men

  1. S

    Fibro is gradually destroying my life

    :(Hi everyone. This my usual time for feeling the need to talk. I have had Fibro for seven years, starting after I had to retire from my deputy head job and from working altogether because of a total calamitous breakdown. That is always rumbling in the background and now my Fibro, due I think to...
  2. S

    New

    Hello, i am new to the forum. Have no one else to talk to that cares. My boyfriend just doesn't get it that I'm tired and sore always and can't do what he always wants to, plus I'm having trouble working and he wants my rent $. Mine started with Mono in May 2015, after a few months of that pain...
  3. S

    IV Vitamin Therapy

    Hello All, Two weeks ago I had the opportunity to try IV Vitamin Therapy when I went to San Diego. My PCP had mentioned this therapy before and after traveling and getting extremely exhausted I called and made an appointment. I was able to speak to a very knowledgeable Dr she went over my...
  4. L

    Newness

    Hi everyone. I have just joined. I do not yet have an official diagnosis. We are waiting to rule out lupus, lyme disease and chronic kidney failure. My doctor, parents, husband and myself believe I have FM. I have been doing many tests for the last 3 months. I am so worn down. I am so depressed...
  5. M

    Fibromyalgia has ruined my life

    :I was diagnosed 15 years ag, withFibromyalgia . I had a doctor who understood me and how much pain I was in. She truly helped me both physically and mentally! Unfortunately she moved and I have been seeing doctor after doctor trying to get help, every sense!. Most of them say that there is...
  6. J

    New to this Forum

    I am a 56 year old mother and grandma. I am learning about this disease and doing everything I can to deal with the pain. I live in the NW and so it is cold here now, and it has been rough already. I am here to learn from others, and find support, as I am finding out that most people dont...
  7. S

    Diagnosed 3 years ago but still lost!

    I was diagnosed by a pretty crummy rheumatologist who basically went off of some blood tests taken by my GP and then felt my joints (which always hurt) and said that I had Fibro. I had no idea what that was and she didnt tell me. I stopped seeing her because she didnt listen to me and didnt seem...
  8. S

    Diagnosed 3 years ago but still lost!

    I was diagnosed by a pretty crummy rheumatologist who basically went off of some blood tests taken by my GP and then felt my joints (which always hurt) and said that I had Fibro. I had no idea what that was and she didnt tell me. I stopped seeing her because she didnt listen to me and didnt seem...
  9. E

    I'm in denial

    I've done quite a bit of research on fibro because I suspect my husband may have it, although the VA hasn't given him a diagnosis, he does have an rx for Lyrica and Cymbalta. But that's another can of worms. I was diagnosed with depression and anxiety in college, hypothyroidism when I was 22...
  10. J

    I think I might have fibromyalgia

    Hi all. I am new here. I have been thinking that I have fibromyalgia. I went to my new primary care (nurse practitioner) and told her that I thought I had it. She sent me for blood tests (all normal but sed rate was on high side) and that was that. I asked for a rheumatology referral and...
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