So I had my check up a few days ago and my rheumy said I'm not where he wants me to be symptoms wise on the plaq. My symptoms are better on it than without it, but I'm still having quite a bit of symptoms along with new ones. One of the main ones is severe hand pain and swelling. Just really severe pain in each finger joint and on the back of my hands and wrists. My hair is still falling out and my feet and knees are still killing me. I've only been on the plaq for 2 mos and he wants me on it for 2 more, until June, and then see if we need to add another med or switch. For people that added a med to plaq or switched, which med did you add/switch to? Did it help? I'm a little scared of immuno suppressant drugs.
I'm also having really vivid nightmares and dreams on the plaq. Like bloody, zombie, bombs exploding people's heads off, being shot, crying dreams/nightmares. I mentioned this to the dr and he didn't seem too concerned but it's really starting to bother me. I take 200mg once in the morning and once before bed. Any suggestions?
Graves Disease 2007, Ceilac's Disease 2008, Lupus 2012.
"Не дай мне Бог сойти с ума."
God, please don't blow my mind. - Aleksandr Pushkin