pcp

  1. S

    discouraged with Rheumatologist

    I am new to this forum --am happy to have found someone who recognizes the pain I am in. I was diagnosed with Fibro in 1994 by a specialist who has since passed away. My PCP does not believe in Fibro so I went to the new Rheumatologist in the area because his ad said he treats Fibro. I was so...
  2. T

    Meds for Pain

    For my fibro related pain, I currently have been taking Tramadol 100mg 4xs daily and Tizanadine 1-4mg, they are scored, as needed. I also take Cymbalta 60 mg once daily. Anyway, to get to the point, the medication no longer seems to manage my pain. I've been taking the medication for over a year...
  3. D

    Did my doctor really just say that?

    So I just moved to a new location which meant that I had to find a whole new set of doctors and it has been painful, a different kind of pain from the flu-like achy all over electric nerves on fire whole body pain. This is more the - want to pull my hair out, scream, be belligerent but biting my...
  4. K

    Hello - ~20+ years of fibro, new here

    Hello, my name is Kat and I am from Texas. I am nearly 32 years old and cannot remember a life without some sort of daily pain or ache. I was first diagnosed with Chronic Fatigue Syndrome when I was around 11 years old. The official fibromyalgia diagnosis came much later though the doctors said...
  5. 6

    No pain/pressure points. Do I not have fibro then?

    Mine started shortly before my mom died last year (nov). It felt like bone pain--shoulders, forearms, outer hips, knees, hands, fingers, feet, legs. I thought initially it was b/c I had stopped my cal/mag suppliment (on account of supposed IBS triggering). I went back on it and the pain went...
  6. M

    Need new PCP who knows Fibro

    Good morning, I just signed up for the group and have Fibro, spinal stenosis, degenerative disk disease and I'm also a long time sufferer of depression. I'm currently looking for a new PCP and someone to take over my pain management. It's been difficult because I'm also a recovering alcoholic...
  7. T

    What if it's not Fibro?

    I don't really know where to post this. I guess I'm just venting about my worries so I'm putting it in here. I've been in pain and dealing with fibro symptoms for almost 3 years now (I know many of you have suffered much longer). My psychiatrist (who also does primary care) has diagnosed me...
  8. T

    Who can help treat fibro?

    Hello. I'm new to the forum. Just finally desperate enough to try to reach out for help. Here is some history (and sorry if I ramble or don't make sense, I'm having a bad day and feel like my brain isn't functioning at it's full capacity. Several years ago I started noticing unexplained...
  9. M

    28 and newly diagnosed

    Hello all! I am a 28 yo female and have just recently been diagnosed with FMS and MPS. I have been in a chronic state of pain for the last 2.5 years and, as many of you know, it's been a long ride to get a diagnosis. I have seen a PCP, orthopedist, neurologist and pain management doctor. I...
  10. M

    Head Rushes

    Hello all, Does anyone get head rushes from time to time? I sometimes get head rushes where it feels almost like an electric shock through my brain. For a short period of time, I am very cofused, don't remember where I am or what is happening around me. We're talking bout just a minute or...
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