I ask this question to those who may have experience in this since you probably had the same tests done. So my journey started back in 2016 with constant fatigue and after a year of being told I had anxiety/post partum, a ER doctor ran blood tests for autoimmune diseases. It came back that I was ANA positive and my sedimentation rate was slightly elevated at 22. So I went to a rheumatologist where they ran several tests and yes I was ANA + with a low titer and slightly elevated RNP markers which… read more
I’ve alway heard Fibromyalgia was not autoimmune but neurological. I’ve always thought FMS mine as well be autoimmune but i’ve never had a doctor confirm it as so. Where did you get this info from? I’d be interested to learn more @A MyFibroTeam Member
With over 10 million people affected worldwide, I hope that the medical community will soon have a break through on exactly how to treat Fibromyalgia to make patients lives more comfortable. Maybe even find a cure. Those are the things Im concerned with. Whether they classify it as autoimmune or not doesnt change how it affects my body, or my life but if they can figure out how to alleviate pain and help us return to our normal lives, that will be incredible.
You mentioned some autoimmune but have you been checked into hashitmotos {thyroid}, MS. there is also an autoimmune that attacks the pituitary. Make sure your pituitary hormones are checked as well as fibro symptoms have similarities with Cushings and Addisons which is to do with your cortisol levels.
@A MyFibroTeam Member. It would make so much sense if it was autoimmune. If you check out the extremely long list of symptoms with Fibro, they are the same as with autoimmune diseases. In fact many people are misdiagnosed with a autoimmune disease or Fibro all the time.