Definitely this would benefit FM! It will give NIH and CDC a chance to continue with a better budget. It's the smaller budget illnesses that get the huge impact when the money is cut. 20% of 4 million is much harder loss on CFS and FM than 20% of 80 million.
Definitely this would benefit FM! It will give NIH and CDC a chance to continue with a better budget. It's the smaller budget illnesses that get the huge impact when the money is cut. 20% of 4 million is much harder loss on CFS and FM than 20% of 80 million.
I hope everyone here saw this thread ! I believe this bill would not only benefit CFS patients, but other patients as well... possibly fibromyalgia.
"CFHIV" Very funny, I'm chuckling. Hey what did you do to be so special - linked with another illness? Some of us only have AIYHCFS (all in your head CFS).
I haven't gotten my toy surprise yet - and it's been a couple of years :(. They don't send out that many alerts, so it's nice that way.
Platelet, can I say "great minds think alike?". Okay, too cheesy for me, but thanks for the comment. It's good to know it was a good idea. I swear the advocacy is what gave me the words to explain to my family and friends so that they'd understand...
Well, I'm working on learning my body to go to bed at a decent hour, so off I go. Chris, do you have the CFS night owl problem where you tend to go to bed very late? And some folks like me wake up early, at about 5 1/2 hours sleep, but too tired.
Thanks, Curls ! You know what is funny ? I was thinking about e-mailing this information to you, Chris and others here. I already sent my e-mail to my Congressmen and then forwarded it to everyone I know.