Important message . . . We need everyone to participate!

[Guest guest]

Deb Pettitt is the woman who is doing the study of women getting explanted . . . She's top notch! . . . She heads a clinical research company . . . got sick from implants . . . and want to know why! - Rogene dpettitt@... Hey There!I just wanted to find out if you could post for the support group that on the media page of

ww.womenunderstudy.com there is a serious adverse event page for women who have suffered a long term disability from this approved medical device. This is what the FDA uses to wage taking a drug or device off the market. These reports are so powerful if we can manage to get more women to participate and complete and fax to the FDA. Let's clog up the fax line at the FDA with these forms!!! THE SERIOUS ADVERSE EVENT REPORTING FORM IS WHAT THE AGENCY LOOKS AT...OBVIOUSLY THE ONLY THING!! Deborah A. Pettitt, RN, BSN, CCRAYork

Clinical ConsultingDirector Of Women's HealthWK: (504) 866-2060FX: (504) 866-0888CELL: 1-888-473-5273 (note from Ilena ... to send MedWatch form, please go to: http://www.fda.gov/medwatch/report/consumer/consumer.htm