cfs

Electromagnetic Hypersensitivity Syndrome, this is something I think all sufferers of CFS and fibro should look into. Many of the symptoms are shared. In fact, a great many are. Take a look at when your symptoms are at their worse. 1. do they occur more at the PC, it might not be your chair...

I am a firm believer in the dangers of tap water. I know people say that bottled water is just as bad. That might be the case, I am not a tech. However, When I had CFS and Fibro, going to bottled water made a change for the better for me. I lost a lot of the aches and pains that I had. I...

This post is concerned with information and news concerning what chronic fatigue is and what is being done to improve the symptoms. This topic here is for news and general information. While chronic fatigue goes along with fibromyalgia, some people are only diagnosised with it, without having...

Hi. New here. I had a flare up on Friday March 29. I have had FM and CFS for 10 years. I thought I felt bad, but was in a car. Accident Apr 6/2012. These horrible flare ups started I Jan 2013. Now this weekend again. Can hardly walk, my balance is of, my headache is bad but the electric shocks...

Hi I was diagnosed with fibromyalgia and CFS in the autumn of 2012. On one hand it was shock, but on the other hand it was nice to know that all the things I've been experiencing are real and not just in my head. I am looking forward to getting to know other sufferers and be of mutual health...

Dear new friends... I was diagnosed with CFS and Fibromyalgia in 2005... It took about 5+ years to come to that conclusion... It was a long and painful journey... But I am here now and I am good.... Susie

Just wanted to say a quick "hello" to all. I'm a retired nurse and have had fibro since 1980, CFS since 2005, and CMP must be forever. I have been doing research on these topics for the past two years. I have written a 12 month Topical Support Group Curriculum for FMS, CFS, and CMP. We...

Hello! I was diagnosed with fibro/CFS in 1992 after I contracted chicken pox at age 28 and then a couple years later mononucleosis. In 1997, one month after I got married, I relapsed with mono and had a rather severe case. Fibro has steadily worsened ever since. I am interested in connecting...

Hello to all. I was diagnosed with Chronic Fatigue Syndrome then Fibro almost 21 years ago. This is the first time joining any kind of support group or forum. I look forward to learning from you and I hope that I will be able to add something to the group. Best wishes to you all.

I was first diagnosed with fibro in 2011 :( it took about 9 months to get the diagnosed. The sad thing about it is I had just got ten married in Dec 2010. Then I went down hill. I just turned 50 last July so its been a long bumpy road to this point. I am so glad my friend turned me on to this...