"One million children have been diagnosed with this new and controversial diagnosis – “childhood bipolar.” And one million children are being treated for “childhood bipolar” disorder and more and more at younger and younger ages."
The primary promoters–inventors, one might say– of diagnosing children with "bipolar" disorder, who for over a decade, aggressively promoted the biopolar diagnosis and use of antipsychotics in children, were disciplined by Harvard University and its affiliated Massachusetts General Hospital.
The Alliance for Human Research Protection speaks out against a US government-proposed anthrax vaccine experiment on children. Such an experiment would sacrifice children’s welfare, much as canaries sent into the coal mines were sacrificed.
To date, the available evidence about the safety and efficacy of the anthrax vaccine is resoundingly negative. Three US government anthrax vaccine initiatives represent a reckless deviation from the precautionary principle of medical ethics and fiscal responsibility.
April 27, 2011: US Department of Health and Human Services Letter to National Biodefense Science Board seeks OK to Expose children to serious risks of Anthrax Vaccine.
July 1, 2005: Sen. Jeff Bingaman Letter of complaint to the Secretary of of Health and Human Services Stopped proposed Anthrax Vaccine Trial. in children.
Following our March 15 Infomail/ post, "Inside Psychiatry’s Battle to Define Mental Illness," we received an e-mail from Dr. Allen Frances, objecting–in essence retracting his statements in an article in WIRED magazine by Gary Greenverg. Our response to Dr. Frances follows his communication.
"From the start, the [Tri-University Schizophrenia Practice Guidelines] project subverted scientific integrity, appearing to be a purely scientific venture when it was at its core, a marketing venture for Risperdal."
Medicine has been derailed from its Hippocratic tradition, science has been utterly corrupted by commercial interests, and doctors are disregarding patients’ interests. Patients are losing ground, no longer do they have a choice about the medical treatments that they get, or finding an ethical doctor whose recommendations are not tainted…
Introducing John Abrams, MD, author of Overdosed America.
FDA’s lax approval process for medical devices has shielded surgeons and manufacturers who have made a killing from a lucrative business venture. FDA has even awarded the seal of approval years after the rings were implanted in patients while still in the experimental stage–without their knowledge or informed consent.
U S Federal Court ordered an overhaul of mental health care for veterans, who are killing themselves by the thousands each year because of what the court called “unchecked incompetence” of the Department of Veterans Affairs.
Public Citzen petitioned FDA Commissioner to immediately removal from market Pfizer’s Alzheimer’s drug, Aricept 23 mg dose, because of serious safety hazards and failure to demonstrate efficacy. The petition also urges FDA to add a label warning on Aricept and generic donepezil (5 mg and 10 mg) stating: "Use of 20 mg per day is counter indicated."
