Emmie’s Crew
Kristen Robinson
Kristen Robinson
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.
EMMIE’S CREW
Emmie was diagnosed with CF in May of 2024 at 11 years old. She has two of the rarest mutations in the world and does not qualify for medications that help others with more common mutations. We will continue to fight, advocate, and push for medical advancements for her to have the longest, best life!
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.
EMMIE’S CREW
Emmie was diagnosed with CF in May of 2024 at 11 years old. She has two of the rarest mutations in the world and does not qualify for medications that help others with more common mutations. We will continue to fight, advocate, and push for medical advancements for her to have the longest, best life!
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