“Can’t wait to see everyone there, and thanks supporting me! -Daniel McGinnis Just a reminder that the Cystic Fibrosis Walk for Daniel McGinnis is tomorrow morning! All details are in the attached flyer! Event opens at 8:00am, program and walk starts at 9:00am. Parking is across the street from the park, and we are asking people to wear purple and/or Ghostbuster!
My Great Strides Story
Daniel McGinnis
Fundraising for Fort Worth Great Strides 2026
Daniel McGinnis
Hi, my name is Daniel and I’m 10 years old 💙
I have cystic fibrosis, and every day I have to do treatments to help me breathe and stay healthy. But I don’t let that stop me from being a kid—or from being a Ghostbusters fan! 👻
This year, I’m leading my own team called “Daniel’s Germbusters” for the Great Strides to help raise money for the Cystic Fibrosis Foundation.
We’re walking to help find a cure so kids like me can have healthier, easier lives.
I would love your help!
👟 You can join my team and walk with us
💙 You can donate to support our team
📣 Or you can share this post to help spread the word
Every step we take helps fight cystic fibrosis—and that’s something even bigger than catching ghosts!
Thank you for helping me be a real-life hero 💪👻
#DanielsGermbusters
#GreatStrides2026
#CureCF
#WhoYaGonnaCall
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.
MAY
17
17
Comments