I haven’t been on here for a while because they told me I don’t have ls. Now the new doctor is telling me it could be ls. But she won’t know for sure until we get the biopsy results back. I am never having a biopsy again. I was in so much pain that I called my mom in tears. I’m 27. Such a awquward place to be in pain. The best part was I didn’t know they were doing a biopsy. Anyway this is so frustrating and annoying and uncomftorable. Between the itching sometimes pain during sex and sometimes pain in general. Idk what else to do. The cream this new doctor has prescribed isn’t working. Still using it cause I’m desperate. I waited four months to get in to see her. I kind of want to go to Boston. Funny thing is I hate doctors and hospitals and yet I work in a hospital. But anyay. The other thing that is scaring me is that I was told the tissue could scar over. Which means sex could be unbearable. Let’s face it you can’t have children without passionate romance. That scares the crap out of me because I do want kids. Then I always try to look on the bright side. There’s always someone out there whose worse off than me.
I strongly recommend seeing
Dr. Alice J Watson at Brigham and women’s hospital in Boston. She is excellent !!!! She specializes in LS. You will probably have to wait to get in to see her but it is worth it.
Really? Maybe I should give them a call.
Yes I highly recommend her. I saw her mysejf and I’m extremely picky about doctors. I was misdiagnosed with LS. It turns up it was inflammatory vitligo. It’s very rare. It can mimic the signs of LS such as whieting and itchiness. She did a biopsy just to double check. She is a very smart compassionate doctor and her medical assistant is great. It’s a piece of mind.
They can’t get me in until November. But my primary doctor is sending over the referral. Maybe I should just wait till I get the biopsy results from the other doctor. I don’t know.