Why am I running the 2026 Chicago Marathon for the CFF?
After a lifetime of seemingly disconnected and confusing symptoms, a 2017 genetic test revealed that I had two cystic fibrosis mutations in trans -- which indicated a diagnosis of cystic fibrosis.

The months that followed were filled with uncertainty and fear. During that time, I leaned heavily on the resources and community I found through the Cystic Fibrosis Foundation (CFF).

Fortunately, further medical testing revealed that I don’t have the full clinical presentation of CF. Instead, I was diagnosed with CFTR-related disorders — a condition that, in 2017, was newly emerging in medical understanding. Even now, I continue to rely on the CFF to help me navigate this evolving spectrum of disease.

I reflect almost daily on how differently my life could look because of my genetics — and I carry deep respect for the profound impact this disease has on so many lives and families. While my genes didn’t gift me with natural endurance speed, I run to protect my lungs, to safeguard my health, and as a personal expression of gratitude for what my body is capable of.

Running for me is, in many ways, a small miracle — one I don’t take for granted, and one I want to use for the power of good. Please help me in this goal by supporting the CFF.