Welcome to my personal fundraising page!
If you're new...welcome! If you've supported me at any point over the past 14 years, thank you! Together we've raised over $174,000 since 2010.
My business partner and friend since middle school, Scott Bell, was diagnosed with Cystic Fibrosis as an infant. When Scott was born, the life expectancy for someone with CF was under 20. Today, thanks to organizations like the Cystic Fibrosis Foundation and generous donations from people like you, the life expectancy for someone with CF is 56 (up 3 years from last year!).
What's more, in late 2019, the FDA approved a drug that benefits many (but not all) of the CF Community. In short, the drug has helped Scott end his daily regimen consisting of hours of physical therapy and inhalant drugs. Although not "officially" a cure for Scott and those that share his form of CF, it is nothing short of a Miracle.
Please consider making a Donation to help the CF Foundation continue its research to find similar drugs for those in the CF Community that are still in need. In addition, the ultimate goal is to find a Cure for the underlying genetic mutation that causes Cystic Fibrosis. We’ve come so far, but there’s still much work to do.
Finally, if you happen to be in Montgomery, AL on Saturday, May 4th, please join us to Walk for a Cure at The Tipping Point at Hampstead.
Thank you!
Nathan & Ashley Yates
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.