Susan Pomeroy

My Great Strides Story

Some of you may remember, I’m sure most of you won’t, but last year I walked for Team Bush. I’m so very happy to say that this year I’m walking for Team Gavin! Gavin Is a is an adorable seven month, old baby, full of smiles and loving life. He’s doing extremely well with his baby CF treatments. Before we know it, he will be able to start taking the CF meds that have made life better for so many others living with CF. While the advancements in the last decade have been huge, we still hold out hope for even better options, and maybe someday a cure.  Please consider donating to this worthwhile cause. Any amount, no matter how small, is very much appreciated.

Cystic fibrosis affects the lungs, pancreas, and other organs. The symptoms can vary from person to person, and as people with CF live longer than ever before, their disease can become more complicated, leading to serious health issues. 

The Cystic Fibrosis Foundation has made extraordinary progress — including fostering the development of more than a dozen CF treatments — but these treatments are not a cure and not everyone can benefit from them. We must keep going.

Your support makes a difference.

By donating to my fundraising goal, you will help advance our mission for a cure for all. Please consider joining us and helping make CF stand for Cure Found.