Why toxic positivity doesn’t help in cystic fibrosis: https://bit.ly/47rl22d
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
October 30, 2025 at 1:45 PM
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Understand how cystic fibrosis affects your airways: https://bit.ly/47tlL2X
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
October 29, 2025 at 5:15 PM
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Find out how cystic fibrosis is diagnosed early and accurately: https://bit.ly/4nqf084
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNewsToday #Bionews
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNewsToday #Bionews
October 28, 2025 at 8:12 PM
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Breaking down the real costs of cystic fibrosis: https://bit.ly/4o9BDPr
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNewsToday #Bionews
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNewsToday #Bionews
October 26, 2025 at 3:44 PM
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A fresh take on cystic fibrosis and life expectancy: https://bit.ly/3WVPJrq
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
October 24, 2025 at 6:30 PM
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Merging Art and Advocacy: https://bit.ly/47BeLCg
Filmmaker and author Ashley Wilson has lived with cystic fibrosis since birth, and she’s using her art to bring hidden truths to light.
#CysticFibrosis #CysticFibrosisAwareness #ChronicIllnessCommunity #BioNews #CysticFibrosisNewsToday
Filmmaker and author Ashley Wilson has lived with cystic fibrosis since birth, and she’s using her art to bring hidden truths to light.
#CysticFibrosis #CysticFibrosisAwareness #ChronicIllnessCommunity #BioNews #CysticFibrosisNewsToday
October 21, 2025 at 3:42 PM
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Navigating Two Big Changes: https://bit.ly/46WUjvC
#CysticFibrosis #CysticFibrosisAwareness #Menopause #ChronicIllnessCare #CFCommunity #CysticFibrosisNewsToday #Bionews
#CysticFibrosis #CysticFibrosisAwareness #Menopause #ChronicIllnessCare #CFCommunity #CysticFibrosisNewsToday #Bionews
October 17, 2025 at 1:03 PM
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Get inspired: https://bit.ly/3W9oYzv
Tré LaRosa shares how using AI tools like ChatGPT has helped lighten the load of managing daily care and nutrition, without replacing his medical team.
#CysticFibrosis #CysticFibrosisAwareness #ChronicIllnessCare #CF #CysticFibrosisNewsToday #Bionews
Tré LaRosa shares how using AI tools like ChatGPT has helped lighten the load of managing daily care and nutrition, without replacing his medical team.
#CysticFibrosis #CysticFibrosisAwareness #ChronicIllnessCare #CF #CysticFibrosisNewsToday #Bionews
October 16, 2025 at 4:04 PM
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#tbt To last week when our team at CCHS wore yellow for wear yellow for CF day.
#CysticFibrosis #cysticfibrosisawareness #Yellow #outfitinspiration #teachingteam #hospitalschool #ThrowbackThursday #EduSky #EduSkyUK #Disability
#CysticFibrosis #cysticfibrosisawareness #Yellow #outfitinspiration #teachingteam #hospitalschool #ThrowbackThursday #EduSky #EduSkyUK #Disability
June 19, 2025 at 8:32 AM
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CF: genetic condition; causes thick, sticky mucus, clogging lungs, digestive tract; leads to chronic infections, digestive issues, complications like neuropathy
https://www.foundationforpn.org/may-is-cystic-fibrosis-awareness-month/
#cysticfibrosis #cysticfibrosisawareness #neuropathy
https://www.foundationforpn.org/may-is-cystic-fibrosis-awareness-month/
#cysticfibrosis #cysticfibrosisawareness #neuropathy
May 19, 2025 at 4:24 PM
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Happy #cysticfibrosisawareness month!
I'm an #artist. I sit and draw. & then I do breathing treatments that requires me to sit.
Some might think I chose art because of my CF, it was a coincidence.
Speaking of art, here is a page I am currently working on. #NeedhamComics #MonkeyBoy #CysticFibrosis
I'm an #artist. I sit and draw. & then I do breathing treatments that requires me to sit.
Some might think I chose art because of my CF, it was a coincidence.
Speaking of art, here is a page I am currently working on. #NeedhamComics #MonkeyBoy #CysticFibrosis
May 11, 2025 at 7:44 AM
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Happy #CysticFibrosis Awareness Month! Recently I was asked by #UCSD's Adult CF clinic to design a shirt for the running team "Breath Easy" for their #GreatStrides Run, by #CysticFibrosisFoundation. So, I designed a robot #Nebulizer.
#cysticfibrosisawareness #TheSimpsons
#MrPlow
#cysticfibrosisawareness #TheSimpsons
#MrPlow
May 11, 2025 at 7:18 AM
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It has been a journey... Thanks, @emilysentourage.bsky.social for including me in the #CFAwarenessMonth campaign this year! 💜
#cysticfibrosis #fight4cure #cysticfibrosisawareness #crossoutcf
www.emilysentourage.org/the-cf-broth...
#cysticfibrosis #fight4cure #cysticfibrosisawareness #crossoutcf
www.emilysentourage.org/the-cf-broth...
The CF Brother Who Became a CF Scientist
During CF Awareness Month, Emily’s Entourage invites members of the cystic fibrosis (CF) community to share their stories. Today’s blog post highlights the story of Miquéias Lopes Pacheco, PhD, a brot...
www.emilysentourage.org
May 1, 2025 at 9:43 PM
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Happy #CysticFibrosisAwareness Month!
When I was born, my parents were told I might not make it to 18. I remember the summer we learned about Pulmozyme at CF camp—we threw a party. We truly believed a cure was around the corner. That was 1993.
When I was born, my parents were told I might not make it to 18. I remember the summer we learned about Pulmozyme at CF camp—we threw a party. We truly believed a cure was around the corner. That was 1993.
May 1, 2025 at 6:34 PM
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#EternalSpotlight #CelebrateLife #RIP #JulianBenson #CaptainSparkle #CysticFibrosisAwareness #IrishTelevision
April 28, 2025 at 2:39 AM
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Every story of strength starts with a choice. 💪
For @cystic_ninja, living with Cystic Fibrosis, he could’ve let it control him. Instead, he used it as fuel and made it to the American Ninja Warrior Finals. 🏆
#CYACommunity #AmericanNinjaWarrior #CysticFibrosisAwareness
For @cystic_ninja, living with Cystic Fibrosis, he could’ve let it control him. Instead, he used it as fuel and made it to the American Ninja Warrior Finals. 🏆
#CYACommunity #AmericanNinjaWarrior #CysticFibrosisAwareness
March 14, 2025 at 1:10 AM
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We’re getting everything set up for the big Paddle Out show tonight at the Golden Bough Theatre in Carmel! 🌊🎬 See you soon! 💜✨ #PaddleOut #LivingBreathFoundation #CysticFibrosisAwareness
March 8, 2025 at 10:55 PM
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Feb 28 is Rare Disease Day!
#cysticfibrosis #rarediseaseday #cf #comic #cfawareness #cysticfibrosisawareness
#cysticfibrosis #rarediseaseday #cf #comic #cfawareness #cysticfibrosisawareness
February 28, 2025 at 5:15 PM
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Miss America 2025, Abby Stockard, received a heartfelt commendation from the Alabama Senate for her remarkable advocacy and dedication to healthcare, inspiring many with her journey and impactful work.
Learn more here!
#AL #CysticFibrosisAwareness #CommunityImpact
Learn more here!
#AL #CysticFibrosisAwareness #CommunityImpact
Alabama Senate honors Abby Stockard for winning Miss America title
Senator Wagner commends Abby Stockard for her achievements as Miss America during legislative session.
citizenportal.ai
February 8, 2025 at 11:34 AM
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Our new Self Love Salve is here! ✨
& A portion of proceeds will be donated to the Cystic Fibrosis Foundation, so every jar supports both self-care and a great cause. 💜
Available now at Abby’s Apothecary! #SelfLoveSalve #GiveBack #CysticFibrosisAwareness
& A portion of proceeds will be donated to the Cystic Fibrosis Foundation, so every jar supports both self-care and a great cause. 💜
Available now at Abby’s Apothecary! #SelfLoveSalve #GiveBack #CysticFibrosisAwareness
February 5, 2025 at 6:52 PM
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