fun

  1. Q

    anger

    do you ever feel anger towards your body. because im pissed. im mad im so tired and im mad that im not fun and i can't work or have sex more or eat what i want or get stupid drunk or climb mountains or try acid or get a whole tattoo sleeve or do everything ive wanted to do. i crave adventure and...
  2. S

    19 with fibro and cfs...

    I am 19, and have had fibromyalgia for about 5 years now... When i was first diagnosed, it was extreme and they thought that i had lupus or arthritis, I was missing tons of school because there were days that i could barely walk. The past couple years have been less severe, but its still with...
  3. M

    blood in stool

    Does IBS include blood in stool? So much fun.
  4. Tipnatee N

    Hello, I'm new here too , living drug free with FM nice to meet you all!

    Of course it's not that I want to live drug free with fibromyalgia, but I'm broke and now homeless too lol what can I say , gotta stay optimistic somehow right? :wink: I did most research on supplements, food, and lifestyle. Sometime I gets good days sometimes I don't ( some are pretty bad) ...
  5. S

    Really tired of the vicious circle

    Last night I was supposed to go to a party, and I had agreed to bring the coleslaw. I tried to pace myself all day, getting the things done I had to do but not over doing it, and made sure I had time to rest for 2 hours before time to leave for the party, but I could tell as the time approached...
  6. P

    New member and need support

    Hi, I'm new to forums and have never discussed my illnesses with strangers before. I am so alone with my new diagnosis of FM from a rheumatologist. I have been suffering for years and put it down to arthritis. My GP is too busy, my husband thinks it's just pain so take a pill, my friends are...
  7. S

    The Depression Letter

    Reading the Fibromyalgia letters made me think I should write one like it, only talking about Depression. So I just now did. And here it is: I have spent more of my life depressed than I have spent being not depressed. Most people don't think that is possible, but believe me, it is. Many people...
  8. D

    Another like Sageys

    Dear Miserable Human Being, Hi, my name is Fibromyalgia, and I’m an invisible chronic illness. I am now ‘velcroed’ to you for life. Others around you can’t see me or hear me, but YOUR body feels me. I can attack you anywhere and anyway I please. I can cause severe pain, or if I am in a good...
  9. AbbyRose

    It all makes sense now

    Hi everyone. I'm Abby. I was officially diagnosed in February of this year by a rheumatologist, but my family doctor put me on Lyrica before Christmas. I've been in pain for years, but blamed myself for it. I was (and am) overweight, and that's society's first answer to any fat person's health...
  10. J

    New Symptoms?

    Hello, I am newly diagnosed as of January. However, I have been in pain for over a year, and felt "funny" for two years. I am suffering from RLS, muscle twitches only when I lay down, crawling feeling all over my body, achy joints, burning skin, and fibro fog. The last two days I have...
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