SuperFriends fighting to find a cure for Cystic Fibrosis #CysticFibrosis
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Joined March 2014
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SuperFriends4CF retweeted
Hey #SuperFriends, please give this a RT. Someone needs these numbers. Thank you. #13reasonswhys3 #MondayMorning #SuicideAwareness #SuicidePrevention #InternationalDogDay
SuperFriends4CF retweeted
Hope inspires happiness. 💜 So does #FiveFeetApart. Get your tickets now: fivefeetapartfilm.com/ticket…
SuperFriends4CF retweeted
Picture on the right was taken 6 years ago and changed my life. I was type 2 diabetic with an A1C over 11. 6 years later my AIC is 5.7. No longer need meds for type 2 Diabetes because I no longer have it. #Diabetes #diabetesawareness
SuperFriends4CF retweeted
✨NEW VIDEO✨ What would happen if a person with #cysticfibrosis was on reality TV? 🎥
@CFAware @cftrust @CfAdventurers @SuperFriends4CF @CF_Foundation
SuperFriends4CF retweeted
Anton Yelchin Foundation donates $1 million to USC Adult Cystic Fibrosis Clinic thr.cm/25QG1R
SuperFriends4CF retweeted
.@CFNewsToday shares how the Foundation is taking a comprehensive approach to tackle the challenge of infections, including committing $100M to infection research over the next five years with the launch of our new Infection Research Initiative. #NACFC on.cff.org/2NRxtJN
SuperFriends4CF retweeted
Hopefully one day Cystic Fibrosis and Diabetes gets the same attention as Susan G. Komen. Should all ha e equal love. #JustSayin
SuperFriends4CF retweeted
Scientists have found a new rare cell type in the windpipe that may be a better target for treating #cysticfibrosis. #CFresearch on.cff.org/2M66gGw
SuperFriends4CF retweeted
Promising phase 2 clinical trial results announced today for acebilustat, a potential anti-inflammatory drug for people living with #cysticfibrosis. #CFresearch on.cff.org/2M9AqWa
SuperFriends4CF retweeted
A new lung cell type has been found – and might be involved in cystic fibrosis
go.nature.com/2OzOee8
SuperFriends4CF retweeted
Traveling when you have #cysticfibrosis often comes with unexpected hiccups. Clay Pickering, an adult living with CF, shares how on his first international trip, his port landed him in trouble with airport security. on.cff.org/2v6Nsxp
SuperFriends4CF retweeted
The STRONGEST factor for success is self-esteem : Believing you can do it, believing you deserve it, and believing you will get it • The mind is the most powerful part of our bodies! ||… instagram.com/p/Blt9w8IhlFB/… – at Santa Monica, CA
SuperFriends4CF retweeted
The future belongs to those who believe in the beauty of their dreams ✨ || We did it!!! #Fight2Breathe is officially a Los Angeles organization! 🌴🌊• It’s been incredible to be able to… instagram.com/p/Bln4z4SB7SV/… – at Culver City, CA
SuperFriends4CF retweeted
THANK YOU to all who attended a walk for Walk Weekend in Auburn Hills, Findlay, Remus, Grand Rapids & Grand Haven. Even a little rain couldn’t stop the great momentum we had going. We appreciate each and every one of you, from your fundraising efforts to showing up to walk!
SuperFriends4CF retweeted
Diagnosed with Cystic Fibrosis at six months old, Joe Mitchell felt he had a fairly normal childhood with the exception of having to take a lot of... tcpalm.com/story/specialty-p…
SuperFriends4CF retweeted
Vertex Awards $400,000 in Scholarships to People Living with Cystic Fibrosis and Their Immediate Family Members businesswire.com/news/home/2…
SuperFriends4CF retweeted
Our NC advocates on the Hill ready to speak with Senator Burr. #CFadvocacy #cysticfibrosis #MarchOnTheHill
SuperFriends4CF retweeted
Want to hear the latest on #CFresearch and science? Register for the #CFFVLC livestream today: on.cff.org/VLC2018
SuperFriends4CF retweeted
Hey #SuperFriends, please RT. My friend's son is missing in Waterford, Michigan and she needs our help. It takes 3 seconds to RT this
