This is an irrefutable statement: Since the CDC has recommended the hepatitis B vaccine right after birth for all newborns and infants in 1991, autism cases have skyrocketed. Today we are going to consider this connection.
Is there a connection between the hepatitis B vaccine and autism? Let’s consider a philosophical argument. If A causes B, and B causes C, can we conclude that A causes C? This appears to be a valid argument. Let’s look at this argument in a specific context.
If (A) Hepatitis B vaccination causes significant increase in vaccine injury, notably (B) Type 1 diabetes, and (B) Type 1 diabetes leads to an increased rate of (C) autism cases, then can we conclude that (A) Hepatitis B vaccination is causing an increase in (C) autism cases?
Many doctors are reluctant to give their own children hepatitis B vaccine.
While it is true that most doctors follow the recommended CDC vaccine schedule for their own children, an inordinate number of doctors are not following the schedule, especially when it comes to hep B vaccine after birth of their newborns. Why the hesitancy? What do they know that we do not know? Why would they not want their children to “be protected” from this virus and its disease?
According to a study found in Miller’s Review of Critical Vaccine Studies, by Neil Z Miller 2016, page 284 titled “Many pediatricians do not vaccinate their own children according to official recommendations,” here are some quotes regarding pediatricians:
“ …34% deviated from the officially recommended timing of vaccinations for their own children.”
“Many pediatricians did not vaccinate their own children against hepatitis B (32%) or Hib (29%).”
While these quotes are easily found in Neil Miller’s book, they can also be found according to the actual study which he so graciously includes:
Posfay-Barbe KM, Heininger U, et al. How do physicians immunize their own children? Differences among pediatricians and non-pediatricians. Pediatric 2005 Nov; 116(5): e623-33. The whole study can be found here:
Most doctors and most people have good reasons for deciding on what they do, especially regarding the health and safety of their own children. Health care professionals know more than most of the general population about the true effects of vaccines on children, and their hesitancy in getting some of these vaccines should be considered as a warning signal for the rest of us who have not been trained in healthcare or medicine.
In the case of the hep B vaccine, perhaps they realize this vaccine is not needed at this time of life for children not born of hep B infected mothers. They rightfully have concluded that hep B is not a contagious childhood disease, and infants and young children have no realistic way of being exposed to hepatitis B virus. Here is a list from the CDC on how a person can become infected with hep B virus. This information can be found on this link:
Vaccine Information Statement: Hepatitis B Vaccine – What you need to know
“Hepatitis B is spread when blood, semen, or other bodily fluid infected with the hepatitis B virus enters the body of a person who is not infected. People can become infected through:
- Birth (if a pregnant woman has hepatitis B, her baby can become infected)
- Sharing items such as razors or toothbrushes with an infected person
- Contact with the blood or open sores of an infected person
- Sex with an infected partner
- Sharing needles, syringes, or other drug-injection equipment
- Exposure to blood from needlesticks or other sharp instruments.”
From this list, it is easy to conclude that hep B is not a contagious disease for young children, and there is only one way a child can be realistically infected by hep B as an infant, and that is by birth from an infected mother. Any vaccine injury caused by hep B vaccine for other than birth from a hep B infected mother is an unnecessary injury. For more information on this topic, please go to my prior blog, which can be found here:
A causes B: (A) Hepatitis B vaccine causes a significant rise in (B) Type 1 diabetes.
There are studies which demonstrate the veracity of this statement. Conversely, there are arguments the Big Pharma side will cite to indicate that this is not a real connection, that it is overstated, and that increased type 1 diabetes rates are due to family history and genetics. This is the usual response to deflect attention away from vaccines as a causative factor of disease that leads many people to conclude that this condition, “… just happens, and it isn’t anyone’s fault.” This is typical of the misinformation the scientific community promotes to push people and their beliefs in a certain direction. It is similar to the genetic theory of autism that they appear to be promoting. But their thinking on this topic is flawed.
The truth is that autism is caused by toxicity. If it were truly a genetic condition, then there could be no cure. The fact that many people have found ways to reduce and/or eliminate toxins from their children’s bodies and cure or lessen their autism proves this as a fact. For one example, Jenny McCarthy alleviated enough of her son’s autism to such a degree that he not only came out of his autistic shell, but he graduated from college and leads a normal life today. Please see the prior blog which goes into this in more detail:
In Miller’s Review of Critical Vaccine Studies, we have two scientific studies which indicate that Hep B vaccine causes Type 1 diabetes. These can be found on page 196, under the heading of this page which is titled: “The hep B vaccine significantly increases the risk of developing type 1 diabetes.”
The first study mentioned is newer, and the quotes from this study that are relevant for this article are:
“In New Zealand, the incidence of IDDM (insulin-dependent diabetes mellitus) in children 0-14 years of age rose by 48% after a hepatitis b vaccination program was initiated.”
“In France, the incidence of IDDM in children 0-4 years of age rose by 61% after a hepatitis B vaccination program was initiated.”
The results from these studies are statistically significant, as they were calculated from whole childhood populations in these respective countries before hep B vaccine programs were implemented, and after their hep B programs became established. It is therefore almost an ideal experiment of vaccinated versus unvaccinated populations. Hundreds of thousands of children were involved in these studies, and the outcome demonstrates, as the author of the paper states:
“There is a 2-4 year delay between hepatitis B vaccination and a rise in the incidence of IDDM, which is consistent with a causal relationship.”
This means there is a cause-and-effect relationship proven here, which indicates that hep B vaccination causes a significant increase of Type 1 diabetes. And not only was this relationship proven in only one population, but rather it was proven in multiple different countries consisting of hundreds of thousands of children, which make the results statistically significant and the results reliable. Only two countries were cited above, but the study actually includes three, which are Italy, France, and New Zealand, and the results from these were consistent with the above noted findings.
The above quotes are from this study: Classen JB. Clustering of cases of IDDM 2 to 4 years after hepatitis B immunization is consistent with clustering after infectious and progression to IDDM in autoantibody positive individuals. Open Pediatr Med J 2008; 2:1-6. The actual study can be found here:
Perhaps this is why a large number of doctors are reluctant to give their own children hep B vaccine. They know that hep B vaccine isn’t needed for infants and young children, aside from hep B positive mothers, and they understand the vaccine injury that may result from this vaccine.
Neil Miller mentions another supportive article for this argument: Classen JB. Diabetes epidemic follows hepatitis B immunization program. N Z Med J 1996 May 24; 109(1022): 195. (Letter.)
While I was unable to find this specific letter as mentioned in Miller’s book, the following link leads to other similar studies. Please click on this link. You do not have to read the studies to understand what the author JB Classen is promoting. Reading the titles will give you enough of a glimpse to see what these studies are about.
Classen JB – Search Results – PubMed
B leads to C: (B) Type 1 diabetes leads to a rise in (C) autism cases.
On page 257 of Miller’s Review of Critical Vaccine Studies we have the title on the top of this page which serves as the conclusion of these studies: “There is a significant link between vaccine-induced type 1 diabetes and the autism epidemic.”
With this conclusion page we have one last study from JB Classen, from Open Access Scientific Reports 2013 May 20; 2(3): 679. The link and title are here:
Quotes from this study:
“There is a direct correlation between the incidence of type 1 diabetes and autism prevalence in children…”
“Simultaneous epidemic of type 1 diabetes and autoimmune/inflammatory autism are likely to have the same root cause.”
A causes C: The conclusion is (A) hep B vaccination leads to an increase in (C) autism.
If A causes B, and B causes C, can we conclude that A causes C? From these studies by JB Classen, we can conclude that (A) hepatitis B vaccine causes a rise in (B) Type 1 diabetes, and (B) Type 1 diabetes leads to a rise in (C) autism cases.
We must give credit where credit is due. Credit is due, first of all, to JB Classen for spending years of his life researching, and then promoting his hypotheses, where he proves beyond the shadow of a doubt that the CDC recommendation for children immediately after birth to get a vaccine for a disease which is not a contagious childhood disease has been causing the increase in autism. Routine hep B vaccination of all newborns has been causing a rise in autism cases.
If you noticed the names on these scientific studies, you can see they have all come from JB Classen. It appears that this one man has made the studies of vaccine injury, Type 1 diabetes, and autism causation a major part of his life’s work. It is time to give this man the credit for bringing these connections to light.
Although his work has been buried by the power of Big Pharma and Big Media working alongside Big Government to bury the truth about vaccine injury from hep B vaccine which appears to cause autism, we now have an administration which may give these scientific studies the credit they deserve. Hopefully, Robert Kennedy Jr. will give this man the credit he is due for his extensive research on these subjects
Also, we must give credit to Neil Z. Miller, author of Miller’s Review of Critical Vaccine Studies 2016, for reviving interest in these studies so that they are not lost in the myriad scientific studies that have been produced over time. Neil Miller’s book is eye-opening on many subjects, and this focus on hepatitis B vaccine being a causative factor for the autism epidemic is only one of many subjects of importance covered in his book. His book is a must read for anyone who wishes to learn more about vaccines and vaccine injury.
It is time to end this madness and this autism epidemic induced by the CDC in 1991. We should change the current recommendation for hep B vaccination to a pre-teen year just before high school. We should test all pregnant women for hep B virus, and only vaccinate those children born of hep B positive mothers. In this way we protect children at risk of hep B exposure at birth, protect older children and young adults from hepatitis B disease at a time of life where it makes sense, and we protect the rest of the children by not giving them a vaccine which is unnecessary for infants and young children, and known to cause vaccine injury, type 1 diabetes, and an increase in autism cases in this country.
A Final Note: JB Classen provides his Theory of the Etiology of the Autism Epidemic.
Hepatitis B vaccine is causing an increase in autism. This does not mean that it is the only contributing factor. In fact, JB Classen makes this point abundantly clear at the end of his 2013 study which has been already noted above, and although I do not completely understand the scientific jargon and the etiology of disease as well as scientists like JB Classen does, I will include it here for those who do:
“Vaccines have shown to cause a large number of cases of type 1 diabetes in both a prospective clinical trial as well as in animal toxicity studies. The pathophysiology is believed to involve vaccine induced macrophage activation, especially by aluminum adjuvants and complex polysaccharides, and resulting in interleukin 1, interleukin 6, and TNF production. It is the belief of the author, based in part on the data present in this manuscript that the epidemics of type 1 diabetes and autoimmune autism are more likely than not to share the same etiological cause.”
This theory goes hand in hand with what JB Classen noted at the beginning of his 2008 study which is also noted above:
“Data from a large prospective clinical trial proved the hemophilus b vaccine (HIB) causes type 1, insulin dependent diabetes (IDDM). Clusters of cases of vaccine induced IDDM occurred starting 36 months after immunization. Clusters of IDDM have also occurred 24 to 48 months following vaccination with several other vaccines including the pertussis and MMR vaccine.”
This theory indicates that toxins within vaccines, especially those which include aluminum adjuvants and complex polysaccharides, induce IDDM and autoimmune autism. Clusters have developed after different vaccinations which seems to indicate that it is the rise of toxicity which occurs in the body after these vaccinations that causes these conditions to occur in children. Since all children are different, IDDM and autism appear at different times according to the differences in the children’s ability to handle these toxins. This goes along with what was stated before, that autism is caused by toxicity.
Based on the above, and on the recent meteoric rise of autism cases, which has occurred in tandem with the hep b vaccine being recommended by the CDC in 1991, it is recommended that:
- Hep B vaccination recommendation by the CDC be changed to a pre-teen year before high school, and only those children born of hep B positive mothers receive the hep B vaccination right after being born.
- Reduce the number of vaccines which include aluminum adjuvants and complex polysaccharides to only those vaccines which are absolutely necessary for children to receive to prevent life threatening contagious diseases. This should reduce toxic exposure from these vaccines and thereby reduce the cases of IDDM and autism.
- Delay the vaccines as long as practically possible for young children, thereby enabling their immature bodies and brains to develop without these toxins affecting their natural growth patterns.