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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

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