fms

  1. M

    28 and newly diagnosed

    Hello all! I am a 28 yo female and have just recently been diagnosed with FMS and MPS. I have been in a chronic state of pain for the last 2.5 years and, as many of you know, it's been a long ride to get a diagnosis. I have seen a PCP, orthopedist, neurologist and pain management doctor. I...
  2. L

    New member MS and FMS

    Hi, Only just been diagnosed with fibro even though I'm sure it started 15 months ago. I also have MS, I was diagnosed when I was 16, I'm now 30. I'd love to chat to someone else that has both and find out how they cope with having bot of them. Because I've had MS for so long I'm pretty good at...
  3. R

    Hello from new member

    I have had FMS for many years. I was diagnosed in 2003 but have had symptoms since I was in my 20s, I am now 60. I'm in constant pain and have headaches daily. Went to Mayo's last week about possible surgery on my spine in my neck but the neurologist stated that it wouldn't help my particular...
  4. S

    anyone ever experience this?

    Yesterday my son said his tongue cramped up. Also he experienced the feeling of walking into a spider web when I highly doubt there was one. He is 9 now but had really bad allergies and asthma when he was a baby. That doesn't seem bad since he turned 4. Anyway, his complaints have grown...
  5. H

    Feeling GOOD!

    This is the first day this year I can say I feel good:smile: January and Febuary I was exhausted every day. Then I had the worst flare up of joint and muscle pain I've ever had. The depression hit and the "crazy" moods you can have jumped on board but this morning I feel as close to a normal...
  6. J

    Do YOU know what brought on FMS?

    I do, an emotional trauma in July 1999. IF, I do indeed deal with this syndrome, that is when it came on. The fight/flight/fright happening. I was attempting to get thyroid "fixed" for 10 yrs prior and I feel thyroid was WEAK and the trauma brought this on. I will add more later to...
  7. J

    Hi all, hope I can help or learn something new

    I've been at this FMS since mid 1999 and on another FM/CFS group for about 8 yrs, but wanted to move to a new group and see how it goes. My bigger challenge I believe NOW, is advancing OA and cleaning up and managing complications from a hip replacement.....grrrrrrrrrrrr And then there is...
  8. S

    the torture table

    I recently had a nerve test done. They start by sending electrical currents throe different nerves. Then they use needles to observe muscle reactivity. On a normal person this is not such a big deal. On anFMS patient...this was torture. Each electrical current was the same feeling as hitting...
  9. S

    Girlfriend with FMS

    Hey everyone, and thanks in advance! I've been with my girlfriend now about 2 years, and I can honestly say she's the person I've clicked most with. Our relationship doesn't have any of the typical issues (mistrust, fighting,etc) so I'm thankful for that. I truly love her and think that she's...
  10. N

    New to support group

    Hey there! I'm really excited that I found this website and will be able to get some much needed understanding. My husband, family and friends are caring but it's different to be able to speak with someone who actually has the same diagnosis as me. I was diagnosed with FMS 10/2014 and had been...
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