A woman with severe ME has started a project to make a documentary about ME/CFS. They've already made a great start, but they need help! There are several ways that we can all help right from our beds and couches.
Check out their video:
Then you can donate to their Kickstarter fund - donations as low as $1 are accepted. Just think - if everyone with ME/CFS donated just $1, they'd end up with millions to make this important documentary!
You can also help by spreading the word. From their Kickstarter page, you can share on Facebook or Twitter or embed the video in a blog post as I've done here. You can also read more about the project on that [age.
They've already made a fabulous start to this important project - just think what they could do with proper funding!
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.
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