Introducing the Social Health Awards Program and NetworkWe are very excited to announce the launch of the Social Health Network and Awards! The Social Health Network is a community for patients, caregivers, and healthcare professionals with the... By Editorial TeamBookmark for later
Traveling with Cystic FibrosisNot to be a downer, but traveling with CF is a headache. Regardless, I have been incredibly lucky to have gotten to visit so many countries across North America. Salt... By Mikayla BianchinBookmark for later
Tips for Summer Caregivers for Kiddos with CFSummer is here and that means your kiddos with CF are home for the next few months from school. Just when you finally feel comfortable releasing control the school year... By Janeil WhitworthBookmark for later
Introducing the Social Health Awards Program and NetworkWe are very excited to announce the launch of the Social Health Network and Awards! The Social Health Network is a community for patients, caregivers, and healthcare professionals with the... By Editorial TeamBookmark for later
Traveling with Cystic FibrosisNot to be a downer, but traveling with CF is a headache. Regardless, I have been incredibly lucky to have gotten to visit so many countries across North America. Salt... By Mikayla BianchinBookmark for later
Tips for Summer Caregivers for Kiddos with CFSummer is here and that means your kiddos with CF are home for the next few months from school. Just when you finally feel comfortable releasing control the school year... By Janeil WhitworthBookmark for later
Introducing the Social Health Awards Program and NetworkWe are very excited to announce the launch of the Social Health Network and Awards! The Social Health Network is a community for patients, caregivers, and healthcare professionals with the... By Editorial TeamBookmark for later
Traveling with Cystic FibrosisNot to be a downer, but traveling with CF is a headache. Regardless, I have been incredibly lucky to have gotten to visit so many countries across North America. Salt... By Mikayla BianchinBookmark for later
Tips for Summer Caregivers for Kiddos with CFSummer is here and that means your kiddos with CF are home for the next few months from school. Just when you finally feel comfortable releasing control the school year... By Janeil WhitworthBookmark for later
The Many Colors of Cystic Fibrosis: Yellow (Part 1)When I was a child, I fell in love with the show Joseph and the Technicolor Dreamcoat and its colorful set design. Since that first viewing, I’ve realized that my... By Nicole KohrBookmark for later Reactions 0 reactions Comments2 comments
Ask the Advocates: Staying HydratedLiving with cystic fibrosis (CF), you learn how important hydration is and the best ways to get your body the necessary fluids. We asked our patient leaders to share their... By Editorial TeamBookmark for later Reactions 0 reactions Comments0 comments
My quiet timeWhen things get bad I have discovered “Quiet Time”. I typically shut off all noise, TV, radio, etc. I like to lay down, close my eyes and most of the...Bookmark for later Reactions 0 reactions Comments0 comments
Fill in the blank: ___________ is something that only someone with CF would understand. Share something that only those living with CF of caring for a loved one with CF would truly understand. Let's raise awareness by talking about topics that are uniquely related...Bookmark for later Reactions 0 reactions Comments6 replies
