← Return to Lichen Sclerosus: Any other women dealing with this disease?

Discussion
Comment receiving replies
@fdixon63

@alju. Hi. After seeing multiple MD's, dentists, etc. over many years it is amazing how few have ever heard of LP. I've had two biopsies over the last 8-10 years but none actually elaborated as to lichen sclerosis, only lichen planus. Two years ago my derm suggested a vulva dermatologist a distance from my home but I was happy to go. She too recommended Amitriptyline. Not sure if it helps the pain but the sleep benefit is wonderful. I have a lump in the vaginal area that I believe the derm called "?milia." I've got scaring there as well and I go back every 4 months or so to, I assume, to make sure no cancers develop.
Also, I've had multiple squamous cancers on my legs and arms (many requiring surgeries) that I'm sure are related to lichen planus.
The sharing this forum provides is amazing. Thanks to all. Faye

Jump to this post


Replies to "@alju. Hi. After seeing multiple MD's, dentists, etc. over many years it is amazing how few..."

It's surprising how much contradicting info is out there on these two problems , LP vs LS which is the less common and locations on the body that are or can be affected, etc. Very confusing. I never heard of a vulva dermatologist before. I will try to find one near me. I agree about this support group. I am so relieved to be able to actually talk to others about this problem . It's been a terrible emotional stressor for me.