@Kina, I already provided the citations
The research you cited doesn't disagree with the science that already exists. You seem to be extrapolating new meaning from the research.
I beg your pardon. I was told that all people with chronic conditions were welcome here... ? I was under the the impression that many of the people here were still struggling to get official diagnosis. Are they viewed as second class citizens here, as well?
Please don't accuse me of treating members as second class citizens. I don't think I deserve that nor did I mean anything by my comment.
It's very difficult for members with ME/CFS who are responding to members who have chronic fatigue or other diagnoses. A lot of what is posted by non ME-patients just doesn't apply to ME patients and responding takes up our energy resources. At times it takes me hours to respond to a post and really I want to know who I am responding to -- do they have ME. This forum is for patients with ME (suspected or diagnosed), carers, and interested researchers. Lately it has become an environment for all sorts to post about general health issues. Yesterday we got spammed with a whole bunch of posts from a very buff and healthy man just because he saw that some posts on the forum had to do with his particular health issue. Members are here to discuss ME so yes we do want to know how your particular health status relates to ME. I wasn't trying to be rude. I genuinely wanted to know how your lymphatic issues related to you posting here.
I am still interested in how you think your lymphatic issues fits in with ME/CFS.
FYI, I developed CFS in 1983. It wasn't very well understood at the time and anyone who supported it was a whack-o. We've sure come a long way, thanks to the efforts of alternative practitioners allopathic practitioners and researchers, alike. In 1998 I received my first diagnosis of Fibromyalgia (and CFS) from a panel of MDs in varying specialties. In 2002 I received a second, confirming Fibro/CFS diagnosis from an eminent West Coast neurologist.
I wasn't questioning your diagnosis, I was wondering how your lympathic issues relate to your diagnosis.
My problems with glutathione "fit into the ME/CFS" paradigm because they are all related immuno-compromised conditions.
Most have no idea what causes ME. One would think that your problems with glutathione, even though related, is a diagnosis unto itself. I wish I had a diagnosis like that.
Lymphadenopathy, like the other examples of more detailed science that I provided you, on the lymph system, is a lot more varied than what a cursory wikipedia or chacha definition reveals.
I learned about the lymphatic system from a few specialist professors at the University of Western Ontario, not stupid Wikipedia. I guess I will bow out of this conversation because you obviously don't want to discuss the science. I just wanted to add that some of the stuff you are posting about the human body doesn't seem quite right. There is a lot of outrageous misinformation about toxins out there. Being a forum, it's fine to question the science behind what members are posting about.
I still have no idea what 'toxins' you are referring to.