MCTD Support Group
Mixed connective tissue disease (MCTD) or Sharp's syndrome is a human autoimmune disease in which the immune system attacks the body. MCTD combines features of polymyositis, systemic lupus erythematosus, and systemic scleroderma and is thus considered an overlap syndrome. MCTD commonly causes joint pain/swelling, Raynaud phenomenon, muscle inflammation, and scarring of...
i finally decided it is because our systems are so confused all the time they dont have the right responses like normal people.
just my ramblings no scienfitic data just personal obseravtion with me and family members.
hope you get a well break soon, it sounds like you are in need of one
This sounds like my issues with fevers. Could this be a drug reaction to your TNF inhibitor? Are you on Remicaide, Humara, Embrell, Cyclosporin, Methotrexate, Cellcept?
These are all auto immune drugs that cam cause the body to build up antibodies and sometimes CAUSE an immune response.It can happen within weeks or sometimes years after starting these. It is frequently ignored or forgotten by Docs that this can happen. It usually means fevers, chills, weakness (my temp went to 103.) Luckily the covering rheumatologist recognized my symptoms as a drug reaction, but not before the stupid er docs did blood culture and an abdomenal CT scan to rule out an abcess that wasn't there. What a pain. But, as soon as the med was stopped ( and I was put on a small tapered dose prednison), I felt so much better.
Hugs,
Louise
Best of luck. Not good news, but misery loves company. ;-)
CJ
Like Pcon, my fevers tend to run low now, about 96.8, and when they hit 98, I feel feverish.
My first symptoms, back in '73 or '74, were fevers, mostly from 99.5 to 100.5. I did have a few bouts with higher fevers, the highest clocking in at 104.5, and I vividly remember hallucinating-- I knew they were hallucinations-- seeing cups and saucers flying across the ceiling, mom staying up with me half the night.
I have noticed-- and again, this is just anecdotal-- that when I am between flares, my normal temperature runs a bit closer to normal-- say, 97..5 or 98. If I am in a flaring kind of mode, my normal temperature drops.
The fevers are really debilitating. It's not like aches and pains or the exhaustion, where you can play hurt... even working or going to school half time with fevers was total agony. And it's strange, because it's not as dangerous as pericarditis or DVT, but it's nasty on quality of life, working, relationships, etc.
Here's the good news: Fevers are rarely part of the clinical picture now. I have OTHER problems, but for me, this was really a feature of the first few years of the illness. So here's hoping anyone suffering from this follows a similar track!
--CAT