Casey Herman
Kyndal was 5 months old when we found out she had cystic fibrosis. She is now 19 and getting ready for college. While we have had many ups and downs due to CF, she has always tried to persevere with a smile on her face. Anyone that meets her loves her! Kyndal is kind, creative, smart, and always ready for an adventure. As a mom, my hope is there will be a cure for CF. No child should ever have to deal with burden of Cystic Fibrosis and with your help, we can find a cure.
While treatment for CF has made great strides, there is still no cure for cystic fibrosis and too many people with CF die young.
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. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Help us find a cure for 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, not only for Kyndal but for everyone with CF.
While treatment for CF has made great strides, there is still no cure for cystic fibrosis and too many people with CF die young.
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. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Help us find a cure for 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, not only for Kyndal but for everyone with CF.
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