Together, we can make CF stand for Cure Found


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Dear Friend, 

Ashley Wilson was diagnosed with cystic fibrosis via newborn screening in 1997.

Growing up, her parents raised her to be open about her life with CF. And through her podcast and YouTube channel, she has done just that: speaking candidly about her life, experiences with CF-related diabetes and CF liver disease, and more.

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Cystic Fibrosis Foundation
4550 Montgomery Ave, Suite 1100N
Bethesda, Maryland 20814

www.cff.org ([link removed])

In 2018, she discovered something she wanted to keep private: her first gray hair. She immediately plucked it.

Ashley continued to pluck her gray hairs as she spotted them, blaming them on the stress of college life. On every trip to the salon, she reminded her stylist to dye them. They made her feel self-conscious. This year, something shifted, and her perspective changed.

"I have learned to appreciate my gray hair rather than trying to cover it up," Ashley said. "Thanks to research and medication, people with cystic fibrosis are getting to experience growing older and having more special moments."

Ashley has so much more she wants to experience – like finishing her degree in cinematic arts and technology, pursuing acting opportunities, and traveling.

Our dream is that one day, every person with cystic fibrosis will have the chance to live a long, healthy life – gray hair and all.

Friend, you can help move us one step closer to our shared dream: Make your gift today ([link removed]).

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4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US

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