CF Foundation | Reflections from Bryan Johnson

Published on juli 6, 2020 by

“There are so many organizations out there that are just…organizations. The CF Foundation is a family. You laugh, cry, share memories, and you look forward to opportunities. With every new technology, drug, and treatment that comes it gives you more and more hope. You can see the little things that happen and the impact of what you’re doing—it’s exponential.”

As we celebrate 65 years of progress, Bryan Johnson, who has a niece and nephew with cystic fibrosis, shares how he got involved with the Foundation and his hopes for the future.


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