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"A woman from southwestern Michigan spoke about her battles with insurance companies, hospitals refusing to treat her, and going to court to obtain short and long-term disability where the insurance company had hired a doctor to claim that #MECFS does not exist." #CFS #MyalgicE
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Some extracts from the public testimony to the December US CFS Advisory Committee (#CFSAC) meeting in December 2017 meaction.net/2018/01/15/the #MEcfs #CFS #MyalgicE #CFSME #CFIDS
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My private insurance cancelled me 10 days after I had a port placed for IV treatment. They had 3 different reasons they gave, was illegal, but only legal recourse would be to find class action (impossible) to join. Lost everything that year. #pwme #mecfs
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