Taylor King
Hi Everyone,
It’s been a while since my family and I have participated in a Cystic Fibrosis Great Strides Walk, and just as long since I’ve written an update—so here we are!
Life has been full of change and growth, and I’d love to share a little about where I’ve been and where I’m headed.
In the spring of 2022, I graduated from the University of Utah with a Bachelor of Science in Marketing. Closing that chapter was bittersweet, but I felt an overwhelming sense of accomplishment and gratitude for an incredible four years. After saying goodbye to lifelong friends and packing up everything I knew in Salt Lake, I took a leap and moved to Denver.
Why Denver? Growing up, I visited Colorado often to see family and always felt drawn to this place. When it came time for a fresh start after college, Colorado felt like the perfect next step—familiar yet new, with family close by and everything I loved about Northern Utah: mountains, hiking, biking, snowboarding, and, of course, snow! A remote full-time job made the move possible, and just like that, I started an exciting new chapter.
Since moving here in the summer of 2022, I’ve fallen in love with another city all over again. I’ve spent my days snowboarding at the most beautiful resorts, hiking through the breathtaking Rockies, exploring downtown Denver, and meeting incredible new friends. My sense of independence has skyrocketed, and I can confidently say—I’m incredibly happy!
Through all these changes, one thing has remained constant: my commitment to my health. I’ve always made my treatment and medications a priority, balancing work, life, and fun while taking care of myself every step of the way.
The Cystic Fibrosis Foundation has been a life-changing force in my journey. Thanks to groundbreaking advancements like Trikafta, the life expectancy for people with CF has doubled in my lifetime alone—from around 30 years old to over 60! That kind of progress is nothing short of incredible.
This is all made possible by hardworking doctors, nurses, selfless volunteers, generous donors, and supportive communities. The CF Foundation’s mission is simple: “To Make CF Stand for Cure Found.” I truly believe a cure is coming in my lifetime. With your support, we can get one step closer.
90% of every dollar donated goes directly to research, care, and education programs for Cystic Fibrosis. No matter the size, your donation makes a real difference—not just for me, but for the entire CF community.
After nearly three years in Denver, I knew it was time to get involved with my local CF community. I have an incredible team of doctors, amazing friends, and a life I love. This year, I’m thrilled to experience my very first Great Strides Walk in Colorado! My family has participated in walks in Nevada and Utah, and now it’s time to walk in the Mile High City.
I’d love for you to join me on May 10th at Sloan’s Lake as we take strides toward a cure.
Thank you for catching up with me, and for considering a donation to help change lives. Your support means the world!
See you soon!
Love,
Taylor King
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There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.
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.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Will you help us end cystic fibrosis?
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.
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