Sue Lepper
Our handsome grandson, Caleb, was 15 in January and is a freshman in high school. He is a typical teenage boy except he was born with Cystic Fibrosis. He starts and ends every day with chest percussion and medications.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.
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward. Caleb is the recipient of that research and science and benefits from the amazing drug,Trikafta. More
“wonder drugs” are in the pipeline for Caleb and the many other CF mutations that still need a miracle.
Thank you for being a part of our dream. Come walk with us on May 17, 8:30a, at the beautiful Suwanee Town Center, Suwanee, Ga. We press on until a cure is found for everyone with CF.
With deep appreciation,
Sue
Caleb’s Grandma
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.
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward. Caleb is the recipient of that research and science and benefits from the amazing drug,Trikafta. More
“wonder drugs” are in the pipeline for Caleb and the many other CF mutations that still need a miracle.
Thank you for being a part of our dream. Come walk with us on May 17, 8:30a, at the beautiful Suwanee Town Center, Suwanee, Ga. We press on until a cure is found for everyone with CF.
With deep appreciation,
Sue
Caleb’s Grandma
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