Is there anyone here willing to share their experience with mucous?
I was diagnosed with MMP in December, 2019. I see a dermatologist at Johns Hopkins who specializes in pemphigus and pemphigoid. I take CellCept to suppress my immune system, and I feel very good. My biggest problem has been caused by the Covid pandemic. Because I take an immuno-suppressant medication, I am highly vulnerable to Covid. The Covid vaccine is not likely to have much benefit for people who take immunosuppressants.