I also have CFS, diagnosed for about a year and half before the PN was diagnosed. I incur all the symptoms you describe except the swollen glands and vision trouble. I'll have to ask my doctors about any link. Take care

I had thought and I could be wrong but the trigger point test is not always accurate in dx. I remember a doc thinking I had fibro which I don't or myofacial pain. I am not sure the difference but maybe you want to research that as well.

I too, have CFS.

The least of my symptoms is swollen glands, but that happens too. I have been experiencing the sore throat all week, usually at work. I just woke up from a nap, having fallen asleep after sitting down on the couch after supper. I am much better now about staying asleep...I don't know why this worked, but I gave up dairy, for other reasons, and my insomnia went away. I have a headache, every hour of every day, it never goes away. Just last week I was evaluated by my optimetrist for trouble with my vision, I am seeing a glare in my right eye. Forget about my memory, it seems nearly non-existant.

My PN has probably been around for 10 years or more, just getting an official diagnoses a few years ago. My CFS was diagnosed this last Feb. I don't know that they go hand in hand...it's possible for one person to deal with many problems...lucky us huh?