fms

  1. P

    Emotional Stressors

    I am fairly new to this forum but not new to FMS. Even tho I was diagnosed with FMS in the early mid-90s, this condition still perplexes me. I was wondering how emotional stressors affects other FMS patients? I find that whenever I have an emotional event in my life, I am thrown into severe...
  2. B

    Today...this is how I feel!

    So this is how i feel. I had a bad sleep and the day is not starting off good. I am very tired and very cold. I have a terrible headache. I can't think properly and can't remember and can't think about too much at once of what i have to do or it gets me upset. My whole body hurts. My hair...
  3. K

    emotional strain

    I was first diagnosed with FMS in 2006, but I'm certain I had it much longer. The symptoms, stress, and extreme fatigue are so debilitating. I feel isolated and others seem to think I'm some type of hypochondriac. I'm always at the doctor's offices hoping to get better.
  4. J

    Might lose my job because of FMS

    Hi everybody, It's been a while since I posted here. I think I was trying to live as normally as possible knowing that I had Fibro. I was diagnosed in October 2014 and gave my diagnosis letter to my boss who was fully understanding as she had a family member with fibro but her case was worse...
    • Josee51
    • Thread
    • anxiety back diagnosis family family member flare fms good job support understanding
    • Replies: 8
    • Forum: Moan, complain and vent
  5. B

    New Member - Hello to Everyone!

    Looking forward to reading and hearing about what everyone has experienced or is currently experiencing with Fibro, Chronic Fatigue, and Pain. Lord knows it is such a challenge living with this every day and incorporating it into your daily life. I have done sooo much work over the past few...
  6. O

    New to group.

    Hello everyone, it's so nice to have found this group. I've been a FMS sufferer for over 15 years. It seems to get worse as the years go by. The typing is a little difficult tonight, but I will continue to visit and share with you as well as be a source of support. :)
  7. S

    One for the ladies only!

    Hi all I have been diagnosed with CFS/ME and FMS for just over a year. I have just recently had a bout of thrush which I haven't suffered fromantic since diagnosis. I couldn't face being pulled around by the Dr and the following week of pain so I went to the chemist and I bought an oral pill...
  8. P

    Loss of support from family and friends

    [INDENT]Hello ... I'm PhillyFibro, and have had FMS for nearly 30 years. It was like a bad nightmare for 7 years before I was diagnosed in 1994. OK, so I wasn't a nut job, there's a real illness here. I believed knowing what was happening would be a giant help. But it took years to find...
    • PhillyFibro
    • Thread
    • about me anxiety counseling cry digital early family fms friend good heart hope job loss of family & friends meds problem shower sick sleep support
    • Replies: 8
    • Forum: Welcome new members
  9. S

    Help. Just moved here. Need a doctor

    . Diagnosed with FMS 01/1996 and CFS 08/1996. I was 36, in the prime of my career. It was not a gradual onset but sudden, one day fine, got the flu, apparently kicked it all off. I was in bed first two years while mainstream doctors worked to find medications that at least got me moving...
  10. L

    FMS Doctor in Colorado Springs?

    Can Anyone recommend aa good FMS doctor in Colorado Springs? Searching hasn't proven to be very helpful in finding someone that actually cares.
Back
Top