Folk
Well-Known Member
I've always wondered about what difference would money make for people with CFS/ME or similar diseases.
Apart from not having to work and being able to rest more. Do you think money would change your condition? How?
I mean there's stuff like Rituximab going on, and we'll only have the results in 2017 (and that will still be the start of the journey). So would you try stuff like that if money wasn't a problem? And if that didn't help, try other experimental treatments util find one that does the trick?
Or perhaps going to ME specialist after ME specialist or something like that and see what they have to offer?
Apart from not having to work and being able to rest more. Do you think money would change your condition? How?
I mean there's stuff like Rituximab going on, and we'll only have the results in 2017 (and that will still be the start of the journey). So would you try stuff like that if money wasn't a problem? And if that didn't help, try other experimental treatments util find one that does the trick?
Or perhaps going to ME specialist after ME specialist or something like that and see what they have to offer?