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Thursday, 09/23/2010 1:22:48 AM

Thursday, September 23, 2010 1:22:48 AM

Post# of 130743
"The MPDD is approved by the FDA. What is necessary is to marry this device with the proprietary intervention therapy developed by Dr. Marcus which itself has its genesis in the treatment therapy pioneered by Hans Kraus, MD, the physician who
treated President John Kennedy for his Addisons Disease. Together, this intervention potentially can help millions of people around the world suffering from chronic back and neck pain and avoid unnecessary surgeries that are often unsuccessful in eliminating pain. I am one of those who had been diagnosed with compressed/bulging discs in C-2-C-7 and have tried many types of therapies including acupuncture, nerve blocks, facet injections and, recently was a candidate for a spinal fusion. Dr. Marcus’ MPDD and therapy changed all of that and I have been pain free for months. I also know that Dr. Marcus has had great results working with veterans of Iraq and Afghanistan who sustained significant painful back and neck injuries as a result of combat operations in those theaters of operation so the potential for benefit is clearly there. But as we all know, medicine in this country requires new innovative therapies pass muster with some of the most rigorous clinical trials in the world, so these things often take time. If shareholders are really interested in learning more about the MPDD and accompanying therapy, they should come to Dallas November 18-19 to the World Congress on Disabilities (www.thewcd.org) and attend the lecture given by Dr. Marcus on this subject. Indeed, attending the WCD will give you and any other shareholder who attends a first class perspective on the scope of what we do both in the civilian and military sectors. And yes, having FDA approval is generally regarded as a very important step in the process of gaining acceptance in the international and domestic medical community."
-Joe Valenzano, CEO EPGL

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