medications

  1. FemaleFibroCEO

    Thanks for allowing me to join! I am a busy CEO of a women owned business

    I feel like I have come girl circle in the last five years with no relief. I have been to GM doctors, chiropractors, rheumatologist, spinal specialist all to no avail. I had a c5/6 spinal fusion in 2011 which shows everything exactly in tact but my body functions seem to be getting weaker daily...
  2. M

    Treatments other than medications?

    I am fairly new to fibro - was diagnosed right at a year ago. I just found you guys yesterday (yay!). I have struggled tremendously with medications - the side effects on some are horrible, others do nothing for me. I think I have come to the conclusion that I need to stop expecting a miracle...
  3. J

    Out of "Remission"...

    So, I'm new here, but I'm not new to Fibro. I was diagnosed in October of 2007 while living in NYC. It was brutal. Just so much pain and no answers on how to fix it. The fibro makes me so sensitive to medications I couldn't take anything but AdvilPM and Tramadol - and even that was hit or miss...
  4. P

    What does your symptom timeline look like?

    Hi everyone, I am new to this website. I was recently diagnosed with FM and Im hoping to get to know some of you on here as I think a support group is very important to have. In my case, I've had a very difficult time these last three years with all my seemingly random symptoms and problems. I...
  5. M

    No doctor really cares

    I'm super new in here so please bare with me. I was recently diagnosed with FM. I have been in so much various pain for the past 5 years. I was seeing a family doctor who just gave me vicodin and nothing else for 3 years. She would not increase the dose or add new medication with it. I was so...
  6. E

    HOW do i get them to understand?

    I know i am new here, as yesterday was my first post, but after i got home from work last night, in the worst pain yet, i got upset because my fiance simply does not understand! I don't know what to do, simply asking for a back rub seems as tho its a burden, he says why do you hurt so bad? or...
  7. S

    Blood Tests Okay But Still Having Issues

    Hey all, I have been traveling down this road for nearly 2 years, it started with a motorcycle accident, went into a year of bladder symptoms (urgency, frequency, diagnosed with pelvic floor but still having problems after PT) this whole time I had fog and other issues. NOw that I am trying to...
  8. M

    First time

    This is my first time on this or any other support forum. I am admittantly a little nervous. Well, here goes nothing: I have spent most of my life with no insurance. I knew that I had pain, but I didn't know what it was or why. I haven't had the easiest life, so I figured that the pain i felt...
  9. MercyL

    Brain Fog

    I find my concentration extremely compromised when the arthritic aspect of my pain asserts itself during the winter months, and rainy days. Thing is, it even happens when my medications are working well! I assume that the unstable atmosphere overloads the part of my brain that sends out the...
  10. M

    Hi

    Hi I was online looking for info on my missing brother when I found this forum. I am so excited about finding this site. I was diagnosed with Fibromyalgia about 7 years ago, don't ask me for the exact date because i can't remember lol darn fibro fog. I had suffered for years before that. I...
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