Growing up with cystic fibrosis, I’ve had to do things a little differently than other kids my age. And while living with CF isn’t easy, I’ve been blessed with friends and family who support me.

My world was turned upside down in just a few weeks when a routine exacerbation quickly escalated into a lung transplant. I wasn’t prepared to tackle a transplant, but with time and support from my ...

Help make CF stand for Cure Found.

When my newborn was diagnosed with cystic fibrosis, I was overwhelmed by a whirlwind of emotions — from grief and anger to love and hope.

Growing up with CF made school challenging — not only because of hospitalizations and absences, but also because my teachers and classmates often didn’t understand what cystic fibrosis was.

I feel lucky to have finally received my CF diagnosis as an adult — but I often think of my sister, who lived a lifetime of illness without ever getting the answers she deserved.

The Cystic Fibrosis Foundation has awarded Corbus Pharmaceuticals up to $25 million to develop a potential anti-inflammatory drug that aims to reduce the frequency of pulmonary exacerbations for ...

Breastfeeding a child comes with a lot of challenges, dedication, and love. Breastfeeding a child with cystic fibrosis brings all of these aspects to a different level. As a first-time mom wanting to ...

The additional funding will support a Phase 2 clinical trial for an inhaled antisense oligonucleotide drug for people with cystic fibrosis who have the splicing mutation 3849+10Kb C-to-T.

When I moved away for college, I was determined to prove that I could manage my CF all by myself. But I was thrown for a loop when I was unexpectedly diagnosed with CF-related diabetes.