Join the Discussion: https://bit.ly/4rErM6r
#CysticFibrosis #CFCommunity #CFNewsToday #Bionews #CysticFibrosisDiagnosis #RareDiseaseCommunity
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You deserve support without needing to prove the need.
#CysticFibrosis
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Why toxic positivity doesn’t help in cystic fibrosis: https://bit.ly/4mlvBtz
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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Spread CF awareness: https://bit.ly/4qdb9No
Cystic fibrosis can affect many parts of the body, and symptoms can look different from person to person.
#CysticFibrosis #CF #CFAwareness #CysticFibrosisCommunity #RareDisease #ChronicIllness #CysticFibrosisNewsToday #Bionews
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What’s your take?: https://bit.ly/47sjWEJ
#CysticFibrosisNewsToday #Bionews #CysticFibrosis #CFCommunity #CFWarrior #CFLife #MentalHealth
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Love and disability meet in this cystic fibrosis story: https://bit.ly/4fe3YjU
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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Fatigue in CF isn’t tired; it’s body-deep depletion.
#CysticFibrosis
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Parenting with CF: https://bit.ly/4brKoAB
Jen Cogliano reflects on raising her daughter while living with cystic fibrosis, from daily treatments and hospital stays to choosing age appropriate honesty and focusing on presence over fear.
#CysticFibrosis #CysticFibrosisNewsToday #Bionews
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Today is #65RosesDay raising awareness for #Cysticfibrosis. In today's @irishexaminer.bsky.social I spoke to the family of a young girl with CF about how much joy she brings to their lives, how her condition shaped the family, & their hopes for her future.@cfireland.bsky.social
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What it's really like waiting for a lung transplant: https://bit.ly/4ff126r
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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Color coding your sputum is an actual skill we never asked to learn.
#CysticFibrosis
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Household routines shift around treatments without question.
#CysticFibrosis
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Having a rare genetic condition doesn’t define a person’s worth. https://bit.ly/4oygcHv
#CysticFibrosis #CFCommunity #CFLife #CFAwareness #CFNews
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Clothes that fit one month and not the next, classic CF reality.
#CysticFibrosis
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Prof James Chalmers talks about bronchiectasis and a clinical trial he is leading called AIRTIVITY® that is looking at a new treatment, for people with or without CF.
Read our blog to find out more.
➡️ https://ow.ly/iqcP50YFwrw
#ResearchWednesday #CFTrust #CysticFibrosis #Bronchiectasis
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Stay hydrated—especially if you live with cystic fibrosis: https://bit.ly/40GWL5S
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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Share Your Thoughts: https://bit.ly/4p4tPik
#CysticFibrosis #CFCommunity #CFNewsToday #Bionews #Healthcare #ChronicIllness
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Words matter when you’re living with cystic fibrosis: https://bit.ly/41eBlx3
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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Chime in here: https://bit.ly/47IpYjg
#CysticFibrosisNewsToday #Bionews #CysticFibrosis #CFCommunity #CFWarrior #CFLife #GeneEditing
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Leave a 💨 if coughing fits have interrupted your plans this week.
#CysticFibrosis
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How life after transplant looks with cystic fibrosis: https://bit.ly/4mjsceW
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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Salt & CF: https://bit.ly/4qOoAVa
People with cystic fibrosis lose more salt through sweat than most, making balance a daily priority.
#CysticFibrosis #Bionews #CysticFibrosisNewsToday #CFLife #CFCommunity #CFWellness #SaltWithCF #ElectrolyteHealth #CFNutrition #CFSupport
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Leave a 👎 if you experience sinus trouble that never really goes away…
#CysticFibrosis
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Jump Into Conversation: https://bit.ly/4rDrTPF
#CysticFibrosis #CFCommunity #CFNewsToday #Bionews #ChronicIllnessSupport
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Some days feel like a never-ending cycle of cough, breathe, repeat.
#CysticFibrosis
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After a double-lung transplant, Jennifer Bleecher was able to walk her daughter down the aisle—without oxygen, without fear, just love. https://bit.ly/47iCRAn
#CysticFibrosis #CFCommunity #CFLife #CFAwareness #CFNews
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Caring takes courage: https://bit.ly/49YkSCi
Ed’s reflection on life with his daughter Jasmine is a powerful reminder of what caregiving really looks like day to day.
#CysticFibrosis #CFAwareness #CaregiverAwarenessMonth #CaregiversMatter #BioNews #CysticFibrosisNewsToday #Bionews
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What makes living with CF rare and extraordinary: https://bit.ly/40FQGXg
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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CF families speak a language all their own.
#CysticFibrosis
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The shared grief within the CF community: https://bit.ly/4ff12mX
#CysticFibrosis #CysticFibrosisAwareness #CFWarrior #CysticFibrosisNews #Bionews
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