Untrue. I have Gupta. It is not an additional $50 a year.
Ugh, you're wrong. It is an additional $50 a year. From the site:
I am not reading testomonials. I have talked on the phone with multiple people/friends whom are much better.
The ME/CFS community can only keep ignoring these cases and calling them sporadic for so long.
For every "friend who got better" there are dozens on here and IRL who have tried stuff like this and feel like they were scammed. Why is it that none of these people have published their methodologies in the scientific literature, or subjected their techniques to broader scientific study? How come they don't seem to have any understanding of the underlying mechanisms at play? If they made their work public they could help millions of people instead of just those with the means to pay them - and surely a remunerative tenure-track post at a top university would follow due to their forthcoming scientific reputation.
When you are better you are mostly not hanging out on health boards.
I improved dramatically with a handful of treatments that my postings on here detail. a year and a half ago I was pretty much unable to exercise except for walks here and there, I had almost no social life, and I was often missing work. Now I am working full-time without much issue, exercising almost daily (including competitive soccer and mountain biking), and have a satisfying social and dating life. I still have constant symptoms and bad days, so it's not all perfect. I come back here not only to stay abreast of the research, but also because I care about this community and want us all to get better from advances in medicine through scientific research - the only way most of us will ever see meaningful improvement. These will be the treatments developed on top of the foundations laid by Dr. Davis and his collaborators, along with the broader scientific community.