Guest guest Posted September 15, 2004 Report Share Posted September 15, 2004 I WOULD LIKE TO FIND A DR. WHO REALLY KNOWS THIS CONDITION- I COULD GO TO BERGEN COUNTY NEW JERSEY, OR WESTCHESTER COUNTY NEW YORK- ANYONE KNOW? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2004 Report Share Posted September 17, 2004 > I WOULD LIKE TO FIND A DR. WHO REALLY KNOWS THIS CONDITION- I COULD > GO TO BERGEN COUNTY NEW JERSEY, OR WESTCHESTER COUNTY NEW YORK- > ANYONE KNOW? I just copied my post from last week to another woman in the NY area: I've done a lot of internet research and found names through the NVA. There seem to be only a handful of vulvodynia specialists in NYC: I have been to Dr. Ledger in NY (Cornell NY Hospital; he is nice and knowledgable but after 3 oral meds didn't help me right away he didn't really know/care what else to do), now I'm going to see Dr. Gae Rodke (she wrote the Vulvovdynia survival guide w/ Glazer). I have also heard good things about Goldstein (he has a web site. www.ourgyn.com), he is in NY only somtimes and is expensive (non of these people take insurance). And I've heard good things about a Dr. in Philly: Kellogg-Spadt. If you come across Dr. Peacocke, be careful, she seems to have a very narrow view on vulvar pain and doesn't deviate from her treatment even if it doesn't help. I've heard she has helped many women but I've also heard many disappointed patients (through internet groups like this). I saw her for 1.5 years and had to eventually give up (she's a dermatologist specializing in vulvar pain). Lastly, a well repected specialist is Dr. is at the University of Rochester, NY. If you want to start Physical Therapy/Biofeedback: Pamela on Also, join the National Vulvodynia Association, they will send you info and a list of specialists in your area, there should be someone in NJ, and they put you in touch with a support group. Good luck. bel Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2004 Report Share Posted September 18, 2004 In a message dated 9/18/04 10:20:40 AM, VulvarDisorders writes: << Also, join the National Vulvodynia Association, they will send you info and a list of specialists in your area, there should be someone in NJ, and they put you in touch with a support group. >> P.S. This list hasn't been updated in quite awhile, it's not worth the $40 - if that's the only reason you're joining the NVA. Tara's list on her website is a much better source. Debbie Tiger Quote Link to comment Share on other sites More sharing options...
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