what kind of specialist do you see for your OLP?
Posted , 8 users are following.
I have an appt Aug 8th to see a dermatotogist. But that seems weird for something in my mouth??
0 likes, 20 replies
Posted , 8 users are following.
I have an appt Aug 8th to see a dermatotogist. But that seems weird for something in my mouth??
0 likes, 20 replies
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linda32054 donna18720
Posted
You definitely want to see a dermatologist! I had seen a primary care doc and an ENT specialist, dentist and oral pathologist until finally I figured out I should see a dermatologist and he is the one who was able to help me. After all it's a skin disease and none of the others knew enough about it to be helpful.
nicola_66716 donna18720
Posted
linda32054 nicola_66716
Posted
donna18720 linda32054
Posted
that makes sense to see an immunologist. And I guess that it is still skin in your mouth too. I'm so confused and just want to stop suffering. I have been dxed with olp, multi nodular goiter, vaginal atrophy which I wonder if that is not really also lp. I can barely eat right now. The gel the oral surgeon gave me does nothing.
linda32054 donna18720
Posted
Nope, the oral surgeon did nothing for me either. It wasn't until I saw a dermatologist and he did a biopsy of my mouth that I got on the right medication. Yes, LP is miserable - just keep searching. You are your own best advocate for your health.
ckitefly donna18720
Posted
I recently when to a Rheumatologist because it was suggested to me to see that type of doctor beause they can test for many if all Auto Immune disorders that can be the cause of my OLP. i went on 7/18 and got the ball rolling by taking tons of blood and then started me on a medicatin called Hydroxychloroquine 200 mg ( twice a day) and I have to say, that although the sores in my mouth are still there in the far back ( molar area) they are less inflammed and also the swelling in my inner cheek area and less. I just ate bbq chips and with no pain when normally, I would eat them but felt like my inner cheek area was being cut open with glass. I know the mediation isn't for everyone but for those out there, think about seeing the Rhematologist too. I asked her if she sees people with OLP and she said she has a lot. That was a good sign. Now to get bloods results back and see what that has instore for me in regards to more medicaton but this is a real good start and happy to pass on so others can try same treatment.
linda32054 ckitefly
Posted
I didn't see a Rhemy for OLP, but I did see one for Sjogrens which is just another type of auto immune disease. For OLP I had the best results from seeing a dermatologist.
Good Luck.
donna18720 linda32054
Posted
donna18720 ckitefly
Posted
linda32054 donna18720
Posted
Good luck!
donna18720 linda32054
Posted
linda32054 donna18720
Posted
62 year old body. Your a youngin' in my book. I'm 72 and still rolling along. By the way I forgot to say that the dermatologist might do a biopsy to make sure it's OLP. No worries - it's not that bad.
donna18720 linda32054
Posted
lynn_02499 donna18720
Posted
Miracle!
lynn_02499
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linda32054 lynn_02499
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donna18720 lynn_02499
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linda32054 donna18720
Posted
I just realized that Hydroxychloroquine is the generic for Plaquenil. I then remembered I had heard many people on this forum saying how successful they were with that drug.
I just thought that Hydroxychloroquine was something BRAND NEW. I'll contact my dermatologist and ask for a prescription for Hydroxychloroquine as the drug I'm using (Mycophenolate) has so many awful side effects.
Thanks so much!
donna18720 linda32054
Posted
Isn't this the drug that can hurt your eyes?