Erosive oral lichen planus
Hello
I'm new to the group. I was diagnosed with erosive lichen planus 4 years ago and it has been a nightmare since. Mine has progressed from my mouth to my esophagus, nose and eyes. I've seen so many doctors @ Vanderbilt and St Thomas Hospital who have no idea how to treat my illness. I've. Even advised to go to the Mayo Clinic in Rochester but I'm really not sure what doctor or doctors have experience with treating this disease. Any help would be appreciated
Thanks
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My dermatologist suggested hydroxychloroquine, but i was afraid of the side effects. I will have to ask about the lyderm gel.
Thank you
@joyatbells - Lyderm gel (comes in paste form too, but gel is better applied in the mouth) is a steroid and may have side effects too because my doctor said it should not be taken for more than seven to ten days.
Someone in one of these threads said she used kid’s toothpaste and it helped with the burning when brushing her teeth so I got Crest kid’s toothpaste while I waited for my appointment with the specialist, and that did make brushing teeth more comfortable.
How are u doing now Mary ? X
Yup. I've come to like bubble gum flavored toothpaste.
At Easter I got kids toothpaste that tasted like the yellow marshmallow rabbits. (I lose words!) The ones that taste way better if they're stale. Checking out new kids flavored toothpaste can be fun around the holidays.
My doctor just referred me to a rheumatologist. I'm hoping for some help with oral lichen planus. I have sores in my mouth that make it hard to chew. Hurts a lot. Have tried cyclosporine. Still on it but don't notice s difference.
I use a water pik. I use warm water in the tank, lowest setting. Hold the wand close to the gum, careful in the sore areas.
You know, with all my pain, when I'm not hungry, I forget to notice how much pain I'm in. Like now. Weird, I have a toothache and its like NBD because its just moith pain. I'm used to mouth pain. And its only reading tgis that I'm actually realizing I have a bunch of sores.
I got my teeth cleaned (its her hands pulling on my cheeks that brings tears.) She said I had a large sore beside my tongue. I was surprised I didn't even feel it. Its normal life right now. She was like "you don't feel that?"
I also have CRPS, it crazy what pain we can get used to living with. I'm inder so much stress right now its no wonder I have a mouth full of sores. Thanks, ill do my prednisone/lidocaine swish and spit.
Hi,
I have OLP also! It's painful for me also! In addition to the lesions, the tissue in my mouth feels like it was sanded with coarse sandpaper!!!!
I'm not familiar with cyclosporine treatment for OLP. I use a dexamethasone mouth rinse when my mouth gets really bad. It can only be used for 10 days at a time! It helps!! I also have the Lidocaine rinse which helps for about 7 minutes!! LoL
I haven't taken oral Dexamethasone (steroid) yet. I won't take them unless I absolutely have to. The side effects can be very challenging.
I also have LP on my skin and I have Esophageal Lichen Planus which is "extremely" rare. ELP is so rare it's impossible to find a doctor that has ever had a patient with it.
I wish the best! I hope the rheumatologist will be able to help you!
I use my dexamethosone and lidocaine rinse together and hold it in my mouth as long as possible. Even 30 minutes if I can. I don't use it regularly so I don't think about how many days in a row. I only use it when I'm in a bad Flair and even at that I hate medicine so I might use it once a day?
I was on steroids for covid recently and I all of a sudden realize that I had no sores in my mouth either I had totally forgotten to notice! Yeah being on Prednisone is a dream except for what it does to your mind and to your bones. I also live with bipolar so I have to be really careful when I'm on prednisone. We all do. It can make you feel pretty crazy! But especially if you're bipolar be really careful because it can make you manic. I can't imagine it in my esophagus. I wish more people had heard about it. Sometimes I'm invited over to a friend's house and they're having food that I know I can't eat. I usually try and tell people I can't eat square food and they don't know what that means. Lol. Anything sharp or anything with a point. I'm also trying to be gluten free and sugar free and salt free and I'm finding there's not very much I can eat. I wish gluten free for 20 days now would show better results in my mouth but it's not
I have friends who say "oh yeah I have a cold sore on occasion - its painful." At which time we all know, we just say "yeah."
It feels unbelievable that somebody would have a gazillion cold sores inside their mouth. Have you ever felt like I wish I had one day, one hour, one minute - when I wasn't in pain someplace in my body?
I looked at some artcles. I wanted to suggest that you go to the National Eczema Association website and facebook page. Here if the name and contact number for them. There must be some doctor who can help you. I think you need to do some research and contact this organiztion rather than looking for another doctor who may be clueless.National Eczema Association | 505 San Marin Drive, #B300 | Novato, CA 94945
415-499-3474 or 800-818-7546.