Guest guest Posted March 23, 2002 Report Share Posted March 23, 2002 Hello! My name is Ellen. I'm Swedish and have moved here for 4 months ago. I have vulva vestibulitis, and had it for 3 years. Before I went to London, where I live now, I was very active in to make vulva vestibulitis known i Swedish media and I do a lot of research about it. I wonder how the treatment is for vulva verstibulitis here? I notice my sickness effects me a lot and would really like to meet others who have the same problem.. Are there any groups who meets in London? I'm working with a website about vulva vestibulitis: www.vestibulit.com. It's mostly in Swedish but it has some English texts about different rapports and research material. I would really like to get some more materials about vulva vetsibulitis.. Thank you! Ellen Sundh glanneus@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2002 Report Share Posted March 23, 2002 Hi Ellen, I'm from Germany, but I get the newsletter from The Vulval Pain Society: www. vul-pain.dircon.co.uk There are several support groups in the UK, but I can't find one in London on my list. There are two women from London on the VPS contact list in the last issue of the newsletter: Moi McNally 2 The Terrace Old Ford Rd Bethnal Green London E2 9PH Miss Pamela Wain 50 Langford Court Langford Place London NW8 9DN (Sorry, no telephone numbers) Hope this helps, a. Quote Link to comment Share on other sites More sharing options...
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