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  1. R

    Chronic pain never ends

    Pain that lasts longer than six months. Chronic pain can be mild or excruciating, episodic or continuous, merely inconvenient or totally incapacitating. Symptoms of Chronic Pain The symptoms of chronic pain include: • Mild to severe pain that does not go away • Pain that may be described as...
    • rusty22
    • Thread
    • activity burning chronic chronic pain pain sore symptoms withdrawal
    • Replies: 5
    • Forum: Chronic pain
  2. cinderr

    Is Satisfying Sex Possible With Fibro?

    Does anyone else have this problem? I was once sexually active, very active, I now have difficulty engaging in sexual activity. Does anyone else have this problem?(Am I repeating myself or what?!) The problem is movement and changing positions or just getting in the correct position. There is...
  3. W

    Feeling EXTREMELY down...

    Hi Everyone, First off, I live with FMS, I don't SUFFER from it... I am generally not a complainer, I generally just stuff my feelings of inadequacies, guilt, pain, etc... Why do I stuff them? Well, my family isn't very supportive, and I find it easier to stuff them then to talk about how I...
    • WhoAmI
    • Thread
    • activity depressed disability family fibromyalgia flare fms frustrated frustration good humidity job men missing work pain problem work
    • Replies: 1
    • Forum: Moan, complain and vent
  4. mariposa

    Call Out for Those Suffering This "Achy Week"

    That subject line was kind of awkwardly stated. :-D What I wanted to say is that to anyone having to endure especially horrid pain because of this rainy, gloomy, and dreary week, I am sending positive thoughts your way. Between the rain and storms happening across the US, and tornadic...
  5. A

    What kind of specialist?

    My family doctor diagnosed me a couple years ago and has me on Cymbalta for pain. The pain has gotten much worse even though my life, activity, diet hasn't changed much. I take either ibuprofen or naproxen at the max dose every day just to function. My dr gave me Ultram but will only give me 10...
  6. D

    Hi Everyone

    Just wanted to say a quick "hello" to all. I'm a retired nurse and have had fibro since 1980, CFS since 2005, and CMP must be forever. I have been doing research on these topics for the past two years. I have written a 12 month Topical Support Group Curriculum for FMS, CFS, and CMP. We...
    • Donna10112
    • Thread
    • activity age cfs energy fms good hope how to information pain research support symptoms wanted work
    • Replies: 5
    • Forum: Welcome new members
  7. GlumshanksGirl

    Never ending battle.

    After over 4 years of strange symptoms that left me writhing in pain, fainting, coping with brain fog and concentration problems, digestive upsets, and more I was finally diagnosed with Fibromyalgia on December 5th of 2012, 2 days after my 27th birthday. Hi, I'm Shi and I am a Fibromyalgia...
    • GlumshanksGirl
    • Thread
    • about me activity brain brain fog concentration coping early encouragement fibromyalgia folding health hope job jobs lyrica pain questions rheumatologist symptoms
    • Replies: 2
    • Forum: Welcome new members
  8. D

    Diagnosed with CFS

    Just introducing myself. Hi I was diagnosed with CFS in 1999, following a couple of years of constant viral infections. I was given various blood tests which all came back negative. My white cells were mapped and found to be working properly in response to each infection, but still new...
    • Detoxing
    • Thread
    • abdominal activity acupuncture age back balance brain caffeine cfs children chronic chronic fatigue syndrome condition counseling cure daily depressed depression diagnosed dizziness early fatigue good health heart helpful homeopathic ibs immediately lost medication medications mental health money oil pain remission rest supplements support tests toxins treatment vision working
    • Replies: 9
    • Forum: Chronic fatigue
  9. G

    Paging Wright!

    I posted this in response to a thread by Inventor and Notme suggested discussing my EMG/NCS results with you. My neuro only sent me a summary, is that helpful to you or would you need something more specific? "Inventor, I've been following your thread closely and feel like I could have written...
    • Guest
    • Thread
    • activity als anxiety back children china cramping daily depression diet doctors emg exercise eye fasciculations fatigue free gluten hair health heart helpful insight insomnia lyme media muscle neuropathy onset rest stupid support symptoms tests tingling twitches wanted
    • Replies: 13
    • Forum: Chronic fatigue
  10. G

    Protomyxozoa Rheumatica

    Protomyxozoa Rheumatica is a parasite discovered by hemotologist, Dr Steven Fry. He believes the organism may cause numerous neurological diseases, including ALS. The following is Part I of the transcript of a recent interview with Steven Fry, MD. Please do not expect your physician or other...
    • Guest
    • Thread
    • acne activity als alternative medicine autism book books brain fog catheter cfs chronic chronic fatigue syndrome clinical complain conditions diabetes doctors doxycycline drugs early energy exercise exhausted fatigue fever fibromyalgia flares foods frustrated frustration good grant happy headaches health healthy heat helpful information looking for medications medicine mercury muscle pain natural neurology pain problem relief research rheumatologist school sensitivity sick specialist story supplements support survey symptoms teen test testing tests therapy understanding wanted website work working worldwide wrong
    • Replies: 0
    • Forum: General discussions about fibromyalgia
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