Support group for people who have Lichen Planus, created by eHealthMe (http://www.eHealthMe.com). To join the group, do any of these: create a post to introduce yourself, ask a question, or simply follow the group.
I have had lichen planus for 3 years and oral lichen planus for over one year. It is so miserable. I just recently stated wondering if it could be caused from taking fish oil capsules. I'm going to stop taking them and see if I have any improvement. Anyone else feel their OLP is or was from taking fish oil capsules?
Post created 5 days 8 hours ago
I would like to find out if I got lichen planus from prescription lsoniazid and what needs to be done so doesn't come back.
Post created 1 month 5 days ago
Can I have Botox if I have lichen planus and oral lichen planus
Question created 1 month 2 weeks ago
Hello, I was diagnosed with Oral Lichen Planus in 2012 after a significant period of chronic stress. I have been on vitamin B injections since then, which has been very helpful. During the past few months I have had severe flare ups of LP on my tongue. After a course of steroids I had a return visit to hospital, where for the first time, the Doctor mentioned Pernicious Anemia. I am very delighted, as perhaps now I can finally get the help I need. Joining this group is a big step forwards. By sharing our knowledge, we can support and learn from each other. Thanks for reading.
Post created 2 months 3 weeks ago
I've had L.p. for about 2 months it started as a small white circle under my arm pit it disappeared an then all of a sudden all hell broke loose my back turned into a puzzle of bumps then shortly after both my legs now my wrist it itches so bad I barley can work went to the dermatologist 2 time with a 40 dollar copay he wants me to keep comi g just to look at me the send me on my way with cream i need help please anyone
Post created 3 months 3 weeks ago
I am a 69 year old female and was the first patient my doctors "cured" hepatitis C with Harvoni when the drug first came on the market in 2014. I was fine for the next 2 years as far as I know and after having a full knee replacement in 2015, I started noticing red spots which were sore and itchy on my leg. It has now traveled to both legs, my body trunk and it looks like I'm starting a break out on my face. I've lost all of my fingernails, some of my toenails, but starting to lose more. My scalp and ears are itchy all the time and I have to clean the hair off my hair brush every couple of days. I have just started investigating the side effects of Harvoni and am sure I'm a victim of the drug as well.
Besides more drugs, does anyone have any information about homeopathic help to reduce this horrible itch. I pray my nails will grow back and that I don't lose all my hair, but I'm devastated and don't feel very positive at the moment.
I pray all of us can get some help.
Post created 4 months 10 hours ago
Why am I the first to say something. Are there more of you out there?
I have AS and was just diagnosed with lichen plants. Like I really need more shit to deal with.
Post created 4 months 3 days ago
I have Lichens Planus and for a long time thought it was connected to taking Malarone and as a colleague is now in the same situation as me, too much of a coincidence.
Post created 5 months 2 days ago
My little boy who is 13 now was diagnosed with Lichen planus after taking Miralax for 4-5 years 1 cap daily.
I just have to wonder if it is related to the Miralax?
Post created 6 months 5 days ago
Hi I've recently been diagnosed with oral lichen planus has anyone found anything to help symptoms thankyou
Post created 6 months 2 weeks ago
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