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Leigh's Foundations or non-profits

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I am starting a non-profit for children with Leigh's and mito

diseases. Do any of you know of any that already exist? I do know of

the UMDF. I would like to know about all the groups that anyone may

have heard of.

" Eli's Angels " is what it will be called. It will distribute

Children's books for the parents to read and many other supportive

things for families facing these ugly diseases. Does anyone have any

interest? E-mail me or come to Eli's website:

http://www.caringbridge.org/co/elijahkurtz

and check for updates as I am processing the paperwork. I am a good

way into seting it up. I hope to have everything filed by the end of

OCT. Then just have to what for the Gov to do thier end.

Ann

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I've started a non-profit organization in the attempt to help other families affected with mito. The paperwork is with my CPA right now after that it goes to the IRS. Hoping to get something back soon. We have decided not to do any fundraising until we have been approved as a 501©3 organization to avoid both federal/francise/state taxes. If you need some help let me know.

robinakurtz1974 wrote:

I am starting a non-profit for children with Leigh's and mito diseases. Do any of you know of any that already exist? I do know of the UMDF. I would like to know about all the groups that anyone may have heard of. "Eli's Angels" is what it will be called. It will distribute Children's books for the parents to read and many other supportive things for families facing these ugly diseases. Does anyone have any interest? E-mail me or come to Eli's website: http://www.caringbridge.org/co/elijahkurtzand check for updates as I am processing the paperwork. I am a good way into seting it up. I hope to have everything filed by the end of OCT. Then just have to what for the Gov to do thier end. Ann Please contact mito-owner

with any problems or questions. __________________________________________________

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