story

  1. T

    New Member

    Hello everyone, I am new to this and was just diagnosed with this last Monday. I have been dealing with this for years however it just gotten to the point whereas walking or standing to long sends the shooting pain from my feet to the top of my body. The headaches or endless. I have bald spots...
  2. R

    Just griping

    :-(I know what to do for a migraine, I've had them since I was 5 yrs old. But when they last for 5 days I get real tired and fed up-if I had any energy I'd scream. I've never understood people--like my sister--who say crying cleanses them, just gives me a migraine and sick stomach. We had to...
  3. T

    New to Group / Fibro Survivor of 21 Years

    Hello. I'm looking to share what I've slowly learned about living with Fibro for the last 21 years. I was diagnosed at 32, had to leave my job at 46, and am fighting to not become an "old woman" at 53. I'm hoping to learn new information, coping strategies (one can never have too many), and...
  4. W

    Hello, New and sharing my story.

    Hello there, I am brand new here and I hope not to make any faux pas during my 'initiation' phase. Lol! I am 27 years old and was diagnosed with Fibro around 2-3 years ago, resulted from an accident at work around 5 years ago which damaged my foot and has left me on crutches ever since. Here is...
  5. Forgetmenot

    Funny things to cheer us up

    inwas talking to my eldest son .who is 18 and his brother who is 16. I was feeling very low when my elder son reminded me of something they both did when there were 6 and 4. We lived on a busy St.and most ppl on the school run,Would pass by my house twice a day. I'd gone in the kitchen I don't...
  6. R

    New member here. Any FMS link to chronic Lymes?

    Hi all. I am a new member, but 'old' in terms of chronological age and duration of FMS. I will not bore you with my lengthy story and the many attempts at beating this thing. I was wondering: what do any of the members here know about chronic Lymes disease and its link to FMS. When I lived in...
  7. yoyowa

    It's Never Lupus - my ongoing, annoying, confusing story

    Hello all! I'm new to the thread and thought I'd introduce myself, vent and discuss because frankly I'm so annoyed I just want to scream. So bear with me. I've always felt a bit off medically. I was born with toxoplasmosis originally but got a then new, experimental treatment which 'cured' me...
  8. M

    My Story

    We all have a story. Some lucky people have one big one, others have more. Some have them at the young age of six, others in their 60. My story happened when I was seventeen, young, teenage, vulnerable, and desperately in love with a sexy guy who has the most beautiful eyes. My story is about...
  9. L

    New member, new story

    Hello! I am a new member although I signed up a long time ago I finally decided to post after some recent crappy events. I decided to share my story with you all in hopes of finding someone who can relate, which I am pretty sure most of you can. But anyway, I apologize for the length of it in...
  10. R

    My Story... so far

    Hi all I have been on the fibro diagnosis roundabout for about a year now. I have other issues which is making diagnosis difficult (according to my gp). I have scheurmanns disease in my upper back and resulting arthritis in different points along my spine. I also have bursitis and other...
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