CFS_for_19_years
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https://www.huffingtonpost.com/entr...030e4b023121e0e92a5?ncid=engmodushpmg00000004
Article continues here: https://www.huffingtonpost.com/entr...030e4b023121e0e92a5?ncid=engmodushpmg00000004The movie is called “Unrest.” The unrest of the title is one of the many symptoms of Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome, often expressed as ME/CFS. It is at one level a touching love story and at another, where its real purpose lies, a cry to be heard.
This mysterious, debilitating disease affects maybe 1 million Americans and has no cure, is hard to diagnose, and there is no therapy other than attempts to alleviate the worst symptoms. It is a disease of the immune system. To get it to have normal life confiscated and replaced with bare existence, pain, confusion and fatigue, which is not ameliorated by sleep, hence the unrest.
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The key to the movie is home footage shot by Brea and her husband, Omar Wasow, as she fell ill. It opens with Brea in extremis crawling across a floor, flattened and in pain. It has a fine admixture of the horrors of the disease and the joy and love of her restricted life with Omar.
The film scores many firsts, one of which, to the best of my knowledge, is it has been certified for continuing education credits for doctors. For a movie that is entertaining as well as instructive, this is an achievement. At an upcoming showing in Atlanta, the audience will be made up entirely of medical professionals getting continuing education credits.