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LayneRoxxx (November 30, 1999 at 12:00 am)
I may have a mild form of this....although it was fairly severe at first and lasted about 2 years.
I still do not exercise very much at all although I enjoy it. If I do the next day I'm tired and braindead.
Some tips - stay away from caffeine. Try taurine at night and tyrosine during the day if you need an extra boost.
PhoenixShield77 (November 30, 1999 at 12:00 am)
Why are doctors diagnosing patients with CFS or Fibromyalgia when it actually is
M.E (Myalgic Encephalomyelitis). Why have the medical organization come up
with a new name (CFS) (CFIDS) years ago for an illness which already existed as M.E
PhoenixShield77 (November 30, 1999 at 12:00 am)
Is this a huge COVERUP by the government? Why have they not funded research for a cure until supposedly now? Its evident that CFS has a negative stigma on the inflicted sufferer of a serious illness, and not a made up one. Doctors dont believe it exists, or are they actually told NOT TO. Without funded research backed by the government it seems to me they are keeping the diagnosed and the public mislead and and in the dark.
PhoenixShield77 (November 30, 1999 at 12:00 am)
I have recently discovered M.E (Myalgic Encephalomyelitis) is caused by Hepetitis B Vaccination.
You can find out more by looking up M.E on google or Wikipedia. I need youre help to uncover the real truth so that we can help educate the ones who are suffering with this syndrome and fight for the right for a cure. Any feedback or comments are appreciated.
I have recently discovered M.E (Myalgic Encephalomyelitis) is caused by Hepetitis B Vaccination.
SAMMYBABYLOVE (November 30, 1999 at 12:00 am)
People who dont understand m.e please shutt up as your annoying! SHAN you go!! i just want to let you i go through m.e each day! ive had it since i was 13 im 23 now!but i am a mild suffer now!, i know what you go through ive been there!i was house bound for over a year but now im a little better im gunna make a change...i hope you will support my cause!!! Next year im doing a big campaign for awareness for m.e/cfs...so watch this space!! just watch me we deserve rights!take care everyone!!
ShanMayteex (November 30, 1999 at 12:00 am)
7universe, you can fuck off yea? cus i have m.e and i ENT lazy you dont have a clue what its liek, i hate it.. i WISH i was back at school. you dont know how lucky you are! so if i was you i'd keep your opinions to yourself you SKET! :( >:(
lovemyscooter (November 30, 1999 at 12:00 am)
My brother and I both have CFS. It's a lonely disorder because everyone thinks you are a lazy hyprocondriac......it's horrible. Thank you for bringing this out.
libgirl2 (November 30, 1999 at 12:00 am)
well done. I've been dealing with this for over 15 years and you're right - it does destroy your life. there is no other way to describe it. thanks for speaking out.
LockedAndLoaded12 (November 30, 1999 at 12:00 am)
I'm 10 and i have CFS, its not fair is what i think, u dont get it from being lazy!
carisa411 (November 30, 1999 at 12:00 am)
Great video. I am 30 yrs old and have had chronic fatigue/chronic EBV for 3 years. It's pretty horrible and I really don't speak with anyone about it either b/c they just won't understand. It's nice to see someone is out there who "gets it." |
