Part 3: Vaccines Cause Autism and Autoimmune Diseases
Part 3: Vaccines Cause Autism and Autoimmune Diseases
They don’t make anyone healthier. To the contrary.
BS”D
I want to share this piece from Unbekoming’s substack:
We don’t need to beat around the bush here.
Autism is a vaccine injury. It’s no more complicated than that. The machine, THEY, have a global campaign to convince you it’s not, but true is true.
Let’s start with a Facebook post from Maready in May 2019 promoting his 2019 book The Autism Vaccine.
One of the most jaw-dropping discoveries I made while researching "The Autism Vaccine" took place in Austria. I was initially intrigued by the autism story when I realized that the first time aluminum had been used in a pediatric vaccine was less than a year before Donald Triplett—the first child ever officially diagnosed with autism—was born. Knowing that recent scientific study has pointed towards elevated levels of aluminum in the brains of children with autism, I began to research when this new ingredient was first added.
The story of WHY it was added is fascinating, but WHEN it was added—1932—is really important. Before that year, you will only find a rare mention of a few kids here and there resembling the modern diagnosis of autism. It was extremely rare before 1932—so rare that even the most prominent child psychiatrist in the country had never seen any children with it. In 1932, the decision was made to add aluminum to a vaccine because it seemed to make it work better. Within a year or two, accounts of parents noticing aloneness in their children or obsession with repetitive patterns and behaviors began to appear.
In Baltimore, a famous child psychiatrist named Leo Kanner began to see children—mostly boys—show up in his clinic with a strange set of behaviors he had never seen before. This coincidence in time was enough to make me want to understand if there was a possible relationship between the addition of aluminum in 1932 and the sudden appearance of children with autism.
I explored this lead for quite a while and became convinced they were related. It seemed unlikely that the one country in the world that made this change would begin to see autism within a year after having done so. What I realized later was that the United States wasn’t the only country to make this change. There was another, and in fact, like the United States, they were struggling with a massive outbreak of diphtheria and had begun to launch nationwide campaigns to have every child in the country immunized—with the new aluminum-containing vaccine.
The United States was using a very nasty type of aluminum called potassium aluminum sulfate, sometimes called potash. Scientists in Denmark had experimented with something different—aluminum hydroxide and noticed that this type of aluminum caused fewer granulomas, or nodules than the American’s potassium aluminum sulfate. In Austria, they noticed this difference, and in their national campaign to immunize their children against diphtheria, they added aluminum hydroxide to their vaccines.
If you don’t know the story, there was another child psychiatrist in Austria who began to see young patients show up at his clinic—their parents confused as to what had happened to their previously healthy children. Hans Asperger was at a loss to explain what was causing these children to experience strange neurological symptoms. He saw over 200 children—every one of them boys, and they closely resembled the children Leo Kanner had seen in Baltimore.
It should strike anyone as remarkable that the two countries which launched nationwide diphtheria immunization campaigns in the 1930s using a new aluminum-containing shot were the very two countries where autism was first noticed and documented. Other countries may have employed the new ingredient in their diphtheria vaccine, but from what I can tell, no one was running nationwide campaigns like the United States and Austria.
This was simply too much for me to accept as coincidence: Two countries began running nationwide immunization campaigns for their children, with a new vaccine that contained aluminum, and within a year or so, those same two countries began to see the appearance of a new neurological disorder that would later be called autism. The United States and Austria—the two countries where the case reports first describing autism appeared. Coincidence? You decide.
If you did not yet read Part 2 of my series, which shows the overwhelming correlation between vaccine dosages and rates of autism, please see it here:
In Part 3, I want to explore in more depth how vaccines cause autism (and touch on autoimmune diseases.)
Thank G-d, I found a meticulously sourced Epoch Times article from February 2023, by Celeste McGovern, titled “Top Doctors Reveal Vaccines Turn Our Immune Systems Against Us,” which provides a wealth of information. I will include 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.
The Significance of Macrophagic Myofasciitis
This mobility or “translocation” of aluminum in the body is perhaps the most disturbing of the mounting evidence in current aluminum research. In 1998, French researcher Romain Gherardi and his colleagues observed an emerging condition of unknown origin that presented in patients post-vaccination with chronic fatigue-like symptoms including swollen lymph nodes, joint and muscle pain, and exhaustion.
Tissue biopsies of the patient’s deltoid revealed lesions up to 1 cm in diameter and unique from similar lesions of other diseases. They went to the lab for analysis and to Gherardi’s astonishment, they mainly consisted of macrophages—large white blood cells in the immune system whose job is to swallow up foreign invaders in the body. Enclosed in the cellular fluid of these phagocytes were agglomerates of nanocrystals of aluminum.
Gherardi and his colleagues began injecting mice with aluminum to see what happened. Their research published in 2013 revealed that the metal particles were engulfed by macrophages and formed MMF [magnetomotive force]-like granulomas that dispersed—to distant lymph nodes, spleen, liver, and eventually the brain.
“This strongly suggests that long-term adjuvant biopersistence within phagocytic cells is a prerequisite of slow brain translocation and delayed neurotoxicity,” writes Gherardi in his February 2015 review of the relevant research in Frontiers in Neurology.
A more frightening animal study of aluminum is that of Spanish veterinary researcher Lluis Lujan’s study of ovine ASIA. After huge numbers of sheep in Spain died in 2008 in the wake of a compulsory multiple-vaccine campaign against bluetongue in Spain in 2008, Lujan set out to find out what killed them—and he began by inoculating them with aluminum.
His 2013 study found that only 0.5 percent of sheep inoculated with aluminum vaccines showed immediate reactions of lethargy, transient blindness, stupor, prostration, and seizures—“characterized by a severe meningoencephalitis, similar to post-vaccine reactions seen in humans.” Most of them recovered, temporarily, but postmortem exams of the ones who didn’t revealed acute brain inflammation.
The delayed onset “chronic” phase of the disease affected far more of the sheep—50–70 percent of flocks and sometimes virtually 100 percent of animals within a given flock, usually including all of those who had previously recovered.
The reaction was frequently triggered by exposure to cold and began with restlessness and compulsive wool-biting, then progressed to acute redness of the skin, generalized weakness, extreme weight loss, and muscle tremors, and finally, entered the terminal phase where the animals went down on their front quarters, became comatose and died. Post-mortem examinations revealed “severe neuron necrosis” and aluminum in the nerve tissue.
See Epoch Times article:
See this paper:
Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity
https://pubmed.ncbi.nlm.nih.gov/23609067/
Abstract
We have examined the neurotoxicity of aluminum in humans and animals under various conditions, following different routes of administration, and provide an overview of the various associated disease states. The literature demonstrates clearly negative impacts of aluminum on the nervous system across the age span. In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer's and has been linked to this disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice. In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome.
Remember the list of 38 vaccine ingredients in Part 2? Aluminum isn’t the only troublesome component.
The milk protein can also be very problematic. Interestingly, according to Vinu Arumugham, “Cow's milk protein contaminated vaccines cause 75% of autism cases.”
Discussing autoimmunity caused by injecting foreign proteins in the human body, Vinu writes:
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). A milk-free diet reduces IgG4 levels thus improving CFD.
A milk-free diet downregulates folate receptor autoimmunity in cerebral folate deficiency syndrome
Cerebral folate deficiency in the developing brain results in autism:
Cerebral folate receptor autoantibodies in autism spectrum disorder
By using folinic acid (not folic acid), you can get folate to the brain through an alternate pathway, bypassing the FRA antibody blockage:
Autism pathogenesis: Piecing it all together, from end to beginning …
Immunization with homologous xenogeneic (animal/plant/fungal) antigens causes the development of autoimmune diseases.
This has been known for at least 45 years.
Vinu quotes a previous article:
Important findings: 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.
Returning now to Unbekoming’s post “Jamison’s Story,” which I started with, as he brings very powerful pieces from Handley’s “How to End the Autism Epidemic:”
Handley:
When we were newlyweds, my wife Lisa and I knew we wanted three or four kids. Our first son, Sam, was born in 1999 in Berkeley, California, and by early 2001 a family routine was settling in. We understood what it meant to be parents. Sleepless nights were routine. Our personal hobbies took a back seat.
Jamison took longer than expected. When he finally arrived in August 2002, a little more than thirty-three months younger than his big brother and almost a year behind “schedule,” I was overjoyed. Two boys? My sons would always have each other. A lifetime of wrestling matches, shared sports, and being dudes together was imminent. I couldn’t wait to watch and share in the fun. It was a euphoric time.
But on the night following Jamison’s two-month “well baby” visit—during which he received six separate vaccines—his health deteriorated rapidly and never rebounded. He developed eczema all over his body. He didn’t sleep for more than twenty minutes at a time. After a few sleepless nights, I had to move out of the master bedroom and sleep with Sam so I could make it up for work the next day. Lisa endured the crazy nights alone, waking with Jamison every time, trying to feed him back to sleep.
As time went on, Jamison developed dark circles under his eyes. His stomach became distended, and he was really skinny, almost emaciated. He sweated like crazy at night. The eczema persisted. He was constantly leaning on furniture (we later learned he was trying to ease the pain he was feeling in his gut), and he had frequent ear infections. He was always on antibiotics.
Our life, and our family, began to collapse. By late 2003, as Jamison’s health continued to decline, I would call home from business trips to brutal reports from Lisa about Jamison’s health. After one trip I returned home to California to a Post-it note on the kitchen counter from Lisa. “Went to Portland, sorry.” She had fled home to Oregon with the kids to be with her parents.
I remember the moment when our nanny said something. She was nervous. She was only twenty-one years old, a college junior. “I’m worried about Jamison,” she told me. “He’s not playing with things the way he used to.” I disregarded this comment—from the person who spent hours a day with my son —not yet ready to face the fact that something was terribly wrong.
A few months into 2004, our family bottomed out. Now eighteen months old, Jamison was sick, needy, never sleeping, and his behavior was changing for the worse. He’d run along walls, back and forth, turning his eyes to the side. He was spinning in circles, playing with toy trains in odd ways, stuffing himself with foods loaded with carbohydrates, alternating between diarrhea and constipation, and looking sicker than ever. He had been an early talker, but now his words had disappeared. Why was he no longer saying “juice” or “ball” or “doggie”?
“There goes our son with autism,” Lisa declared. She was half-joking, trying to rationalize his odd behavior. She didn’t know what “autism” meant, and neither did I. Wasn’t that the guy from Rain Man? She knew something was wrong, though. Inside, I was starting to worry, too. It wasn’t normal, the things Jamison was doing. The specter of the “A word” began to hang over our house.
Getting an appointment to have Jamison screened for autism was excruciating. The University of California, San Francisco, medical center and every other place we tried had multi-month waiting lists. When UCSF had an unexpected cancellation, we rushed in and got our answer: autism, the severe kind. The presiding doctor, famous in her field, told us to expect institutionalization. And probably no speech. Good luck; it will be a hard road. We asked about diet and some other things we had been reading about, and she said it was just a placebo for parents.
For a while Lisa and I told no one. We’d suppress our cries to try to show Sam, now four years old, that we were OK. As soon as he was napping or sleeping, we’d cry until the tears ran out. Every morning I woke up believing it was a nightmare. I was in a daze; the world had stopped making sense. Why was this happening to my son? So many dreams were being shattered at once about his life and his future. I felt my vision narrowing as the grief took over. Jamison was slipping away. He stopped recognizing us or acknowledging our comings and goings. It was unbearable.
I called my parents, living in Virginia, and said, “I need you right now.” They arrived the next day. When I met them at their hotel, I fell into their arms and wept. They would give Sam love and care while Lisa and I figured out what we were going to do for Jamison. Autism had arrived. Dr. Lynne Mielke greeted us in the waiting room of her office. She looked with concern at Jamison; he was doubled over on a small ottoman in the waiting room, applying pressure to his gut, as he often did. “Poor baby,” she exclaimed, “his belly must really be hurting him.” Lisa and I looked at each other, puzzled. We’d never thought about that simple explanation. It would be the first of many things Dr. Mielke would teach us about what had actually happened to our son.
Lisa had dragged herself to the computer first, while I still wallowed in misery. She started reading. “You need to read this stuff; kids are recovering!” she yelled at me. I finally joined her. Recovery? That certainly sounded better than the prognosis from UCSF. We set up two computers, side by side, in a narrow home office so we could research together. Two Stanford geeks, putting their well-honed research skills to work. There we sat, late into the night or into the morning, rubbing elbows and comparing notes, for weeks on end.
The things we learned challenged all of our beliefs. We learned there were two camps in the autism world. In the first camp, autism was a genetic condition, sort of like Down syndrome. If you had autism, you always would. Parents would be well served to accept their child’s fate and maximize the joy in life that they could.
The second camp was the opposite. Autism was an environmental illness, mostly (but not only) caused by a recent massive uptick in the number of vaccines given to kids. Autism was essentially a label for a set of symptoms that included many other “comorbid” conditions, such as allergies, gut distress, poor sleep, and malnutrition. If you treated many of these physical symptoms, some or all of the things we call autism could disappear. Recovery from autism was very possible in this world, and there were doctors claiming that they were doing just that: recovering children with autism.
This information was deeply disturbing and confusing. Naively, we returned to our pediatrician and UCSF with this newfound research. They told us everything we were reading about vaccines and special diets was nonsense. We didn’t understand. Both sides couldn’t be right. How could there be experts telling us something that wasn’t true?
As Lisa and I read, researched, talked, listened, and considered the arguments and information coming at us, what we came to was this: The “autism is genetic” story didn’t make sense. There is no “autism gene,” and the genetic research done up to that point provided no answers and still doesn’t today. Moreover, the rate of autism has reached epidemic levels, and there’s no such thing as a “genetic epidemic.” Mark Blaxill, an autism parent, said it well, “You can’t explain all of this as a genetic disorder since the dawn of time.”1 There had to be a cause.
The second camp—that autism is primarily environmental—made so much more sense to us. Jamie was so sick all the time! We’d watched him decline, time and again, after vaccine appointments. We went back over his pediatric appointment history and the symptoms we’d seen emerge; they corresponded completely. The parent stories we were reading online sounded exactly like Jamie’s story, and many parents were also reporting their children were recovering, once they found the right type of doctor, usually a “Defeat Autism Now!” or “DAN!” doctor. We chose to see the DAN! doctor closest to our California home, Dr. Lynne Mielke down the road in Pleasanton.
The American Academy of Pediatrics (AAP) has never recognized that children can recover from autism.
If they did, then it wouldn’t be genetic, would it!?
In 2004 DAN! doctors were viewed as medical outcasts and shunned by the mainstream community. This made us very wary. We’d see Dr. Mielke, but we’d proceed with extreme caution; the last thing we wanted to do was cause Jamison additional harm. What if the UCSF doctors and our pediatrician were right? What if it was all quackery?
Dr. Mielke didn’t fit the picture our mainstream doctors had tried to paint. She had gone to Indiana University’s medical school and then completed her psychiatry residency at UCLA. She’d been a practicing psychiatrist until she watched her younger son disappear into autism after his vaccine appointments, just like Jamison. Desperate to help him recover, and armed with a medical degree, her research led her to the DAN! movement growing across the country. As her son’s symptoms started to improve, she decided to open a clinic to help other children. Dr. Mielke was polished, professional, and organized. Our first meeting with her left us utterly flabbergasted.
Unlike the pediatricians and UCSF diagnosticians who had dismissed our questions about the vaccine-autism rumors and special diets that we were gathering during our research, Dr. Mielke quickly confirmed them. “Yes, it’s the vaccines. For most of the kids, that’s what pushes them over the edge,” she told us matter-of-factly. What was her evidence? Hundreds of patients with the same story as her son and Jamison and the medical tests to support the theory that vaccine injury—not genetics—was creating a generation of children with more autism than the world had ever seen.
More importantly, she was also bearing witness to many of her patients improving, and some recovering completely, by following what was known as the DAN! Protocol, a combination of diet, nutrition, and detox that had been spearheaded by the San Diego–based Autism Research Institute. She wanted to do tests on Jamison that our mainstream doctors hadn’t even considered, and she was particularly focused on healing his gut. Why hadn’t the other doctors even mentioned that?
We decided to give it a try. Dr. Mielke’s son and our son had the same backstory. We would only do interventions that posed no risk to Jamison’s health. Removing gluten and dairy posed no risks. Within two weeks of our first visit with Dr. Mielke, a combination of diet, nutritional supplements, cod liver oil, and probiotics had flattened Jamison’s belly, and he’d stopped leaning on furniture. Eye contact started to return. The dark circles under his eyes were going away. His awareness of the world around him was returning.
Encouraged, we became students of biomedical treatment for autism, which means you treat the medical symptoms a child with autism is experiencing, like poor sleep, gut distress, food allergies, or recurrent ear infections. Elbow to elbow on our matching computers, Lisa and I researched everything that might work to save Jamison. He had just turned two, and we felt that recovery was a real possibility for him. He was getting better and better.
You’d think witnessing Jamison’s health improve would make us ecstatic, and in a sense it did, but our feelings were also far more complex than that. Watching Dr. Mielke’s prophecies bear out in Jamison’s improved health was like falling down a rabbit hole and losing faith in the world we thought we knew, all at once. How could we be getting advice from autism experts that was so contradictory? How come UCSF didn’t seem to care if a doctor just thirty miles away was recovering children from autism? Why weren’t these doctors all talking to each other and sharing ideas and information?
More unbearable than the thought that Dr. Mielke and the hundreds of other DAN! doctors across the country were wrong was the feeling that she was right. Were vaccines the primary trigger for an epidemic of autism? Were we really doing that to kids? The scale of damage was nearly incomprehensible. This would be a recurring theme for us on this journey. We’d meet highly intelligent parents, doctors, and scientists who would tell us that, yes, that’s exactly what’s going on. It was two different realities.
The mainstream press paints this issue as crazy, desperate parents looking for someone or something to blame, but that’s not accurate or fair, and it doesn’t help kids. Over the course of fifteen years, I’ve been astonished by the things prominent scientists, doctors, politicians, and parents have said about the connection between vaccines and autism. The community of people who know the truth has grown massively since Jamison was diagnosed. For many the knowledge required them to pay the ultimate price: witnessing their own child decline after being vaccinated. Many of these highly educated, intelligent people would tell me, “I never would have believed it if it hadn’t happened to me.”
In retrospect I shirked my duty to research vaccines properly. You don’t think of a vaccine as a medical procedure, but that’s what it is. I hadn’t done a shred of primary research about vaccines prior to vaccinating my children. I remembered being vaccinated as a kid and thought, “I’ve been vaccinated, and I’m fine.” I trusted the authorities, who all seemed to be saying that vaccines were safe and effective.
I had no idea that in 1986 vaccine makers were given blanket indemnity from liability by the US Congress. I didn’t know the vaccine schedule in the United States had tripled since the mid-1980s. Or that the US government had paid out
$3.6 billion for vaccine injuries. Or that other developed countries gave many fewer vaccines, and had much less autism. I didn’t know the hepatitis B vaccine, often given on day one of life, only provided protection for four years. Or that autism, ADHD, asthma, and allergies were all skyrocketing, and that their rise corresponded to changes in the vaccine schedule. I couldn’t know that biological science would show how a vaccine can injure an infant’s brain—because it hadn’t been published yet. And I certainly had never read the many published studies showing how vaccines can result in autoimmunity and neurological damage.
Most significantly, I believed the narratives that appealed to emotion and trust in authority that we often hear about vaccines.
One more excerpt from the intro to Handley’s book:
Interestingly, the belief that vaccines can cause autism isn’t the fringe topic many mainstream media articles make it out to be. In the 2016 election of the 128 million people who voted for either Hillary Clinton or Donald Trump, 24.3 percent of them believe this statement is true: “Vaccines have been shown to cause autism.” That’s 31.3 million people.5 It’s not a conspiracy theory, as I hope this book will show you through sound logic, data, and scientific studies.
That said, what you’re about to read may challenge many things you believe to be true. I know how that feels. I trusted my doctors. I listened to authorities. I struggled to accept that people would lie. Yes, I’m incredibly angry about what happened to my son, and about the ridiculous number of children now affected by autism, but I’m not angry because I need someone to blame. I’m angry because after fifteen years of immersing myself in the scientific literature, beating down the doors of the most knowledgeable doctors and scientists in the country, weighing every argument I encountered, and witnessing the experiences of so many families, including my own—essentially eating, breathing, and living autism—I know that autism is preventable and recoverable, but we’ll never end this epidemic until we reckon with the lies and obfuscation that enable it.
So the first step to ending the autism epidemic is to be honest about how it started, and expose the lies told, time and again, to distract and confuse the issue. We need to name names and hold people and institutions accountable. We need to look at common arguments—that the rate of autism isn’t actually increasing and that the science is settled, for example—and intellectually dismantle them in a logical, fact-based way. We need to look at the role of the media, Big Pharma, and trusted institutions such as the Centers for Disease Control and Prevention (CDC) and the AAP. We need to follow the money. This is what I cover in part one.
The second step is to understand the clear and compelling scientific evidence that supports the connection between vaccines and autism. What many people don’t know (because the mainstream media doesn’t report this) is that since 2004 there has been a revolution in the understanding of the cause of autism, based on the rapid-fire publication of a number of biological studies that point to an “immune activation event” in the brain—immune activation being the whole point, by the way, of vaccination. Does that mean vaccines are the only cause of autism? No. Other things can cause immune activation events; it just appears that vaccines do it most consistently and devastatingly.
What many people also don’t know is that recently some highly respected scientists—experts who were relied on to testify against parents in the National Vaccine Injury Compensation Program’s “vaccine court”—have recently switched sides and now support the view of so many parents that vaccines can indeed cause autism. They have amended their views based on evolving science. Their words carry tremendous weight, and I hope this book helps put their comments, many of which have never before seen the light of day, into proper context. This is what I cover in part two.
The third step to ending the autism epidemic is to develop a constructive plan for how we protect future generations from a devastating epidemic now impacting one in thirty-six American children based on what we understand about the cause of autism and where families and doctors have experienced success in recovery. This is what I cover in part three.
The autism epidemic is ultimately a failing of our public health officials. In the United States the Centers for Disease Control and Prevention—a federal agency within the Department of Health and Human Services—is not only responsible for implementing our national vaccination program but, in a twist of bitter irony, is also responsible for tracking the number of children with autism. It’s as if the expression, “the fox guarding the henhouse” had been waiting its whole life for this moment. Sadly, the CDC’s failings are further enabled by scientists, doctors, and many members of the media willing to parrot the same old lies that obscure an honest discourse about the epidemic and how to end it.
(The footnotes are in Unbekoming’s article link posted further up.)
I want to let my readers know that by Divine Providence, I became connected with a wonderful woman who (many years ago) had researched and found an effective detox program for her her autistic son. Thank G-d, he is currently well and functioning normally.
I started a WhatsApp autism/neurological vaccine injury information/support chat recently for people to be able to connect with Raquel and learn how she was able to help her son, and connect with other parents, as well. If you are a parent and want to join the WhatsApp group, please email me for the link at truth613@substack.com.
Please look out for Part 4, G-d willing.
Just fabulous info! I’ve been studying this for about 25 years. Thank you for tackling this in just the right way.
Handley’s book is exceptional. And the links to articles are priceless.
Thanks!
https://vinuarumugham.substack.com/p/how-vaccines-cause-autism-a-visual