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 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.

This month is a celebration of you — the individuals, families, and supporters who make up the CF community. You can join us by sharing your accomplishments, milestones, and hopes for the future on ...

The Clinical Specimen Resource Library is intended to facilitate sharing of patient-derived specimens and lab-derived resources managed outside of the CF Foundation. This is designed to be a ...

Pain is a common issue for many people with cystic fibrosis. People with CF can experience a range of different types of pain from CF. Your CF care team can work with you to develop a plan to decrease ...

Nosis Bio, an inaugural winner of the Foundation’s Golden Ticket Competition, receives funding to further explore design of novel ligands, which are specialized molecules that could help more precise ...

Today, Vertex released positive preliminary clinical trial results for the potential triple-combination therapy VX-445 plus tezacaftor/ivacaftor (Symdeko®). Positive results were announced today from ...

The Cystic Fibrosis Foundation recently announced that there are almost 40,000 people living with CF in the United States. Not only are there more of us with CF, but we are now living longer. Based on ...