Definite caution to anyone getting a sauna as treatment, if you have POTS or heat sensitivity like me try before you buy. Saunas and hot tubs are a Nono for POTS patients anyways with the blood pressure, heart rate, and fainting (in fact the doc gave me advice to even take showers as mild as I could get them unless using for muscle relief occasionally).Warm and dry - I could see infrared sauna's, music rooms, maybe total immersion tubs - all really good foods - an organic garden right there! It would be great!
The biggest thing would be not having to worry about how I will survive financially in my senior years. Being able to afford not only a roof over my head and decent food, but also dental care, dentures and hearing aids if needed, medications. Those things won't even be a consideration for me if things don't improve financially.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?
The best i ever felt was when I could afford to go to an osteopath, who did iv supplement, homeopathic injections and recommended a number of gut improvement supplements i can no longer afford. My current insurance is an hmo, all i can afford and he's expensive for out of pocket care.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?
I think to an extent it could - having an indoor pool, massage therapists, cooks, etc would be helpful but to see a significant difference in CFIDS symptoms money could only give you the chance for improvement.
Money doesn't improve anybody health. your everyday routine like exercise, diet routine and other daily activities improve your health situation.