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Re: Anyone been told 'it's in your head'??From: Denise (anonymous@obgyn.net)Tue Aug 10 21:40:46 2004
Hi, I'm glad you're trying another doctor. I am in the same boat. It takes so much work and you're already exhausted from the pain and run-around from other doctors. Make sure you have a copy of every record of your own. Then you can make copies yourself and take them where you need to and save time (they have to do this...you do not have to have a doctor's name to release your records to...just say you have to combine records chronologically from several doctors and you need them yourself, if you get resistence). Write down everything you can think of as far as symptoms (maybe keeping a journal would help here). Combine your records, for past history, and symptoms in some kind of logical form on paper. Then when you see the doctor, you have all info ready and hopefully eliminate some of the trial-and-error method by the doctor. If you use endo research, make sure you qualify it by its credible source (the doctor's name who wrote the article or paper, medical web sites like university hospitals, JAMA, New England Journal of Medicine, ACOG, etc.). Most doctors hate the fact that patients "read up on the internet" because they think they are basing decisions on what someone else said on a forum (although this forum is great). Some other resources for valid endo info based on expert research and clinical studies are the Endometriosis Research Center, the Endometriosis Association, the Center for Endometriosis Care, National Women's Health Information Center, and some medical university sites (include clinical study search). Hope this helps a bit. Take care, Denise --endo diagnosed 1987
At Tue, 10 Aug 2004, Amy wrote:
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