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← Return to Oral Lichen Planus
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Autoimmune Diseases | Last Active: 6 days ago | Replies (31)
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@diana70 Welcome to Mayo Clinic Connect! I think that you will find that there are many discussion on oral lichen planus. I have a few resources for you. This first one is by the Autoimmune Organization. They should have help for you.
https://autoimmune.org/resource-center/finding-a-physician/
This site is from GARD (genetic and rare disease org)
https://rarediseases.info.nih.gov/
And, finally, NORD ( national organization for rare diseases)
https://rarediseases.org/
Take some time and read through the other discussions on OLP.
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Thank you for the information. I would have thought being near John Hopkins would give me access to some specialists, but I have had no luck. OLP is a painful condition. It feels like having a mouthful of canker sores. I can’t figure what caused this current flare. I have been stressed because of the need for recent dental work. The flare up is on the side that didn’t have the dental work.