By: Carol Geraci
The new CDC CFS/ME Website is scandalous, dangerous and reprehensible. The CDC is now adopting the UK’s treatment protocols for CBT, GET, professional counseling and they even say that lifting light weights and stretching can help people with CFS feel better. The CDC is sending doctors to the UK’s St. Barts website for treatment guidelines (including NICE).
They lie about XMRV, serious infections, immune and neurological dysfunction in patients. This is a serious misrepresentation of how severely ill patients are. The CDC CFS website is where treating doctors look for clinical guidelines, testing and treatments. It is also where the media looks for information and your families!
CDC CFS/ME New Website Denies XMRV
The CDC fails to mention the XMRV studies from NIH, FDA, Harvard, National Cancer Institute, WPI and Cleveland Clinic. The CDC denies any connection between XMRV and ME/CFS!