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Welcome to Britnie’s Top 30 Under 30 Home Page! |
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 You may have already heard… but I am so excited to announce that I will soon be honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding young professionals for their career and philanthropic accomplishments, Nashville’s Top 30 under 30. I am super pumped and hope that you all will join in on my excitement. In accepting this, I have committed to raise money to help the Foundation realize its mission of controlling and curing cystic fibrosis (CF). There are several ways that you can support me and help me meet my goal – by making a donation to this page, by purchasing a ticket to the big event on April 11th at the Hutton Hotel (and making sure that I have the loudest cheering section) or by sponsoring the event. If you would like more information on any of those options, please email me at Britnie@AerialDevelopmentGroup.com
I have learned a lot about CF, what it looks like in our world and what we can do by contributing to the foundation. Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than ten million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but your help is needed now — more than ever — to help keep up the momentum of this life-saving research. When the Foundation began in 1955, most children with CF did not live to see their first day of elementary school. Today, the median predicted age of survival for a person with CF is in the mid-30s. This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day. To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation! |
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| Below is a list of donors who have donated to support me. Thanks to everyone for your support! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Nashville’s Top 30 Under 30, Cystic Fibrosis Foundation
