cfs

  1. D

    Rebuilding muscle and strength

    So we have had an amazing thread on exercise intolerance that's had the most replies ive seen for ages. So those of you who understand i haven't been able to exercise much for over 2 years and i have limitations based on joint issues....so i cant squat or get on the ground or bend around as in...
  2. D

    So bad for so long

    Has anyones fibro /CFS got so bad for so long that they feel like there is no hope and depression and anxiety set in. I have been house bound for over 2 years and the stress of being like it makes me feel so unhappy and anxious like i have no control over my life at all. I have done the'...
  3. W

    Can Surgery cause fibromyalgia/CFS and does using CPAP machine make the pain worse?

    40ish male, not over wieght and still working Quick History, 2014 cancer surgery, tumour removed, skin flap, graph. 2015 apporx 18 months later, rapid weakness, vision and muscle fatigue issues 2016 after MS clinic, Neurology, rheumatology, multiple MRI's every known body scan, blood test...
  4. B

    Dr. Pridgens Famvir + celebrex treatment

    Anyone here tried antiviral treatment for fibromyalgia, or know someone who has? I've been reading about Dr. Pridgen and his antiviral + celecoxib combo, and its some interesting stuff. There Is also a Dr. Wyller in Oslo university looking into the herpes simplex and its connection to ME/CFS.
  5. vickythecat

    Raising Awareness and Taking Action

    Hi, Aren't we all frustrated how time and time again doctors have not taken us seriously? Or how fibromyalgia is not considered serious enough for certain benefits, social help, disability payments, referrals to occupational/physical therapists etc? Or how people around us just see this outer...
  6. vickythecat

    disability, benefits and feeling guilty

    Hi, I am not entitled to disability or any benefits in the country I currently live in, as fibromyalgia, CFS, nerve damage or my lifelong mental health issues (BPD, major depression, social anxiety, PTSD) are not considered 'enough' to be entitled. Sad, really really sad. I am very lucky that I...
  7. S

    19 with fibro and cfs...

    I am 19, and have had fibromyalgia for about 5 years now... When i was first diagnosed, it was extreme and they thought that i had lupus or arthritis, I was missing tons of school because there were days that i could barely walk. The past couple years have been less severe, but its still with...
  8. I

    Need some advice

    I am a bit lost and feel totally lazy and guilty right now. I would like some advice if possible. I am a male in my mid 30s and i have been diagnosed with hypothyroidism about 9 years ago, and addison disease about 7 years ago. I did well for the first 3 years with addison. I was working full...
  9. E

    finding good doctors

    So I'm pretty sure we can't have a "wall of shame" board for all the dictors (doctors) we have almost all ran into. But now after another move to another state it would be great to be able to see a list of doctors that other CFS/FMS patients have had good treatment from. When my...
  10. A

    New and I don't feel myself

    "They" tried to diagnose me with fibromyalgia/CFS about five or six years ago and I denied that I had it. I slogged through those five years, surviving, not living. Now I have reached full circle and am ready to admit that either or both fibromyalgia and chronic fatigue account for my symptoms...
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