

My Breathe Team Story
Linda Murphy
Fundraising for 2025 AJC Peachtree Road Race
Linda Murphy
I'm participating in Atlanta's Peachtree Road 10K July 4th in memory and honor of Andy Lipman.
I'll be walking in this, my first 10K, (not running as Andy always did) but even walking it is outside my comfort zone! It is only Andy that could inspire me to even attempt this!
This would have been Andy’s 29th AJC Peachtree Road Race, a remarkable feat for anyone, but particularly for a person living with CF. I'll be walking and fundraising for the CF Foundation in his memory, less than 6 months since he passed suddenly from an aneurysm.
Andy made, and will continue to make, a profound difference in so many ways - for the CF community and humanity as a whole - hero, warrior, mentor, inspirer, encourager, motivator, writer, coach, advocate, organ donor, devoted family man, and friend. He spread awareness of CF not only through his own personal CF journey, but in sharing the stories of so many fellow CF warriors from around the world, sharing in their triumphs and struggles in his CF Warrior Project books and in so many other ways. In this picture I’m with Andy and his mother Eva at one of his book interviews and signings 5 1/2 years ago. It was a happy day spreading awareness of cystic fibrosis.
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. There is currently no cure for cystic fibrosis. 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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