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“I just heard from the NDIA [National Disability Insurance Agency] who have denied my claim based on the fact they have 'overwhelming evidence' that ME/CFS is not a permanent condition and can be effectively treated with 'sleep, proper diet, CBT and GET.”
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From: "Post-Exertional Malaise (PEM) and Graded Exercise Therapy (GET) in #MyalgicEncephalomyelitis/#ChronicFatigueSyndrome (ME/CFS)" by S. Eyssens 2017 emerge.org.au/wp-content/upl #MEcfs #CFS #MyalgicE
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So sorry. This is complete and utter bull shit. There is no way those things would cure my daughter. England is still in the Middle Ages in regards to ME/CFS.
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Maybe they don't have or want to tax large corporations or billionaires their fair share. Therefore, they cannot meet their moral or governmental obligations?