by
Lance D Johnson (NaturalNews.com )
Young, healthy women who experience amenorrhea, ovarian failure, and
infertility have likely been damaged by Merck’s HPV vaccine. A new study
published in the
Journal of Toxicology and Environmental Health analyzed
data on pregnancy outcomes, comparing women who received an HPV vaccine
with those who did not. The data analysis is titled,
“A lowered probability of pregnancy in females in the USA aged 25 who received a human papillomavirus vaccine injection.”
The study, uninfluenced by pharmaceutical money, analyzed data on 8
million women aged 25-29 living in the U.S. from 2007 and 2014.
According to the analysis, conception rates would have fallen by 2
million if 100 percent of the females in the study would have received
the HPV vaccine. The study warns that the HPV vaccine has a negative
influence on fertility and more research is “warranted.”
Despite mounting evidence of harm, Merck seeks to fast-track Gardasil on new age group
Despite these grave concerns, the Food and Drug Administration (FDA)
is currently fast tracking the process by which the Gardasil-9 is
approved for use in women and men ages 27 to 45. Merck’s application for
approval has been granted
priority review, and is scheduled
for an approval date of October 6, 2018. So, much important information
about Gardasil’s risks will be suppressed as the FDA moves quickly on
behalf of Merck’s business interests.
When Gardasil was initially licensed, many post-marketing reports poured in, claiming that vaccine recipients endured primary ovarian failure after vaccination. The cases of Gardasil vaccine damage that have been identified and reported to
the U.S. Vaccine Adverse Events Reporting System (VAERS) are in excess
of 58,000. Many cases have resulted in emergency room visits, seizures,
and the diagnosis of autoimmune conditions. Additionally, approximately
11,000 cases have been filed, documenting “serious” disability and
sudden death. Women should no longer be subjected to Merck’s deadly
experimentations. Gardasil is an experimentation because the risks are
concealed and the vaccine is fast-tracked for approval. (Related: Merck accused of fast tracking Gardasil for financial gain; judge orders the drug company to prove the effectiveness of this vaccine.)
One of the greatest dangers of vaccination, which is not studied by
the drug companies or the FDA, are the prevalence of stealth viruses
within the vaccines. While they do not impact the animal tissue in the
vaccine or infect the animals used in the vaccine studies, these viruses
can be dormant and revert to infectious form in humans. Watch “The criminalization of science whistleblowers: An interview with Judy Mikovitz, PhD.
Aluminum adjuvant: one of the most alarming issues of vaccine science
One of the biggest problems with the Gardasil vaccine is the use of
aluminum as an adjuvant.
The adjuvant is used to force the immune cells to respond to the
antigen in the vaccine. Without the adjuvant, the immune response to the
vaccine pathogen would be weak. The problem is that the
aluminum is taken up into the immune-responsive cells and
is carried throughout the body. This may cause the immune system to
attack itself, as the aluminum persists as a threat in the body. This
metal causes problems in the brain of humans. Studies show that brain
tissue from autistic children contains
high amounts of aluminum.
Aluminum is exponentially more dangerous through injection, than
through ingestion. To suppress information on the harmful effects of
vaccines, the drug companies base their vaccine safety on ingested
aluminum amounts, not the impact of injected aluminum. There’s a big
difference. Equally disturbing, GlaxoSmithKline and Merck spike their
placebos with aluminum adjuvants to make the vaccine appear less
dangerous. This shortcut helps the drug companies cut observation
periods so they can conceal the risks of aluminum adjuvants in their HPV
vaccines.
The devastating, traumatic failures of Gardasil are being suppressed
and young women are suffering at the deceptive science of these devilish
institutions. Despite the growing body of evidence of harm from
Gardasil, Merck is seeking fast-track approval to unleash their vaccine
on another vulnerable age group of the population. The FDA, ignoring the
evidence of Gardasil’s harm to women’s ovaries and fertility, cannot be
trusted to evaluate the drug company’s “science.” A moratorium should
be issued on all HPV vaccines until there is sufficient evidence to
prove the vaccine is no longer causing ovarian failure, autoimmune
conditions, infertility, seizures, and death.
Read FDA.news for more headlines about the FDA’s dangerous junk science.
Sources include:
TandFOnline.com
GreenMedInfo.com
GreenMedInfo.com
Vaccines.News
GreenMedInfo.com
HippocraticPost.com
WorldMercuryProject.org
Vimeo.com
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