

Welcome to Garrett Graff's Page
Garrett Graff
I am honored to announce my selection to the STANDOUT Triangle Class of 2025. STANDOUT is a professional development and leadership program of the Cystic Fibrosis Foundation that recognizes young professionals throughout the Triangle area for their contributions to the community.
As part of this honor, I’m raising critical funds and awareness in the fight against cystic fibrosis (CF). CF is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. A defective gene causes a buildup of thick, sticky mucus in the lungs, pancreas, and other organs, often leading to repeated infections, hospitalizations, and shortened lifespans.
The Cystic Fibrosis Foundation is a global leader in advancing CF research and care. Their work has led to remarkable progress — including the development of more than a dozen approved treatments — and has helped significantly extend life expectancy for people living with CF. Still, many individuals do not benefit from these existing therapies due to their specific genetic mutations or disease severity.
That’s why I’m participating in STANDOUT — to continue pushing forward. Harper is a young girl in our community living with CF, and her story reflects the strength and resilience so many in the CF community show every day.
I would be honored to have your support in three ways:
- Make a donation – Every dollar goes directly to the CF Foundation to fund research, care, and ultimately, a cure.
- Join me at the STANDOUT Gala on Friday, November 14 at MacGregor Downs Country Club. Tickets are $150 and include dinner, drinks, and entertainment — all in support of an amazing cause.
- Help spread the word – Share my page with your friends, family, and network to raise awareness and amplify this mission.
Thank you for helping me make a difference in the lives of those living with CF. Together, we can continue to advance progress and bring hope to families like Harper’s.
To learn more about CF and the work of the Cystic Fibrosis Foundation, visit www.cff.org.
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