Posted by tina on January 6th, 2011 at 8:00 pm
ME/CFS patients are no longer invisible, no longer silent. From their beds and wheelchairs, many disabled patients worked together to place the first-ever ME/CFS ad in The Washington Post.
The recent studies show that more research funding is needed to prevent the next mother, father, or child from becoming chronically ill with this devastating disease.
Time for the US and UK governments to take the following actions:
Provide more funding for biomedical ME/CFS research;
Develop a national rese...