Chad Eddy (@ceddy8) header
Chad Eddy (@ceddy8) profile picture

Chad Eddy

@ceddy8

All or nothing. Club soda with lime; shaken, not stirred. 2022 @ChiMarathon finisher. Professional @EOSWorldwide Implementer. #AllIn🐯 #curecf💜

 Bexley, OH
linktr.ee/ChadEddy
Joined July 2009
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  • Followers613
Cystic fibrosis is a progressive, genetic disease. People with CF have inherited two copies of the defective CF gene — one copy from each parent. Both parents must have at least one copy of the defective gene. #CFAwarenessMonth
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The edge is in the inputs. The person who consumes from better sources, gets better thoughts. The person who asks better questions, gets better answers. The person who builds better habits, gets better results. It's not the outcomes. It's the inputs.
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After you conquer the streets of Chicago, you’ll carry the city with you around your neck, with landmarks etched into the medal. This is the ultimate representation that you are a @BankofAmerica #ChicagoMarathon-er. Where are you going to take your #MedalMonday photo?
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This week we’re celebrating #65Roses Day! Just as each individual rose forms a beautiful bouquet, each monthly gift contributes to making CF stand for Cure Found. Help us grow our bouquet by joining the CF Foundation’s monthly giving program. Go to: on.cff.org/3NK02IA
Image from Cystic Fibrosis Foundation - West Florida Chapter (@CFF_WestFlorida)
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We have committed more than $109 million to infection research through the Infection Research Initiative in a little over three years. #CFResearch
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Would you believe in the year Hank Aaron passed away, the @braves won 44 games before the All-Star break, 44 games after the break, and won the World Series the 44th week of the year. Aaron, of course, wore #44. Maybe the Braves had a secret weapon after all.
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Boys soccer District Semi-Finals TOMORROW vs Granville 7:00 AT HOME❕ Student section will be in the stands behind the end zone (where the band is for football) ⚫️⚫️⚫️⚫️BLACKOUT⚫️⚫️⚫️⚫️
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Boys soccer All-League honors 1st team: James McCann Nick Eddy Griff Wagenbrenner 2nd team: Sam Powers Grayson Fletcher HM: Liam Kauffman Ethan Nguyen
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Chad Eddy retweeted
Ted Lasso (@TedLasso) profile picture
Ted Lasso
@TedLasso26 Sep 2021
I like to think grief is the price we pay for truly loving someone. And it’s worth every penny.
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OHIOANS - Early Voting begins today until Nov 2nd. 🗓 Need info about how to vote? SPREAD THIS PSA. 👇 Your vote counts - make sure your voice is heard this November.

HOW TO VOTE IN OHIO | 2020 Election PSA

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Since 1965, the term "65 Roses" has been used by kids of all ages to describe #cysticfibrosis. Here's why. 🌹 #CFawareness on.cff.org/2z6UtmK
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Please listen and pass along!
SiriusXM NHL Network Radio (@SiriusXMNHL) profile pictureSiriusXM NHL Network Radio@SiriusXMNHL21 Dec 2019
Former NHLer Steve Ludzik on The Power Play with @stevekouleas talking about his end-stage liver disease and how he is looking for a live living donor with blood type 0. For more info: Phone: 416-340-4800 ext. 6581 Web: livingorgandonation.ca Email: [email protected]
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With $500,000,000 in funding, the Foundation is setting out the Path to a Cure – an ambitious research agenda – and challenging industry to develop treatments for the underlying cause of disease for all people with #cysticfibrosis. on.cff.org/2Jyk3Dk
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“This is a moment to celebrate and to reflect on how working together, and against great odds, we have effectively transformed a genetic disease in a single generation, making #cysticfibrosis the greatest story in medicine" - Dr. Michael Boyle on.cff.org/33T80Im
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Tonight, 7pm, @Bexley_Mens takes on the Centennial Stars at home in the District semi-finals. Come out to Carlton Smith Field to support the Lions in their final home game of the year! #GoLions
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OUT NOW! We are thrilled to share Claire’s story with the world. Thanks to Nick Reed & @YouTube for your amazing vision & support. On the one year anniversary of her passing, we are so thankful for the impression she made on the world & miss her every day. bit.ly/YoutubeClaire
Image from claire wineland (@clairewineland)
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The Foundation has increased its award to Arcturus Therapeutics to up to $15M to develop an inhaled RNA therapy that could potentially help all people living with #cysticfibrosis produce a normal CFTR protein, regardless of their mutation. #CFresearch on.cff.org/2KzhKjg
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Since 1965, the term #65Roses has been used by the CF community to inspire hope and to describe their disease
Image from CFF Central Ohio Chapter (@CFF_CentralOH)
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One month from today, we'll celebrate #65Roses Day (6/5)! Learn more about the history behind the term, and stay tuned to see how you can get involved. 🌹 on.cff.org/2UXgKZb
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Check out the most recent Patient Registry reports for information on #cysticfibrosis health trends: cff.org/Research/Researcher-…

Patient Registry

The CF Foundation Patient Registry collects information on the health status of people with cystic fibrosis who receive care in CF Foundation-accredited care centers and agree to participate in the...

cff.org
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