Thanks for the welcome Sorry this doesnt seem so social, just wasnt sure where to post this.

Lets see, I have been tested for sure for RA and Lupus as autoimmune disorders go. They also checked me for lyme at the begining. Im not really sure what the other tests were to be honest. My old family physician refused to refer me for the 1st 3 years...he said he thought he could treat it but just waited till an evil flare hit gave me steroids and narcotics and sent me home. The rhumetologist said since the tests came back negative that all I had was fibromyalgia... Though I have yet another lab slip in the car for another round of tests. The symptoms keep increasing and he seems not to care so, not sure what to do. We honestly dont have a lot of options here.(MT) short list of symptoms in case any of you out there have any ideas. Joint inflamation, joint pain, joint stifness, muscle weakness(new), fatigue, extremely dry skin, lips and eyes, even a small ammount of twitching in muscles in my legs. Ive had a list of unexplainable problems from sinus tachycardia, kidney swelling and stent placement, unexplained breathing problems and rashes that lasted months for no reason. Also from what Im told unlike fibro, during my pregnancy I was in complete remission(eded badly though IUGR and preeclampsia, micro preemie short 5 days on earth)

As for a chair, I am thinking of getting something that is going to last quite some time and that is going to make me as comfortable as possible during these flares. I was kinda hoping for suggestions from chair users as to what they have found in the form of comfort. I will definitly be looking into pads

Thanks sorry so long