Raising $1 million for the @CF_Foundation. An annual #hockey tournament for men, women, and kids, silent/live auction, and more! #CysticFibrosis #CureCF

Columbus, OH
Joined January 2011
Our fearless founder is at it again! Let's do this, let's make CF "history"! 👇 @CFF_Chicago
On Oct 9th, 2022, I'm hitting the streets of Chicago with "Team CF" for the 2022 Chicago Marathon, to raise money for the @CF_Foundation and to make CF "history" (a thing of the past). To be a part of history with me, click here: 👇 on.cff.org/3ed3USB
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Hey, y'all! Give @65HoursForCF a follow and follow our next journey to #MakeCFHistory.👇
Let the training begin. Long run Monday! In August, I hit the streets for my 6.5 x 6.5 x 65 passion fundraiser for the @CF_Foundation. ✅️6.5 Miles. ✅️Every 6.5 hours. ✅️For 65 hours. ✅️For CF. Follow me for more updates on how to support and participate. 🙏
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May is Cystic Fibrosis Awareness Month. In August, I'll be running 6.5 miles every 6.5 hours for 65 hours to raise $1,000,000 for the @CF_Foundation . #CureCF
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Hey @hoka @higdonmarathon @CF_Foundation let us know what you think of our shoe game for the upcoming @RunFlyingPig half marathon. 👇
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12 years ago we came here to support the @CF_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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Make CF History retweeted
A beautiful day! Over $130k raised for the @CF_Foundation @CFF_Chicago at the 2022 @ChiMarathon.🙏🙏 We will be the generation that finds a cure for CF.💪💜 @higdonmarathon #MedalMonday #CureCF #BreatheEasy
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✅the @davidgoggins 2022 4x4x48 Challenge That was one small step for my niece Gabby💜, 90,260 steps (50 miles) for the @CF_Foundation and #TeamCF @CFF_Chicago Donate here:👇 fightcf.cff.org/goto/MakeCFH… #CureCF #4x4x48Challenge
Let's do this! 👇 #CureCF
Today is my birthday, and I'm asking for your support. This October I'm running in the Chicago Marathon as a part of @CFF_Chicago #TeamCF. It's my mission to make CF "history" (a thing of the past). Join me in the fight to #CureCF: ➡️fightcf.cff.org/goto/MakeCFH… #RunTilItsDone
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4 years later, today isn't any easier. Nor should it be. Nor will it be. Life is precious. Breathe easy, Gabs. ➡️ youtu.be/Gm09A1XGh6I #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.
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Stay hydrated when you exercise! People with #cysticfibrosis lose more salt in their sweat than people without CF.
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Wishing everyone a very merry Christmas! May our "65 roses" Santa make all our wishes come true -- a cure for CF soon! #CureCF #MakeCFHistory
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
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Autographed copy? Order at PayPal.Me/Cassalina and your personalized book arrives in 3 days!$20 pb, $30 hrdcopy. Pls note which book.
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Don't know why they say '65 Roses' in place of 'Cystic Fibrosis" brev.is/Zfk5 #cfawareness
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Have you read Beyond Breathing? Check out the reviews: amzn.to/1J7bpBl #CysticFibrosis #BookReview
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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?” ~ @clairewineland RIP. #CureCF #MakeCFHistory
Claire Wineland, who inspired countless people around the world with her honest talk about illness and mortality while living with cystic fibrosis, has died just a week after receiving a lung transplant. She was 21. cnn.it/2CgDr6E
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It comes in waves, grieving does. Somedays you can carry it around, like a brick in your pocket. Other days it pins you down and all you can do is hope it doesn't crush you. Breathe easy, Gabs. youtu.be/Gm09A1XGh6I #CureCF #MakeCFHistory
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