The Queen B herself, the madame, the Diva, miss little Sass Ella was diagnosed with Cystic Fibrosis when she was still growing in her mother’s belly. Having no idea what CF was, we researched the diagnosis and were scared to say the least. However, we were determined to find the perfect balance of keeping her healthy, and letting her enjoy her life to the fullest. Anyone who's ever met Ella knows that's exactly what she does - she lives life to the fullest! This angel is a ray of sunshine wherever she goes. She has brought so much laughter and happiness into the lives of her friends, family, teachers, and everyone who has the pleasure of knowing her. We thank God for the medicine, treatments, and continuing research being done to help her and other CF patients stay as healthy as possible. The Great Strides Walk is her favorite event all year because she gets to be surrounded by ALL the people she loves! Come walk with us, and have some fun with Ella at Great Strides :)
Donations and t-shirts are optional, and of course appreciated. Your presence at the walk means more to Ella than you'll ever know!
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There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. We walk for them. Will you join us? All we need you to do to become a member of our team is click on the
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To help minimize the risk of COVID-19, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: