My Great Strides Story
Kristine Mcmullen
Kristine McMullen
Although our girl Georgia is 16+ months, she will forever affectionately be referred to as “baby Georgia” in our house. Our boys, Callan and Colson, love to play with their “baby” ‘cousin’- whether it be cabin weekends and sharing snacks, New Years Eve glow-stick dance parties, or watching the Super Bowl together - we relish the time we get to spend with the Wehr’s.
Our kids (3 & 4.5) know nothing of CF or how it affects Georgia, and we walk and stride for a life where she feels this way: minimally impacted and deeply loved and supported - for decades of cabin weekends, snack-sharing, and superbowls ahead.
Ryan and I are forever in awe of our the friends we get the added blessing to call family, Emily and Steven, and the strength and perseverance they demonstrate daily in how they not just care for Georgia, but dedicate themselves to finding a cure and advocating for Georgia.
Any donation - monetary, steps, prayers, or well-wishes mean the the world to Team Georgia and to fighting CF & finding a cure. Thank you for considering!
A little more on CF:
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.
Our kids (3 & 4.5) know nothing of CF or how it affects Georgia, and we walk and stride for a life where she feels this way: minimally impacted and deeply loved and supported - for decades of cabin weekends, snack-sharing, and superbowls ahead.
Ryan and I are forever in awe of our the friends we get the added blessing to call family, Emily and Steven, and the strength and perseverance they demonstrate daily in how they not just care for Georgia, but dedicate themselves to finding a cure and advocating for Georgia.
Any donation - monetary, steps, prayers, or well-wishes mean the the world to Team Georgia and to fighting CF & finding a cure. Thank you for considering!
A little more on CF:
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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