SuperFriends4CF

SuperFriends fighting to find a cure for Cystic Fibrosis #CysticFibrosis

[David Herro @DavidHerro]

Hey #SuperFriends, please give this a RT. Someone needs these numbers. Thank you. #13reasonswhys3 #MondayMorning #SuicideAwareness #SuicidePrevention #InternationalDogDay

[SuperFriends4CF @SuperFriends4CF]

@OpenHerLungs 💚💚💚

[David Herro @DavidHerro]

I'll take Kick Cancer's Ass for $500...

[Five Feet Apart @FiveFeetApart]

Hope inspires happiness. 💜 So does #FiveFeetApart. Get your tickets now: https://t.co/IH9AtoBHlK

[David Herro @DavidHerro]

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

[Nicole Kohr @cystic4real]

✨NEW VIDEO✨ What would happen if a person with #cysticfibrosis was on reality TV? 🎥

@CFAware @cftrust @CfAdventurers @SuperFriends4CF @CF_Foundation

[The Hollywood Reporter @THR]

Anton Yelchin Foundation donates $1 million to USC Adult Cystic Fibrosis Clinic https://t.co/OF2plsKfOL

[Cystic Fibrosis Foundation @CF_Foundation]

.@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 https://t.co/HAddQaj6oR

[David Herro @DavidHerro]

Hopefully one day Cystic Fibrosis and Diabetes gets the same attention as Susan G. Komen. Should all ha e equal love. #JustSayin

[Cystic Fibrosis Foundation @CF_Foundation]

Scientists have found a new rare cell type in the windpipe that may be a better target for treating #cysticfibrosis. #CFresearch https://t.co/8mNSawuwur

[Cystic Fibrosis Foundation @CF_Foundation]

Promising phase 2 clinical trial results announced today for acebilustat, a potential anti-inflammatory drug for people living with #cysticfibrosis. #CFresearch https://t.co/NjGI6P4Srr

[Nature News & Views @NatureNV]

A new lung cell type has been found – and might be involved in cystic fibrosis
https://t.co/HnduTOGV0U

[Cystic Fibrosis Foundation @CF_Foundation]

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. https://t.co/7UafKDnQC9

[Caleigh Sarah Haber @TeamCaleigh]

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! ||… https://t.co/kVV2iapTl2

[Caleigh Sarah Haber @TeamCaleigh]

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… https://t.co/ApnW0Ww2Pu

[SuperFriends4CF @SuperFriends4CF]

Check out Andrea Yumang's profile on #Zillow https://t.co/wOnmRnoglj

[CFF Michigan Chapter - Serving Michigan & NW Ohio @CFF_Detroit]

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!

[CysticLife @CysticLife]

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... https://t.co/IuVw5h68XF

[SuperFriends4CF @SuperFriends4CF]

May is also #EDS Awareness Month

[CysticLife @CysticLife]

Vertex Awards $400,000 in Scholarships to People Living with Cystic Fibrosis and Their Immediate Family Members https://t.co/kc154b68Nh