HPV, Tetanus Vaccine Causes New Disease: New Vaccines Worse?

by Heidi Stevenson

The vaccine junta is not only unconcerned with vaccine-induced diseases, it’s massively gearing up this vaccine arms race against the human race. It’s known that tetanus vaccine causes a new disease, antiphospholipid syndrome. New adjuvants are composed of phospholipids, a potential disaster.

The tetanus vaccine causes a new disease known both as Hughes syndrome and antiphospholipid syndrome (APS). It’s an autoimmune condition that can attack any part of the body, though is best noted for heart attacks and killing fetuses. It’s likely that APS will become more common with the new generation of vaccine adjuvants now being produced.

The sufferers of (APS) are mostly women, and its diagnosis is often made as a result of multiple pregnancy losses. As is typical of new diseases, research is focused on finding a genetic cause, in spite of the fact that the connection with vaccines is well known and documented.

As the name implies, APS is a condition in which phospholipids, natural and necessary substances required by every part of the body, is seen as an infectious agent by the immune system. So, this substance that exists in every cell becomes subject to attack. Symptoms include:

  • Blindness
  • Cardiovascular:
    • Deep vein thrombosis (clots in veins)
    • Phlebitis
    • Thrombocytopenia (deficiency of blood platelets, causing bleeding & bruising)
    • Atherosclerosis
    • Pulmonary embolus (clots in the lungs)
    • Heart valve abnormatilies
    • Stroke
  • Headaches & migraines
  • Miscarriages
  • Neurological disorders:
    • Epilepsy
    • Chorea (sudden uncontrollable jittery movements)
    • Transverse myelitis (inflammation of the spinal cord)
    • Multiple sclerosis
    • Cognitive dysfunction
  • Skin disorders, including mottling, ulcers, and necrosis

APS can also be diagnosed—more accurately, misdiagnosed—as lupus erythematosus, which is another vaccine-induced condition.

APS and Vaccines

One study calls Hughes syndrome the “classical antiphospholipid syndrome”[1]. That study refers to similarities between plasma protein beta-2-glycoprotein-I (β2GPI), which is attacked in APS, and the tetanus vaccine. That is, the tetanus antigen has parts that are virtually identical to β2GPI, which is found virtually everywhere in the body.

Another study documents how APS can be induced in laboratory animals with tetanus vaccination[2]. Many large number of other studies document and investigate the connection between vaccines and antiphospholipid syndrome[3,4,5,6,7,8].

These studies leave little doubt that APS is caused by vaccines. That should come as little surprise, since it was first identified as a disease during the 1980s. If this disease existed prior to vaccines, it was so rare that it was unknown. Now, it can take its place among a growing list of vaccine-induced conditions, including rheumatoid arthritis, macrophagic myofasciitis, multiple sclerosis, autism, and siliconosis. The list keeps growing and many believe that all these conditions should be included under a single name, autoimmune/inflammatory syndrome induced by adjuvants, or ASIA.

Why New Generation Vaccines Are Especially Worrisome

Phospholipids are a primary part of your body, forming part of the membrane of every cell, among other functions. They’re under attack in APS. As can be seen with regard to tetanus vaccine, APS can be induced by the antigen when the epitope—the part of the antigen forming the pattern that autobodies are designed to attack—is similar to a particular part of the body.

What’s frightening is that phospholipids are becoming a primary ingredient of vaccines in the form of a new generation of adjuvants made via recombinant DNA by diddling with a part of pathogenic bacteria called outer membrane vesicles (OMVs).

OMVs allow for designer vaccine antigens and adjuvants. OMV adjuvants are, of course, being promoted as the safest ever developed. That safety claim is based on the fact that they’re so much like the body already. This is the same claim that’s been used to promote squalene, which, as we’ve recently seen with the tragic cases of narcolepsy in children after the squalene-laced flu vaccine, Pandemrix, was unleashed in Europe, can devastate lives. Gaia Health explained the issue in How the Flu Vaccine Causes Narcolepsy.

Squalene is a lipid. That’s what makes it so dangerous. OMVs are even more precisely analogous to human tissue, because they are not only lipids, they are phospholipids—which are precisely what the body attacks in APS. Therefore, we can anticipate that there will be ever-more cases of APS as we see the approval of ever-more OMV-based vaccines, which are in the pipeline now.

Have no doubt: these vaccines will be approved. The first one, Cervarix, is already out there—and it’s been deemed safe, in spite of evidence to the contrary.

People with APS are suffering from phospholipid antibodies that are erroneously destroying parts of the eye, cardiovascular system, brain, nerves, skin, reproductive system—in short, any part of the body. This self-destruction is induced by vaccine technologies. These technologies are presumed safe without adequate, if any, testing. Just how many people must suffer before this travesty is ended? When will the clearly mad purveyors of these technologies step back and question what they’re doing?

The fact is that there are not just one, but several generations of people who don’t even know what good health is. Worse, each successive generation is growing sicker than the previous one. And worst of all, the vaccine junta is not only unconcerned, it’s massively gearing up this vaccine arms race against the human race.

Sources:

  1. When APS (Hughes syndrome) met the autoimmune/inflammatory syndrome induced by adjuvants (ASIA)”Lupus, M Blank, E Israeli, Y Shoenfeld, doi: 10.1177/0961203312438115.
  2. Vaccine model of antiphospholipid syndrome induced by tetanus vaccineLupus, L Dimitrijević, I Živković, M  Stojanović, V Petrušić, S Živančević-Simonović, doi: 10.1177/0961203311429816.
  3. β2 glycoprotein 1 (β2GPI), the major target in anti phospholipid syndrome (APS), is a special human complement regulatorBlood, Katharina Gropp, Nadia Weber, Michael Reuter, Sven Micklisch, Isabell Kopka, Teresia Hallström and Christine Skerka, doi:10.1182/blood-2011-02-339564.
  4. Anti-β2 glycoprotein I (β2GPI) autoantibodies recognize an epitope on the first domain of β2GPIPNAS, G. Michael Iverson, Edward J. Victoria, and David M. Marquis.
  5. Anti-phospholipid antibodies following vaccination with recombinant hepatitis B vaccineClinical and Experimental Immunology, J Martinuč Porobič, T Avčin, B Božič, M Kuhar, S Čučnik, M Zupančič, K Prosenc, T Kveder, and B Rozman, doi:  10.1111/j.1365-2249.2005.02923.x
  6. Immunomodulatory and physical effects of phospholipid composition in vaccine adjuvant emulsions.
  7. ‘ASIA’ – autoimmune/inflammatory syndrome induced by adjuvants.
  8. Infections and vaccines in the etiology of antiphospholipid syndrome.
  9. Hughes Syndrome Foundation
  10. Antiphospholipid syndrome
  11. Learning About Antiphospholipid Syndrome (APS)
  12. The antiphospholipid syndrome (Hughes’ syndrome)
  13. APS Foundation of America

Vaccines cause autoimmune disorders!

…bless you all…

Disease Caused by Vaccines

When people are subject to repeated vaccines, they predictably simulate a situation of suppressed cell-mediated immunity and heightened antibody responses. Why? Because that’s the goal of vaccination. If you make a list of the diseases that are characterized by suppressed cell-mediated immunity and heightened humoral immunity, you’re talking health conditions like asthma, allergies, eczema and autoimmune diseases including Crohn’s, Vitiligo, Multiple Sclerosis, Sjogren’s syndrome, Hashimoto’s, etcetera.
We cannot and will not eradicate all disease with vaccines. We have merely traded acute illnesses from which most recover for chronic illnesses for which modern medicine has no cure.
Ask your grandparents or parents how many children did they know in 1940’s or ’50’s who had allergies, and the answer is basically none. Now, it’s anywhere from 20 to 40% of children have some sort of chronic illness.
Fifteen percent of children suffer from asthma. (1) Something is wrong with this picture.
So how did we get here? Many of today’s chronic diseases are characterized by excessive antibody production.
How did we get that? Well that was the point of the vaccination program. That’s the goal. Why would you expect anything else to happen? Many of you may respond, “This has never been proven.”
Actually, the fact that vaccines produce more illness has been proven. Longitudinal survey studies comparing the health of vaccinated versus unvaccinated children have repeatedly shown statistically significant vaccinosis – illness produced in an individual after receiving a vaccine. In a 1997 study in New Zealand, 1265 children were surveyed. Twenty-three percent of the vaccinated children experienced asthma and thirty percent suffered from allergies, while the unvaccinated children did not have a single incident of these illnesses. (2) In a 2004 British
Study of 30,000 children, vaccinated children had a 5.04 increased risk of asthma, while the unvaccinated only had a .36 percent prevalence. (3) In a 2011 German Study of 8000 children, vaccinated children had at least two to five times more diseases and disorders than unvaccinated children.
In patients with an autoimmune disorder, the immune system can’t tell the difference between healthy body tissue and antigens that need to be attacked. The result is an immune response that destroys normal body tissues. This response is a hypersensitivity reaction similar to the response in allergic conditions. Vaccinations have been shown to induce autoimmune disorders.
Interestingly, there’s a study out of Kobe University in Japan where they took mice and put them on a rigorous
vaccination program. They wanted to see if they could develop excessive antibodies as seen in autoimmune disease. And they found that at a certain threshold they could consistently and reliably induce autoimmune disease by simply giving enough vaccinations. (4)
The Kobe University study authors concluded:

Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s
immune ‘system’ by repeated immunization with antigen to the levels that surpass the system’s
self-organize criticality.

In other words, they found that, not only is vaccination a possible or even probable cause of autoimmune disorders, but that chronic diseases are the inevitable result of vaccinations!
This study was done with mice. This begs the question, ‘Has this been replicated in humans?’ Unequivocally yes. This experiment has been done and it’s called the last 70 years.
Autoimmune diseases have increased in quantity and variety as the number of vaccinations has increased over the last 70 years. There are over 100 autoimmune diseases. Studies with monogenetic twins have revealed that genetic influences only account for 25–40% of the disease risk making environmental influences the predominant factors. (5) Regardless of genetic vulnerability, one’s environment determines whether genes for autoimmunity are expressed.
There is a reason the fastest growing subset of diseases in the US and the world are autoimmune diseases. This is because we’re producing them. It’s a growth industry. As vaccines have increased in number, so have the number of cases of autoimmune disease.
Currently, there are 38 vaccines on the recommended schedule, with even more in some US states. There are many more vaccines in development. I predict a worsening epidemic of allergies, asthma, autoimmune and other diseases caused by an atrophy of the cell-mediated immune response as more vaccines are added to the vaccine schedule. We are only seeing the tip of the iceberg with vaccine-induced disease.

  1. Channick, R. More Astham Inhalers going to School: New State Law Eliminates Need to Doctor’s Written Permission. Chicago Tribune. October 1, 2012.
  2. 6 Kemp, T et al. Is Infant Immunization a Risk Factor for Childhood Asthma or Allergy? Epidemiology. 1997 Nov 8: 678-80. http://www.ncbi.nlm.nih.gov/pubmed/9345669
  3. 8 McKeever TM et al. Vaccination and Allergic Disease: A Birth Cohort Study. American Journal of Public Health. June 2004, Vol 94, No. 6, pp 985-989. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1448377/
  4. 11 Novaccine.com. Reactions/Conditions. http://www.novaccine.com/reactions-conditions/
  5. Karopka, T, Fluck, J, Mevissen, H, Glass, A.  The Autoimmune Disease Database: a dynamically compiled literature-derived database. BMC Bioinformatics 2006, 7:325  doi:10.1186/1471-2105-7-325. http://www.biomedcentral.com/1471-2105/7/325

    …bless you all…