  • Adjuvants are not new. Many commonly used vaccines in Canada contain an adjuvant. Adjuvants have been used for several decades to boost immune response to vaccines. However, adjuvants have not previously been used with influenza vaccines in Canada.
  • The WHO has indicated that it has no special concerns about the safety of adjuvanted H1N1 vaccines in general.
  • New Brunswickers should continue to protect themselves and those around them by washing their hands thoroughly and often, coughing or sneezing into sleeves, staying home if sick, and keeping common surfaces clean.
  • Persons at high risk of complications from influenza-like illness should seek medical attention promptly. Those at risk include pregnant women, people with underlying medical conditions such as diabetes, or those with compromised immune systems.
  • Persons with influenza-like symptoms should stay home and minimize contact with family members as much as possible. If symptoms worsen, they should visit their physician or nurse-practitioner, a walk-in clinic or the nearest hospital emergency department.
  • It is recommended that persons with influenza-like symptoms limit contact with other people, including other household members until they are free of symptoms and are feeling well.
  • Those experiencing influenza-like illness should consider ending self-isolation when they are able to participate fully in all of their normal daily activities.
  • It is important for New Brunswickers to understand that if they do not have influenza-like symptoms it is safe to go to work and school, to participate in activities and to socialize.
  • More information on the H1N1 flu virus may be found online, or by calling the 24-hour H1N1 line, 1-800-580-0038.
  • 09/10/08

    MEDIA CONTACT: Danielle Phillips, media relations, H1N1 Pandemic, Department of Health, 506-444-3821, flumedia@gnb.ca.




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More Autism on the Way? Swine Flu Vaccine Adjuvants, Thimerosal and Autism

Pregnant women will be at the front of the line for the Swine Flu vaccine in many countries. Mercury in thimerosal crosses the placental barrier. So thimerosal will not be used in the Swine Flu vaccine right? WRONG!. Thimerosal will be used and its negative effects, including possibly autism in some of the women's children, could be enhanced by the aluminum adjuvants used in the vaccines.

Australian scientist Vera Scheibner Ph.D., has described the effects of aluminum adjuvants including the enhancement of mercury toxicity and possible autism implications amongst a host of other health issues in The Terrifying World Of Vaccine Adjuvants:

Adjuvants are formulated compounds, which when combined with vaccine antigens intensify
the body’s immune response. They are used to elicit an early, high and long-lasting immune
response. “The chemical nature of adjuvants, their mode of action and their reactions (side
effect) are highly variable in terms of how they affect the immune system and how serious their adverse effects are due to the resultant hyperactivation of the immune system. While
adjuvants enable the use of less *antigen to achieve the desired immune response and reduce vaccine production costs, with few exceptions, adjuvants are foreign to the body and cause adverse reactions”, writes Australian scientist Viera Scheibner Ph.D, (1) The most common adjuvant for human use is an aluminum salt called alum derived from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific literature reveals that the neurotoxic effects of aluminum were recognized 100 years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer’s disease and other neurological disorders.

The article cites Boyd Haley for the proposition that vaccines which contain both aluminum adjuvants and mercury based preservative, greatly magnify the neurotoxic effects. The article comments on squalenes used in vaccines and a process called molecular mimicry and ties molecular mimicry to the autism epidemic:

Tying molecular mimicry to the autism epidemic, many children have regressed into autism spectrum disorders after injection with the triple live virus MMR (measles,mumps,rubella) vaccine. Dr.Vijendra Singh’s research at Utah State University suggests that auto-antibodies are attacking myelin in these children. He has shown that many autistic children have auto-antibodies to brain myelin basic protein (MBP) as well as elevated levels of measles virus antibodies. “Immunoblotting analysis showed the presence of an unusual MMR antibody in 60% (75 of 125) of autistic children, but none of the 92 normal children had this antibody. In addition, there was a positive correlation (greater than 90%) between MMR antibody and MBP auto-antibody, suggesting a causal association between MMR and brain autoimmunity
in autism. This is one of the most important findings in autism to date, which prompted us to link measles virus in the etiology of the disorder”, writes Dr. Singh. (8,9,10)

These excepts are a small selection of the information contained in this article which I recommend for reading by anyone who is interested in reading beyond the standard public health authority assurances about the possible consequences of the still not tested Swine Flu Vaccines. Although I have extracted sections directly referencing autism the article covers many other issues associated with vaccine adjuvants.




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