CFF North Texas

In honor of CF Awareness Month, KC White, Board Chair of the Cystic Fibrosis Foundation, joined the Valder Beebe Show to raise awareness about cystic fibrosis. youtube.com/watch?v=KtRTYt…

During Cystic Fibrosis Awareness Month, we are inspired by the resilience of the CF community.

Act Now. #CFAdvocacy

Genetic therapies — including mRNA therapy, gene therapy, and gene editing — could potentially benefit everyone with CF, regardless of mutation. Learn more about our research into genetic therapies. on.cff.org/48bovSc

Rep. @JudgeCarter, on behalf of her brother with #cysticfibrosis, Hope Scarborough from Lubbock, TX urges you to pass the PASTEUR Act to jump-start the development of new antibiotics. #CFadvocacy

@RepArrington, on behalf of her brother with #cysticfibrosis, Hope Scarborough from Lubbock, TX urges you to pass the PASTEUR Act to jump-start the development of new antibiotics. #CFadvocacy

Senator @JohnCornyn, on behalf of her brother with #cysticfibrosis, Hope Scarborough from Lubbock, TX urges you to pass the PASTEUR Act to jump-start the development of new antibiotics. #CFadvocacy

Rep @RonnyJacksonTX, on behalf of her brother with #cysticfibrosis, Hope Scarborough from Lubbock, TX urges you to pass the PASTEUR Act to jump-start the development of new antibiotics. #CFadvocacy

Way to go, Avery Gray! We’re so proud of you for representing the #cysticfibrosis community during @CF_Foundation’s 14th annual Teen Advocacy Day. Thank you for sharing your story with @RepVanTaylor this morning. #CFadvocacy

Thank you to our Wine Opener Presenting Sponsor, Puttery. We appreciate your commitment to help us cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives. Purchase your tickets to The Wine Opener today: events.cff.org/thewineopener

We are awarding up to $15.9M in additional funding to Eloxx Pharmaceuticals Inc. to support more clinical trials of ELX-02, a potential therapy for people with #cysticfibrosis who have nonsense mutations. #CFresearch on.cff.org/3LpSb1C

"It’s me vs CF, and as long as I keep putting one foot in front of the other, it doesn’t matter how slow I move. I know I’ll never be the fastest. I know I’ll never be the strongest. But I also know I’ll never give up." Read more about Jennifer: facebook.com/CFFNETX

Mark your calendars! 📅 Sign On Week runs Feb 7-11. We can’t wait to welcome back all of our teams in-person. Now is the time to start thinking about your 2022 team - grab your teammates and make sure they're ready to register next week! 🤩

We have surpassed $100 million in research funding through our Infection Research Initiative, created to help address the chronic and intractable infections that are a hallmark of #cysticfibrosis. #CFResearch on.cff.org/33UdrN8

The first 5 runners to sign up for Team CF at this year’s Cowtown Marathon on the weekend of Feb. 26 will receive: ✔️ Team CF t-shirt ✔️ CFF branded neck gaiter/buff ✔️ Moisture wicking shirt (for race day) All distances are available. To sign up: fightcf.cff.org/site/TR?pg=ent…

Through the astounding support received by you and our CF community, our North Texas & Shreveport chapter raised $1.6 million this year! We offer our sincerest thank you for all you have done to help us find a cure for CF & we cannot wait to see what we will accomplish in 2022!

Help us achieve our shared dream that one day, every person with cystic fibrosis will have the chance to live a long, healthy life. Donate today: give.cff.org/north-texas/do…

DOUBLE YOUR DONATION THIS #GIVINGTUESDAY When you give today, your gift will be matched, dollar-for-dollar, up to $250,000, thanks to the generosity of the Stremick family, whose 16-year-old granddaughter, Ella, has CF To double your impact: give.cff.org/north-texas/do…