Hi

My name is Sarah

I was diagnosed with Cystic Fibrosis at birth. Today, I am a high school sophomore, and thanks to an amazing medical team and incredible breakthroughs in research, I live a normal life just like any other kid. In fact, most people don't even know I have CF until I tell them!
Staying active is a huge part of my health. I play volleyball year-round and regularly hit the gym to give my lungs the exercise they need. I am also surrounded by a wonderful circle of family and friends who support me daily. I enjoy shopping :) , driving with friends, going to the beach, and best of all going to my boyfriend's sports games. My boyfriend, Jack, makes an impact on my health journey. He talks to me through long, scary appointments, reminds me to take my medicine, and always finds fun things for us to do to keep me smiling.
All the donations made to Cystic Fibrosis research have provided the funds needed for miracle medications like Trikafta, which I take daily. Trikafta helps prevent lung infections and reduces mucus buildup. While it does have some side effects, it has allowed me to completely eliminate several other medications I used to depend on.
It is because of this organization and fundraisers like this one that I am able to afford this life-changing medication. With your continued support, I hope to live a long, full life like any other kid. Thank you for your donations!

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure. There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.