Lichen planus
I was diagnosed about two yrs ago with lichen planus an auto imune disease they say it is very rare and not contagious yet my younger brother has it also. I have the skin lichen planus as well as oral lichen planus which affects my gums, cheeks, and tongue. It is very , very painful. I had a very large back surgery in April and I got lichen planus sores on my back as a result of the trauma from surgery my incision that is twenty inches long healed but my sores from lichen planus are still open. I don't know how to get them to heal and right now I have just developed an outbreak in my mouth. The pain is so deep in the nerves that I feel like my teeth are going to explode and I can feel my pulse under my teeth. I can't explain the pain and I am begging for someone to tell me if they found anything that helps with the pain. Also I never heard of lichen planus , what can I expect from this disease? How often will I have outbreaks? will it ever go away? Should I have my teeth pulled out or will dentures make it even worse? Not too many doctors seem to know much if anything about this auto imune disease.
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Thank you. I found a an article on Medical News Today that lists meds that can cause LP. One is beta blockers which I take for blood pressure (I never knew that) another is inflammation meds which would have been the cataract med. If you have cataract surgery maybe you could have one eye done and see if you do fine and have other eye done later. I had no idea I would have a reaction and had eyes done back to back with great results. I now have the breakout in my face and treating with a Facial spot lighter and moisturizer. It is better. Can now cover with a cover stick and foundation. Hope yours goes into remission .Hugs and Prayers
Thanks, ema12 @ema12 Good advice to have the eye surgery in stages I think. We'll have to see if the virus goes away in time for surgeries next year or not. Anyway, I hope we both continue to be in a place where we can live with the annoyances of LP. Take care and hugs back to you! Linda
You mentioned rosacea and I gave a friend who had it and puts the medicine metro gel on it. I have some since my breakout in face is like rose Ema. Will let you know if it helps. Sleep well.
Oops. Have a friend who has it .....
Great, ema12 @ema12. Much appreciated. Sweet dreams.
My burning mouth did go away. My lp went into remission for about 15 years. Just went to oral surgeon for my gums. He gave me a prescription for LIDEX GEL. I am picking it up today. Fingers crossed. Just keep trying to lower stress and support your immune system. Not many people have even heard of lichen planus. I am glad I found this blog and can share ideas. Just found a lady talking about lp in slow wound healing. Told her about this blog. She also has oral lp. We are in this together.
Hello. My doctor has started me on a regime of folic acid daily except on one day in the week, only, I take 6 pills of methotrexate. So far, I feel it has helped. I don't seem to itch as much and some of the spots on my legs are drying up. I am praying that this will be totally successful. Any relief is better than nothing, however. Good luck,
@jlclaussen Welcome back to Mayo Clinic Connect, a place to give and get support.
It sounds like you have news of success to share. Congrats that your treatment is working.
Other members like @ema12 @lidnaj @markymark911 may be able to benefit from your knowledge and experience. May I ask the process you went through to get the correct treatment?
I have been under medical care with my Dermatologist. It has been a process of trying different medicines. I also have meds for the itching, and for my scalp. I seem to be at a point where I am able to at least tolerate my lichen plantus. However, I understand that it will probably be an ongoing problem. I hope my information is helpful to your situation. Judy
I have had LP for several years and finally got it under control with Methotrexate. But I find eating mushrooms trigger an attack with me so I stay away from them. I am on just two 2.5mg. pills a week now (down from 8 pills a week) and on Stelara injection every 12 weeks.