Andy Lipman; Obituary, Death: It is with profound sadness that we announce the passing of Andy Lipman, a true inspiration and a beacon of hope for individuals living with cystic fibrosis (CF). Andy passed away at the age of 49, a remarkable accomplishment for someone who was diagnosed with CF, a genetic disease that profoundly impacts the lungs and digestive system.
His life was defined not by the limitations of his diagnosis, but by his boundless spirit, determination, and unwavering commitment to living life to the fullest. Andy was born with CF, a condition that affects thousands of people around the world. Doctors often told him that his time would be short, but Andy refused to be defined by the prognosis. Instead, he dedicated his life to defying the odds, raising awareness about cystic fibrosis, and advocating for a cure.
His journey was a testament to the power of hope, resilience, and a positive mindset. From the very beginning, Andy set out to surpass expectations. He achieved what many considered impossible, living far beyond the median life expectancy for someone with CF. On his 38th birthday, Andy surpassed the expected lifespan for people with cystic fibrosis, a milestone that celebrated both his incredible perseverance and his refusal to give in to the challenges of the disease.
By the time he reached 49, Andy had defied the prognosis that so many others with CF face, becoming an enduring symbol of hope for those struggling with the condition. Andy was not just a survivor; he was a true advocate for the CF community. He attended the University of Georgia, where he graduated with a degree in Business Administration. But his education extended far beyond the classroom—Andy became a role model and an inspiration for countless others who were battling the same disease.
He didn’t just want to survive; he wanted to live, and to help others live, too. He embraced an active and fulfilling lifestyle, achieving physical feats that seemed unimaginable for someone with cystic fibrosis. He carried the Olympic torch, ran in the Peachtree Road Race every year since 1997, completed triathlons, and maintained a rigorous workout routine.
These accomplishments were not just personal milestones—they were a declaration of his commitment to defying the limitations of CF. As an author, Andy chronicled his journey in two powerful memoirs, Alive at 25: How I’m Beating Cystic Fibrosis and The Drive at 35: The Long Road to Beating Cystic Fibrosis. Through these books, he shared his experiences, offering hope, strength, and insight to those facing similar challenges.
Andy also created the CF Warrior Project series, which celebrated the resilience of others living with cystic fibrosis around the world. His words inspired a movement—a community of warriors who, like him, refused to let CF define them. In addition to his writing, Andy co-founded the Wish for Wendy Foundation in honor of his sister, Wendy, who tragically passed away from CF at just 16 days old.
Through this foundation, Andy helped raise over $4.5 million for cystic fibrosis research and awareness. His dedication to the CF cause earned him the Alex Award from the Cystic Fibrosis Foundation in 2017, recognizing his tireless advocacy and the immense impact he had on the CF community. Andy’s public speaking engagements were another way he shared his story and amplified the message of hope for those living with CF.
In 2019, he made a memorable appearance on The Today Show, where he shared his personal journey and encouraged others to fight for a cure. His voice resonated with millions, offering strength to those who needed it most. But Andy’s greatest joy came from his family. Despite the challenges of CF, Andy and his wife, Andrea, were blessed with two children, Avery and Ethan, through IVF.
These miracles brought indescribable happiness to his life, and he was a devoted father and husband, always showing that love, determination, and the support of family could overcome even the greatest obstacles. He was a role model for his children, teaching them the values of perseverance, compassion, and living each day to its fullest.
Professionally, Andy was the President of Andy Lipman, LLC, and had a successful career at DiversiTech. He was also deeply involved in his community, serving on the boards of the Georgia Chapter of the Cystic Fibrosis Foundation and the University of Georgia’s Terry College Business emeritus board of directors. Andy’s contributions to both his professional community and the CF community were invaluable, and he was widely respected for his leadership, generosity, and unwavering commitment to making the world a better place.
Andy’s life was profoundly changed in 2019 when he began taking Trikafta, a breakthrough medication for cystic fibrosis. This life-changing treatment significantly improved his lung function, allowing him to experience a quality of life that had previously seemed out of reach. Trikafta gave him the chance to live with greater vitality and energy, and it was a reminder of the power of medical advancements and the hope they bring.
Though Andy’s battle with CF has come to an end, his legacy will live on in the countless lives he touched, the movements he inspired, and the awareness he raised. He leaves behind a loving family—his wife, Andrea; his children, Avery and Ethan; his parents, family, and friends—and a community that was profoundly shaped by his courage and determination.
Andy Lipman’s legacy is one of hope, perseverance, and unwavering love for his family, his community, and all those who battle cystic fibrosis. He leaves behind a world forever changed by his passion for life and his commitment to making a difference. Andy will be missed, but his spirit will continue to inspire us all to live boldly, to never give up, and to cherish every precious moment.
In lieu of flowers, the family asks that donations be made to the Wish for Wendy Foundation to continue the fight for a cure for cystic fibrosis. Rest in peace, Andy. You were a warrior, and your fight has left a lasting mark on the world. Your courage will never be forgotten.
