Autoimmune Diseases Support Group

Do any of you with OLP also have “burning mouth syndrome “ - the feeling of having eaten pepper all of the time? Just curious.

Hello I have had OLP for many years. It always presented on the side of my tongue or inside my cheeks. In 2016 I got...

I read on another site about great success with this drug. She knows OLP isn't curable, but says all of her symptoms have disappeared with...

I am a new member of the Group. Thank you for the chance to share and to learn. I have Two Questions for the group:...

I am so frustrated with my current dentist. I am loosing teeth - six in the last year and another currently needs to be pulled...

Are there any sucess stories out ther for OLP. I just quit Low dose Naltrexone after taking for 3 months. While I think it works...

I’ve been treated for erosive Oral Lichen Planus for several years. I see a dermatologist at UAB in Birmingham, AL who specializes in OLP. I...

Hi! I was recently diagnosed with systemic LP. I would love to connect w/ others who are also trying to understand & manage a systemic...

Greetings! I've just re-read EVERY post & response here re: OLP, and made a list of multiple meds and treatments that folks have found helpful....