Phoenix Rising has been there for me since my daughter was struck down with CFS at the age of 11. I am not familiar with what charitable activities Phoenix Rising might do beyond providing one of the most vibrant, active, knowledgeable forums that I've ever encountered, but frankly, that's enough! The self educated M.E. / CFS sufferers on Phoenix Rising can knowledgeably discuss all of the current research on the disease, report their experiences using medical treatments and "alternative treatments", discuss genetic SNPs and their implications, and the best protocols to follow if you have a problem genetic mutation. They provide extensive discussions of methylation and detox, how to follow protocols and how to interpret your symptoms. I have never found another forum that provides such comprehensive and in-depth discussion of an illness. Phoenix Rising deserves FIVE STARS.
Whoa, Man! Where do you get your $$$? What percentage of it goes to admin and what goes to serve your clients?
This is actually a blog with an internet forum attached which belongs to one individual. I would like to see the financial reports. If Phoenix Rising actually does any charity work, I have never seen it.
Suffering with a poorly understood debilitating neuroimmune illness has wrecked havoc in my life. Phoenix Rising opened up my world to other sufferers just like me. They provided not only much needed information on medical care, treatments, and the latest research, but also a warm and supportive on-line community that reaches out to each other on a daily basis.