Welcome to Team Sarah Grace! We are a group of family and friends who have come together to honor, support and love little Sarah as she faces the biggest fight of her life. As her lucky aunt, let me thank you for visiting our page!!
Life is full of blessings if you just know where to look for them! I know nothing is ever easy but when I compare my daily walk with that of my precious niece Sarah Grace, I am reminded of how lucky I am and the wonderful opportunity I've been given.
Thirteen years ago, Sarah Grace was born with cystic fibrosis. The diagnosis came as a shock to our family, and the battle she faces every day is real. But Sarah Grace is a brilliant fighter. Small and mighty at birth, SG has grown into a powerful and determined young woman who lives every day to the fullest and inspires me with all she accomplishes. A terrific student, an innovative and creative robotics competitor, a scrappy lacrosse player, and a loving and thoughtful young woman with a genuine heart for others, SarahGrace makes me proud every day.
A huge thank you to everyone who has been a part of this journey with us over the years. We would love to have you join Team Sarah Grace for the 2024 Great Strides event on Saturday, May 4th at Shelby Farms. Last year was our first at Shelby Farms and the location was spectacular and the day so much fun!! I know this year can only get better as we come together for our 13th walk, and 13 just happens to be Sarah Grace's lucky number!!
If you’re able to join us, please mark your calendar and save the date for Saturday, May 4. I just know this year’s event is going to be the best yet, and we’d be honored to have you as a part of the team.
If you’re able to join Team Sarah Grace, please officially sign up to ensure you receive future correspondence about the Great Strides event. Thank you in advance for helping us fight the good fight for Sarah and everyone who is living with CF. And please pray that CF will soon stand for Cure Found.
With tremendous thanks,
Shelley
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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.