I am incredibly honored to be participating in the Cystic Fibrosis Foundation’s Chicago Magnificent fundraising event, but for me, this is about so much more than a fundraising challenge.

It’s about my niece, Sydney.

Watching someone you love live with cystic fibrosis has a way of changing your perspective. I’ve seen the strength, resilience, and determination that CF requires—not only from Sydney, but from my sister, Christine, and her husband Steve, who have been by their daughter’s side through all of it. I’ve seen how much this disease can ask of a person and a family, and I’ve also seen just how much hope research and medical advances can bring.

That is why I am stepping up and committing to raise at least $5,000 for the Cystic Fibrosis Foundation. And honestly? I don't just want to meet that goal. I want to absolutely blow it out of the water.

Every donation, no matter the size, helps support research, medical care, and programs that are working toward a future where cystic fibrosis no longer dictates what someone can do, how long they can live, or what their family has to worry about.

More than 40 years ago, children with CF often didn't live long enough to attend elementary school. Today, people with CF are living into adulthood and beyond because of incredible advances in research and care. But there is still more work to do—and we need a cure for every person living with CF.

I’m asking you to join me in this fight.

Donate if you can. Share this page. Talk about cystic fibrosis. Help me spread the word.

Because someday, I want Sydney—and every person living with CF—to look back and know that we helped create a world where CF is no longer something they have to fight.

Let’s make some history. 💜

Thank you for standing with me, Sydney, and the entire CF community.