I’m walking in a cystic fibrosis fundraiser on May 16 at Fort Williams Park in Cape Elizabeth, home of Portland Head Light, for CF Awareness Month.

This one is personal.

I was diagnosed with cystic fibrosis as an adult in 2023. Even with milder CF genes, it has led to serious complications, including lung disease, severe bowel issues, and major surgeries such as a lung resection and spinal fusion related to an ongoing fungal infection that requires lifelong treatment.

On top of that, I manage multiple chronic conditions every day. It has meant additional surgeries over the years and a constant balance of treatments, symptoms, and the unknowns that come with them.

Cystic fibrosis is a life-shortening genetic disease that affects the lungs and other vital organs. While progress has been made, there is still no cure.

I’ve started things off with a donation and will be walking to help support research and better treatments.

If you’re able to help, whether by donating or sharing, I’d really appreciate it. Every step gets us closer.