shak8
Senior Member (Voting Rights)
I thought last night that a barrage of letters to editors for personal opinion pieces in newspapers would get out the word about what having ME is like.
I think people are glued to newspapers and other media. Is now a good opportunity to reach a lot of people and tell our personal stories and the science, or lack of, behind ME/CFS?
I think people are glued to newspapers and other media. Is now a good opportunity to reach a lot of people and tell our personal stories and the science, or lack of, behind ME/CFS?