VACCINES :THE LIES AND THE LAW

I AM INCENSED BY THE RECENT SINGLE STUDY THAT "MAY" SHOW, "MAY", THAT HAVING MEASLES COMPROMISES THE IMMUNE SYSTEM FOR UP TO THREE YEARS.

I CAREFULLY READ THAT STUDY AND IT FAILS ON MANY LEVELS, AS I AM CERTAIN OTHERS IN THE SCIENTIFIC/MEDICAL COMMUNITY WILL BE POINTING OUT IN A FEW DAYS.
ONCE THAT HAPPENS, WHEN OTHERS IN THE SCIENTIFIC AND MEDICAL COMMUNITIES SHOOT DOWN THIS 'STUDY', I WILL POST THEIR COMMENTS HERE, AS AN UPDATE.

LET IT BE NOTED THAT THE "JOURNAL" THAT POSTED THE CURRENT "STUDY" DID NOT DO SO UNTIL 6 MONTHS AFTER ITS SUBMISSION, AND THAT THE STUDY HAS NOT BEEN ACCEPTED BY THE LANCET, JAMA, NOR A PEDIATRIC JOURNAL, TO DATE.

IN THE INTERIM, PLEASE ASK YOURSELVES, WHY, WHY NOW, HAS THE MEDIA AND SOME STATE GOVERNMENTS AS WELL AS THE CDC, THE WHO, AND PHARMACEUTICAL COMPANIES SO VICIOUSLY ASSAILED AMERICANS' RIGHT TO FREE WILL CHOICE AS TO WHETHER OR NOT TO VACCINATE THEIR OWN CHILDREN OR THEMSELVES?

IN OVER 60 YEARS THAT I HAVE BEEN AWARE OF "THE NEWS", I HAVE NEVER SEEN SUCH A HARANGUE, SUCH AN ATTACK ON FREEDOM OF CHOICE, AND NOT IN ALL PREVIOUS YEARS COMBINED CAN I RECALL AS MANY ARTICLES, ON-AIR DEBATES, AND SESSIONS OF STATE AND FEDERAL CONGRESSES ADDRESSING THE IDEA TO FORCE AMERICANS TO BE VACCINATED. 

WHAT NEXT? 
WILL THEY FORCE US TO BUY CERTAIN VEHICLES BECAUSE THEY'RE SAFER, OR PASS LAWS TO MAKE US ALL GET TESTS TO SEE IF WE HAVE "HIGHLY COMMUNICABLE DISEASES", OR GENETIC DEFECTS? 

THINK ABOUT THAT... MAYBE YOU WILL SEE THINGS IN A NEW LIGHT. 

FOR NOW, I WANT TO USE THE CDC's AND OTHER'S OWN WORDS TO SHOW YOU THE FALSE LOGIC AND BLATANT HALF-TRUTHS APPLIED TO THIS BUSINESS ABOUT "ALL MUST BE VACCINATED OR THE WORLD WILL END" HYSTERIA AND HYPE.

FIRST, ALTHOUGH MANY ARE SCREAMING THAT PARENTS WHO CHOOSE NOT TO VACCINATE THEIR CHILDREN WILL CAUSE PANDEMIC, SUCH HAS NOT BEEN THE CASE IN ALL THE TIME SINCE VACCINES WERE FIRST OFFERED. 

IN OVER HALF A CENTURY THIS HAS NEVER BEFORE BEEN AN ISSUE, NOR HAS IT HAPPENED!

TO THAT MYTH THAT THE UNVACCINATED CAN END THE WORLD AS WE KNOW IT, ANTI-VACCINE PARENTS MAY ASK: 
"HOW THE BLOODY HELL CAN MY UNVACCINATED CHILD INFECT YOUR VACCINATED KID?"  

GOOD QUESTION!
HOW, INDEED?

AH, BUT THE RETORT OF THE VACCINE PUSHERS, FANGS BARED HAS BEEN,
"WELL, SOMETIMES EVEN THE BEST VACCINES FAIL!"

THEN, HOW DO WE KNOW IT'S NOT THE VACCINATED KIDS, THE ONES WITH "FAILED" VACCINES, INFECTING THE UNVACCINATED, AS WE SAW RECENTLY WHEN IT WAS FOUND THAT THE VACCINATED SPREAD MEASLES AND WHOOPING COUGH IN TAT LEAST TWO INSTANCES DURING "OUTBREAKS"? 

[AND, BTW, TWO OF MY GRANDCHILDREN ATTENDED ONE OF THE ARKANSAS SCHOOLS THAT WAS CLOSED BY PERTUSSIS OUTBREAK...TWO YEARS IN A ROW!
BOTH WERE VACCINATED, BUT BOTH ACQUIRED PERTUSSIS AND WERE ILL FOR WEEKS.. AND PASSED IT ON TO THEIR TODDLER SIBLING AND MOTHER, WHO WERE ALSO VACCINATED.] 

"According to CDC reports, “most routine childhood vaccines are effective for 85% to 95% of recipients.   For reasons related to the individual, some will not develop immunity.”
It is not uncommon for a small portion of the vaccinated population to be infected, However, that does not prove that vaccinations are not effective."

SO RANTED ONE WEBPAGE I VISITED.

"DOESN'T PROVE VACCINATIONS ARE NOT EFFECTIVE"?

YES, YES IT ASSUREDLY PROVES JUST THAT! 

PERHAPS WHOEVER WROTE THAT RANT FAILED READING COMPREHENSION?

IF, AS THE CDC SAID, VACCINES ARE EFFECTIVE 85% TO 95% OF THE TIME, THEN, IN 5% TO 15% OF THE VACCINATED, THE VACCINE FAILED, i.e. WAS INEFFECTIVE.

SIMPLE MATH. 
SIMPLE LOGIC. 
READ.

AND IF VACCINES FAIL, AND THE CDC ADMITS THEY DO, THEN THOSE WHO ARE VACCINATED DON'T KNOW IF THEIR VACCINE "TOOK" OR NOT?
WHY NOT DO A FOLLOW-UP, SEE IF THE VACCINE WORKED? 

BECAUSE OTHER STUDIES HAVE SHOWN A GREATER FAIL RATE?
BECAUSE THEN WE MIGHT SEE THAT THERE ARE MORE THAN 15% OF THE VACCINATED WHO ARE STILL SUSCEPTIBLE TO DISEASE AS SOME STUDIES HAVE SHOWN? 

AMERICANS ARE SELDOM AFFORDED LOOKS AT EUROPEAN OR ASIAN PEER-REVIEWED STUDIES ON THIS TOPIC.
THAT'S A SHAME ,AS MANY FINE ONES HAVE BEEN DONE.
ANY THAT DISAGREE WITH VACCINE MANUFACTURERS ARE RIDICULED AND DENIED, BUT THAT DOES NO NEGATE THE FINDINGS.

WHAT PHYSICIANS KNOW THAT YOU MOST LIKELY DO NOT...
I WANT YOU TO LOOK WITH ME AT THE LIST OF "ADVERSE REACTIONS" THAT ACCOMPANIES EACH BATCH OF MMR VACCINE YOUR DOCTOR GETS. 

AFTER THIS, WE'LL LOOK AT THE HARMFUL EFFECT OF THE VIRAL PROTEIN IN VACCINES, AT THEIR FAILURE RATE, THE SIDE EFFECTS, THE DEBATE OVER ADDING ALUMINUM TO THE VACCINES, HOW THE MEASLES VACCINE ITSELF SUPPRESSES THE HUMAN IMMUNE SYSTEM, AND THE LACK OF STUDIES DONE ON LONG-TERM EFFECTS OF THE MMR VACCINE.

REMEMBER, THE FOLLOWING LIST IS PROVIDED BY MERCK, WHO MANUFACTURES THE MMR VACCINE: 

Adverse Reactions
The following adverse reactions are listed in decreasing order of severity, without regard to causality, within each body system category and have been reported during clinical trials, with use of the marketed vaccine, or with use of monovalent or bivalent vaccine containing measles, mumps, or rubella:

[NOTE: THESE, AS IT STATES ABOVE, ARE LISTED IN DECREASING ORDER OF SEVERITY WITHIN EACH CATEGORY...FOR EXAMPLE, UNDER DIGESTIVE SYSTEM, ITS DECREASING ORDER REACTIONS, ETC]

Body as a Whole

Panniculitis; atypical measles; fever; syncope; headache; dizziness; malaise; irritability.

Cardiovascular System

Vasculitis.

Digestive System

Pancreatitis; diarrhea; vomiting; parotitis; nausea.

Endocrine System

Diabetes mellitus.

Hemic and Lymphatic System

Thrombocytopenia (see WARNINGS, Thrombocytopenia); purpura; regional lymphadenopathy; leukocytosis.

Immune System

Anaphylaxis and anaphylactoid reactions have been reported as well as related phenomena such as angioneurotic edema (including peripheral or facial edema) and bronchial spasm in individuals with or without an allergic history.

Musculoskeletal System

Arthritis; arthralgia; myalgia.
This type of [arthralgia] involvement as well as myalgia and paresthesia, have also been reported following administration of MERUVAX II.
  In women, incidence rates for arthritis and arthralgia are generally higher than those seen in children (children: 0-3%; women: 12-26%),{17,52,53} and the reactions tend to be more marked and of longer duration. 
Symptoms may persist for a matter of months or on rare occasions for years.

Nervous System

Encephalitis; encephalopathy; measles inclusion body encephalitis (MIBE) (see CONTRAINDICATIONS); subacute sclerosing panencephalitis (SSPE); Guillain-Barré Syndrome (GBS); febrile convulsions; afebrile convulsions or seizures; ataxia; polyneuritis; polyneuropathy; ocular palsies; paresthesia.

Experience from more than 80 million doses of all live measles vaccines given in the U.S. through 1975 indicates that significant central nervous system reactions such as encephalitis and encephalopathy, occurring within 30 days after vaccination, have been temporally associated with measles vaccine very rarely. 

The Centers for Disease Control and Prevention has pointed out that "a certain number of cases of encephalitis may be expected to occur in a large childhood population in a defined period of time even when no vaccines are administered". 
However, the data suggest the possibility that some of these cases may have been caused by measles vaccines. 

Post-marketing surveillance of the more than 200 million doses of M-M-R and M-M-R II that have been distributed worldwide over 25 years (1971 to 1996) indicates that serious adverse events such as encephalitis and encephalopathy continue to be rarely reported.

There have been reports of subacute sclerosing panencephalitis (SSPE) in children who did not have a history of infection with wild-type measles but DID receive measles vaccine. 

Cases of aseptic meningitis have been reported to VAERS following measles, mumps, and rubella vaccination. A causal relationship between the Urabe strain of mumps vaccine and aseptic meningitis has been shown, there is no evidence to link Jeryl Lynn™ mumps vaccine to aseptic meningitis.

Respiratory System

Pneumonia; pneumonitis (see CONTRAINDICATIONS); sore throat; cough; rhinitis.

Skin

Stevens-Johnson syndrome; erythema multiforme; urticaria; rash; measles-like rash; pruritis.

Local reactions including burning/stinging at injection site; wheal and flare; redness (erythema); swelling; induration; tenderness; vesiculation at injection site.

Special Senses — Ear

Nerve deafness; otitis media.

Special Senses — Eye

Retinitis; optic neuritis; papillitis; retrobulbar neuritis; conjunctivitis.

Urogenital System

Epididymitis; orchitis.

Other

Death from various, and in some cases unknown, causes has been reported rarely following vaccination with measles, mumps, and rubella vaccines; (see CONTRAINDICATIONS). 

Under the National Childhood Vaccine Injury Act of 1986, health-care providers and manufacturers are required to record and report certain suspected adverse events occurring within specific time periods after vaccination. 

However, the U.S. Department of Health and Human Services (DHHS) has established a Vaccine Adverse Event Reporting System (VAERS) which will accept all reports of suspected events.

 A VAERS report form as well as information regarding reporting requirements can be obtained by calling VAERS 1-800-822-7967. 

<End adverse reactions list>

THE LATEST HYPE TO TRY TO GET ALL PARENTS TO SUBJECT THEIR CHILDREN TO THE ABOVE POSSIBILITIES IS ALL ABOUT MEASLES, THE DISEASE, CAUSING LONG-TERM IMMUNE SUPPRESSION.
THREE YEARS SEEMS TO BE THEIR FAVORITE CRY.

THE MEASLES VACCINE ITSELF CAUSES SUPPRESSED IMMUNITY!
WE'VE KNOWN THAT SINCE AT LEAST 1969!

THE PROBLEM IS, THERE HAVE BEEN ZERO LONG-TERM, FOLLOW-UP STUDIES THAT SHOW HOW LONG SUCH IMMUNE SUPPRESSION LASTS AFTER THE MMR VACCINE!

IN FACT, DAMNED FEW, ALMOST NO LONG-TERM STUDIES HAVE BEEN DONE TO SEE WHAT HAPPENS TO VACCINATED CHILDREN!
THEY WERE NOT REQUIRED BEFORE FDA APPROVAL!

JUST ONE OF MANY STUDIES THAT SHOWED IMMUNE SUPPRESSION AFTER VACCINATION:

EFFECT OF MEASLES VACCINE ON IMMUNOLOGIC RESPONSIVENESS
P Fireman, G Friday, J Kumate - Pediatrics, 1969 
 The American Academy of Pediatrics

"The attenuated measles virus temporarily suppressed the cutaneous delayed hypersensitivity reaction to purified protein derivative for 1 to 4 weeks; in addition, the delayed hypersensitivity reactions to candida, vaccinia, diphtheria toxoid, poison ivy, and 2,4-dinitrochlorobenzene antigens were also temporarily suppressed for 1 to 4 weeks. A modest depression of total leucocyte counts, including small lymphocytes, was noted for 1 to 3 weeks; at the same time, the capacity of lymphocytes from patients who received live measles vaccine to respond in vitro to stimulation with purified protein derivative, candida, and ragweed antigens was suppressed without decrease in their in vitro response to phytohemagglutinin. 

The mechanism of the suppression of delayed hypersensitivity by live measles vaccine appears dependent on a viable virus since killed measles vaccine had no demonstrable effect on pre-existing cutaneous delayed hypersensitivity or on the in vitro lymphocyte responses. 

This study demonstrates that live attenuated measles virus interferes with the capacity of the recipient to express cutaneous delayed hypersensitivity without suppression of humoral antibody."  

LIVE ATTENUATED VACCINES...A HISTORICAL PROBLEM

Live vaccines are usually avoided in patients with compromised immune systems.
WHY?

FROM MAYO CLINIC
"Vaccines help stimulate your immune system to fight off certain diseases. 

A compromised immune system can't recognize and fight off bacteria, viruses or other germs the way a healthy immune system can.

[LOOK! NO MENTION THAT THE MEASLES VACCINE CAN FURTHER SUPPRESS AN IMMUNE SYSTEM!]

Beware of live vaccines!

Your doctor may avoid giving you live viral vaccines, such as measles-mumps-rubella (MMR) or chickenpox (varicella) vaccines, because the live viruses may cause complications if you're immunocompromised.  

Measles-mumps-rubella (MMR)

Not recommended for immunocompromised adults."

FROM THE WORLD HEALTH ORGANIZATION [WHO]:

"Available since the 1950s, live attenuated vaccines (LAV) are prepared from living micro-organisms (viruses, bacteria currently available) that have been weakened under laboratory conditions. 

LAV vaccines will replicate in a vaccinated individual and produce an immune response but usually cause mild or no disease. 

STOP RIGHT THERE!

"LAV VACCINES WILL...USUALLY CAUSE MILD OR NO DISEASE."

WHY, YES, YES IT DOES!

MERCK'S PACKAGE INSERT FOR PHYSICIANS SHOWS US HOW MANY DISEASES THE MMR CAN CAUSE!

THANK YOU, WHO.

AND WE KNOW THE VACCINE CAUSES REPLICATION OF THE VIRUS INSIDE THE HUMAN BODY, THANKS, BUT WHAT CAN THAT DO? 

FROM ANOTHER 'STUDY':

"We have shown that T cells infected with measles virus produce an antiproliferative cytokine that can limit clonal expansion of the antigen-specific T cells.

We show that infection with as few as five infectious viral particles added to 10,000 EBV-transformed B cells can inhibit their proliferation. 

Similarly, five infectious viral particles used to infect 1,000 B cells used as APCs can reduce antigen-specific T-cell proliferation.

This is the first example of a virus causing a cell to produce a factor that inhibits APC function.

Jacobson et al. found that much of the CTL response in humans to measles virus was major histocompatibility complex class II restricted , and they identified the restricting element as HLA-DR2. 

They suggested that the CTL response was skewed to the internal viral proteins such as the nucleocapsid protein. "

JUST 5 INFECTIOUS MEASLES VIRUS PARTICLES CAN AFFECT 10,000 HUMAN CELLS.

HOW MANY VIRUS PARTICLES IN A DOSE OF VACCINE? 

INTERESTINGLY, LITTLE REALLY 'NEW' DATA (APART FROM THE ABOVE STUDY AND SEVERAL OTHERS HERE AND ABROAD) EXIST IN THIS "NEW" STUDY ON IMMUNE SUPPRESSION GOING ON FOR YEARS, AS OPPOSED TO WEEKS OR MONTHS, AS WE KNOW IS A RESULT OF THE MMR VACCINE.

ABOUT THOSE "INTERNAL VIRAL PROTEINS...OUR BODIES HATE THOSE AND REACT STRONGLY, SOMETIMES FATALLY SO, AGAINST THEM! 

Anyone who understands the basics of biology will know that all vaccines by their very definition are antigens and every antigen by definition must be a FOREIGN PROTEIN.

NOWHERE IN NATURE ARE FOREIGN PROTEINS ALLOWED TO ENTER THE BLOODSTREAM WHOLE AND INTACT! 

 They are always first digested in your intestinal system and broken down into its constituent amino acids, dipeptides and tripeptides. 

Any interference or tampering with these laws of existence, such as injecting foreign proteins, has great potential to bring calamity to your health and cause autoimmune diseases like autism.. 

This is precisely what may be happening with our massive reliance on vaccine injections.  

WHERE LIES THE BULK OF A HUMAN IMMUNE SYSTEM? 

LET'S START WITH A DIAGRAM CREATED FOR CHILDREN:

THAT'S NICE.  

HOWEVER, IT DOES NOT SHOW THE REALLY IMPORTANT ASPECT OF THE HUMAN IMMUNE SYSTEM...THE GUT...THE LARGE, AND THEREBY ALSO, SMALL, INTESTINES! 

THEREIN LIE THE MANY BILLIONS OF PROBIOTIC (MEANING "FOR LIFE") BACTERIA THAT WE ALL MUST HAVE TO LIVE, TO EVEN BEGIN TO MAKE IT OUT IN THE WORLD. 

 "Most people don’t know that 60-70% of their immune system is located in the gut as a vast network of lymph tissue referred to as GALT (gut associated lymphatic tissue). 

The probiotics in our gut are constantly interfacing with the GALT and essentially priming the immune system for contact with other bacteria. 

They serve as a way for the body to learn how to respond to bacteria without actually having to suffer an infection. 

This becomes particularly important in young children whose immune system is in constant state of development until about age 7."

REMEMBER THAT STATEMENT ABOUT CHILDREN'S IMMUNE SYSTEM BEING A WORK IN PROGRESS UNTIL ABOUT AGE 7! 

SO, WHILE THE HUMAN BLOODSTREAM REJECTS WHOLE PROTEINS AND SERIOUSLY REBELS AGAINST ANY, SOMETIMES SUCCUMBING DURING THE STRUGGLE, THE HUMAN GUT CAN FAR MORE OFTEN AND FAR MORE EFFECTIVELY HANDLE IT!

AND THAT IS WHY WE EAT PROTEINS AND DON'T INJECT THEM.

WHERE DO VACCINES ATTACK FIRST? 

THE HUMAN BLOODSTREAM!  

THEREIN LIES A MAJOR PROBLEM WITH VACCINES. 

THEY ATTACK OUR IMMUNE SYSTEM IN ITS WEAKEST PLACE, AND CREATE ABSOLUTE CHAOS.

OUR GOVERNMENT DOES NOT DENY ALL SIDE EFFECTS FROM VACCINES.

IT EVEN LISTS A FEW <HERE>.

LET'S LOOK AT THE MMR VACCINE'S KNOWN SIDE EFFECTS: 

MMR VACCINE SIDE-EFFECTS
(MEASLES, MUMPS, AND RUBELLA)

Mild Problems

• Fever (up to 1 person out of 6)
• Mild rash (about 1 person out of 20)
• Swelling of glands in the cheeks or neck (about 1 person out of 75)

If these problems occur, it is usually within 7-12 days after the shot. They occur less often after the second dose.

Moderate Problems

• Seizure (jerking or staring) caused by fever (about 1 out of 3,000 doses)
• Temporary pain and stiffness in the joints, mostly in teenage or adult women (up to 1 out of 4)
• Temporary low platelet count, which can cause a bleeding disorder (about 1 out of 30,000 doses)

Severe Problems (Very Rare)

• Serious allergic reaction (less than 1 out of a million doses)
• Several other severe problems have been reported after a child gets MMR vaccine, including:
  • Deafness
  • Long-term seizures, coma, or lowered consciousness
  • Permanent brain damage

WHY AREN'T WE GIVEN STATS ON HOW OFTEN DEAFNESS, SEIZURES, COMA, BRAIN DAMAGE HAVE BEEN REPORTED LIKE THEY GIVE US STATS ON ALLERGIC REACTION?

BUT WAIT, THERE'S ANOTHER MEASLES VACCINE. 

MMRV VACCINE SIDE-EFFECTS

(MEASLES, MUMPS, RUBELLA, AND VARICELLA)

Moderate Problems

Seizure caused by fever (about 1 child in 1,250 who get MMRV), usually 5-12 days after the first dose. 

They happen less often when MMR and varicella vaccines are given at the same visit as separate shots (about 1 child in 2,500 who get these two vaccines), and rarely after a 2nd dose of MMRV.

Temporary low platelet count, which can cause a bleeding disorder (about 1 child out of 40,000).

Severe Problems (Very Rare)

SEVERAL severe problems have been reported following MMR vaccine, and might also happen after MMRV. These include severe allergic reactions (fewer than 4 per million), and problems such as:

Deafness.

Long-term seizures, coma, lowered consciousness.

Permanent brain damage.

AGAIN, NO STATS ON FREQUENCY OF OCCURRENCE OF THESE "RARE" SIDE EFFECTS AFTER THAT ONE "ALLERGIC REACTIONS" STAT...AND, DO "ALLERGIC REACTIONS" INCLUDE FATAL ANAPHYLACTIC REACTION? 

NOTICE HOW LIFELONG DEAFNESS, SEIZURES, COMA AND PERMANENT BRAIN DAMAGE ARE CALLED MERE "PROBLEMS".

THE CFR KNOWS

A 2014 report published by the Council on Foreign Relations (CFR) openly states "that the most highly vaccinated populations are also those with the greatest number of outbreaks for those same infectious diseases. This was especially the case for measles, mumps, rubella, polio and pertussis outbreaks."

The Office of Medical and Scientific Justice (OMSJ), having thoroughly analyzed the conclusions presented in the CFR report, determined that even the CFR isn't convinced that herd immunity is a scientifically legitimate concept.

The OMSJ concluded that given "the repeated incidences of infectious outbreaks in populations with 94% or more vaccine compliance [the alleged threshold when herd immunity is activated], and the emergence of new viral strains, the concept of herd immunity should be forgotten.

"The Office offers several possibilities to explain the report: 1) vaccines are increasingly becoming ineffective and causing 'immune dysfunction,' and 2) 'vaccine antigen responses' may be reprogramming viruses while weakening the immune systems of the most vaccinated individuals."

HOW DO VACCINE MANUFACTURERS PROPOSE TO ADDRESS THAT? 

APPARENTLY WITH SILENCE.

WHILE THE CDC IS CONSTANTLY IN THE MEDIA TALKING ABOUT HOW QUICKLY THOSE BAD OLD "NEW FLU STRAINS" ARE MUTATING, THE CDC SAYS DAMNED LITTLE ABOUT THE MUTATIONS AMONG THE COMMON VIRUSES THAT CAUSE CHILDHOOD DISEASES! 

WE SEE "NEW AND IMPROVED" FLU VACCINES EACH YEAR...WHY NOT THE SAME FOR MEASLES, PERTUSSIS, ETC?

Scientists: MMR Vaccine Should Not Have Been Licensed

Sunday Herald, London,
December 10, 2000

"Senior clinicians, including a former medicines regulator at the
department of health, argue that the MMR should not have been licensed in
1988 because there was insufficient evidence of its safety and the decision
to license it was "premature."

Dr Scott Montgomery an epidemiologist at Karolinska Hospital in Stockholm, Dr Peter Fletcher, who was a senior professional medical officer for the department of health in the early 1980s, are critical of the level of evidence supporting the introduction of the jab.

"Being extremely generous, evidence on safety was very
thin, being realistic there were too few patients followed-up 

for sufficient time. Three weeks is not enough, neither is four weeks." 

Caution should have ruled the day, answers to some important 

questions should have been demanded and encouragement should have been given to conduct a 12-month observational study on 10-15,000 patients

and a prospective monitoring programme set up with  a computerised primary care database.

The granting of a product licence was definitely premature." 

Another of the reviewers, Professor Duncan Vere, a clinical pharmacologist and former member of the Committee on the Safety of Medicines, agrees that the observation periods for the tests of MMR were too short.

"In almost every case, observation periods were too short to include

the time of onset of delayed neurological or other adverse events," he said.

"Interaction between vaccines had not been considered adequately in children with multiple vaccinations and potentially ill-developed immune systems.

 He adds: "It is possible that a group of children exists who are developing a disorder with gastroenteritis, abnormal reactions to measles virus and neurological disease. 

In the present condition they are highly likely to be vaccinated. 

The existing data throws no light on the question and new

comparative studies are needed to seek an answer to it." 

AS I SAID BEFORE, STUDIES FROM ABROAD ABOUND THAT ANYONE MAY FIND AND READ ONLINE.

THAT JAPAN QUITE EARLY ON STOPPED THE MMR SHOULD CAUSE AMERICANS TO QUESTION ITS SAFETY.

CDC WHISTLEBLOWER'S

"I will have to present several problematic results relating statistical associations between the receipt of the MMR vaccine and autism."

-Dr. William Thompson, Senior CDC Scientist, Vaccine Division (In letter to Dr. Julie Gerberding)

January 28, 2015

It was a shocking surprise last year when a senior epidemiologist at the CDC, Dr. William Thompson, acted upon his moral conscience and released thousands of pages of CDC documents with research data to Congress that unveil the agencies long history of fraudulent studies and medical cover-ups that hid the serious failures and health risks of vaccines. 

Dr. Thompson is a distinguished scientist who has worked at the CDC since 1998. Prof. Brian Hooker, a specialist in molecular and cellular systems, and the first person to be contacted by Dr. Thompson, stated during a recent broadcast that the released documents are not simply a smoking gun. Rather it is a “wildfire.”  Dr. Thompson is currently cooperating with members of a Congressional subcommittee. 

Dr. Anne Schuchat from the CDC has stated, “We know there are places around the country where there are large numbers of people who aren’t vaccinated. 

However, we don’t think those exemptors are driving this current wave. We think it is a bad thing that people aren’t getting vaccinated or exempting, but we cannot blame this wave on that phenomenon.” 

CDC BLEW ITS OWN WHISTLE, THEN REMOVED THE PAGE FROM ITS WEBSITE.

THE PAGE WAS ARCHIVED AND YOU MAY SEE IT FOR YOURSELF <HERE>.

• SV40 was discovered in 1960. Soon afterward, the virus was found in polio vaccine.


• More than 98 million Americans received one or more doses of polio vaccine from 1955 to 1963 when a proportion of vaccine was contaminated with SV40; it has been estimated that 10–30 million Americans could have received an SV40 contaminated dose of vaccine.


• SV40 virus has been found in certain types of cancer in humans.

I WISH TO PAUSE AND ADDRESS THE CONTAMINATED POLIO VACCINE. 

IN ANOTHER BLOG, I STATED THAT MANY OF MY 70+ CLASSMATES AND I WERE VICTIMS OF THIS VACCINE.

I AM A THREE-TIME CANCER SURVIVOR, NONE WERE METASTATIC. 

MY FIRST CANCER WAS DISCOVERED 4 YEARS AFTER THE VACCINE.

WHEN ALL OF US STUDENTS GOT THIS VACCINE, OUR PARENTS WERE ALSO INVITED TO BE VACCINATED.

ALL WERE.

OF MY ENTIRE FAMILY WHO WERE VACCINATED AT THE SAME TIME, INCLUDING MYSELF, MY PARENTS, A SIBLING, AN AUNT, AN UNCLE, TWO GRANDPARENTS AND 5 COUSINS, 13 INDIVIDUALS, I AND ONE MALE COUSIN, ARE THE ONLY SURVIVORS.

ALL OTHERS DIED FROM CANCER. 

ALL.

THE CDC LIED AND STUDIES HAVE ABSOLUTELY LINKED MILLIONS OF CANCERS TO THAT DAMNABLE SV40.

THE EVIDENCE IS IN OUR DNA!

THE CDC ALSO, AT ONE TIME, ADMITTED THAT THE MMR CAUSES AUTISM.

AGAIN, IT REMOVED ITS "RESOURCES FOR CONCERNED PARENTS".

… rubella (congenital rubella syndrome) is one of the few proven causes of autism.”  Walter A. Orenstein, M.D. US as Assistant Surgeon General, Director National Immunization Program in a letter to the UK’s Chief Medical Officer 15 February 2002.

HE WAS QUOTING THE CDC! 

rubella virus is one of the few known causes of autism.” US Center for Disease Control.

The current President of Merck’s Vaccines Division, Julie Gerberding confirmed to CBS News when she was Director of the US Centres for Disease Controlthat:

Now, we all know that vaccines can occasionally cause fevers in kids. So if a child was immunized, got a fever, had other complications from the vaccines. And if you’re predisposed with the mitochondrial disorder, it can certainly set off some damage. Some of the symptoms can be symptoms that have characteristics of autism.“

HOUSE CALL WITH DR. SANJAY GUPTA – Unraveling the Mystery of Autism; Talking With the CDC Director; Stories of Children with Autism; Aging with Autism – Aired March 29, 2008 – 08:30   ET

MERCK'S DIRTY TRICKS...BUSTED!

October 12, 2009

MERCK WAS 'BUSTED' FOR PUBLISHING SEVERAL ISSUES OF A FAKE JOURNAL.

The claim that Merck had created a journal out of whole cloth to serve as a marketing tool was first reported by The Australian about three weeks ago. 

[NOTE: THE STORY WAS ONLINE AT THE FOLLOWING WEBSITE BUT NOW GIVES A "FORBIDDEN" NOTICE WHEN ATTEMPTS ARE MADE TO ACCESS IT. http://www.theaustralian.news.com.au/story/0,25197,25311725-5013871,00.html ]

It came to light in the context of a civil suit filed by Graeme Peterson, who suffered a heart attack in 2003 while on Vioxx, against Merck and its Australian subsidiary, Merck, Sharp & Dohme Australia (MSDA). In testimony provided at the trial last week Dr. George Jelinek, an Australian physician and long-time member of the World Association of Medical Editors, reviewed four issues of the journal that were published from 2003-2004. An "average reader" (presumably a doctor) could easily mistake the publication for a "genuine" peer reviewed medical journal, he said in his testimony. "Only close inspection of the journals, along with knowledge of medical journals and publishing conventions, enabled me to determine that the Journal was not, in fact, a peer reviewed medical journal, but instead a marketing publication for MSD[A]."

YOU MAY STILL READ ABOUT THIS HERE:

MERCK'S FALL FROM GRACE

IT WAS NOT THE FIRST TIME MERCK'S ATTEMPTS TO SILENCE PHYSICIANS WAS REVEALED.

A CBS REPORT LED TO THE DISCOVERY OF SOME SHOCKING EMAILS FROM MERCK.

SEE THOSE DOCUMENTS <HERE> AND ALSO <HERE>.

IN THE CASES OF HANNAH POLLING AND BAILEY BANKS, THE COURTS FOUND THAT HIS CONDITION (ACUTE DISSEMINATED ENCEPHALOMYELITIS) WAS CAUSED BY THE MMR VACCINE. 

The Concession Report declared that Hannah had an underlying mitochondrial condition which contributed to her “autistic-like” symptoms.

A PDF FILE SHOWING THAT AND MUCH MORE, <HERE>.

FAR ABOVE IN TEXT SOMEWHERE IS A REFERENCE TO THE JERYL LYNN STRAIN OF THE MUMPS VACCINE.

"This story has a long timeline.  It starts with the mumps vaccine that Merck’s eminent vaccinologist Maurice Hilleman, MD, came up with using a strain he developed from his five year old daughter—commonly referred to as the “Jeryl Lynn” strain—that has been manufactured by Merck since 1967.

In essence what transpired is the vaccine virus was “passaged” over the years through various growth medium or animal cells that caused the vaccine to lose its potency—let’s say ‘watered down’—and it became non-effective against the “wild” mumps virus. However, Merck had contended its MMRII vaccine was 95 percent effective. " 

However, other Merck vaccines contained the ‘watered down’ mumps vaccine.  They included the quadravalent vaccine ProQuad, and the trivalent MMRVaxpro Merck sold to European markets.  In 2005 the FDA recalled Merck’s ProQuad."

Long story short, FDA finally was able to sort out the mess with the help of the whistleblowers who became plaintiffs along with the United States of America ex rel., in the original complaint [Civil Action No.10-4374, U.S. District Court for the Eastern District of Pennsylvania] filed August 27, 2010.

One interesting factoid I found in the complaint is how the 1986 vaccine law probably came about.  Merck and the CDC were haggling about certain aspects of disclosing diminished efficacy and Merck made some suggestions in 1970 that CDC agreed to.  It basically was this: 

“It provided a way to assure that the CDC could purchase Merck’s vaccines without Merck being subjected to personal injury claims for failing to warn individual vaccinees or their parents about the safety and efficacy of vaccines administered through government vaccination programs.” [Complaint pg.32, clause 106]

ALUMINUM, NOW THAT MERCURY IS "ONLY" FOUND IN FLU VACCINES

While vaccines available in the US today exist with no Thimerosal (50% mercury), virtually all vaccines still contain aluminum, which has been linked to impaired neurological development in children.

Aluminum has not replaced thimerosal as a vaccine preservative; it has always been used in vaccines.

In the recent past, most US children got exposed to both thimerosal and aluminum simultaneously with the hepatitis B, Hib, DTaP (diphtheria, tetanus and pertussis) and pneumococcal vaccines.

Combining mercury with aluminum increases the likelihood that the mercury will damage human tissue.

According to a recent report by Michael Wagnitz, an American chemist, “Currently eight childhood vaccines that contain aluminum ranging from 125 to 850 micrograms (mcg). These vaccines are administered 17 times in the first 18 months of life, an almost six-fold increase compared to the vaccine schedule of the 1980s.”

Wagnitz adds, “According to the American Society for Parenteral and Enteral Nutrition, based on IV feeding solutions, a child should not exceed a maximum daily dose of 5 mcg of aluminum per kilogram of weight per day.

That means if a child weighs 11 pounds, the child should not exceed 25 mcg in a day. This level was determined to be the maximum safety limit based on a study published in the New England Journal of Medicine titled “Aluminum Neurotoxicity in Preterm Infants Receiving Intravenous Feeding Solutions.”

The hepatitis B vaccine, administered at birth, contains 250 mcg of ALUMINUM!


In a 1996 policy statement, “Aluminum Toxicity in Infants and Children,” the American Academy of Pediatrics states, 

“Aluminum can cause neurological harm. 
People with kidney disease who build up bloodstream levels of aluminum greater than 100 mcg per liter are at risk of toxicity. The toxic threshold of aluminum in the bloodstream may be lower than 100 mcg per liter. 

What level of aluminium toxicity is contained in vaccines routinely given German, French and other children in the EU is not known. It might be time for a public demand for such information to be disclosed, and before governments launch mass vaccination campaigns for untested vaccines against a non-proven H1N1 Swine Flu threat. "

ALUMINUM TOXICITY IN HUMANS 
NEUROTOXICITY WELL ESTABLISHED
(PubMed)

The neurotoxic properties of aluminium are well established; however, the evidence surrounding the potential association between aluminium and neurological disorders in humans is much less clear. 

... infants and children may be at higher risk for toxicity due to aluminium...

Modest evidence of an effect exists for reproductive toxicity following oral exposure, for neurological toxicity following either oral or injection exposure, and for bone toxicity following injection exposure. 

There is a large body of literature, mostly in the form of clinical reports, which documents the adverse effects of non-occupational aluminium exposure in individuals with impaired renal function. These patients are typically exposed to aluminium through dialysate fluid or medicinal sources. Anaemia, bone disease, and dialysis encephalopathy are the most commonly reported complications of aluminium exposure in this population.  

Aluminium hydroxide is used widely in pharmaceutical and personal care products. 

Aluminium has not been classified with respect to carcinogenicity; however, “aluminium production” has been classified as carcinogenic to humans by the International Agency for Research on Cancer (IARC). 

Apart from the potential that aluminium might interact directly with molecules implicated in Alzheimer's Disease (AD) and related neurodegenerative disorders, studies in animals have revealed potential mechanisms by which aluminium might indirectly impact on the function of the nervous system.

Increased oral aluminium absorption has been suggested in Alzheimer’s disease (AD) and Down’s subjects. 

Absorption of aluminium from intramuscularly (i.m.) injected aluminium hydroxide and aluminiun phosphate adjuvants is significant, and may eventually be complete. Tissue aluminium concentration increases with age.

Following i.v. injection, ~ 0.001 to 0.01% of the aluminium dose enters each gram of brain and ~ 100-fold more each gram of bone. Brain aluminium uptake across the blood-brain barrier (BBB) may be mediated by Tf-receptor mediated endocytosis (TfR-ME) and a Tf-independent mechanism that may transport aluminium citrate. There appears to be a transporter that effluxes aluminium from the brain into blood. 

Aluminium distributes into the placenta, foetus, milk, hair, and can be quantified in all tissues and fluids. 

The presence of aluminium in vaccines was found to be associated with macrophagic myofasciitis (MMF) at the site of i.m. injection. The toxicity of aluminium is affected by chelating agents and ligands although the mechanisms underlying toxicity remain unknown.

Aluminium accumulation in lysosome-like cytoplasmic granules of retinal neurons in rats exposed to very high doses of aluminium was reported. 
Severe atrophy of the retina and loss of photoreceptors was also noted.

From animal studies and the clear association of aluminium exposure and DAE, it is clear that high levels of aluminium in CNS can lead to neurotoxicity. 

From the present data, however, it is difficult to determine what level of exposure poses a risk for human health or which systems are most vulnerable. Based on projections from studies in dogs, individuals with sustained aluminium levels in serum that are 10-fold higher than the average range, or 1-2 μg/L, may be at increased risk for bone abnormalities. 

Whether general effects of aluminium on metabolic processes depress metabolism or reduce nutritional efficiency remains to be resolved.

There is little reported for aluminium compounds in the way of immunotoxicity. 

There may be an altered immune response to challenge following excess aluminium exposure and this may be influenced by the health and hormonal status of the dam with increased susceptibility to bacterial infection seen in pregnancy."

GROWING MEDIA FOR VACCINES... "CELL MEDIUM" FROM CHICKENS, PIGS, MONKEYS, COWS, HUMAN EMBRYOS, OH MY! 
THE THINGS THEY GROW VACCINES IN! 

FROM THE PACKAGE INSERT OF THE MMR VACCINE:

The growth medium for measles and mumps is Medium 199 (a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum) containing SPGA (sucrose, phosphate, glutamate, and recombinant human albumin) as stabilizer and neomycin.

DITTO FOR THE RUBELLA PART OF THE MMR:

The growth medium for rubella is Minimum Essential Medium (MEM) [a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum] containing recombinant human albumin and neomycin. Sorbitol and hydrolyzed gelatin stabilizer are added to the individual virus harvests.

Each dose of the vaccine is calculated to contain sorbitol (14.5 mg), sodium phosphate, sucrose (1.9 mg), sodium chloride, hydrolyzed gelatin (14.5 mg), recombinant human albumin (≤0.3 mg), fetal bovine serum (<1 ppm), other buffer and media ingredients and approximately 25 mcg of neomycin. The product contains no preservative. 

MERUVAX1 II (Rubella Virus Vaccine Live), the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.

   

On the thimerosal/mercury issue, and only because that is still in flu vaccines and a few others, all that needs to be said has been said and can be summed up thusly:

Attributed to Dr. Boyd Haley:

"You couldn't even construct a study that shows thimerosal is safe... It's just too darn toxic. If you inject thimerosal into an animal, its brain will sicken. If you apply it to living tissue, the cells die. If you put it in a petri dish, the culture dies. Knowing these things, it would be shocking if one could inject it into an infant without causing damage."  

AND YES, YES, ALL THAT HE SAID HAS BEEN PROVEN.

AS I SAID, I WILL UPDATE THIS BLOG BY START OF NEXT WEEK AFTER I FIND RESPONSES TO THE PSEUDO-SCIENCE OF THE MEDIA-LAUDED REPORT THAT HAVING MEASLES CAN LEAD TO YEARS OF IMMUNOSUPPRESSION. 

TO THOSE WHO READ THIS AND CHOOSE TO VACCINATE ANYWAY, GOOD LUCK! 

I CERTAINLY HOPE YOUR CHILDREN FARE WELL.

BUT JUST AS YOU HAVE YOUR RIGHT TO CHOOSE, SO DO ALL.

EVERY AMERICAN PARENT HAS A RIGHT TO DETERMINE WHETHER OR NOT HE/SHE WANTS TO SUBJECT THEIR CHILDREN TO THE LIKES OF MERCK AND ITS VACCINES.

TO SET UP A HOWL THAT THE FEDERAL GOVERNMENT FORCE ALL PARENTS TO VACCINATE THEIR CHILDREN IS OBSCENE!

AND CRIMINAL! 

IF YOU ARE A DEVOUT BELIEVER IN THE SAFETY OF VACCINES, IMAGINE HOW YOU WOULD FEEL IF THOSE OPPOSED TO VACCINES FOUND A WAY TO FORCE YOU TO STOP VACCINATING YOUR CHILDREN! 

DO AS YOU PLEASE, LET OTHERS DO THE SAME, AND PREPARE YOUR MINDS FOR THE POSSIBILITY THAT YOUR CHILD WILL DEVELOP THE VERY THING THE MAKERS OF VACCINES SWEAR TO YOU THEY DO NOT CAUSE.

I SINCERELY PRAY WITH ALL MY HEART THAT YOU WILL BE ABLE TO LIVE WITH THE GUILT SHOULD THAT HAPPEN.

A DEAR FRIEND AND COLLEAGUE WAS NOT ABLE TO LIVE WITH THE GUILT AFTER HER SON BECAME DEAF AFTER HIS MMR.

HE WILL NEVER KNOW HIS MOTHER.

HER LOSS BROKE MANY HEARTS.

I PRAY NO ONE ELSE ON EARTH WILL CONSIDER HER "WAY OUT".

THERE IS ALWAYS, ALWAYS HOPE!

VACCINATED OR NOT, MAY ALL OUR CHILDREN BE SAFE! 

PERHAPS NOT CITED (hyperlinked) ABOVE, OTHER SOURCES FOR THIS BLOG:

~ http://cid.oxfordjournals.org/content/early/2014/02/27/cid.ciu105  

Twice-vaccinated individual spread measles to others.

~ http://www.ccg-nicosmits.nl/pdf/weten/Vaccination%20Causes%20Autism.pdf

ADMISSION BY U.S. SURGEON GENERAL AND THE CDC THAT RUBELLA VACCINE CAUSES AUTISM.

~  http://www.ncbi.nlm.nih.gov/pubmed/25391635 

~  http://cid.oxfordjournals.org/content/early/2014/02/27/cid.ciu105

~  http://www.washingtonpost.com/national/health-science/measles-cases-are-spreading-despite-high-vaccination-rates-whats-going-on/2014/06/23/38c86884-ea97-11e3-93d2-edd4be1f5d9e_story.html

~  http://articles.mercola.com/sites/articles/archive/2012/04/17/pertussis-vaccine-for-whooping-cough-effects.aspx

~  http://www.cdc.gov/media/releases/2012/t0719_pertussis_epidemic.html

~  http://www.ncbi.nlm.nih.gov/pubmed/11268375

~  http://link.springer.com/article/10.1007%2Fs12026-014-8574-4#page-1

~  http://www.greenmedinfo.com/blog/breaking-news-millions-children-infected-vaccine-safety-experts-rotateq-vaccine

~  http://sanevax.org/hpv-not-cause-cervical-cancer/

~  http://www.ncbi.nlm.nih.gov/pubmed/25429011

~ http://naturalsociety.com/97-compliance-chicken-pox-vaccine-still-causes-outbreaks/

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