cfids-fibro sleep
I regularly read a mailing list about CFIDS/Firbomyalgia news. I don’t always understand everything talked about, and so a lot of skimming happens, but sometimes I find really good stuff. Here’s a few things that jumped out at me this evening.
CFIDS-Fibromyalgia Self-Help - Treating Sleep
That got me searching because I thought I’d heard that people with Fibro didn’t go into delta sleep barely at all.
Living with FMS: The Big Picture
That sounds more like what I remember reading.
I’m starting to think that the headaches that I’m having now may have something to do with a related Fibro condition, Headache Due to Myofascial Trigger Points.
Comments
I sent a CFS book your way a while back (September 22nd actually). Did it ever arrive?
Posted by: Kymberlie R. McGuire | October 25, 2003 01:03 AM
We could be wired wrong. Who knows. I do know that I have never been able to go into delta sleep. My mind is definitely way too active. It takes me forever to fall asleep, unlike my husband who is out in 5 minutes. Since I started taking Trazodone, I’ve been able to sleep so soundly I don’t hear his snoring, anymore! I don’t think I could manage without it. I do wake up with headaches pretty frequently. And it stays the entire day. What’s that mailing list you read? I’d like to check it out.
Posted by: Rayne | October 30, 2003 03:05 PM