In 2020, we welcomed our first child to the world, Violet Louise. Shortly thereafter, Violet was diagnosed with Cystic Fibrosis. Since becoming the most important part of our lives, we have made it our mission to help support those who support her.
The Cystic Fibrosis Foundation is a huge support system for those impacted by Cystic Fibrosis and as a family, we do everything we can to help support their mission. Over the last two years, we have participated in the Great Strides Walk in Chicago, where we raised a combined total of over $50,000 and were recognized as the Rookie of the Year for our area in 2020.
This year, Violet has been selected as the Ambassador for The Greater Illinois Chapter of The Cystic Fiborsis Foundation. We are so very proud of her and are even more inspired now to find a cure.
I hope you will consider donating to our fundraiser as we walk in hopes of changing the meaning of CF from Cystic Fibrosis to "Cure Found".
Thank you so much from our family to yours!
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.