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We are excited to fund the second stage of this work with the potential to be a game changer in gene therapy for CF. In stage one, the team identified novel transporter viruses specific for human lungs. Head here to read more: cure4cf.org/research-proje…

With Trikafta now delivering life changing benefits for many people, more women with CF are becoming pregnant. Head here to read more: cure4cf.org/research-proje…

D-Day is coming soon and now is the time to get ready! Head here and download your battle plan with step-by-step instructions on how to get involved and help spread the word. cure4cf.org/d-day2023/

Let's deep dive into gene editing! 🧬 Genes are part of DNA molecules which make up every cell in every living organism.🧡 To learn more, watch this video from our colleagues at the CF Foundation youtu.be/dq_Lb_r6pOw

Over the past week we've shared the successful recipients of our 2023 Holckner Family CF Impact Grant where we awarded $708,873 towards life changing research. Share this post and help us spread the word so that we can continue to support research that works to find a Cure.

The team at the Sydney Children’s Hospital Network, led by Dr Jagdev Singh, have some exciting news. The second patient has now received a phage treatment specifically targeted to the type of pseudomonas found in their lungs. cure4cf.org/phage-therapy-…

Tomorrow is the day: D-Day! Friday is the day to donate because every dollar donated will be matched by our generous corporate partners. The more you give, the more they match. Double the donation. Twice the fight.

D-Day is here. 🧡 Join us today, on D-Day as we work together to raise $150,000, our biggest fundraising challenge yet where our amazing partners will dollar-match every donation we receive for 24 hours. Donate Now: …stic-fibrosis-foundation.giveeasy.org/d-day-2023?cus…

Prof Selvadurai from The Children's Hospital at Westmead is Co-Investigator of the Accelerating Gene Therapies for Cystic Fibrosis and an awardee of the 2023 Holckner Family Grant Round. Read his fight statement 👇 and help him find a cure by donating cure4cf.org/d-day2023/

With the incredible support of you, our #CFArmy, we're already half way to our $150,000 goal! We're so excited to see how far we can go! 🧡 Donate now:…stic-fibrosis-foundation.giveeasy.org/d-day-2023?cus…

Dr Elena Schneider-Futschik from the University of Melbourne is one of our 2023 Holckner Family Grant Round Awardees and is exploring the safety and effectiveness of Trikafta in pregnancy on mothers and their babies. 🧡 …stic-fibrosis-foundation.giveeasy.org/d-day-2023?cus…

We're getting so close - we've just hit 90% of our goal! 🧡 Our #CFArmy couldn't be any better - but let's not stop until we've reached our goal of $150,000! Donate now: …stic-fibrosis-foundation.giveeasy.org/d-day-2023?cus…

You guys are incredible, we couldn't have done this without you! 🧡 And we’ve still got a few more hours to go! Donations are still open until 10am tomorrow morning if you'd like to join our #CFarmy and donate! Donate Now: …stic-fibrosis-foundation.giveeasy.org/d-day-2023?cus…

We set the bar at $150,000, our biggest goal yet and you raised it to $161,932! 💪 This means that we can fund over 2400 hours of life-changing research.🔬 We are forever grateful to every single person who donated and supported D-Day 2023.

Kick start the summer of 2024 running with epic views & sunsets at Portsea Twilight! 🏃 Join our #CFArmy in this year’s Portsea Twilight run and help us get closer to finding a cure. 🔶 Sign up portseatwilight24.grassrootz.com/cure4-cystic-f…

The Cure4CF team is taking a well deserved break over the holidays, and we hope you will be too! Our office will be closed from December 22nd and will re-open Monday 8th January, ready for an amazing 2024! 🧡🎁

This Christmas, help us get one step closer to finding a cure by asking your loved ones to make a donation to Cure4CF in lieu of giving you a present. 🎁 Find out more cure4cf.org/fundraise-for-…

Wishing our wonderful #CFArmy and wider CF Community a very Merry Christmas. 🎄 While presents and Christmas cheer are great, there's only one Christmas wish on our minds - a cure for cystic fibrosis. We know that our CF Army won't stop until we have found one. 🧡

We believe that a world without cystic fibrosis is within our reach. 🔶 Meet our current researchers and find out more about the innovative projects they’re working on in the fight to pave a future free from cystic fibrosis: cure4cf.org/current-resear…

Happy New Year to our #CFArmy! 🎇 Our New Year resolution is to make 2024 even bigger than 2023! It's a lofty challenge given we uncovered two amazing research projects. You can read more about them here - cure4cf.org