Mary Offiler
Our grandson, Henry, was born on January 21, 2016. Within the first few weeks of his life, he was diagnosed with Cystic Fibrosis. While we were caught off guard (to say the least) with his diagnosis, we have found solace in the spirit of the CF community. The Cystic Fibrosis Foundation offers hope and promise to those living with CF. Our hope for our grandson is that he is able to enjoy life to its fullest as the CFF works to find a cure for this disease.
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short.
This year Henry celebrated his ninth birthday. Our birthday wish for Henry is to help him have many, many more. Please join us in bringing hope to those who live with CF.
As our team name says, "Henry's Engines" is ready to ZOOM ahead to find a cure for CF! Let's make 2025 the year it happens!
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.
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