cfs

  1. H

    Weirdest thing with Candida

    I know this isn't specifically related to Fibro/CFS. But many sufferers also have Candida issue so this will be of interest to many. One very strange thing that I've noticed is that after taking a mid-afternoon nap the candida overgrowth on my tongue has almost completely vanished. In addition...
  2. W

    Eating Fresh Food and More Vegetables has Helped My CFS

    Recently I made a thread about what foods to eat to feel less fatigue. I have started to stay away from frozen foods and start making some vegetable (brocooli and cheese, tomato) soup and pasta. I am eating out less and I drink milk everyday. I am feeling better and am sleeping less. Still...
  3. T

    New Here

    Hi, I was diagnosed with Fibro/CFS in Sept 2002 after a viral infection that lasted 3 months. I also found out I have had a genetic immune deficiency since birth. I am being treated by a pain specialist for chronic pain and a doctor who specializes in Fibro/CFS. Despite having good doctors...
  4. R

    Fibro/CFS and Multiple Chemical Sensitivity

    After viewing a half a dozen posts, I came to realize something extremely important. 1) people rely on our un-educated doctors too much 2) people are hoping for miracle drug that cures all 3) no one mentioned food intolerances/sensitivity 4) elimination diet were hardly mentioned 5) if I ever...
  5. B

    Hello

    Hello everyone, I'm Tricia aka Boo. I'm new to the forum; not to fibro. I was diagnosed in 1997 with Fibro and CFS. I've been married for 24 years and we have 2 amazing children. Our daughter is 23 and a RN; our son is 14 and just started his freshman year of high school. In fact, I went to...
  6. C

    New Fibro Symptoms?

    I was diagnosed back in 1991 with CFS/Fibro. Over the years I have avoided medication as much as possible, I do not tolerate pain meds well at all. about 2 1/2 years ago I started having Blood Pressure spikes going as high as 220/180 and debilitating headaches unlike any I had ever had over the...
  7. L

    How long did it take you to find medocation that works?

    How long did it take you to find medication that works? I'm at the end of my rope here, I really am. Quick background: I'm 18, male, been having symptoms for a little more than a year now, and I just got diagnosed on July 30, with fibro, CFS, and orthostatic intolerance. Since last year the...
  8. L

    Urgent Lyrica Question!

    I'm 18 and I was just diagnosed with FM and CFS on July 30th. My rheum started me on Lyrica Thursday night, and today I was reading about side effects. First off, I'm seeing that most people expereince side effects before the drug starts working. That's horrifying, to be frank, but not as...
  9. K

    Sharing Fibro Info

    Hi All, I wanted to share a few things with the forum that I hope will help even 1 person. This is truly a frustrating condition for patients and doctors with very little relief and no magic pill. First, a few things that have helped the pain, meds don't seem to work on me at least. Getting...
  10. K

    New here...flare up!

    Hi all. I have been battling this beast for 12 years, but was only diagnosed a few years ago (CFS diagnosis in 02). All these years, I've had flare ups, but some just seem to be worse. My vent for today is this: My husband has severe PTSD. He is 100% disabled veteran, but sometimes I just need...
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