WARNING LABEL ☠️: Vaccines Cause Autoimmune Diseases like Type 1 DIABETES, plus Autism, SIDS, and Higher Mortality in Children (Part 5)
Please tell the world!
BS”D
I just recently learned of two young children, both from families I know, newly diagnosed with diabetes - on the same day. Several days later, I got a call from the mother of an 8 year old girl who became diabetic a year ago.
WHAT IS GOING ON? This isn’t normal! Kids were very rarely getting diabetes in our grandparents’ days. Childhood diabetes has now exploded.
Something has obviously caused this drastic change for the worse. What is it?
Type 1 Diabetes is an autoimmune disease, and as you may have know, it is well established that immunizations can result in autoimmune diseases.
For example:
Predicting post-vaccination autoimmunity: who might be at risk?
https://pubmed.ncbi.nlm.nih.gov/25277820/
Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity
https://pubmed.ncbi.nlm.nih.gov/23609067/
This quote is from Vinu Arumugham’s substack:
Vaccines have a fundamental flaw. They violate basic Nobel-winning immunology from 1913. Predictably, they cause allergies, autism, asthma and autoimmunity.
“Never inject alien proteins into humans.” -Dr. Charles Richet, Nobel 1913.
Steve Kirsch published an article last week specifically linking Type 1 diabetes to children’s vaccines.
Steve says:
I recently interviewed a mother, Debbie Nease, whose son was perfectly normal. He got a vaccine shot and within days, he was a type I diabetic. Is this just an isolated anecdote? It turns out it isn’t.
We know from many studies that vaccines are the primary cause of auto-immune diseases. For example, my survey of over 10,000 kids showed an OR of 22 which means that 95% of autoimmune diseases, in general, are caused by vaccines. Anyone can replicate that survey in 24 hours, but nobody in mainstream medicine will dare to do this.
The same survey showed that kids who were vaccinated were about 4.7 times more likely to get diabetes than kids who avoided all vaccines (and the k-shot).
The clincher is that there is a pediatric clinic in America which has had thousands of fully unvaxxed kids over the last 25 years. The rate of type 1 diabetes in that practice is zero.
Could there be other causes of type 1 diabetes? Of course. But the pediatric clinic is evidence that the vast majority of type 1 diabetes is preventable and the main intervention is stopping the shots.
Here is some of the evidence Steve presented (see link to his article for more.)
• The control group study showed no diabetes in 1,000 people who were fully unvaccinated:
• When you remove the suspected cause, the problem appears to completely disappear. A pediatric clinic with no vaccines has no type I cases in 25 years. This is hard for anyone to explain. It will be written up and submitted to the medical literature. When you combine this fact with the 4.7 odds ratio in the point above, it’s very clear that 75% or more of type 1 diabetes is caused by the vaccine.
• The climbing rates of type I diabetes worldwide with no explanation as kids get more and more shots over time:
• The explanations for the climbing rates of type I diabetes don’t fit because there isn’t a causal link established between any of these factors and type I diabetes. According to this Healthline article, “these factors include the early introduction of cow's milk, short duration of breastfeeding, and perhaps even pollution.” So where is the study showing a later introduction of cow’s milk and a longer duration of breastfeeding fixes the problem?
• Too many “coincidences” among parent reports where their child developed diabetes shortly after vaccination.
Here is Steve’s article:
Dr. Pierre Kory titled his presentation on our July 30th program “Why I Would Not Give My Child Any CDC Recommended Vaccine.”
I urge you to watch the 1.5 hour talk by this brilliant doctor - who believed in vaccines and their safety, until he did more research and changed his mind.
https://rumble.com/v33ge0z-july-30-talking-about-childhood-vaccines-with-dr.-pierre-kory-md.html
For those who missed previous articles about vaccines causing autoimmune diseases, or want to review, here is much more information on the topic:
A Midwestern Doctor wrote on July 21:
The most common side effect of vaccinations are autoimmune disorders. This makes sense, since vaccines work by stimulating the immune system to respond to something, and autoimmune disorders result from excessive activation of the immune system. Although there are many different mechanisms at work here, at this point, I believe the primary ones are as follows:
1. If the immune system develops an immune response to a target protein (an antigen) it will often also develop an immune response to other antigens with similarities to the target antigen, a process known as molecular mimicry which is well recognized to occur with certain infectious organisms (e.g., the bacteria which causes rheumatic fever). Certain vaccine antigens have a higher overlap with human tissue and hence have a higher rate of autoimmune complications.2. Vaccines are typically composed of a target antigen under the theory that exposing the body to the antigen will eventually cause it to develop an immune response to an infection which also has that antigen. Antigens tend to be expensive to produce, so it is often not economically viable to produce enough of the antigen for each vaccine to elicit the needed antibody response.
There are two common solutions to this approach. The first is to create a self-replicating antigen (e.g., with an infectious virus that contains the antigen or an mRNA gene therapy) so enough of the antigen is produced to solicit an immune response. The second approach is to use an adjuvant—a cheap compound like aluminum that provoked the immune system to attack anything there and thereby significantly decreases the amount of antigen needed and thus the cost of the vaccine.The problem with adjuvants is that they will also often provoke the immune system to develop undesirable responses as well (e.g., allergies to pollens circulating at the time of vaccination or autoimmunity to human tissue resembling parts of the vaccine antigen).
3. In medicine, it is often expensive and time consuming to prove a medication will yield a long term benefit. For this reason “surrogate markers,” changes which appear quickly and are assumed to correlate with improved health benefits are evaluated instead. Unfortunately, in many cases, changes in surrogate markets do not actually correlate with a tangible benefit.In the case of vaccines, the surrogate marker is antibody formation. This creates a situation where vaccine manufacturers do whatever is needed to create an antibody response—something which can often be highly problematic. For example, with the HPV vaccine, a major design problem was it not eliciting a sufficient antibody response. This problem was “solved” by using a stronger aluminum adjuvant, which achieved the desired surrogate marker but also had the side effect of creating an extremely high rate of autoimmune complications in the HPV vaccine recipients (making it arguably the most dangerous vaccine on the market prior to the COVID-19 vaccines).
Many have argued an epidemic of neurological and autoimmune disorders characterize the modern age. For example:
Under Dr. Fauci’s leadership, the allergic, autoimmune, and chronic illnesses which Congress specifically charged NIAID to investigate and prevent, have mushroomed to afflict 54 percent of children, up from 12.8 percent when he took over NIAID in 1984.
One of the primary culprits for this change was Fauci brokering a 1986 deal that incentivizing a flood of unsafe childhood vaccines to enter the market:
(BW: A Midwestern Doctor had a similar graphic in his original article but I substituted this one, as it’s clearer.)
A Midwestern Doctor also mentions the critical point that typically, when a pharmaceutical harms someone, it is relatively subtle and hence hard to recognize.
In this meticulously sourced Epoch Times article from February 2023, by Celeste McGovern, titled “Top Doctors Reveal Vaccines Turn Our Immune Systems Against Us,” there is a wealth of information. Here are excerpts.
The Trouble With Aluminum
Aluminum has been added to vaccines since about 1926 when Alexander Glenny and colleagues noticed it would produce better antibody responses in vaccines than the antigen alone. Glenny figured the alum was inducing what he called a “depot effect”—slowing the release of the antigen and heightening the immune response.
For 60 years his theory was accepted dogma. And over the same time, the vaccine schedule grew decade on decade, but few ever questioned the effects of injecting aluminum into the body, which is strange considering its known toxicity.
A PubMed search on aluminum and “toxicity” turns up 4,258 entries. Its neurotoxicity is well documented. It affects memory, cognition, psychomotor control, damages the blood-brain barrier, activates brain inflammation, depresses mitochondrial function—and plenty of research suggests it is a key player in the formation of the amyloid “plaques” and tangles in the brains of Alzheimer’s patients. It’s been implicated in amyotrophic lateral sclerosis and autism and demonstrated to induce allergy.
Further:
With these new observations, researchers began investigating the adjuvant effects of aluminum and in the past decade, there has been a flurry of research. Far from being a sandbag that holds the antigen for a while and then gets excreted, it turns out that aluminum salts trigger a storm of defense action.
Within hours of injection of the same aluminum oxy-hydroxide in vaccines into mice, for example, armies of specialized immune cells are on the move, calling in grid coordinates for more specialist assault forces.
Within a day, a whole host of immune system commandos are in play—neutrophils, eosinophils, inflammatory monocytes, myeloid and dendritic cells, activating lymphocytes and secreting proteins called cytokines. The cytokines themselves cause collateral damage but they send out signals, directing cell-to-cell communication and recruiting other cells into action.
If the next phase of the attack is launched—fibroblast growth factor, interferons, interleukins, platelet-derived growth factor, transforming growth factor and tumor necrosis factor might all be engaged. There’s evidence that poorly understood and pesky inflammasomes, (currently a topic of cutting-edge cancer causation research) such as the NOD-like receptor 3 are activated too, but it’s all still too early to say exactly what they’re doing.
New research emerging from the University of British Columbia has found that aluminum adjuvant injected into mice can alter the expression of genes associated with autoimmunity. And in their recent study published in the Proceedings of the National Academy of Sciences, immunologists at the University of Colorado found that even host DNA is recruited into the aluminum assault, that it rapidly coats injected alum, triggering effects that scientists have barely scratched the surface of understanding.
See Epoch Times article:
Remember the list of 38 vaccine ingredients in Part 2? Aluminum isn’t the only troublesome component.
Discussing autoimmunity caused by injecting foreign proteins in the human body, Vinu Arumugham writes:
Animal protein containing vaccines cause autoimmune diseases even when the vaccine does not contain an adjuvant. Adjuvanted vaccines only make the problem worse.
Vaccines interact to cause autoimmune diseases.
Immunization with homologous xenogeneic (animal/plant/fungal) antigens causes the development of autoimmune diseases.
This has been known for at least 45 years.
Jacob et al. found 293 chicken proteins + bovine proteins in the influenza vaccine.
Similarly, one can expect hundreds of bovine proteins in the DTap/Tdap vaccines as casein or casamino acids derived from bovine milk is used for culture. One of those milk proteins is the bovine folate receptor alpha protein. Cow's milk protein contaminated vaccines (DTap/Tdap, Prevnar 13, ActHiB) therefore cause IgE mediated sensitization to bovine folate receptor alpha (FRA). Once sensitized, upon consuming milk, the person starts making IgG4 antibodies directed against FRA. These IgG4 cross-react with human FRA in the choroid plexus, block folate uptake to the brain thus resulting in cerebral folate deficiency (CFD).
I mostly focused on diabetes and autoimmunity in this article, but there is so much proof of the vaccines causing Sudden Infant Death Syndrome, increased mortality in children, and autism, that there can no longer be any question about it: our children have a much better chance at life and health without these injections.
I regret that my children are vaccinated.
Please see the powerful articles on SIDS, all-cause mortality, and autism below, and please share!
https://childrenshealthdefense.org/defender/infant-vaccines-all-cause-mortality/
1 in 36 Kids Have Autism, CDC Says
One in 36 (2.8%) 8-year-old children — 4% of boys and 1% of girls — have an autism spectrum disorder (ASD), based on an analysis of data from 2020, published today by the Centers for Disease Control and Prevention (CDC).
The trend has persisted for decades. Autism prevalence in the 1990s, which was 1 in 1,000 children, already represented a tenfold increase over the condition’s estimated prevalence in the 1970s.
Here is what 1 in 36 “looks” like.
Dr Chris Exley has a sub stack. He's studied aluminum for decades. He's another scientist who's lost funding and job to prevent dangers of this in jabs.
Exactly correct. Look at the Amish kids. No vaccines, no autoimmune disease, no autism, no ear infections, no SIDS.
There are also a few old time honest pediatricians who will tell you privately that the unvaccinated children in their practice are healthier and better developed than the vaccinated.