Lichen sclerosis--Has anyone else been told they're in remission?
Last week, after my latest 6 month check-up, my doctor told me I was in remission. She said I have the option of continuing twice a week applications of the clobetasol or not using the steroid until a flare-up occurs. I'd like feedback from others on what they've done and how that's worked out for them. Thank you for all input.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
@ronag my flare ups are random and can occur any time, usually when I am stressed. Sometimes they last several days and sometimes just a day. Taro Clobetasol ointment has worked for me each time.
I only take when I need it. The skin there is thin and it may cause you to want to rub. Don’t. Just put the cream on. Gently. It does come and go for me. Best of luck to all of you.
@cher51 for me, the ointment works better than the cream.
It is ointment I use. I respond to people in a short period of time. So sorry. Thank you.😀
Even in remission you should use clobetasol twice a week for life to prevent structural changes. I learned the hard way. I have a completely hooded clitoris and reabsorbed inner labia. Most docs still don’t know how to manage lichen. Look to the LSSN community and Dr Jill Kraft to learn how to manage lichen.