Guest guest Posted July 24, 2002 Report Share Posted July 24, 2002 The reality of the situation is that the protocol is available in only two places in the US, and while the protocol as it STANDS NOW will probably improve all children only some of those children will normalize. The organization is divided into two groups; The Parent Coalition (many of us are on this list) who are volunteers and the Medical Research Board. The parents job is to raise awareness and the medical side of the organization's job is to treat patients and research the protocol and drugs that will improve the protocol possibly dramatically. The Medical Board has a plan that will ultimately end up with, I think, about ten clinics throughout the US, training for Physicians, and drug trials (they already have 5 drugs they want to test and FDA approval). OK, so why isn't this happening now? MONEY. The medical board has some investors but they need a little more money to get started. How much? About what Enron or World Com frittered away in a day. A million would be nice and two even better. So if you want this to happen contact everyone you know who is in the position to invest or knows someone who is. We have a plan for Canada as well so if you want to get involved with that contact at dmccreary@... Dr. Goldberg is one person. He has a large, very busy practice. His overworked staff hits the door running and doesn't let up until the day is over. Dr. Goldberg cannot see his patients, train and oversee physicians, and research new drugs at the same time. This goes for the other Docs on the Board who are also clinicians. If enough money is raised there will be clinics throughout the US which will treat Autistic Spectrum Disorders, and Chronic Fatigue Syndrome but also be doing research in other immune modulated diseases such as MS, Rheumatoid Arthritis, Lupus, etc. If you know of a potential investor contact at DGreg21541. While you are looking for investors buy the tapes (Dec 2001) from . Net website, and have a video conference in your area. You may not know of investors but someone else who sees the tapes might! All parents have the right to know that there is a viable treatment available and that only money is standing in the way of making that happen. Forward the press release to every media source that you can. This is the richest country in the world we could set this up with a fraction of what is wasted every day. Contact me if you have specific questions. Kathy on Parent Coalition VP Quote Link to comment Share on other sites More sharing options...
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