Joint inflammation SLE/MCTD
Hi!
So, they suspect that I have SLE or MCTD due to my symptoms and ANA pattern.
My issue is that they can’t diagnose until all boxes are ticked and I don’t know when that will be. I’m currently in a flare that has been lasting for a year now. Rheumatologist, immunologist, neurologist and GI specialist are all treating different symptoms. I just really want to be able to move my body more but my joints are killing me.
It’s my shoulders and knees mainly. However, it cannot be seen from the outside and my inflammation blood markers are fine as well. They did find bursitis in one shoulder about a year ago (without being able to see anything from the outside). I had steroid injections, which helped my shoulder until it didn’t anymore.
Rheum won’t do more imaging due to it all looking fine from the outside but the pain is only getting worse (and spreading tbh, wrists, fingers, elbows, ankles and hips) and keeping me up at night.
NSAIDS are horrible for my stomach so I can’t take them when I need them. Diclofenac gel it is.
Is or was anyone in a similar situation and what did you do? I just want to move my body so bad.
Thanks!