Navigating Daily Life with CF
In this powerful episode of Our Fight to Breathe, host Caleigh Haber sits down with her close friend Nick Di Brizzi Jr., a double lung and kidney transplant recipient who has turned his journey with cystic fibrosis into a mission of hope and service. Nick, an actor, athlete, and founder of the Breathe Like a Boss Foundation, shares nearly a decade of friendship and parallel recovery with Caleigh as they explore what it truly means to live—not just survive—with chronic illness.
This conversation offers rare insight into the realities of life before and after transplant, the challenges of managing complex medical needs, and the transformative power of community support. Nick and Caleigh discuss the daily heroism required to navigate chronic illness while maintaining hope, purpose, and connection to others who understand the fight.
Key topics covered:
- Daily management strategies for cystic fibrosis and post-transplant life
- The role of exercise, mindset, and community in long-term health outcomes
- Navigating the emotional and physical challenges of chronic illness
- Finding purpose and giving back through advocacy and nonprofit work
- The critical importance of organ donation awareness
- Building resilience through faith, family, and peer support
Whether you're living with chronic illness, supporting someone who is, or seeking to understand the patient experience, this episode offers valuable perspectives on resilience, community, and the power of turning personal struggles into sources of strength for others.
Medical disclaimer: This podcast is for informational purposes only and should not replace professional medical advice.
Creators and Guests
Host
Caleigh Haber-Takayama
I'm Caleigh Haber, a cystic fibrosis warrior, two-time double lung transplant recipient, and passionate advocate for the chronic illness community. Born with CF, I've navigated countless surgeries and medical challenges while choosing to live each day to the fullest in honor of my donors and with deep gratitude for my supportive community. Through Fight2Breathe and my podcast "Our Fight to Breathe," I advocate for the cystic fibrosis, organ transplant, and rare disease communities, working to raise awareness and inspire others to thrive despite their challenges.
Guest
Nick Di Brizzi
Nick Di Brizzi Jr. is a Chicago-based actor, athlete, and founder of the Breathe Like a Boss Foundation who lives with cystic fibrosis. Diagnosed as a toddler, Nick is nearly nine years post double lung transplant and also received a kidney transplant from his brother in 2021. He is known for roles in television shows like Fargo and for representing Illinois at the Transplant Games of America, where he has earned multiple medals. Through his foundation, Nick helps others with respiratory illnesses access fitness resources, aiming to improve health without financial burden. His journey of resilience and kindness inspires and uplifts the cystic fibrosis and transplant communities.