learning

  1. A

    Struggling today

    I'm new here & wanted to say hello & introduce myself. Still learning my way around this site. I'm 49 was in a severe car accident in 1992. They did not know of FMS then so was diagnosed with Myofacial Disease. Anyway, 15 Dr.s, shots, Chiropractic, etc etc etc ... I was finally diagnosed with...
  2. R

    Got room for one more?

    Hello all! Although I'm new here I'm not new FMS it's many frustrations. I was diagnosed in 2009. Currently on disability leave from work and will probably retire very soon. I was also diagnosed with Rheumatoid Arthritis (in 2005) and Sjogren's (two months ago). I had Ulcerative Colitis in my...
  3. QuentinCroft

    Hi fom Sunny Coast QLD Australia - Partner of FM patient

    Hello - New here of course and looking forward to learning as much as I can about FM. I'm a partner of an FM patient and would like to gain more insight to becoming a more effective partner. Already some threads have helped on here. Although I love my wife unshakably - I cringe at some of my...
  4. B

    Just Joined

    Hi, I was diagnosed with Fibro from a Rheumatologist about 20 years ago. I was so bad at the time that every morning I woke up I felt like a truck had run over me. My Medical doctor was very understanding and did many tests to rule things out like Lupus, MS ect. They all came back clean so...
  5. L

    Hi

    Hi, Have had fibro for 30 years ...my family has a genetic form..my mother had it, older sister and 1 daughter. I usually cope with this disease with a dr. Who somewhat gets it..and studying alternative therapies and learning to help myself. this year started out pretty stressful which does...
  6. lynnnelson

    Low-Dose Naltrexone (LDN) - Amazing and Good Clinical Studies!

    Greetings, I'm diagnosed with Hashimoto's and Fibro and have extreme pain and fatigue. The pain is in all major joints with aching, soreness and stiffness in all muscles. Brain fog and anxiety along with my low functioning thyroid (what's left of it). The autoimmune #'s were off the charts...
  7. C

    Throat Issuee

    Hi everyone haven't been on here for a few weeks. Still learning how to deal with having fibro along with costocondritis. I can now say that the costo isn't as hateful as it once was but the fibro, well you all know how it is. It seems like as soon ass I start to get used to having fibro out of...
  8. C

    Newbie intro

    Hi all! I'm new here. I haven't explored the forum much yet, but am looking forward to learning from others' wisdom and knowing I'm not alone. I was officially diagnosed with fibro by my family doc about a year and a half ago, though I suspect I've had it a lot longer. My physical therapist...
  9. MysticMoon

    Hi, New to the Forum but Not to Fibro

    I was diagnosed with FMS several years go after a surgery that I never seemed to recover from. It took many frustrating dr visits, a multitude of tests, and years of fighting to get the treatment that works for me. While I do not have my entire life back, I am at a place where I can function...
  10. Gerbentrelle

    "Young, wild, and [chronicly in pain]"

    I have been treating my fibro/CFS for 2 years and a myriad of mental health diagnoses for 8 years. At the age of 20, I have gotten to a manageable state in all of my illnesses while juggling fibro, depression, and college. I don't have many loved ones that have any interest in learning about my...
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