Our local chapter puts on multiple events a year to raise money to fund research to find a cure for cystic fibrosis. Help us make CF stand for cure found!
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.
https://t.co/YI4ZPfz7u3
Today, we, along with our coalition partners, are urging Congress to take immediate action and #PassPASTEUR, legislation key to fighting the public health crisis of antimicrobial resistance and protecting Americans from deadly superbugs. #CFAdvocacy https://t.co/daZ8oes3yP
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. https://t.co/nZu4X27WTt
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: https://t.co/oYHb82RyEK
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 https://t.co/qC75Tuo3L6
"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: https://t.co/SqODMqizUQ
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 https://t.co/mpcpHwYMmM
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: https://t.co/LYueo3elKX
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: https://t.co/1Hr3jJ2Lgd
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: https://t.co/1Hr3jIL9RD