Autoimmune Disease Epidemic – by Dr. Sherri Tenpenny

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Autoimmune diseases are the third most prevalent disease category, exceeded only by cancer and heart disease. There is a 20% chance of a person developing an autoimmune disease in their lifetime, and four out of five of those persons will be female. In 2000, autoimmune disease deaths were the eighth leading cause in women under the age of 65 years.

According to the nonprofit Autoimmune Association, the term “autoimmune disease” refers to more than 100 ailments that affect up to 50 million Americans. In simple terms, these illnesses manipulate the body’s immune system, leading to the development of autoantibodies that attack healthy tissue

Autoimmune illness can manifest as exasperating fatigue, persistent pain, and depression. The most common (or most familiar) autoimmune diseases include rheumatoid arthritis, multiple sclerosis (MS), scleroderma, lupus, Sjögren’s syndrome, autoimmune thyroid disease (Hashimoto’s disease), and type 1 diabetes Having an autoimmune disease often leads to social isolation due to the inability to participate normally in life. These symptoms can wreck promising careers and, sadly, can often, completely disrupt family dynamics.

Source: NIH

The U.S. does not have a national registry for autoimmune diseases. According to a December 2023 article published in Scientific American databases in Denmark and Italy have been use to estimate the following:

According to the International Journal of Celiac Disease (2015). These observations point to a stronger influence of environmental factors as opposed to genetic factors on autoimmune disease development. Research suggests the increase in autoimmune diseases is related to changes in our environment, unhealthy lifestyles, upsurges in obesity, sleep deprivation, air pollution, exposure to toxic environmental chemicals, and infections.

Something is missing from that list.

Adjuvants are substances added to vaccines to enhance their immune response, ie their ability to produce a quantitative amount of antibody. Aluminum was first used in human vaccines in 1932 and was the only adjuvant in use in licensed vaccines for approximately 70 years.

Adjuvants have been assumed to act by a combination of mechanisms, including forming a depot to hold the antigen locally for a longer period of time; 2) the induction of cytokines and chemokines; 3) the recruitment of immune cells; 4) the promotion of the transportation of the antigen to lymph nodes; and 5) the induction of local inflammation. It appears that adjuvants activate innate immune responses.

Despite its extensive and continuous use, the immune mechanism of action of aluminum remains incompletely understood. (2015)

We’ve been loading kids, adults, and animals with aluminum for nearly a hundred years, and we don’t know how it works? That means we don’t really know why we put it in the shots.

It’s just a guess. A theory.

Instead of viewing this with jaw-dropping horror on what aluminum and other adjuvants may be doing to the immune system, researchers continue to look at these questionable mechanisms for help in designing other types of adjuvants.

Beyond aluminum, other adjuvants used in vaccines are squalene (MF59 – Novartis), AS01, AS03, AS04 (GSK), and various mineral oil emulsions. Mineral oil adjuvants induce the most pervasive autoimmune disease, with approximately 60% of patients developing autoimmune diseases, such as SLEsystemic sclerosis (SSc), rheumatoid arthritis (RA), dermatomyositis (DM) after given injections of vaccines that contain mineral oil. Most mineral oil-aduvated shots are found in Latin America.

A syndrome called ASIA, which stands for autoimmune/autoinflammatory syndrome induced by adjuvants, is an admission of autoimmunity caused by vaccination. First described in 2011, typical clinical symptoms of ASIA are:

Chronic fatigue, arthralgias (joint pain), myalgias (muscle pain), pyrexia (fever), sicca symptoms (dry mouth, dry eyes), and cognitive impairment, including mental fogginess, memory deficits, and/or atypical neurological symptoms.

An international registry for ASIA syndrome was also established in 2011, with well-defined diseases observed in 89% of patients. Between 2011 and 2016, 4,479 ASIA cases were added to the registry, with the most severe cases associated with the HPV vaccine (aluminum), influenza vaccine (mercury), and mineral oil adjuvants.

Another source sites that the most common vaccines to be related to ASIA syndrome are those directed to influenza virus, HPV, HBV, diphtheria-tetanus-pertussis (DTP), MMR and Bacillus Calmette-Guerin (BCG).

Source: Licensed vaccines with or without adjuvants.

When I presented the 40 Mechanisms of Injury – how the COVID jab can harm, even kill you – in July 2021, I divided the injuries into four categories:

  1. Category 1: Acute death within 24-28 hours after a jab – from blood clots, pulmonary embolism, strokes, or heart attacks.
  2. Category 2: Spike protein disease. When Pfizer release its first tranche of documents, a 38-page document was included that contained more than 1200 different conditions and diseases that had been observed even before the Pfizer jab had been released. Most of these were caused by the permeation of a foreign protein in the blood, named the spike protein. These conditions have now been given an official name: spikeopathy – toxicity caused by the spike protein.When the COVID jabs were first released, essentially January 2021, I said we would sadly see a big uptick in “spikeopathies” and deaths, about 3 years after the person had three shots: two shots and a booster. That would begin in around 2024….it’s what we’re seeing now. Ed Dowd’s newly released, updated book, Cause Unknown, includes stats from 2023. A 10 percent increase in excess deaths would have been a 1-in-200-year event. But what we’re seeing is a 40 percent increase. Soberingly predicted.
  3. Category 3: This is the slow but continuous appearance of more and more autoimmune diseases. In 2020, a prominent immunologist/researcher demonstrated that 28 of 55 tissue types reacted to SARS-CoV2 antibody, including skin, gastrointestinal, pancreas, liver, heart, muscle, joint, thyroid, brain, enteric nerve, tight junction proteins and cellular components, meaning, the antibody to either the infection or the antibody generated against the jab particles could induce autoimmune disease. A prominent immunologist told me at the time, “DrT, we’re in trouble. We’re going to be seeing massive illness over the next 10 years.” We’re already seeing reports that COVID-19 vaccines may cause rare autoimmune diseases, including autoimmune glomerulonephritis [kidney disease], autoimmune rheumatic diseases [joints], and autoimmune hepatitis [liver].
  4. Category 4: The catch-all for all other types of injuries including turbo-cancers and infertility.

To learn more about the 40 Mechanisms of Injury and WHY it is important to keep this information in mind, you can purchase the full webinar from Brighteon by going to these links:

The Interview The Course OFFER ENDS ON MARCH 19, 2024

In April 2023, an article published in the journal, Autoimmunity Reviews minced no words and got straight to the point: (this study is worth reading)n

Growing evidence suggests that COVID-19 vaccination may cause new-onset autoimmune diseases, including autoimmune glomerulonephritis (kidney disease), autoimmune rheumatic diseases (many), and autoimmune hepatitis (liver disease).…In this review, we provide evidence that vaccination induces autoimmunity and summarize possible mechanisms of action, such as molecular mimicry, activation by bystanders, and adjuvants. Our objective is not to refute the importance of vaccines, but to raise awareness about the potential risks of COVID-19 vaccination.

Of course, the authors had to throw in the normal caveats:

  • “Nevertheless, the causal relationship between COVID-19 vaccines and these autoimmune diseases remains to be demonstrated,” and
  • “Our objective is not to refute the importance of vaccines,” and
  • “The benefits of COVID-19 vaccination significantly outweigh the theoretical risks,” and
  • “We strongly encourage worldwide vaccination to build immune protection in the population.”

Scientists are so strongly throttled to maintain the party line that they dare not say,

“When is this deadly nonsense going to stop?!!?”

 

Source: Autoimmune Disease Epidemic – by Dr. Sherri Tenpenny


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