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<blockquote data-quote="Hound dog" data-source="post: 436398" data-attributes="member: 84"><p>Yay! I'm glad you reached your goal. That's great.</p><p></p><p>No clue on the foundation thing.........but honestly the needing a lot of money sounds about right. We have Anna's Army here in town which is a foundation for Cystic Fibrosis started by the little girl's mom to actually at first help them pay for treatment and such........then when the little girl passed it sort of blew up and became the foundation as the town rallied around the parents who are doing this so their child's death isn't in vain. Fund raisers are the main source of income, although people also just plain donate. Any school even, especially grade school, always has Anna's Army volunteer's parked at the door. Even at Darrin's art show......Nana bought him dog tags from them and bracelets for Nichole and Aubrey. Anna's Army helps with kids with CF in the area, sort of a local thing, which is why everyone is so on board with it. It's nice that the money stays local and kids here with CF are being helped.</p></blockquote><p></p>
[QUOTE="Hound dog, post: 436398, member: 84"] Yay! I'm glad you reached your goal. That's great. No clue on the foundation thing.........but honestly the needing a lot of money sounds about right. We have Anna's Army here in town which is a foundation for Cystic Fibrosis started by the little girl's mom to actually at first help them pay for treatment and such........then when the little girl passed it sort of blew up and became the foundation as the town rallied around the parents who are doing this so their child's death isn't in vain. Fund raisers are the main source of income, although people also just plain donate. Any school even, especially grade school, always has Anna's Army volunteer's parked at the door. Even at Darrin's art show......Nana bought him dog tags from them and bracelets for Nichole and Aubrey. Anna's Army helps with kids with CF in the area, sort of a local thing, which is why everyone is so on board with it. It's nice that the money stays local and kids here with CF are being helped. [/QUOTE]
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