[Note to moderators: I think this belongs in general news - please move if this is the wrong forum]
New article by David M. Perry (twitter handle @Lollardfish) talking about the film Unrest.
https://psmag.com/social-justice/how-disabled-people-care-for-each-other-when-doctors-cant
A very sympathetic piece towards living with a disability, featuring amongst other a patient with ME and calling it myalgic encephalomyelitis.
http://www.washingtonpost.com/sf/local/2018/01/10/for-some-receiving-disability-benefits-the-desire-to-work-will-never-cease/?utm_term=.3c33bec6f9ab
This blog/ article has a few red flags..........maybe the writer should have done a bit more research or is it deliberate?
Starts off OK ish.....
"British people suffering from Myalgic Encephalitis otherwise known as ME or Chronic Fatigue syndrome (CFS) have suffered from over 30 years of...
http://www.cnn.com/2017/12/17/world/amy-wright-2017-cnn-hero-of-the-year/index.html
Amy Wright is 2017 CNN Hero of the Year
Wright advocates for people with disabilities
She employs dozens of people with physical and intellectual challenges at her coffee shop
“My children are not broken," Amy...
Author has ME/CFS.
http://www.smh.com.au/lifestyle/health-and-wellbeing/not-everyone-with-a-disability-wants-a-cure--nor-should-we-expect-them-to-20171201-gzx8ys.html
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