Guest guest Posted May 16, 2005 Report Share Posted May 16, 2005 E-MAILS FROM MOMS WITH SICK CHILDREN Cc: fuchsmorrissey@... Dear Dr. Krauss, Should I send you each e-mail from women who have had their Dr. say " your child's problem's aren't from the implants " . They really are clueless so what am I to say? Do you really think it is fair to put this burden of explaining how lame the studies are on me?? I have my own health and family to deal with without this as well. Why is it up to me, the consumer, to " prove " my black fungi and bacteria filled implant is unsafe?? I really don't want to bother you with so many e-mails but I need to know who it is at the FDA that I refer these women to for answers. I know Sami is a contact person but she is working part-time. I think this is a full-time problem. The IOM never even looked at the individual reports on our children. THAT IS A CRIME. Please help me. Sincerely, PJ Brent PS Remember if the FDA approves the " new and improved " saline implant you really should do a recall of " old " ones that grow bacteria and fungi and make little babies sick. =========================== Dear , My daughter looked like she had Cerebral Palsy but it was finally diagnosed as CIDP. The pediatric neurologist would have NEVER thought to test for it because it is so rare. Please have your friends ped-neuro speak to mine. His number is 404 256 3535 Dr. Ed Goldstein. Love, PJ =========================== At 09:22 PM 3/4/2000 EST, you wrote: PJ, I forgot one more thing, I wanted to thank you for the information that you sent. I have some friends who breast feed, and I am forwarding this email on to them. This is very important information. Thank you for sending it to me I won't go on and on again, but I appreciate the information. Love, (Name Removed) PS My best friends' daughter-in-law breast fed, and she had implants, her child was born with Cerebral Palsy, and several neurological problems, of course the doctors see no connection to it, but we know differently. I have sent your email to her, she has already called me to thank me for it, she is sending it right away to her daughter in law. Thanks again. ********************************************************* HERE IS ANOTHER E-MAIL AT four, Connor has really funny skin. It is scaly and very dry. Very sensitive to anything even chewing red chewing gum irritates the skin around his mouth. I have to keep his skin really moisturized and use unscented products. I will keep an alert out for the small patches if they start to appear. Thank you for the information. How old was she? My child that lived 45 minutes looked like she had been burned and had scar tissue from the waist down, no genitals, Skin like you said shiny, just looked like melted plastic over the little bones. From the waist up she wasn't that bad, as far as skin. Thank you for responding. ============================= sey wrote: Dear ****** PJ Brent just sent me an email about you and your son. You questioned what are the first signs of scleroderma. I know that others may have different first signs, but for it was tissue that looked like varnished tissue on her legs. They were very, small patches of shiny tissue. Then with the first winter of her life these patches began to merge together. She also had (still has) very, very dry, cracked tissue that will wax and wane. Wherever the very dry tissue went is where the very shiny, varnished skin would go. It looks as though someone put spots of clear fingernail polish on her skin. I had this problem too with my skin my right hand on the last knuckle, but mostly on my right ankle, was also extremely dry-underneath the dry tissue was shiny skin, but my problem reversed itself after I had the mastectomy of both breasts in 1993. I never got my problem documented as I did not know what I was dealing with. As I saw experiencing the same thing I knew like mother like daughter. I have made a big issue out of 's tissue, her small body, large head and her very tiny hands and feet. Doctors at first dismissed my concerns, but I kept questioning what I saw. In 1996 at the age of 6 years old a skin punch biopsy was done which speaks VOLUMES. Hypersilicemia has never, ever been fully investigated in the first place and still to date has not been FULLY investigated...if the companies say that hypersilicemia has a " acceptable risk " then they need to show us mothers and the general public the studies...show us the studies! Because what I and my daughters are going through is not " acceptable " . Neuro problems, growth problems, diseases of autoimmunity like scleroderma in the offspring of a child whose mother had silicone & double lumen breast implants (3M/McGhan in my case) is NOT AN ACCEPTABLE RISK. Anyway, I made sure that I had a doctor who stayed neutral/objective and kept that open-mind. I did not want her (the physician) to side with me or against me...I just wanted her to tell me what she observed. Other doctors who also treat all of us see what has happened. Just hang in there with everything. At some point those in medicine will have to uphold medicine in its greatest/grandest form of DO NO HARM and uphold medicine, science, and research to a higher standard of DO NO HARM...after all they were suppose to do this in the first place and have failed greatly. Shame on those who fail to listen to their patient with an open mind, in a neutral/objective way which is indeed vital in medicine, research and science. Take care, Fuchs-sey Fuchssey@... http://www.sclerodermasupport.com/support/stories/scleroderma/diffuse/cindym.htm (ALWAYS REMEMBER: since when is it an " acceptable risk " in medicine, science and research to pull ones trigger, IN ONES YOUTH, in one's old age OR VIA THE PLACENTAL BARRIER IN THE OFFSPRING? ACCEPTABLE RISKS? Hold on wait a minute, I would call this negligence/self-serving/being medically stupid in its greatest form! " ACCEPTABLE RISKS " , the companies need to greatly define " acceptable risks " with a breast implant of any kind to me and others. What they (the breast implant companies) are doing to the general public and to the INNOCENT children of this earth is far worse than what did with smoking: Aflatoxin/ Aspergillus flavus, Tobacco, Ammonia, The p53 Tumor-Suppressor Gene, which is cancer's missing link. Silicone exerted the immune response in the animal models many years ago way before it happened to any one of us or via the placental barrier in our children- process known as MICROCHIMERIMSM/GVHD fetal cells in autoimmunity along with a possible " two hit " theory meaning with OR without a genetic predisposition and how many " hits " did it take to cross the threshold to a chronic disease. What about HERVs, ALUs and jumping genes?....as again allow me to remind you, hypersilicemia was never, ever fully investigated in the first place and has not been FULLY investigated to date. They are bushwhacking the general public...this is sick medicine. The human body is speaking volumes, is anyone listening? They should if they wish to uphold their oath of DO NO HARM) Quote Link to comment Share on other sites More sharing options...
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