As you may know, the ME/CFS Worldwide Patient Alliance has been sponsoring a contest for patients to create videos that can be used as a Public Service Announcement (PSA) for ME/CFS. The winning video will be sent to TV stations all across the nation.
Six excellent videos have been created and entered in the contest, but now MCWPA needs your help!
Use this link to the MCWPA Discussion Forum, where you will find a Discussion Topic created for each of the PSA contest entries. Click on the link to watch the YouTube videos, then leave your thoughts and opinions on each one in the discussion forum. Entrants will then have a chance to revise their videos, based on your feedback, before final voting on the winner. Sounds like fun, right? Go on over there now and let your voice be heard! This is your chance to add your own thoughts to a national ME/CFS awareness campaign.
I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. Our younger son fully recovered after 10 years of mild illness. Our older son still has ME/CFS and also has Lyme disease plus two other tick infections. This blog is about how our family lives with chronic illness, with a focus on improving our conditions and enjoying our lives in spite of these challenges.
1 comment:
Thanks for the information Sue.
I tried to comment on your post yesterday but was unable to. Probably my internet connection.
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