Recombinant
retroviruses contaminate vaccines and modify human/animal genomes
Viral modifications to human genome are
introduced by recombinant retroviruses that may be contaminating all
live vaccines.
Some killed virus vaccines may not be
completely killed. Adjuvants stimulate
chronic inflammation by their tissue persistence, ASIA.
Medical history is replete with poorly publicized
failures and tragedies that have not been analyzed and taught to doctors
giving them a false sense of confidence in risky vaccine technology. Contrary view: 2017
Update Paper calls XMRV ME/CFS link into question. False positives vs. retroviral capability to modify
genomes. 100% vaccination provides a
sure path to total deployment of latent, unknown retroviruses with unknown
pathogenic payloads.
Glyphosate also provides another threat to human and
animal genomes. Animal
Genome Threats modify genomes in unknown ways. This science is out of
control and modifying our reproductive integrity in unknown adverse ways through
the food supply.
Vaccine recipes promote passing viruses
and unknown contaminating retroviruses through a chain of growth stages in
hopefully uncontaminated animal tissue cells. Contamination is the rule, not the exception.
The suspected recombinant nature of HIV retrovirus may possibly be
confirmed by the reproducible production of a recombinant
mouse leukemia retrovirus, XMRV related retrovirus family.
ME/CFS/Fibromyalgia patients with
disrupted immune systems and infected immune cells (B,
T, macrophage & mast cells) have
been matched with a high percentage (>50% to >80%) positive tests for
XMRV family retroviruses in the patients’ blood, for patients showing immune
system dysfunction, mitochondrial dysfunction, high HHV family virus titers,
and/or high cytokine activity. (Ref 1)
The ME/CFS epidemic, spread contagiously
and passed to children via human genome pathways, is hypothetically traced to a
recombinant retrovirus-contaminated experimental
polio vaccine tested at Los Angeles County Hospital in 1934 that led to a lawsuit
settlement. A nondisclosure agreement suppressed the facts. Retroviruses are capable of recombinant
propagation and of infecting human and
animal DNA with copies of themselves, so the infection can be passed to the
infected animal offspring. Human US XMRV contagion is estimated to be about 6%
or more, except among groups that have never been vaccinated.
The false news is that vaccines are
safe; Many of our smarter scientists
know how and why they are not.
However, the UN’s WHO-led vaccine lobby
has suppressed the truth and promoted the lie.
---Suzanne Humphries Refs
Shall the sins of the pro vaccine cult
descend to the children of the innocent to the Nth generation?
Perversity of Unintended Consequences
The quest for 100% vaccinations has lead
to the retroviral RNA contamination of the human genome and to known and
unknown cascading morbid autoimmune defects, without limitations.
Mandated vaccinations promote a cumulative destruction of the integrity of
human and animal genomes, passing the ME/CFS defects to the offspring.
For over 75 years, ME/CFS has lacked an
infection-linked cause. Now it is likely seen as a vaccine experiment run wild
in 1934 that can be replicated at will.
Further vaccine safety mistakes are now revealed in a fundamentally
flawed virus payload replication recipe, prone to animal retroviral
contamination. And to occasional new recombinant RNA virus production. Other vaccine production contamination
mistakes have led to reported vaccine viral contamination episodes. SV40
is one example. GWI
vaccine contamination. AIDS epidemic in US made worse by early Hepatitis B vaccine
contamination with HIV-1.
Worldwide, a pro-vaccine,
UN/WHO-promoted, public health collusion mandates 100%
vaccination. This is a massive crime against humanity in the name of
protection from hypothetical, (not real) future epidemics. The escalating
morbidity cascade is crashing our (US) medical delivery systems by increased
costs from a cascade of old and new autoimmune diseases.
What we do not know (repressive
scientific ignorance) can definitely hurt all of us. Ignorance and denial
of toxicology science applied to vaccine adjuvants leads to ASIA
(adjuvant stimulated chronic inflammation) and worse. Numerous quality control
lapses for vaccines have also been reported. Contamination
Adjuvants, like aluminum in
flu shots, are cumulatively toxic, they are moved by phagocytes past the blood
brain barrier, and contaminate the brain, promoting tissue contamination,
oxides, inflammation, causing Alzheimer's and Parkinson's symptoms by depleting
antioxidants like vitamin C. Flu shots every year for everyone are
cumulatively poisoning our tissues and brains. So are the 64+ vaccine
doses by age 18 mandated for our children. More are planned, without limits.
The justifications for new vaccines are
theoretical, the harms from ignored toxicology science are real.
A fact-based rising groundswell by
doctors against the vaccine mandates is to be found in lectures on Utube. Article
Scroll down for an index to a
Synthetic Seminar on the subject.
Retroviral XMRV Plague
Mother daughter propagation of
ME/CFS-promoting, contaminated vaccine initiated, retroviral-caused, genome
modifications are already with us. I met such a mother two days
ago. Her life is malady plagued, so is her daughter's.
The 70+ year US occupation of Germany has
introduced a slow passage of the 1934, Los Angeles County Hospital staff's
ME/CFS stealth contagion of the XMRV-related retro-viral genome
modification into the German population from the US military families. XMRV
related virus is now growing naturally in the German population. So are the
related DNA modifications to their genomes from the retrovirus. References
About 6 to 8 percent of the US public is
infected by the ME/CFS retrovirus (XMRV associated retrovirus). This is over 20
million persons (~2014). Autism rate (2016) is about 2 percent of the children,
but Autism plus ADHD is much higher rate, comparable to the ~8%
retrovirus infection rate. Rising special-needs costs are consuming the budgets
of school systems in the US, Scotland, and world wide. ADHD is Autism lite.
The probable and actual effects to the
XMRV related viruses 6% to 8% epidemiological statistics are: (Plague)
Predictable Rise in Autoimmune Diseases in Late Life
For those infected with the XMRV
associated retrovirus with subclinical symptoms, later-life ME/CFS/Fibromyalgia
emergence and other neural inflammations (MS/IBS/ALS/etc) are another
consequence. The XMRV like virus lives/replicates in T and B immune cells and
cloaks itself in blood so it is nearly undetectable. Except when
stimulated by a vaccination or an adjuvant shot.
Cumulative adjuvant tissue toxicity
excites the infected immune system and the Retroviruses emerge to replicate.
Vaccinations
stimulate the infected immune cells to replicate and the latent virus awakens
to plaque the host and cause chronic disabilities.
Vitamin C dependency (higher than normal
needs) increases greatly. High dosage ascorbate is an antiviral
antibiotic. -- Klenner
Read Plague by Dr Judy
Mikovits. Review
The book provides a unified explanation of how we became infected with a
multitude of morbidities.
This reference describes the
mechanism of vaccine induced maladies
Viral modifications to human genome are introduced by recombinant retroviruses
that are contaminating all
live vaccines.
This is because multiple payload virus
growth passes through mouse and other animal tissue and brain cells are used to
grow the attenuated target virus used in the vaccine production. Any
intrinsic infections of the mouse cells are also replicated and end up in the
vaccine payload. How recombination
of retroviruses works.
Some
"killed" RNA viruses in vaccines are more resistant to sterilization
methods and may survive, alive, in the vaccine payload. Viruses
and Virus Nucleic Acid Contaminate Many Vaccines References
Could retroviral contamination be the
cause of Gulf War Illness syndrome? If so the virus(es) are still unknown
because they were so hard to detect. Perhaps modern analysis of frozen blood
samples will find them
Retroviruses in blood are really hard to
detect unless you are a highly skilled virologist, like Dr Mikovits. But
several papers have shown ~50% to over 80% associations with CFS patient blood
and XMRV associated virus, when samples were selected based on immune system
abnormalities. They also show the 6% to 8% XMRV-related virus strains in the
controls that have latent infections but are asymptomatic.
Lets see if the CDC can shift mode here
and start protecting the US citizens in time to prevent a total wipe out of our
civilization by the escalating Autism epidemic. So far the US health
administrators have been using 'studies designed to find nothing' to
"prove" that the 'studies that found the virus' are mistaken. This is
flawed logic. Absence of evidence is evidence of incompetence. "Look
away, nothing to see here" is not a viable medical policy in the face of
an epidemic.
I was searching for a Pareto chart of
Autism/ASD factors and could not find any analysis.
Else vaccine 100% mandates plus problem vaccines
will continue to cause cumulative harm to the human genome in the name of
hypothetical future benefits. Not a good trade at all!
What to Do? [About COPD, Autism, Prostate Cancer, ME/CFS,
Alzheimer’s/Parkinson’s, Opioid Addiction, Diabetes/Obesity, etc]
1.
Stop all/problematic live virus vaccines as a
matter of public safety. It is impossible to test for unknown retroviral
contamination. Safety science must be improved and applied before vaccines can
become safe.
2.
Eliminate obsolete and ineffective vaccines from
the schedule.
3.
Stop all early vaccination where the immune
system has not developed sufficiently.
4.
Use vaccines only to protect against real public
health emergencies, not to possibly protect against hypothetical threats.
5.
Reduce vaccine lobby funding greatly to force
prioritization to most cost effective and least dangerous vaccines.
6.
Sterilize the blood supply if this is practical,
else develop an XMRV test to identify contaminated blood and carriers of the
Virus
7.
Develop and apply anti
retroviral therapies to preserve the health of those infected with the XMRV
retrovirus. Look at HIV therapies that may apply to the XMRV family of viruses.
Do not vaccinate persons who are sick or have retroviral infections of the
immune cells.
8.
Start (Fund) an institute for the study and
identification of all retroviruses: Human and Animal, Complete the sequencing of
their RNA and identify these sequences in the host animal. Identify the
pathogenic sequences and taxonomy.
Apply this knowledge to develop tests for Epidemiology, so the threat to
the genome can be controlled.
9.
Test everyone for XMRV related and other retroviruses
in human blood, tissues, and tumors.
10. Test
everyone for immune dysfunctions and mitochondrial dysfunctions markers prior
to vaccinations. Set guidelines for safe and unsafe based on these test
results. One test might be a PET scan for localized low AA/DHAA values, Stone’s
morbidity index as it applies to vital organs, Heart, Brain, Kidneys, Liver,
lungs, ears, pancreas, etc.
11. Do
not vaccinate these persons/families testing positive for retroviruses that
suppress immune cells. This will avoid vaccine/adjuvant-stimulated
disabilities. XMRV family retroviruses
have emerged as a significant factor in mitochondrial dysfunction (MD) for
immune B, T, and Mast cells. In other reports
MD plus vaccination increases the odds of severe neuro- and other systemic/organ
tissue inflammation, histamine flares, ROS/NOS oxides, ascorbate depletion, and
organ failures for kidneys, heart, liver, gut, etc.
12. Add
high dosage vitamin C to the vaccination protocol to minimize the odds of
SIDS/SBS/anaphylaxis and other reactions.. Use high dosage sodium ascorbate IV
in case of severe vaccine reactions.
See Dr Tom Levy’s Primal
Panacea for details. Apply the
new ascorbate based ER
sepsis protocol to vaccine reactions.
13. Change
the vaccine making recipes to make it certain that uninfected cells are used to
grow viruses for vaccines. If adequate proof of cell purity from retroviruses,
mycoplasma, and other microbes cannot be tested, then do not deploy that
vaccine until proof from live contamination is within the state of the art.
Recent (Oct 2017) testing of research and developmental immortal cell lines has
shown many mistakes in identification and contamination with many live viruses
including MLRVs and XMRV family viruses. This has serious and multifold unknown
consequences in invalidating research and calls many vaccine production
recipes’ safety into question. XMRV family viruses is a notorious contaminant
of virology labs, having an aerosol propagation mode. This makes testing all
vaccines for XMRV contamination a priority quality/safety issue for all
vaccines.
14. Repeal
the 100% vaccination mandates.
15. Curb
the WHO and its dangerous policies. Too much misplaced trust in vaccine safety
and purity.
16. Stop
requiring vaccinations catch up in hospitals as condition for payment of other services
by public funded insurance. Vaccinating the sick causes kidney failure for some
unknown reason. Dr Suzanne Humphries
17. Reeducate
Bill Gates on vaccine tragedies in medical history so he realizes the potential
for harm of unbridled vaccine deployment in a world of unidentified viruses in
animal culture tissues. His pro vaccine support of mass vaccinations has done
both good and harm. He needs to learn more about the dark side of vaccine
failures. So he can maximize the good and minimize the multiple harms.
18. Revise
the vitamin C (AA-Ascorbic Acid) RDA amount to make AA’s RDA
condition-dependent. Provide more AA in
junk food to compensate for many deficits based on condition and
lifestyle: Chronic diseases, Toxins,
Smoking, Alcohol intake, Drug addiction, Age, Hyperglycemia and diabetes, etc,
all conditions contribute to an AA deficit and to antioxidant depletion. AA deficits require a higher intake for
normal health of tissues and organs. Stone’s
morbidity ratio, AA/DHAA, should be much greater than one in blood and
tissues. Blood AA for a 100 kg stressed
rat is about 15 grams per day. Gut to
blood transfer effectiveness is less than 10%.
19. Remove/repeal
vaccine-maker immunity from liability for all products that cause massive harms
to the public. There is fraud in the pro vaccine promotional propaganda.
20. Prosecute
False Claims Act violations and conspirators who have deprived the public of
their lives and health, based on lies about vaccine safety and effectiveness.
21. Seek
judicial decisions to makes the mandatory vaccination laws all
unconstitutional. Real harms vs. hypothetical benefits. Is injustice and
unconstitutional tyranny.
22. Publish
a medical history timeline of all vaccine failures, bad vaccine lots, and mass
tragedies known to medical historians. Make all doctors read this as a part of
their study of the Pro vaccine medical cult, under the topic of “Madness of
Crowds” and mistakes of the group-think medical consensus. Reference: SV40-Cancer, Uganda mass vaccine deaths, Australian
mass vaccine deaths, GWI, HIV
contamination of vaccines, XMRV & ME/CFS & Mitochondrial dysfunction of
Immune Cells.
23. HIV in Hepatitis vaccine for gays, ME/CFS
analysis, Vaccine failures, Autism Pareto chart analysis, GWI
tragedy from contaminations.
24. Remove
public health officials nationally and at the UN that have promoted unsafe
vaccines worldwide. Identify pro vaccine anti-safety ideologists in the
sciences and remove them from posts of influence. Stop claiming no evidence by
cherry picking and removing positive studies and emphasizing invalid or
worthless studies that prove or disprove nothing. Remove pro vaccine propaganda
from the health education information and news services.
25. Promote
the related sciences contributing to vaccine safety on a priority basis. Fund
studies of toxicology and its implications. Accurately measure the cumulative
tissue and organ loads of persistent adjuvants and the rates of depletion of the
inflammation promoting adjuvants and additives. Make PET scan technology available to clinical practices for
measuring the morbidity ratio AA/DHAA. This permits locating organs that have
ongoing inflammation and ascorbate antioxidant depletion, producing pathogenic
effects.
26. Do
a realistic benefit/harm analysis on the Flu vaccines and end or restrict the
programs that are unjustified when the lies and distortions are removed from
the analysis. Flu death statistics appear overstated, Ascorbate is a cure, Flu
vaccine adjuvants are cumulatively toxic, Adjuvants promote chronic
inflammation leading to early dementia and neural inflammatory disabilities.
27. Recognize
that the government vaccine mandates are unconstitutional, counterproductive,
and liable to do great harm. The dark side costs are not affordable, and the
benefits of vaccines for all are overstated and hypothetical.
28. Fix
the bankrupt vaccine insurance fund so it can truly compensate the victims of
dangerous vaccine events. Compensate
the victims of vaccine tragedies from public funds for the massive harms done
to the families of CFS/ME and Autism and other vaccine caused mandated
vaccines. VAERS statistics are biased
by too strict exclusionary rules, gross undercounting by orders of magnitude
and unfair evidence exclusionary rules. The vaccine court is bankrupt based on
charging too little for each dose and too high cost of the tragedies associated
with problem vaccines.
Karl Poehlmann October 24, 2017
Copyright 2017 by KF ^ KM Poehlmann, All Rights Reserved.
References:
http://www.ra-infection-connection.com/StopVaccTyranny.htm
Although this is CDC’s area of responsibility, It
appears that this analysis has never been performed, or if performed it has not
been published. This indicates a gross
dereliction of duty by the agency.