BreatheCon is a unique event to virtually gather with other adults with cystic fibrosis in a welcoming, inclusive space where you can be your authentic self.
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Learn more about previous CF Foundation community conferences.
I have always been very interested in science, eventually leading to my career as a genomic scientist. My curiosity helped me cope with the uncertainties of cystic fibrosis, leading me to many academic, professional, and personal opportunities that gave me a more expansive view of how my different roles and identities can build upon one another.
To the moms of children with CF who feel isolated in their journey — you are not alone. This is my letter to you, from someone who understands.
ResearchCon is for everyone with a personal or professional connection to cystic fibrosis to learn and discuss CF-related science and care alongside others living with and studying the disease.
Hearing from diverse voices is critical as we continue our journey to listen, learn, and take action against racism and discrimination.
Our corporate champions are an important part of our progress — with corporate supporters by our side, we continue to advance our goal — to make CF stand for Cure Found.
With help and support from my parents, I felt empowered to make my first big decision with my cystic fibrosis care: When to remove my G-tube.
Whether focused on physical wellness or connectivity and creativity, there are countless projects led by the community to support and empower people with CF and their loved ones.
At this age, your child with cystic fibrosis is ready to transition from breast milk or formula to whole milk or a high-calorie supplement. Encourage independent eating. Create a consistent schedule and mealtime expectations.