← Return to Oral lichen Planus: What home remedies or medications help you?

Discussion
Comment receiving replies
Profile picture for lpx3 @lpx3

I have had OLP for about 15 years and for most of those years it didn't bother me much but an occasional sore now and then. I always used the fluocinonide gel which seemed to speed healing and help with the pain. And then about 5 years ago it all changed. Now It is oral, vaginal and in my esophagus. all have been biopsied many times and comes back pre cancerous. My mouth and esophagus is the worst. Trying to eat is very hard and painful and my throat is constricted which makes it hard to swallow. I have had 2 metal stents in my esophagus and its been stretched at 20 times. It either gets stuck or I choke. Anywho I could give many more details but here are the things that help me. Lidocaine gel is my friend. salt water is my rinse. Fluocinonide gel for pain. And Clobetasol cream for vaginal flare ups. I do have it a little on my skins and nail but very little PTL. And do have some scalp issues. My primary was clueless and had to find a new dentist. I dont think she is going to help much. My gyn is great. And I see a Pathologist every 3 mouth to keep a close eye on the pre-cancer. I have Crohns so I see a gastro and I have RA and see Rheumatologist . I am reading over you guys say about different things that have worked and maybe one will work for me. Good Luck to all

Jump to this post


Replies to "I have had OLP for about 15 years and for most of those years it didn't..."

@lpx3 So sorry to hear these struggles Flovent HFA 220 had been helping me- by swallowing, not inhaling, to coat my esophagus. That said, GSK discontinued the brand, reselling under generic and my insurance won't cover it. Surgeon suggested I try Budesonide with honey and the yellow packet of diet sugar- but I tried it, a real PITA and not my preference. So I order from Canada. Still expensive. I also have OLP. ELP, and LIchen Sclerosis in my lady bits. I, too, need regular dilations, so far 8 of them, a far cry from your soldiering. What a trooper! Glad you are so even keeled and upbeat about it. This was a great PSA for those of us who can learn from your post. I also need cervical surgery to C5-6 (maybe 4-T1 but worst is C5-6 which is exactly where the plating would go for an ACDF. Only one of 3 surgeons suggested posterior, but even with that, could cause more swallowing issues than I already have. One top notch ns said my swallowing would never be the same..I was grateful to hear his unbiased view. It took a long time to find someone who would say anything about how it would affect my swallowing. Since this is a rare condition, no one cold even tell me if they had worked on such patients before. Hoping for more research, or at the very least clinical studies -but one I knew about at Northwestern funds were slashed. I tried to write to the Senate and Congress to explain why so necessary, but needs to have so many more voices behind us. So many rare diseases, so little funds..