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Welcome to Alexandra Crow's Page

Alexandra Crow

Alexandra Crow

Welcome to my fundraising page!!

Ever since 2015 I have been apart of this amazing group called the Peachtree Society as an honoree, council member, mentor, chairman and NOW and Allstar fundraising for the 2nd time! These past few years I have had the opportunity to meet other amazing young professionals who have a passion to raise money and awareness for cystic fibrosis. This society honors young Atlanta professionals for success in community, philanthropy, and industry while partnering to further the mission of the Cystic Fibrosis Foundation. This year for Peachtree Society All-Stars I get to be apart of Team James Alexander! I am so excited to be back with some of the best fundraisers from the past years of PTS and join forces to continue to raise money and awareness for cystic fibrosis. GO TEAM ALEXANDER!!

As for my WHY I continue to be apart of the PTS and the CF Foundation? Well that’s easy, all the incredible cf families I have met through this program and As most of you know I have been incredibly fortunate in my life to have a best friend, little brother and Hero who had Cystic Fibrosis.  I made him a promise many years ago that whether he was here or not I would help find a cure for CF.  Now I am not a scientist nor a doctor but I still have a passion to fight this disease that took my brother away from us.  I was given the chance to have an amazing relationship with Cole where he taught me what is was like to put my problems aside and help others.  So even though the curing of CF won't help bring him back, the passion that he showed while alive gives me the will to keep fighting for this cure!

Thank you for your support; stay tuned for updates on how you can help!!

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Please help me meet my fundraising goal by making a donation. Your generous gift will be used efficiently and effectively to help support vital CF research, medical and education programs.

Making a donation is easy and secure! Just click the Donate button on this page to make a donation that will be credited to my fundraising efforts. Any amount you can donate will be greatly appreciated!

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. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. 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 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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