"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
Some extracts from the public testimony to the December US CFS Advisory Committee (#CFSAC) meeting in December 2017
https://meaction.net/2018/01/15/the-public-testifies-about-me…#MEcfs#CFS#MyalgicE#CFSME#CFIDS
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