Oral lichen Planus: What home remedies or medications help you?
Anyone in the group suffer from Oral Lichen Planus. I am at my wits end with all these erosive sores in my mouth. I've had two biopsies , one in the inside cheek and one under the side of my tongue. The spot under the tongue is extremely sore to touch and has been for over a year. It scares me because the soreness never goes away, sometimes it isn't as sore but nothing helps. Any home remedies for this dreadful condition?
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Good morning Maryz,
I am about 6 months into treatment for OLP and vag lp. You have so much experience I wanted to ask you about symptoms. I am doing clobetazol 4x week and a liquid concoction of an anti-rejection medication. Some days my gums look "fine" and then they're flaming. I have had episodes of thrush. I am really frustrated. Before my diagnosis with biopsy, I had no lesions, no burning tongue-my dentist just seemed concerned that my gums were so red. He suspected lp and sent me to a specialist and my world turned upside down. Did you go through any allergy testing? I have some metal fillings-the specialist said, no that's not the cause, but I am considering having those replaced just in case it might make a difference. I am not satisfied treating the symptoms-I would like to know the cause and address that. what are your thoughts?
Thank you-I have not made any connections about particular food yet. I need to search and begin at square one to eliminate foods and find out how much time before adding again.
Good morning @microgirl I really do understand your wish to find the cause of the OLP. I would, too! OLP is an autoimmune disease which happens when your immune system gets out of whack. I, too, was shocked when my immune system went crazy and caused lesions on my brain. My research explained that most AD are genetic, but more research needs to be done. I attached a link to the Mayo Clinic site that will provide more information.
https://www.mayoclinic.org/diseases-conditions/oral-lichen-planus/symptoms-causes/syc-20350869
@maryz and any other LP person - how do you get your calcium if you don't drink milk?
@bustrbrwn22 I use lactose-free milk, 2%, tastes great. Also, I've found lactose-free cheddar cheese, yogurt, butter, cookies. It's all out there at the grocery stores and all tastes just fine. I also take Calcium 650 mg and am going to ask my doc for a Vitamin D prescription, since I've read it aids in the absorption of the calcium tablet. I also was on Alendronate for a few years and an planning to request it's return to my list of "must haves".
I am new and notice it has been a while since anyone posted about LP. My mouth had begun to be react to spicy foods and generally become uncomfortable. When I mentioned it to my dentist, he mentioned signs of LP but he didn't think it was active. He changed my toothpaste and mouthwash to Biotene products, which seemed to help. I already had osteoarthritis in my knees from wear and tear (age and weight), so I didn't think much about it again until I developed excruciating pain in the back of my neck. When my neck and ear on one side began to get numb and show no signs of stopping, I went to the ER. After ruling out heart attack and stroke, the doctor diagnosed Shingles! Eventually my jaw and the inner part of it (gums and lining) were becoming numb, and I couldn't feel my outer ear. I had no idea that Shingles could do those things! Gabapentin seems to be the common prescription for relieving pain in the nerve endings. It helped at first, but gave me a foggy feeling. Now when I take it I have terrible and vivid nightmares! I have read about LP and Shingles, and they both seem to be activated by stress. They also have similar symptoms and effects. I am not sure if I have one or both or if one is being activated by the other. I am tired all of the time, and the severity of the pain goes up and down the scale. I have so many things going on in my life, I have not been able to keep up with the groups I follow everyday, but any comments or advice would be appreciated. Thank you for listening to me.
@chari6 thanks for sharing. good to know. I have severe Oral LP and am now being put on hydroxychloroquine because I also have LP all over my skin and now my eyes. The flare-ups never stop. I'll bring this up to my ear dr when she returns my call.
Hello @chari9 you must be quite miserable with both LP and shingles. The combination must be so difficult! LP is an autoimmune disease but the shingles virus is an opportunistic virus that takes advantage of a lowered immune system. Read through this discussion and see what others have done. I’m sure that members @bustrbrwn22 and @artist01 and @microgirl will step up to help you
You might also be interested in this discussion on shingles. The discussion itself is old but the information doesn’t change.
https://connect.mayoclinic.org/discussion/shingles-3/
Other than the Biotene products, are you being treated for LP?
@chari9. Hi Chari. @ I note that @becsbuddy has mentioned my name to you with respect to your LP. I just replied to another member in this thread (I forget the name already. Sorry!) so I hope you can locate my response. Laurie
Hi @chari9 I found the comments Laurie is referring to. She’d replied to @fdixon63 @bustrbrwn22 regarding LP. They are in this group.