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Welcome to Jillian's Jay Walkers, a beacon of hope and support for the Cystic Fibrosis community.

Our mission is to improve the quality of life and well-being of individuals and families impacted by Cystic Fibrosis.

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Our commitment extends beyond awareness and advocacy.

We provide direct support to those affected by Cystic Fibrosis

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Get Support

At Jillian's Jay Walkers, we offer a range of programs designed to support individuals and families affected by Cystic Fibrosis.

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Join us at our yearly fundraising events to support the fight against Cystic Fibrosis. Your participation helps raise crucial funds and awareness.


Support Us

Your support can make a difference. Consider donating or volunteering today to help us continue our mission and support those in need.

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Jillian's Story

Discover the inspiring journey of Jillian Rogers, founder of Jillian's Jay Walkers. A double lung transplant survivor and Cystic Fibrosis warrior, Jillian's story is one of resilience, hope, and dedication. Beyond founding the organization to provide crucial support to CF patients, Jillian also serves on two volunteer boards with the University of Michigan, working with CF doctors, social workers, patients, and nurses to strengthen patient-doctor relationships and improve in-patient care. Her personal triumphs and unwavering advocacy embody the spirit of never giving up. Learn more about her incredible story and how she continues to make a difference in the lives of those affected by Cystic Fibrosis.


Since 2020, we have raised a total of:

We have helped a total of:


30 Families

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Resources & Education

Empowering Through Knowledge

Travel Bag

Traveling with Cystic Fibrosis: Preparation and Safety Tips

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Managing Mental Health: Coping Strategies for CF Patients and Their Families

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Navigating Life with Cystic Fibrosis: Tips and Resources for Patients


Real Stories. Real Impact.

“Jillian’s Jay Walkers is about hope. Jillian is a double lung transplant survivor and an inspiration to so many, including myself.”

– David K.

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