I am 33 years old and have been living with Cystic Fibrosis since I was diagnosed at just 5 months old. Growing up in and out of the hospital shaped who I am today and ultimately led me to become a nurse. Now, I have the privilege of serving as a pediatric hematology/oncology nurse, caring for children and families during some of their most difficult moments; something I understand deeply from my own journey.

I am married to my husband, Ryan, and we have two beautiful children, Ryker (4) and Maddox (almost 1). They are my reason why; my motivation to keep pushing forward, to stay strong, and to continue advocating for a cure.

I am forever grateful to the Cystic Fibrosis Foundation for the incredible advances in medicine that have changed my life and the lives of so many others living with CF. Because of these breakthroughs and access to life saving meds like Trikafta, I have been able to fulfill my dream of being a Mom and a pediatric nurse. 

Being a boy mom means living in a world full of energy, chaos, loud laughter, and the kind of love that runs deep and fierce. It’s scraped knees, endless questions, and tight hugs. Some days are hard. Some days I feel tired in ways I can’t explain. But then I look at them and I remember exactly why I keep going. They are my reason to fight harder, to stand stronger, to be better. They remind me that even on my worst days, I am still their safe place, their comfort, their home. Being their mom is my purpose. And no matter what life throws my way, I’ll keep showing up for them… because they’re everything to me. 💙

Being part of the CF family means being part of something bigger than myself. It means fighting for a future where my children and all families don’t have to live with the weight of this disease. I thank God everyday for my CF team. They listen to me, they advocate for me, and they love Ryker and Maddox like they are their own.  I will never be able to thank them enough.
 
For Maddox’s first birthday, we made a different choice; one that felt more meaningful to our hearts. Instead of gifts, we’re asking for donations to the CF foundation. We are can do is using this moment to teach something bigger from the very beginning; kindness, compassion, and giving.

We are so grateful for everything our boys already have, and we know there are families and children who need support far more. This birthday isn’t just about celebrating a year of life; it’s about sharing love beyond our home and making a small difference where it truly matter.

Thank you for supporting this journey, for walking alongside us, and for helping us take strides toward a cure.