Posted on May 22, 2023
A Midwestern Doctor
Is there a benefit to developing the disease naturally that is prevented by vaccination?
One of the lesser known facts about diseases is that childhood infections are often critical for helping the immune system develop. A variety of diseases that are much more severe in adults than their corresponding “vaccine preventable” childhood infections are observed to result from not catching the disease in childhood. Some examples include:
-Not having a chickenpox infection increasing your risk of glioblastoma (a horrible brain cancer) later in life.
-Not having a mumps infection increasing your risk of ovarian cancer (one of the most deadly cancers for women).
Note: this research substantiating these links and more can be found here.
Vaccine Side Effects
An explosion of chronic illness (particularly of neurological and autoimmune nature) in our society has paralleled the mass vaccination of society.
At this point, we have never had a study performed on the cumulative effects of children receiving the entire vaccine schedule.
Since these studies have thus far never been completed, a variety of less controlled ones (e.g., comparing vaccinated and unvaccinated children in the same medical practice) are published. While these studies show a massive number of complications arise from vaccination, they are typically dismissed as not being valid since they weren’t a controlled study, and in many cases, the authors are attacked (e.g., consider what happened to Paul Thomas). Similarly, I and many colleagues can often immediately recognize children who were never vaccinated (as they are healthier in the body, mind and spirit), yet the changes vaccination create have become so normalized in our society, most doctors now lack the ability to recognize the currently accepted baseline is not normal.
For each vaccine, as we consider the risk of its disease, the efficacy of the vaccine, the effects of developing vaccine immunity within a population, the issues with vaccinating while infected, and vaccine side effects, it should become clear that this is an immensely complex question to answer. There are so many potential risks and benefits of different magnitudes that combining them into a weighted average borders on the impossible.
When I approach this question I use the following algorithm, where each item takes precedence over the ones after it.
I will now briefly discuss some of the vaccines on the current CDC schedule that I feel are the worst offenders.1. Does the vaccine have an unusually high degree of toxicity?
2. Does the vaccine potentially provide an important benefit?
3. Does the vaccine have other reasons to make me concerned about its potential side effects?
4. Does the vaccine actually work?
5. Does the vaccine still work?
GardasilFirst, let’s consider the HPV vaccine and the benefits it created by “preventing cervical cancer.”
While I have seen datasets (when stratified by age) showing Gardasil (and other HPV vaccines) actually increased the cervical cancer death rate in those vaccinated, I will give it the benefit of the doubt here. As the graph shows, cervical cancer rates were already approaching 0 before Gardasil, so it is difficult to say if any of the lives saved were due to it (at this point I believe the cancer prevention attributed to Gardasil is false).
Note: many other diseases whose decline was attributed to vaccination also actually had most of their decline occur prior to a vaccine being available.
This means, in the best case scenario for the vaccine, for 100,000 people you traded killing 89.3 of vaccine recipients in return for saving 2.
Even though this is terrible, the greater issue is that in the original HPV clinical trial, between 2.3% to 49% of the individuals who received Gardasil developed a new autoimmune condition. We do not know exactly where in that range the total number of new autoimmune disorders was, as Merck classified many autoimmune disorders simply as “new medical conditions” (industry trials always reclassify something they don’t want to show up in the final trial with vague labels like this), but other investigations have concluded the 2.3% figure significantly underestimated the rate of new autoimmune conditions.
Diphtheria, Pertussis and Tetanus (DPT)
I am not a fan of the DPT vaccine for the following reasons:
•It is the vaccine most clearly linked to infant deaths (I summarized the extensive degree of evidence substantiating the link that has accumulated over the last century here).
•The vaccine frequently causes permanent brain damage (especially the older version of it). In addition to hearing this from many parents, this happened to two members of my extended family who received the slightly older and more toxic version of it.
•I believe it is one of the primary causes of childhood ear infections (one of the most common complaints parents see their pediatricians for). Many doctors have observed this link, and the best example I heard of came from a doctor and medical missionary who decided to vaccinate an ashram (Indian temple) he was staying in. Before the vaccines, ear infections were non-existent, immediately afterward a large number of children came down with them.
Conversely, I believe the benefit is minimal because:
•The vaccine does not prevent the colonization of any of these bacteria. This is why pertussis outbreaks occur in fully vaccinated populations.
•Diphtheria is now non-existent in the United States, so there is no reason to vaccinate against it (additionally it can be treated with modern antibiotics).
•Tetanus is now very rare (there are approximately 30 cases a year) and it’s actually difficult to say how much the vaccine antibodies protect a person from tetanus (studies have shown that the vaccine produced antitoxin does not prevent tetanus).
As stated above, I do not believe childhood hepatitis B vaccines can be justified. Additionally, the vaccine does create complications and has been repeatedly associated with neuromuscular autoimmune conditions. I believe that this is most likely due to the fact that the antigen used shares a homology with myelin (the coating of nerves), but it may be for other reasons as well.
As discussed above, it is a bit of a debate if the MMR vaccine decreases measles rates, since while regular vaccination does reduce measles rates, permanent immunity to it disappears within the population, and outbreaks will still occur within the vaccinated population. Sadder still, deaths from measles had almost completely disappeared at the time the vaccine for it was introduced (so there was essentially no justification for introducing it), and in effect by creating the vaccine we turned a non-existent problem into a permanent one by doing so. From my perspective, the greatest problem with the MMR vaccine is its frequent association with autism, something I believe is much worse than developing measles and something you are at a much higher risk for than the infection itself.
Two types of polio vaccines exist. The inactivated polio vaccine (currently used in the USA) and the live attenuated one (frequently used in poorer nations). The inactivated one does not prevent you from catching polio, but does to some extent (I don’t know how to calculate the exact figure) prevent a polio infection from causing polio-like paralysis. Since it does not prevent infection, it has no effect on transmission. The live polio vaccine does prevent you from becoming infected with polio, but has the unfortunate side effect of sometimes causing polio in the recipient and spreading the weakened polio virus into the environment.
At this point, the polio virus is mostly extinct, and from 2017 onwards, more cases of polio have resulted from the vaccine than polio itself (note: one of my friend’s relatives developed polio from the vaccine). One of the most tragic examples occurred in India where Bill Gates diverted their health budget to aggressively vaccinating against polio, which resulted in 491,000 children developing a “polio-like” illness.
There is presently no evidence that the (often mandated) influenza vaccine prevents an individual from getting the flu (which, in most cases, is a relatively benign infection) or transmitting it to others. Additionally, there is evidence that the vaccine increases your likelihood of developing a severe case of influenza and developing influenza in the subsequent year. Furthermore, many individuals have developed injuries from the influenza vaccine.
Initially, due to the severity of a Neisseria meningitidis infection, I initially thought the meningococcal vaccine would probably be a vaccine you could make a strong case for. Unfortunately, there are multiple dangerous strains of this bacteria, and one of those strains (strain B) is very difficult to make a vaccine for, since it has homology with tissue of the human body.
Not surprisingly, this has created a selective pressure on the bacteria and now the majority of infections are caused by strain B, which until recently, the scheduled vaccine did not cover (and at this point I am unsure how effective this newer vaccine is). Furthermore, as discussed above, many people carry this bacteria and are asymptomatic—the infection is very rare and the primary group at risk are those with pre-existing susceptibilities, not the general population. Additionally, tonsillectomies (an unnecessary procedure) significantly increase one’s risk for meningitis.
Conversely, the vaccine has a variety of potential autoimmune complications. By far the most common one I encounter is that it causes Crohn’s disease (typically a few months after vaccination), and I think this side effect alone outweighs any potential benefits from the vaccine.
Pneumococcal and Haemophilus influenzae type B (HiB)
These two are probably the most difficult routine vaccines to have a clear-cut position on. This is because:
•These two infections, especially HiB are the vaccine-preventable illnesses that are the most likely to cause severe complications in children. For example, when the HiB vaccine came out, pediatricians around the country noticed a significant decline in the rates of infants with meningitis, which is a big deal. Similarly, in modern-day pediatrics, many of the most common concerning infections doctors encounter are pneumococcal.
•Although these vaccines have adverse effects, they are not as dangerous as those of many other vaccines.
•Because these vaccines work but target an easily mutable part of the bacteria, their adoption triggers their target bacteria to mutate, become resistant to the vaccines, and, in some cases, affect different populations. For example, the pneumococcal vaccine is continually being updated and re-released, with additional strains being covered in each successive version (and I’ve seen multiple vaccinated children with potentially life-threatening pneumococcal infections who had been vaccinated). In the case of the HiB vaccine, it selected for the A strain (HiA), which in some areas was more deadly than HiB, and also selected for strains that affected adults (typically HiB only affects children), leading to severe HiB infections becoming a disease of adults and the elderly.
THANKS TO: https://stuartbramhall.wordpress.com/2023/05/22/inventory-of-vaccine-risks-and-benefits/