My Great Strides Story
Ella Haupt
Ella Haupt
In 2017, my middle child, Calliope Ella, was diagnosed with cystic fibrosis 10 days after she was born. I participate in the Great Strides walk each year because of the enormous impact the Cystic Fibrosis Foundation has had on my experience as a parent of a CF kiddo.
From the moment I met our team at St Vincent's hospital, I was welcomed by a group of professionals who knew how to anticipate my questions and concerns. That support, which is structured by the CF Foundation, has made all the difference in managing a complicated illness.
I'm incredibly thankful for the support of my friends and family in continuing to fund the Cystic Fibrosis Foundation.
From the moment I met our team at St Vincent's hospital, I was welcomed by a group of professionals who knew how to anticipate my questions and concerns. That support, which is structured by the CF Foundation, has made all the difference in managing a complicated illness.
I'm incredibly thankful for the support of my friends and family in continuing to fund the Cystic Fibrosis Foundation.
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