Living with cystic fibrosis means constantly navigating the emotional and physical strain of waiting. Despite the exhaustion and uncertainty, waiting reminds us of our ability to endure in the face of overwhelming challenges.

Linda Bowman, an adult from Boca Raton, Fla., lives with cystic fibrosis and has been an active advocate for the CF community for three decades. She was among the founding members of the Adult Advisory Council and her involvement in the first Community Conference work group helped bring BreatheCon to fruition. She also co-chaired the inaugural CF FamilyCon in 2018. In recognition of her unwavering dedication, Linda received the Cystic Fibrosis Foundation Alex Award in 2017.
Currently, Linda serves on the National Volunteer Engagement Committee, the Care Model Position Paper Committee, and the CF Peer Connect Mentorship program. She also serves on her local chapter board and participates in Community Voice. Linda's passion lies in fostering positive change by amplifying the voices of all those affected by cystic fibrosis, ensuring they are seen, heard, and supported. Linda’s awareness of life's fragility keeps her appreciative of the small blessings.
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Growing up, the term “life expectancy” was always with me, affecting my choices and expectations. Over time, I learned to tune it out and live my life my way.