Join me in funding the research that helps people with cystic fibrosis live longer, healthier lives.​

I was born in 1975 and diagnosed with cystic fibrosis in 1986, at a time when expectations for people with CF were very different. From a young age, CF made it clear it was not going to be an easy journey. It has tried to take me out more times than I can count.

The truth is, I would probably not be here today without my double lung transplant. And even getting to transplant was not guaranteed. I made it to 34 years old because of the research and advancements made possible by the Cystic Fibrosis Foundation, and because of the money raised and given by people who are passionate about improving the lives of those with CF. Every extra year I was able to breathe and stay strong enough to reach transplant was made possible by that commitment.

Today, I am thriving in 2026. I am living proof of how far CF research and care have come, but my story also shows how much further we still need to go.

Cystic fibrosis is a genetic, life shortening disease that damages the lungs, pancreas, and other vital organs. It makes breathing difficult and fighting infections harder, often leading to irreversible lung damage. Too many people with CF still face serious health challenges and life saving lung transplants just to survive.

That is why I am walking.

I am walking to help change the odds for those living with CF so future generations do not have to endure the same health struggles or face the need for a lung transplant to stay alive. There is currently no cure for cystic fibrosis, but together, we can help change that.

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you are supporting the research and science that made my life possible and that will create a better future for everyone living with CF. Thank you for being part of this journey.