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"When you really understand that you can lose everything, it makes you want to live—to create something. It makes you want to be a part of the world. I mean, why not do something big with your life while you still have it?” ~ claire wineland RIP. #CureCF #MakeCFHistory

Don't know why they say '65 Roses' in place of 'Cystic Fibrosis" brev.is/Zfk5 #cfawareness

Have you read Beyond Breathing? Check out the reviews: amzn.to/1J7bpBl #CysticFibrosis #BookReview

I wish people understood that CF doesn’t just impact a person physically. I wish people felt like they could ask me questions. I wish people knew how easily I get sick. on.cff.org/2ClhYaE

Autographed copy? Order at PayPal.Me/Cassalina and your personalized book arrives in 3 days!$20 pb, $30 hrdcopy. Pls note which book.

💜💕 #CureCF #MakeCFHistory

Stay hydrated when you exercise! People with #cysticfibrosis lose more salt in their sweat than people without CF.

Wishing everyone a very merry Christmas! May our "65 roses" Santa make all our wishes come true -- a cure for CF soon! #CureCF #MakeCFHistory

Autographed copy? Order at PayPal.Me/Cassalina and your personalized book arrives in 3 days!$20 pb, $30 hrdcopy. Pls note which book.

💜😇 #CureCF #MakeCFHistory

Let's do this! 👇 #CureCF

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A beautiful day! Over $130k raised for the Cystic Fibrosis Foundation CFF Chicago at the 2022 Chicago Marathon.🙏🙏 We will be the generation that finds a cure for CF.💪💜 Hal Higdon #MedalMonday #CureCF #BreatheEasy

12 years ago we came here to support the Cystic Fibrosis Foundation and be a part of the generation that will find the cure for #CF #cysticfibrosis. Thanks for being a part of our journey. 🙏 #MyTwitterAnniversary

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Hey, y'all! Give 65MilesIn65Hours4CF a follow and follow our next journey to #MakeCFHistory.👇