NEW BLOG - Advocacy: Screaming Out With Half A Breath
After a small break following the new year we are back with a full line up of blogs for 2021! To start things off we're sharing a blog from Founder and Executive Director of the CFLF, Brian Callanan. With Rare Disease coming up on the 28th, Brian writes about his experience advocating and using his voice to share his story of living with CF and empowers others to do the same. Please read and share his powerful blog with others!
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.
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