Posted 4/10/2015 7:37 PM (GMT 0)
Oh my goodness. This reply is off topic from the question, but I want to quickly respond to the comment above. Thank you so much for bringing up Lichen Sclerosus. If only I had read a comment like this years and years ago.
After many years of problems in that area ranging from irritation, itching, or discomfort on the skin to pain during sex and gyn exams, I have just been diagnosed with lichen sclerosus. Previous doctors dismissed my complaints, chalking it up to yeast infections or not being stretched enough. I went many, many years being told "nothing is wrong" and being treated poorly by gyns who did not understand. My relationship during those years was strained because I had no treatment to my pain. I just want to put a PSA here in case anyone down the road may happen to read this and relate to my story...please look into Lichen Sclerosus. I do not know the link between lichen sclerosus and UC, and I am not saying that is the answer to all problems...but us UC gals are more likely to get autoimmune conditions and I can only hope someone could get relief before I did. The length of misdiagnosis has permanently altered my skin.
And to anyone, if the time is ever appropriate, pass this info along to others. Awareness is key!