by Barbara Loe Fisher
As many parents head for the Autism One conference in Chicago next week to learn how to heal their children's vaccine-related brain and immune system dysfunction and worldwide anxiety about the swine flu lingers, the National Vaccine Information Center (NVIC) is opening registration for the Fourth International Public Conference on Vaccination
to be held Oct. 2-4, 2009 at the Hyatt Regency Hotel in Reston, Virginia near Dulles International Airport and Washington, D.C. The largest and oldest non-profit vaccine safety organization in North America, founded in 1982, is sponsoring the event to provide a public forum for open discussion about vaccine issues of concern to parents and health care professionals. The conference theme "Show Us the Science & Give Us A Choice" reflects NVIC's three decade pro- education and pro-informed consent stand defending the right of citizens to make fully informed, voluntary vaccine decisions for themselves and their children.
More than 35 speakers from the U.S. and traveling from Canada, United Kingdom, Italy, Japan, and Kenya will speak about the science, policy, law and economics of vaccination; the human right to informed consent to vaccination; as well as holistic health care options for preventing illness and staying well. Pre-conference state organizing sessions start Thursday evening, Oct. 1, and Friday and Sunday advocacy training, holistic health education and vaccine injury family networking sessions precede a post-conference Monday, Oct. 5 bus trip to Capitol Hill.
Friday, Oct. 2 Highlights: Peggy O'Mara, founder & editor of Mothering Magazine and Jane Bryant, founder & editor of the UK internet news service, One Click, start the first day with a discussion about freedom of the press. The keynote address will be delivered by renowned bioethicist George Annas, JD, MPH, Chair of the Department of Health Law, Bioethics & Human Rights at Boston University School of Public Health. HPV vaccine researcher Professor Diane Harper, MD, MPH of the University of Missouri, Kansas City School of Medicine, will examine informed consent issues involving Gardasil vaccine. Evidence for influenza vaccine efficacy will be reviewed by Italian epidemiologist and physician Tom Jefferson, MD, Cochrane Vaccines Field Coordinator.
Coming all the way from Kenya is cell biologist and vaccine researcher Bonnie Dunbar, PhD, who co- founded the Africa Biomedical Center, to inform the audience about the multi-disciplinary approach to meeting unique health challenges in Africa. She is joined by Canadian pediatrician Colin Forbes, MD, who will recount his more than 40 years of experience caring for children in Kenya and how he helped reduce child mortality in some of the most impoverished child populations in the world.
Returning briefly from a health research position in Japan, MIT doctoral candidate Peter Doshi will outline the impact on democracy of U.S. and global vaccine policies. Human rights activist Shiv Chopra, B.V.Sc., M.Sc., PhD, who was former scientific advisor to Health Canada, and is author of "Rotten to the Core" will give a presentation entitled "Public Health or Corporate Interests?"
During what promises to be an historic conference, pediatrician Bob Sears, M.D. offers an alternative schedule for use of 16 U.S. government recommended vaccines and will debate pediatrician Lawrence Palevsky, M.D., who presents an alternative view of how to maintain health and prevent chronic illness. Holistic health pioneers Joe Mercola, DO and Gary Null, PhD will talk about how good nutrition and understanding how to make healthy life choices is the key to staying well, while holistic veterinarian and immunologist, Richard Pitcairn, DVM, PhD, will teach the audience about how good nutrition and homeopathy can keep pets well and Life University Professor Matthew McCoy, DC, MPH will give a chiropractic perspective on informed consent to vaccination.
"Will the Law Protect Health Freedom?" is the question that constitutional and federal law experts, along with leading medical privacy and health freedom advocates will discuss. Vaccine injury and product liability law will be the topic explored by attorneys, who have won vaccine injury cases in the federal Vaccine Injury Compensation Program, and also have expertise in vaccine contamination and use of experimental vaccines in soldiers. Longtime vaccine choice lobbyists like PROVE President Dawn Richardson will join longtime autism activists M.I.N.D. Institute co-founder Rick Rollens and Unlocking Autism President Shelley Reynolds and others to help parents organize to educate legislators and protect the right to make informed vaccine choices.
During the past few years, there have been calls for elimination or severe restrictions of vaccine exemptions by doctors with ties to the vaccine industry and by government health officials seeking a 100 percent vaccination rate with all government recommended and mandated vaccines. NVIC has long taken a public stand for the basic human right to protect bodily integrity and the October conference provides a public forum not only for those, who want the freedom to make voluntary choices about using pharmaceutical products and medical interventions that carry known and unknown risks, but also for scientists, doctors, journalists and health safety advocates to present information and defend their right and responsibility to investigate and speak about improving vaccine science and policies to protect individual and public health.
The conference is supported by an educational grant from the Albert and Claire Dwoskin Family Foundation, which has made it possible for NVIC to keep the registration fee for those registering by August 30 at $195 for the three day, three night conference featuring top speakers from around the world. There is a low $95 per night hotel rate, which is unheard of in the Washington, D.C. area for a fine hotel like the Hyatt Regency. Meeting and hotel room space is limited in the only hotel in the village of Reston. Conference registration and hotel room reservation is on a first come, first serve basis. For more information about speakers, sponsorship opportunities and registration, go to www.NVIC.org
by Barbara Loe Fisher
Are you grabbing your face mask, stocking up on food and Tamiflu, locking your doors and keeping your TV tuned to the news to find out just how bad the "swine flu pandemic" really is going to get? While Americans are being scared to death, few are noticing how much of their tax money politicians are giving to drug companies
and government health officials to grease the skids to create more experimental flu vaccines and drugs and more effective ways to quarantine
or force their mass use whenever a "public health emergency" is declared in the future.
Call me cynical but not clueless. The bird's eye view I have had for the past 27 years at the National Vaccine Information Center has taught me one thing: the global alliance between Big Pharma and Big Public Health is a prescription for disaster that could extend far beyond a bout with the flu.
The international drama playing out right now before our eyes is an example of how citizens around the world can be easily manipulated by doctors and politicians engaging in fear mongering in the name of disease control to forward agendas that have more to do with ideology, power and corporate profits than health. When the U.S. Director of Homeland Security is the government official doing the talking rather than the U.S. Director of the Centers for Disease Control, put a copy of the U.S. Constitution in your pocket and take a look at federal and state legislation passed since September 11, 2001 to understand which civil rights you don't have anymore when government health officials declare a "public health emergency."
But before we take a look at the threat to civil liberties that pandemic fear mongering poses, let's take a look at how creation of a global human market for influenza vaccines works. It is a blueprint for Successful Marketing 101 (or perhaps it is all just a coincidence).
In 2006, the World Health Organization (WHO) issued an international call for all nations to do whatever it takes to increase public appetite and demand for annual influenza shots
as the main strategy to prepare for an influenza pandemic. In April 2007, the WHO used money
donated by the U.S. Department of Health and Human Services (DHHS) to fund the creation of influenza vaccine manufacturing plants in Mexico and other countries one week after the FDA gave Sanofi Pasteur a license
to produce an experimental bird flu (H5N1) vaccine. Sanofi Pasteur is just one of many drug companies
the U.S. government has given millions of dollars to for the creation of bird flu vaccines.
On February 19, 2009, the FDA's Vaccines & Related Biological Products Advisory Committee (VRBPAC) discussed whether to give approval for the testing of experimental bird flu vaccine on American infants
. VRBPAC consumer member, also NVIC's Director of Patient Safety Vicky Debold,PhD, warned that testing of an experimental pandemic bird flu vaccine on infants in the absence of a real epidemic and without assurances that unapproved novel oil based (squalene) adjuvants (AS03, MF59)
are safe, could pose unacceptable risks in terms of inducing severe immune dysfunction.
On February 27, 2009 it was confirmed that an influenza vaccine maker, Baxter International, had released a mixture of seasonal influenza viruses mixed with unlabeled live bird flu viruses
to facilities in Czechoslovakia, Germany, and Slovenia. Baxter, which is waiting for a license to manufacturer bird flu vaccine, explained it was an "accident" and that no harm was done.
On April 23, 2009, the world heard the first news reports about a mysterious pig (H1N1) and bird (H5N1)and human hybrid influenza virus that was making people sick near a Mexican pig farm. By April 30, the WHO had issued a Phase 5 "Alert"
warning that the world was facing an imminent pandemic influenza epidemic on the strength of several hundred cases of "swine" flu and less than 10 confirmed deaths.
The pandemic flu panic that has an especially strong grip on people living in Mexico and the U.S., thanks to the governments of both countries declaring a "public health emergency," has been a good thing for pharmaceutical companies in the pandemic flu business. Wall Street revealed that the pandemic scare sent stock prices soaring
for drug companies making anti-viral drugs, rapid flu diagnosis tests and influenza vaccines. Sanofi Pasteur, GlaxoSmithKline, Novavax, Baxter, Johnson & Johnson, Roche, BioCryst, and Vical are among the drug companies likely to benefit
from the world pandemic panic.
In all the chaos that has Americans running to drug stores to buy face masks, closing schools to wipe desks down with rubbing alcohol and avoiding public transportation, there is action being taken behind the scenes by politicians and government health officials to prepare the way for implementation of future quarantine and mass vaccination of citizens with experimental vaccines and drugs that have by- passed normal FDA regulations for demonstrating purity and potency of pharmaceutical products. A "public health emergency" has become an excuse to grease the skids and rush to market experimental drugs and vaccines that are not subject to product liability in the civil courts.
The creation of this pharmaceutical company stockholder dream scenario and simultaneous erosion of civil liberties in the name of disease control began in earnest in 21st century America after the tragic events on September 11, 2001. In a time defined by shock, fear, anger and deep sadness, Congress reacted quickly and passed the Homeland Security Act while CDC officials pulled out model state legislation (Model State Emergency Health Powers Act) that gave sweeping new powers to public health officials
to use the militia, if necessary, to quarantine citizens and force them to use experimental drugs and vaccines after the U.S. Secretary of Health declares a "public health emergency."
The stampede in 2001/2002 to re-write long standing public health laws in this country was fueled by reports that terrorists were in possession of weaponized smallpox and anthrax, a fear that was fostered by U.S. government officials and New York Times journalists reporting Iraq had secret stockpiles of weaponized smallpox and anthrax. This myth played a role in public support for the U.S.-Iraq War and persuaded Congress to pass Bioshield and pandemic influenza vaccine legislation
that gave billions of dollars to vaccine manufacturers, the Department of Defense (DOD) and the Department of Health and Human Services (DHHS) to create experimental bioeterrorism and pandemic flu vaccines while protecting drug companies and doctors from liability
for vaccine injuries and deaths that will occur.
The mandated, mass use of multiple vaccines has become big business in the last quarter century since the U.S. Congress passed a law in 1986 shielding vaccine makers and doctors from liability for vaccine injuries and deaths and the numbers of vaccines recommended by the federal health officials for American children multiplied from 23 doses of 7 vaccines to 48 doses of 14 vaccines from birth to age six
. For older children and adults, there are several dozen more federally recommended or state mandated vaccinations.
All of this liability protection and government vaccine mandating has been a boon for vaccine profit- making and public health agency empire building. In 1986, four drug companies made and sold vaccines in America and, by 2007, after corporate mergers and acquisitions there were six drug company giants
making and selling vaccines in the U.S. Today, there are more drug companies seeking to enter the lucrative multi- billion dollar U.S. vaccine market as financial predictions for global profits from the worldwide vaccine business
by 2010 have climbed to more than $20B.
A true global influenza pandemic that could take out projected millions of people is something all nations should prepare for using reasonable strategies to ensure the public health and safety. However, it is a matter of legitimate debate as to whether the primary strategy being urged by the WHO, pharmaceutical companies and government health agencies around the world - ramping up production and use of seasonal influenza vaccine and fast tracking the creation and human testing of influenza vaccines using novel but potentially risky adjuvants and cell substrates - is the way to effectively deal with public health or a future influenza pandemic.
Certainly, the loss of the human right to bodily integrity and informed consent to taking pharmaceutical drugs and vaccines that may pose serious health risks is not justified in the name of controlling pandemic influenza or any other infectious disease outbreak. Politicians should not bow to additional pressure from vaccine manufacturers and public health officials to by-pass normal FDA standards in proving safety and efficacy of pandemic flu vaccines and their components for the purpose of rushing them to market in response to the pandemic panic that has been created. The swine flu debacle of 1976 should have taught Congress that lesson.
A rational perspective that reduces pandemic fear and includes common sense advice for staying healthy in every season is being offered by holistic health doctors, such as Joseph Mercola, D.O.
and physician Congressman Ron Paul, M.D.
The next time you turn on the TV or the radio or search the internet for the latest news on the flu pandemic, take a deep breath and consider all the natural ways to stay healthy and resist influenza or any illness : washing your hands; eating nutritious food; drinking plenty of water; getting enough exercise, rest and sunshine, and lowering stress - which includes not walking around filled with fear, anxiety and dread.