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» LymeNet Flash » Questions and Discussion » Medical Questions » BILL GATES charitable addresses...

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Reno'sBack
LymeNet Contributor
Member # 7367

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Hi, as I posted on General Support, Bill Gates &, his wife, Melinda, are SOLEY going to focus on their charitable organizations in 2 years...even now, they donate 1 BILLION a yearI just read!

~Bill & Melinda Gates Foundation
P.O. Box 23350
Seattle, WA
981o2
(206)709-3100
[email protected]


GRANT INQUIRIES
(206)709-3140

EAST COAST OFFICE
P.O. BOX 6176
Ben Franklin Station
Washington, D.C.
20044

--------------------
~Life's too short, eat dessert first

Posts: 134 | From PA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
LYMESCIENCE
LymeNet Contributor
Member # 9259

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We need to hit them up about Lyme Disease. If we can get them to donate to the Columbia Research Center, say something like a couple million dollars, that would be wonderful.
Posts: 559 | From Cary, NC | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
LYMESCIENCE
LymeNet Contributor
Member # 9259

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In fact, this is something we need to do NOW.

This needs to be a co-ordinated effort, and we need to make as efficient a presentation as possible.

Who knows how much we could get??

My guess is quite a bit. Gates is spending a lot on malaria and HIV.

If we can get a chance to speak with his wife, maybe we can get this thing rolling. I hear she is very sympathetic to the sick who have no one working to help them.

Maybe if we clearly explain the situation to her, and tell that Columbia is the only place that wants to help us, they can make a large donation. I see this as an extremely likely occurance of our getting such a grant if we do this right.

Posts: 559 | From Cary, NC | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Reno'sBack
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Any ideas how we could organize? Columbia would be the ONLY one in the World...we can't afford to pass up this opportunity!

My friend in Hershey is a professional grant writer, but only does educational (school district) grants,

I feel we could get funding if a head of one of our Lyme organizations would meet with the individuals who make this decision.

With a Grant, we, Lymies, could live again! [Big Grin]
~Reno

--------------------
~Life's too short, eat dessert first

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Foggy
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Give them a holler as I'm sure they'd be happy to listen to grant suggestions and fundraising ideas.

http://www.columbia-lyme.org/

http://www.timeforlyme.org/

Posts: 2451 | From Lyme Central | Registered: Aug 2001  |  IP: Logged | Report this post to a Moderator
LYMESCIENCE
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Sure. I think this is a freaking great idea. We allow them to know that Columbia is the only place helping us. We let them know the US government is doing NOTHING AS WE SUFFER.

Columbia University is willing to do something.

Give them a grant so they can help us.

Posts: 559 | From Cary, NC | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
trails
Frequent Contributor (1K+ posts)
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IF we wrote individual letters would that be at all effective? I dont know how to write a grant. But I can tell my story in a page and be rather convincing.
Posts: 1950 | From New Mexico | Registered: Sep 2001  |  IP: Logged | Report this post to a Moderator
   

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