fms

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...

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...

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.

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...

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...

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. :)

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...

[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...

. 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...

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