Join us in supporting the Cystic Fibrosis Foundation and our vibrant 19-month-old daughter, Brooke, as she bravely fights cystic fibrosis.
As Brooke's parents, we couldn't be prouder of the determined, sparkling girl she's becoming. Her personality, a beautiful blend of brightness, warmth, and resilience, inspires everyone she meets. Her light is infectious— smiling through physical therapy, and bravely tackling her medications and food allergies, celebrating every new "safe" food like it’s her own special treat.
She knows what she wants, and we’re certain her courageous energy will guide her through any challenge. While CF once overshadowed our lives, Brooke's radiant spirit now fills our hearts, and her enthusiasm for life outweighs her diagnosis.
Some of Brooke's favorite things include sharing snacks with her closest friends Jet and Benson, chatting with anyone who will listen, being a Sesame Street enthusiast, exploring the cranberry bogs, sporting comfy pajamas, cuddling with Mr. Bunny, and dancing along to The Wiggles.
We're so grateful for the outpouring of support as we participate in our third Great Strides walk, a journey we began even before Brooke's birth. It feels incredible to know we have such a supportive community cheering us on.
As she grows, so does our hope, fueled by the remarkable progress in CF treatment and research. Your donations drive this change, helping secure a brighter future for CF warriors like Brooke.
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This year's Great Strides event will take place at Fort Taber in New Bedford on Sunday, May 19th, at 11:00 AM. We aim to gather a team to surround Brooke and other CF fighters with as much love as possible.
Let's keep pushing until CF stands for CURE FOUND!
With optimism,
Lindsey, Kevin, and Brooke
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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.