For those of you on Facebook, there is a new group being formed to discuss your experience with Dr Rhodes. South Texas Innovative Medicine Discussion Group.
Dr Rhodes is sending letters from his attorney to anyone who is questioning his practice. The Duchennes Muscular Dystrophy group removed discussion of his treatments since they said they could not afford a lawyer in case he sued them. He had moved from RSD to DMD and had generated a lot of interest from parents of suffering children desperate for successful treatment. Nice.

Glad to hear it works for some, but the rest of us should not have to spend $4500 for worthless equipment and a reputable doctor would return calls, emails and letters to try to work something out.

buyer beware.