
Nicole Howard
We’re walking in loving memory of our dear friend Lindsey — a bright light, a fierce
We’re walking in loving memory of our dear friend Lindsey — a bright light, a fierce fighter, and someone who left a lasting impact on everyone who knew her.
Cystic fibrosis is a relentless, life-shortening genetic disease that damages the lungs, pancreas, and other vital organs. It makes everyday things—like breathing and staying healthy—an enormous challenge. While research has brought incredible progress, there is still no cure.
Lindsey's journey with CF was filled with courage, resilience, and love. She faced every setback with grace and never stopped believing in a better future—not just for herself, but for everyone with CF. She was passionate about raising awareness and funds, always holding onto the hope that one day, CF would stand for “Cure Found.”
Your support means more than you know. Every donation fuels research, brings us closer to a cure, and honors the legacy of those—like Lindsey—who inspire us to keep going.
Will you help us continue what she started and bring hope to all those living with CF?
fighter, and someone who left a lasting impact on everyone who knew her.
Cystic fibrosis is a relentless, life-shortening genetic disease that damages the lungs, pancreas, and other vital organs. It makes everyday things—like breathing and staying healthy—an enormous challenge. While research has brought incredible progress, there is still no cure.
Lindsey's journey with CF was filled with courage, resilience, and love. She faced every setback with grace and never stopped believing in a better future—not just for herself, but for everyone with CF. She was passionate about raising awareness and funds, always holding onto the hope that one day, CF would stand for “Cure Found.”
Your support means more than you know. Every donation fuels research, brings us closer to a cure, and honors the legacy of those—like Lindsey—who inspire us to keep going.
Will you help us continue what she started and bring hope to all those living with CF?
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