“YOU BEST START BELIEVING IN GHOST STORIES.
YOU’RE IN ONE.”
CAPTAIN JACK SPARROW
“PIRATES OF THE CARRIBBEAN:
THE CURSE OF THE BLACK PEARL”
Americans go to doctors, whom they trust,
who perform surgery on them in accredited hospitals
using FDA “approved” products.
Americans believe in the system. Americans don’t ask questions.
They trust a system that actually betrays them.
Congress and the FDA facilitate the pharmaceutical industry’s
betrayal of Americans and the health system.
There is greater interest in profitability for industry than
in assuring patient safety.
As for the efficacy (that they work) of thousands of medical devices
implanted in Americans,that is an unknown.
The FDA’s 510 (k) Pre-market Notification submission process only
“establishes” that medical devices are “substantially equivalent”
to a product already approved for sale before 1976.
There is no proof of the safety and efficacy of these medical devices.
No human clinical trials are required.
YOU are the human clinical trial!
"You best start believing in ghost stories. You’re in one!"
Mesh is the never ending nightmare brought to you
compliments of
our United States Congress passing the
Medical Device Amendments Act of 1976
creating the
U.S. Food and Drug Administration’s
510 (k) Pre-market Notification "Approval" Process.
CONGRESS HAS TO REVOKE THIS PROCESS
TO PROTECT AMERICANS!
Contact Your Congressman or Congresswoman!
Ask him or her to support legislation
creating an approval process that fully investigates
ALL Medical Devices and Drugs
BEFORE they are used or prescribed to the AMERICAN PUBLIC!
Ask him or her to stop the use of Americans as Guinea Pigs
for the benefit of the Medical Device Makers
and Pharmaceutical Companies!