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Last October my urogyno told me I had LS because of change in architecture. I had no white patches. After using clob for 2 months she told me she wasn’t convinced that it is LS and to stop using ointment. She told me to see my original Gyno in same office to see if she can offer any other ideas because I still have the awful burning (no itching). She also referred me for a colposcopy this coming Monday
I saw my Gyno today and she did say LS because skin is thin like parchment and my labia is flat. She gave me a milder cortisone cream and aquaphor
I’m very confused and also terrified because I’m sure I’ll have a biopsy to definitely confirm everything. My dr says LS is autoimmune disease. which I read about
I’m 70 years old. I’ve posted here before but it’s been a while
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