My son has CP
I have done intense research on stem cell therapies from Germany, China, Panama, and Mexico. I have met some interesting people. I can say that I have met parent's of CP children saying the very best about stem cell therapy. What I have also discovered that some of these parents direct you to speak to Doctors associated to these clinics directly and indirectly. As much as I try to dismiss my own skeptism, in the back of my mind, I thought, "what are they in it for, and why are they pushing it so hard???" Food for thought everyone, keep your guards up. I just got a call from an independent Doctor that was referred by Parent that claims that Dr. Steenblock's treatment is great. I told him, "Sorry, I would rather deal with Dr. Steenblock directly." It is well complex web out there to lure you in. I just hope I am wrong