Guest guest Posted March 13, 1999 Report Share Posted March 13, 1999 Dear Thankyou so much for getting this extremely sensitive issue into the mainstream of news media. These conditions need so much more publicity, and there is so little out there. Like many others I have found nearly all of my information through use of the Internet. Until September of last year I thought that I was some kind of freak with sexual hang-ups, frigid, even crazy because I did not want sex with the man that I loved very much and that sex was incredibly painful. I am 24 and have had this condition for the past 3 years and have not been able to have intercourse since April 1996, my boyfriend (and now husband) has been very patient, but it has taken a toll on our relationship as I now only see sex in terms of pain and have no Libido. I have seen so many Doctors (10 at the last count), some sensitive but not able to help,some arrogant and insensitive, one suggested that I see a Psychiatrist as " I may have been abused " . I HAVEN " T (and even if I had it does not mean that pain is of a Psychological origin) Vulvar Vestibulitis, Vulvodynia and Vulvar Pain are very real, very painful conditions. Being in such a sensitive and intimate place, it is very difficult to discuss. It's simple to say I've a headache/backache, but how do you explain to someone, even close family and friends that your Vulva feels like it's on fire, that the skin in your vagina feels like it's ripping when you attempt intercourse? After 3 years of treatments, [topical steroids (betnovate), anaesthetic gel (lidocaine), repeated Diflucan, canesten cream (anti-fungal), amitriptyline, metronidazole (antibiotic) erythromycin (antibiotic) Laporoscopy, Sigmoidoscopy, changing contraceptive pills, changing washing powder/bath & showers gel, stopping using tampons] I had surgery in January of this year performed by a wonderful doctor who is a member and past president of the International Society for the Study of Vulvovaginal Disease (ISSVD). While surgery is most definitely the first option, and should not be rushed into without exhausting other treatments, it has been shown in the literature to be between 70-80% successful for appropriate candidates. I am very optimistic, I can't bear to think of it now working. The mailing lists that I have been on, Vulvar Disorders and the VulvarPainForum have been a constant force of support, compassion, and information dissemination. We all have learnt so much from each other. This publicity from MSNBC is exactly what this condition needs Thankyou for discussing it, I hope that this is the beginning of open discussion, Sally Chang Houston, TX Quote Link to comment Share on other sites More sharing options...
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