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My Great Strides Story
Jenessa Kildew
After a perfect delivery and first day with our baby girl, we were quickly swept in to an emergency surgery at the local children’s hospital and a two-month NICU stay while her bowels healed and we were introduced to her diagnosis of cystic fibrosis. We had heard of the disease before, but truly did not know what it meant. The surgeon tried to tell us that there was newfound hope on the horizon for those born with CF today, but it was extremely difficult to believe and understand at the time as the new therapies were still so fresh and not yet tried with young children. We became quickly immersed with administering several new medications, performing Chest Physiotherapy (CPT), placing feeding tubes, and becoming abnormally aware of our surroundings in regards to germ exposure. Not only were we navigating being new parents, but now we were learning an entirely new language and thrown in to a world we never knew existed. Sometimes it felt insurmountable and the future seemed so uncertain.
Today, cystic fibrosis is woven in to our lives but no longer feels dominant. Riley is our sweet, energetic, and brilliant little girl that works hard each and every day with hours of treatments and taking medications. She is also our little girl that rides bikes, runs and plays with friends, dresses up as princesses, does arts and crafts, bakes treats and loves to chatter the day away.
Our family is able to lead this kind of life thanks to the amazing medical advances of today and the mission of the Cystic Fibrosis Foundation.
-Jenessa, Mom to Riley
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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