Hi, my name is Mia and my team and I are GOING TO FIND A CURE FOR CF! We are part of the Skylar Striders CFF Great Strides WALK TEAM every year and also lead a Compassion Mission called "Flip Out for Skylar” in another nonprofit I am in called Small Hands Big Hearts United.
I am asking you to please make a donation to my page to help me find a cure! Also, please register for the walk or volunteer to help set up on walk morning. Let's do this together and show Skylar how much we love her!
Our team in SHBHU also has a Compassion Mission called “Flip Out for Skylar” and we have been growing this for 10 years now. We make custom flip flops in the colors of the CFF logo. Skylar is a founding member of SHBHU and is also our friend, role model and inspiration. She has Cystic Fibrosis but she doesn't let that define her. Skylar was the SHBHU Ambassador Teen PTT President for four years and made what SHBHU is today. She is an example to ALL who meet her of how to be a leader, show compassion to others and live a life with purpose. If you know Skylar, you know she is ALWAYS laughing. We have always said that Skylar is always flipping out over something but in a good way with a huge smile on her face! She is now a college student at PFEIFFER COLLEGE and graduating May 11th.
I love her and her entire family so I want to tell you how you can help raise money to find a cure for Cystic Fibrosis. The CF foundation supports the development of new drugs to fight the disease, improve the quality of life for people with CF, and ultimately find a cure for Skylar. We will raise money to help do this year round.
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. I walk for them and hope you will support me in my efforts. Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis.
Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. Your gift is 100-percent tax deductible.
Love,
Mia
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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.