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Original Message
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Another rush to avert imminent and terrible crisis with what once again is shaping up to be a halfassed bumbling "plan" that isn't really a plan at all. The only difference?...this time they are going to be pumping the Stimulus package into your blood stream....how well did Santa's "Recovery Package" work?....we got sold a bill of goods with all that shovel ready bullshit that ended up being payoffs to states that brought the votes in and billions of dollars worth of non stimulating crap like a couple of tens of millions to protect the Harvest Mouse in San Fran Nancy's district and Cash for Clunkers aka the used American car Destruction Program...hey...! Lets burn down Cleveland and then re-build it! That will create jobs! and then we'll have.....what we started with before we burnt it down, no value added and the huge cost all for?....nothing but spending to replace what we already had....idiots....
You trust these retards to whip together 200 million doses of the fastest, cheapest vaccine ever made and shoot that shit into you?...cause I don't...and I won't be getting any flu shot.
On a personal note....Gillian Barre syndrome virtually killed my grandfather. He was moving to Florida from upstate NY right at the time the Swine flu scare was going down....his doctor talked him into getting the shot because of that move....he was never the same again and was indeed diagnosed with GBS....this was one of them old school hardass old guys that when I was a teenager I'd go up and stay with him for a week or two in the summer and help out doing heavy work clearing his land which he was always making more wooded brushed out and unusable portions into treed and clear usable area....this guy was up and out EVERYDAY at 6:00 AM mowing parts of the 5 acres of grass....then he'd wake me up around 9:00 and we'd eat a huge breakfast and breakout the heavy gear and chain saw trees...hual em out...hual out boulder sized rocks...etc etc...till dinner around 6pm and let me tell ya....that was one tough old dude....we'd knock back a beer or 2 after dinner...cause I was like only 16 so 2 was my limit..by his rules...lol....He'd go to bed around 9:00... and I was off to bang the local mountain gurls....lol....and he knew it.....so he figured I needed a few more hours sleep in the morning....rofl..
Just one of those tuff old salty birds that could prolly drink more whiskey, out hunt, out fight and out fuck most of us punkass teenagers who thought WE were hot shit...
Soon after he got that shot?...it wasted him....he was weak and had all sorts of health issues until it finally killed him about 10 years later....couldn't even walk after a time and had to be in a wheel chair.....I went down to visit him a few years before he died and he was in rough shape and it was all because of the Gullian Barre syndrome shit....he had a big handful of pills he had to take cause his blood pressure went to shit...and had tons of other problems that he never had before......and since he had company....we were drinking Johnny Black....so he swills down all these pills with the Whiskey and by then I could see it was hard for him to even lift the glass.......so I say...ummmm Grandpa...don't you think that maybe all them pills with whiskey will mess you up?...he said....I'm already messed up...fuck it....
So I've seen first hand what that can do...and it's not something you want to have happen to you or yours because as far as "side effects" go...one that more or less destroys your entire nervous system from the bottom up slowly is a pretty freakin bad one.....
>>>>>>>>>>
By Dr. Mercola
According to Kathleen Sebelius, Secretary of the U.S. Department of Health and Human Services, your children should be the first target for mass swine flu vaccinations when school starts this fall.
This is a ridiculous assumption for many reasons, not to mention extremely high risk.
In Australia, where the winter season has begun, Federal Health Minister Nicola Roxon is reassuring parents the swine flu is no more dangerous than regular seasonal flu. "Most people, including children, will experience very mild symptoms and recover without any medical intervention," she said.[ii]
Sydney-based immunization specialist Robert Booy predicts swine flu might be fatal to about twice as many children in the coming year as regular influenza. Booy estimates 10-12 children could die from the H1N1 virus, compared with the five or six regular flu deaths seen among children in an average year in Australia.[iii]
“Cure the Disease, Kill the Patient”
Less than 100 children in the U.S. die each year from seasonal flu viruses.[iv] If we use Australia’s math, a very rough estimate would be another 100 children could potentially die of swine flu in the United States in the coming year.
If children are the first target group in the U.S. per Sebelius, that means we’re about to inject around 75 million children with a fast tracked vaccine containing novel adjuvants, including dangerous squalene, to prevent perhaps 100 deaths.
I’m not overlooking the tragedy of the loss of even one child to an illness like the H1N1 flu virus. But there can be no argument that unnecessary mass injection of millions of children with a vaccine containing an adjuvant known to cause a host of debilitating autoimmune diseases is a reckless, dangerous plan.
Why are Vaccinations Dangerous?
The presumed intent of a vaccination is to help you build immunity to potentially harmful organisms that cause illness and disease. However, your body’s immune system is already designed to do this in response to organisms which invade your body naturally.
Most disease-causing organisms enter your body through the mucous membranes of your nose, mouth, pulmonary system or your digestive tract – not through an injection.
These mucous membranes have their own immune system, called the IgA immune system. It is a different system from the one activated when a vaccine is injected into your body.
Your IgA immune system is your body’s first line of defense. Its job is to fight off invading organisms at their entry points, reducing or even eliminating the need for activation of your body’s immune system.
When a virus is injected into your body in a vaccine, and especially when combined with an immune adjuvant like squalene, your IgA immune system is bypassed and your body’s immune system kicks into high gear in response to the vaccination.
Injecting organisms into your body to provoke immunity is contrary to nature, and vaccination carries enormous potential to do serious damage to your health.
And as if Vaccines Weren’t Dangerous Enough on Their Own …
… imagine them turbocharged.
The main ingredient in a vaccine is either killed viruses or live ones that have been attenuated (weakened and made less harmful).
Flu vaccines can also contain a number of chemical toxins, including ethylene glycol (antifreeze), formaldehyde, phenol (carbolic acid) and even antibiotics like Neomycin and streptomycin.
In addition to the viruses and other additives, many vaccines also contain immune adjuvants like aluminum and squalene.
The purpose of an immune adjuvant added to a vaccine is to enhance (turbo charge) your immune response to the vaccination. Adjuvants cause your immune system to overreact to the introduction of the organism you’re being vaccinated against.
Adjuvants are supposed to get the job done faster (but certainly not more safely), which reduces the amount of vaccine required per dose, and the number of doses given per individual.
Less vaccine required per person means more individual doses available for mass vaccination campaigns. Coincidentally, this is exactly the goal of government and the pharmaceutical companies who stand to make millions from their vaccines.
Will There Be Immune Adjuvants in Swine Flu Vaccines?
The U.S. government has contracts with several drug companies to develop and produce swine flu vaccines. At least two of those companies, Novartis and GlaxoSmithKline, are using an adjuvant in their H1N1 vaccines.
The adjuvant? Squalene.
According to Meryl Nass, M.D., an authority on the anthrax vaccine,
“A novel feature of the two H1N1 vaccines being developed by companies Novartis and GlaxoSmithKline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.”[v]
Novartis’s proprietary squalene adjuvant for their H1N1 vaccine is MF59. Glaxo’s is ASO3. MF59 has yet to be approved by the FDA for use in any U.S. vaccine, despite its history of use in other countries.
Per Dr. Nass, there are only three vaccines in existence using an approved squalene adjuvant. None of the three are approved for use in the U.S.
What Squalene Does to Rats
Oil-based vaccination adjuvants like squalene have been proved to generate concentrated, unremitting immune responses over long periods of time.[vi]
A 2000 study published in the American Journal of Pathology demonstrated a single injection of the adjuvant squalene into rats triggered “chronic, immune-mediated joint-specific inflammation,” also known as rheumatoid arthritis.[vii]
The researchers concluded the study raised questions about the role of adjuvants in chronic inflammatory diseases.
What Squalene Does to Humans
Your immune system recognizes squalene as an oil molecule native to your body. It is found throughout your nervous system and brain. In fact, you can consume squalene in olive oil and not only will your immune system recognize it, you will also reap the benefits of its antioxidant properties.
The difference between “good” and “bad” squalene is the route by which it enters your body. Injection is an abnormal route of entry which incites your immune system to attack all the squalene in your body, not just the vaccine adjuvant.
Your immune system will attempt to destroy the molecule wherever it finds it, including in places where it occurs naturally, and where it is vital to the health of your nervous system.[viii]
Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene.[ix] MF59 (the Novartis squalene adjuvant) was an unapproved ingredient in experimental anthrax vaccines and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets.[x]
The Department of Defense made every attempt to deny that squalene was indeed an added contaminant in the anthrax vaccine administered to Persian Gulf war military personnel – deployed and non-deployed – as well as participants in the more recent Anthrax Vaccine Immunization Program (AVIP).
However, the FDA discovered the presence of squalene in certain lots of AVIP product. A test was developed to detect anti-squalene antibodies in GWS patients, and a clear link was established between the contaminated product and all the GWS sufferers who had been injected with the vaccine containing squalene.
A study conducted at Tulane Medical School and published in the February 2000 issue of Experimental Molecular Pathology included these stunning statistics:
“ … the substantial majority (95%) of overtly ill deployed GWS patients had antibodies to squalene. All (100%) GWS patients immunized for service in Desert Shield/Desert Storm who did not deploy, but had the same signs and symptoms as those who did deploy, had antibodies to squalene.
In contrast, none (0%) of the deployed Persian Gulf veterans not showing signs and symptoms of GWS have antibodies to squalene. Neither patients with idiopathic autoimmune disease nor healthy controls had detectable serum antibodies to squalene. The majority of symptomatic GWS patients had serum antibodies to squalene.”[xi]
According to Dr. Viera Scheibner, Ph.D., a former principle research scientist for the government of Australia:
“… this adjuvant [squalene] contributed to the cascade of reactions called "Gulf War Syndrome," documented in the soldiers involved in the Gulf War.
The symptoms they developed included arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis), Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhoea, night sweats and low-grade fevers.”[xii]
Post Vaccination Follow-Up Might as Well Be Non-Existent
There is virtually no science to support the safety of vaccine injections on your long-term health or the health of your children. Follow-up studies last on average about two weeks, and look only for glaring injuries and illnesses.
Autoimmune disorders like those seen in Gulf War Syndrome frequently take years to diagnose due to the vagueness of early symptoms. Complaints like headaches, fatigue and chronic aches and pains are symptoms of many different illnesses and diseases.
Don’t hold your breath waiting for vaccine purveyors and proponents to look seriously at the long-term health consequences of their vaccination campaigns.
[link to articles.mercola.com]
USAToday.com, Swine flu shots may go to kids first, Sebelius says, June 16, 2009 [link to www.usatoday.com]
[ii] ABC.net.au, Health minister reassures parents over swine flu, July 2, 2009 [link to www.abc.net.au]
[iii] Google News, AFP, Australia urges calm after child flu death, July 2, 2009, [link to www.google.com]
[iv] Meryl Nass, M.D., July 4, 2009 [link to anthraxvaccine.blogspot.com]
[v] Meryl Nass, M.D., July 3, 2009 [link to anthraxvaccine.blogspot.com]
[vi] Rense.com, Vaccines, Autism, and Gulf War Syndrome, August 15, 2005 [link to www.rense.com]
[vii] The American Journal of Pathology, The Endogenous Adjuvant Squalene Can Induce a Chronic T-Cell-Mediated Arthritis in Rats, 2000 [link to ajp.amjpathol.org]
[viii] Vaccination Liberation, Adjuvant Index Page [link to www.vaclib.org]
[ix] Autoimmune Technologies, News Release: SQUALENE FOUND IN ANTHRAX VACCINE, [link to www.autoimmune.com]
[x] Autoimmune Technologies, Gulf War Syndrome: ANTI-SQUALENE ANTIBODIES LINK GULF WAR SYNDROME TO ANTHRAX VACCINE [link to www.autoimmune.com]
[xi] ScienceDirect.com, Experimental and Molecular Pathology, Volume 68, Issue 1, February 2000, Pages 55-64 [link to www.sciencedirect.com]
[xii] Adverse Effects of Adjuvants in Vaccines, by Viera Scheibner, Ph.D., 2000 [link to www.whale.to]
H1N1 vaccines with novel adjuvants being developed for potential mass use
The US government has contracted with at least 5 pharmaceutical manufacturers to develop and produce H1N1 vaccines, using a variety of platforms and manufacturing methods. This is an excellent approach, since at this point no one knows which will succeed and how long it will take to obtain desired quantities of vaccine.
A novel feature of the two H1N1 vaccines being developed by companies Novartis and Glaxo-Smith Kline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.
Each company has its own proprietary adjuvant, acquired in each case at high cost and intended for the high-stakes business of rapidly producing vaccines for novel pandemics or biological warfare threats.
Novartis' adjuvant is named MF59, and Glaxo's is ASO3. We know they work beautifully to strengthen vaccine efficacy. But how safe are they?
That is a very difficult question to answer. Novartis claims MF-59 has been used safely by over 40 million people. However, FDA has not seen fit to approve even a single US vaccine that contains these novel adjuvants.
One European vaccine contains MF59, and two European vaccines contain ASO4, which is a Glaxo adjuvant related to ASO3. Fluad (with MF-59) is only licensed for use in the over-65 population. This age group responds weakly to standard flu vaccines, and whether standard flu vaccines actually reduce flu cases in this age group is controversial. So a stronger vaccine may be indicated for this group. And as we age, we are much less likely to develop autoimmune disorders, so potential autoimmune side effects should also be less in this age group.
However, in the 12 years since Fluad was approved in Italy for older adults (and later in the EU, but not be every country in the EU) no other vaccine containing MF-59 has been licensed... even though MF-59 has been used in a large number of vaccine trials. Virtually all the scientific literature on this adjuvant has been produced by scientists working for the manufacturer, precluding an unbiased assessment of safety at this time.
Glaxo's ASO4 is used in Fendrix (a Hepatitis B vaccine). Fendrix may only be used for people with kidney disease. Patients on kidney dialysis have a high rate of Hepatitis B infection, and a weak immune system. So they are good candidates for an especially potent vaccine against a disease to which they are highly susceptible, and these recipients are unlikely to develop autoimmune complications.
Cervarix is a vaccine directed against several strains of human papilloma virus (HPV), licensed in both Europe and Australia, which contains ASO4. It is difficult to assess Cervarix' safety at this point in time, as data are limited. It is worth noting that FDA has delayed giving Cervarix a US license twice.
The June 19, 2009 Science magazine discusses use of these "next-generation," antigen-sparing adjuvants for an H1N1 pandemic. It quotes Norman Baylor, director of FDA's Office of Vaccine Research and Review, who noted that antigen-sparing strategies benefit populations, not individuals. "You have to think about those trade-offs," Baylor said.
Posted by Meryl Nass, M.D. at 6:36 PM
[link to anthraxvaccine.blogspot.com]
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