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Camden is our grandson and he will be 15 years old in June. He is an awesome young man, very headstrong and determined. Camden's strong will and determination is exactly what he needs to fight Cystic Fibrosis. He does his treatments and takes his meds without hesitation. It has been a way of life for him from the very start.
Camden has a spunky little sister named Charlee Grace . He is a great big brother and Charlee loves him dearly. She already knows like the rest of us how special her big brother is.
Camden loves baseball, football, track and playing golf with his Dad. He has a very special Momma that he loves so much. Our hope is for a cure in the near future and that is the reason our family works so hard to raise money and try to bring awareness to this disease. We know that our fundraising will be used by the Cystic Fibrosis Foundation to help find a cure.
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. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Please support me!
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. 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.
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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.