Thank you to everyone who joined us in celebrating #CFAwarenessMonth ! We appreciate all of you for sharing your stories and helping us raise CF awareness all month long. Together, we can make CF stand for Cure Found.

“It is [about] having a team in your corner, lifting not only you but your whole family up, providing support, and cheering you on.” - Karen Swartz, CCLS Hasbro Children's Hospital

📝: bit.ly/4e130GC

#AllInAllTogether #CFAwarenessMonth

SAVE THE DATE!
🚲
As we end #CFAwarenessMonth , we’re excited to announce our 10th Annual #GlowRideforCF will take place this year on September 21 in Hermosa Beach! Get ready to GLOW with us at our most electric event!
Stay tuned for more details, but for now- mark your calendars!

Today closes out #CFAwarenessMonth , but our commitment to the cystic fibrosis community continues. 🫁💪

In honor of #CFAwarenessMonth coming to a close #BEFAthlete Avery Flatford and her teammates all wore purple ribbons during their region play in support of their teammate and

Today’s #SciencEE features John Lueck, PhD, EE Grant Recipient!

Thanks to our 2024 #CFAwareness Month Tier 2 sponsors — Boehringer Ingelheim, Viatris, 4D Molecular Therapeutics, ReCode Therapeutics, @Baxter_Intl., and Enterprise Therapeutics! #CrossOutCF #CFAwareness

Vacation Vibes

#CFAwarenessMonth

As #CFAwarenessMonth comes to an end, the Right to Breathe campaign is heading to the European Cystic Fibrosis Society in #Glasgow .

At ECFS we will amplify voices like Lukas, still denied lifesaving treatment due to high costs.

Show your support - read his story⬇️ righttobreathe.net/post/patients-…

As #CFAwarenessMonth comes to a close, we want to THANK YOU for coming on this journey to learn more about #cysticfibrosis . Your commitment to #accelerate lifesaving advances and #CrossOutCF once and for all means so much! Stay up-to-date on the latest >> bit.ly/4aeeQus

#CFAwarenessMonth You might have heard of the miracle drug Trikafta for patients with cystic fibrosis. While it has done amazing things for most, unfortunately Bradley & approximately 5-10% of CF’ers do not qualify b/c they have rare mutations that this drug has no effect on. 🙁

In Canada, 62.5% of patients who received a first lung transplant from a deceased donor survived at least 5 years. donateyourorgans.ca #LeaveWell #CFawarenessmonth

“My fear is that there’s going to be an outbreak of an #antibiotic -resistant infection that people just can’t fight off and it’ll become the next pandemic,” Benchea said about the urgent need for new antibiotics. #CFAwarenessMonth pew.org/3SxFQPU

Mayor Krantz has proclaimed the month of May as Cystic Fibrosis Awareness Month in #MiltonON !

Flags are being raised today at Town Hall to bring awareness to Cystic Fibrosis (CF) and raise funds to help find a cure. #CFAwarenessMonth

Regardless of the progress made, we know there’s more work to be done. Our scientists are working to advance potential therapies for people living with #CysticFibrosis . Take a look inside our San Diego labs.
#CFAwarenessMonth #GoingtheDistanceInCF

May is CF Awareness month.

Because of improved medical treatments and care, more than half of people with CF in the US are over 18, but we still have work to do here and around the world.

Until it’s done!

#cysticfibrosis #CFawarenessmonth #njhealth

Doing our nightly treatment. Did u know that CF’ers have to do daily chest physiotherapy to try & break up mucous in their 🫁 in hopes of keeping them healthy? Bradley has spent around 2500 HOURS of his short life hooked to this machine doing treatments! 🤯😢🤯 #CFAWARENESSMONTH

Had a great time raising the Cystic Fibrosis (CF) flag with Liam to mark the CF Awareness Month.

Let’s recognize the resilient spirit of the CF community. Together, we can make CF stand for Cure Found.

#CFAwarenessMonth

As #CFawarenessmonth comes to an end, we just wanted to take a minute to say THANK YOU to everyone that has supported our little man on this journey! We couldn’t do it without y’all! #CureCF #BradleysBattleBuddies 🫶🏻

This #CFAwarenessMonth we want to shine a spotlight on amazing non-profits & orgs making strides for our community, including Cystic Fibrosis Foundation!
The CF Foundation is driven by a dream that one day, every person with cystic fibrosis will have the chance to live a long, healthy life.

Take a deep breath. Didn't that feel good? Now think about the almost 1,000 people waiting for lung transplants... You can bring them closer to their own deep breaths when you register as an organ donor at gorecycleyourself.com! 🫁 #LungHealth #CFAwarenessMonth #WorldAsthmaDay

Cystic fibrosis is considered as an invisible disease. Looking at most CFers you wouldn’t know from the outside how rough their body is going through things on the inside. Not all battles are ones you can see 🫁
#cfawarenessmonth