This week we are so excited to share a blog from a new guest blogger, and CFLF Grant Recipient, Charlotte Ward. Charlotte is 15 years old and was diagnosed with Cystic Fibrosis at birth. She is an avid swimmer and has received three Recreation Grants to improve her swimming skills. Please read and share her very inspiring blog about her journey with CF and the many things that swimming (and CF) have taught her about who she is!
Choose an activity that YOU love, and your $100 donation will go 100% to fund a grant in that activity! Only $10,000 more is needed to reach our 1,000th award!
"Many people have explained how surfing can be a natural saline treatment, and I can feel it working even though I am not thinking about my CF while having fun."
CFLF assists in providing avenues toward healthy and active lifestyles through recreation, thereby empowering and educating people with Cystic Fibrosis on the critical psychological, social, and emotional connections between their lifestyle and their health.
This collaboration between the CFLF, CysticLife and Essential Image Source Foundation captures the lives and stories of people who push themselves beyond the perceived limits of their Cystic Fibrosis.
CFLF assists in providing avenues toward healthy and active lifestyles through recreation, thereby empowering and educating people with Cystic Fibrosis on the critical psychological, social, and emotional connections between their lifestyle and their health.
CFLF assists in providing avenues toward healthy and active lifestyles through recreation, thereby empowering and educating people with Cystic Fibrosis on the critical psychological, social, and emotional connections between their lifestyle and their health.
CFLF assists in providing avenues toward healthy and active lifestyles through recreation, thereby empowering and educating people with Cystic Fibrosis on the critical psychological, social, and emotional connections between their lifestyle and their health.
CFLF assists in providing avenues toward healthy and active lifestyles through recreation, thereby educating people with Cystic Fibrosis on the critical psychological, social, and emotional connections between their lifestyle and their health.
