Looking for a support network for Lichen planus sufferers? I have muddled through for too many years, managing and fighting with the constant itch and pains associated. I suffer orally (albeit manageable out with flare ups) and in my lasy regions. It is a drain. I manage mainly with cold compress and steroid creams for bad flare ups. But I am willing to try any proven methods to make life easier and the condition more manageable x
Lichen planus: Looking for a support network for... - MY SKIN
Lichen planus

Written by

AngeAnge
To view profiles and participate in discussions please or .
1 Reply
•
Hi AngeAnge I also suffer with this problem. Really uncomfortable at the moment got Steriod tablet to dissolve gargle in areas of mouth. But unfortunately upsetting my Stomach. Waiting for Facial/Maxillo to see me after Covid etc.
If you want to message me be glad to chat some more. All the Best.
Not what you're looking for?
You may also like...
Vulvovaginal lichen planus
Anyone have this condition,it's truly horrendous but I haven't had a definitive diagnosis due to...
Lichen Planus misery
I have had Lichen Planus on body for last six months. Have been prescribed steroids, which I have...
Eczema flare up in Spring
Does anyone else suffer an eczema flare up during the change in seasons, particularly at the end of...
Rash,sticky skin,and perennial abscess
quite a bit to get through I'm a male in my mid 50s,I have a constant feeling my skin feels sticky...
Kind moisturisers for seborrehic dermatitis
(I hope I spelt that right)
Hello all, I struggle from seborrehic dermatitis on both sides of my...