From: Katharine Cushing [hcushing@tampabay.rr.com]
Sent: Friday, March 23, 2001 11:11 PM
To: fdadockets@oc.fda.gov
Subject: DO THE RIGHT THING!! 

I am a consumer, a mother, a citizen of America and I demand that you do the right thing in regard to our public health and well-being!!!!  The FDA has not always been reliable in doing the RIGHT THING - DO SO NOW!!!  You are required by law to protect the public interest and as such you must make genetically engineered products KNOWN to Americans so that they are WISE in their purchases!!!  You have been negligent in the past to the DEATH of many Americans due to cancers, and risks from all types of products - cigarettes, saccharine - DO THE RIGHT THING FOR THE CONSUMER!!!!!  WE DEMAND IT!!
 
* The FDA must require mandatory pre-market comprehensive 
  environmental review. Unlike conventional pollutants, 
  where a given amount of pollutant causes a limited amount 
  of damage, a small number of mutant genes could have a 
  population explosion and reproduce forever, causing 
  unlimited and irreparable damage.

* The FDA must require mandatory pre-market long-term health 
  testing. GE products could be toxic, cause allergic 
  responses, have lower nutritional value, and compromise 
  immune responses in consumers.

* The FDA must require mandatory labeling of GE products. 
  Without mandatory labeling, neither consumers nor health 
  professionals will know if an allergic or toxic reaction 
  was the result of a genetically engineered food. Consumers 
  would be deprived of the critical knowledge needed to hold 
  food producers liable should any of these novel products 
  be hazardous.

* The FDA must end its cozy relationship with the industries
  it purports to be regulating. People have been allowed to 
  work for a biotech company, then work for the FDA writing the 
  regulatory rules on that company's product, then go back to
  working for the company.  Ninety-two percent of FDA advisory 
  committee meetings had at least one conflict of interest.