Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a debilitating disease that Marcie and I live with everyday. Millions more - friends like us, and likely other dear friends of yours - are stricken in the prime of their lives with this destructive, often-lifelong illness. This is a health care cause that needs all of our attention and help.
Please consider doing a few things to help the 1M+ Americans (2M+ worldwide), mostly women, who suffer with ME/CFS:
1. Learn about ME/CFS:
Check out a six minute summary of how ME/CFS affects patients.
See one life robbed (trailer), and go further by watching her full length critically-acclaimed feature film Unrest on Netflix or Amazon Prime.
Amazing the magnitude of the destructive impact of this disease....
2. Chip in to our year-end campaign to raise $10,000 for SolveME/CFS (SMCI).
John is Chair of the board of this terrific organization which is leading the charge to attract and fund talented ME/CFS researchers, and advocate for higher levels of private and federal funds to grow the research effort.
GIFTS MADE BY DEC 30 WILL BE DOUBLED by our personal matching gift.
Thanks so much for your support for this great cause.
Marcie & John Nicols
P.S. No gift is too small or too large!