Hi Serentiy, I know your pain so very personally, and please accept my deeply sincere sorrow for your suffering. When I was diagnosed with CFS 40 years ago; they didn't believe it was anything but a behavioral issue. I was a nurse, and used all my predilections to alternative remedies, since medicine offered nothing but stupidity. What is aching so much to see, is how young you were when diagnosied; yes, it is a real and researched diagnosis now; research going along neurological, immunological, mitochondrial issues of cellular production and more more more; all to say; this is one hell of a disease of misery. By now, despite treating symptoms, still working sometimes partime, injecting myself with homeopathy to get by the days; and as the years progressed, one after another affected and needing increasing symptomatic half measure treatments. I understand you are reaching a rough point, the accumulated effects of time on the organs. It's possible that your depression was part of the now diagnosed neurological issues; which they are debating the causes of diligently, at last. It's called myalgic/encephalitis. If and why the lining of the brain becomes inflamed is of question, in this case it causes the lack of strength of muscles, increasing the fatigue, and requiring ever more rest. To get it so young, I can see the consequences of striving for some kind of life. But, there are new protocols emerging: there are affects on organs that can be minimized by methods some of which I could share. Sometimes, I say I must be the oldest living survivor, as now the age of death is averaged to be 55, and the suicide rate 5x the national average. I'm here Serenity, because all of the meaning of life has been stolen, replaced with peace only in sleep, and nightmares of each day. Perhaps though, I can help you in some way since I have been through it. Please let me know, and, I'm glad to have found someone who truly can understand the suffering that calls for peace.
Cleo