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My CF Climb Story

Dawn Whitfield

Fundraising for Philadelphia CF Climb

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Dawn Whitfield

I'm once again climbing a lot, a lot, a lot of steps on November 8th (or at least trying)! But that climb will be nothing compared to the fight people with CF go through in their lives just to breathe and live an everyday life!
Cystic fibrosis is a rare, life-shortening, genetic disease found in about 30,000 people in the U.S., which causes persistent lung infections and limits the ability to breath over time. Those living with this disease are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers all struggling each day just to breathe and live normal, healthy lives.
Sixty-five years ago, most children with cystic fibrosis did not live long enough to attend elementary school, but thanks to Foundation-based research and care, many people with CF are now living into their forties and beyond achieving milestones once thought not possible, such as attending college, pursuing careers, and having a family of their own. While there has been significant progress in treating this disease, there is still no cure and too many lives are cut far too short.
I met Mary on a brewery tour in Bucks County many, many years ago. Since then, I have watched her fight this disease with the support of her wife, Jess. Mary is a true inspiration. Learn more about Mary's journey here.

To support Mary and all others fighting CF, I am once again fundraising and climbing on November 8th. Help make a difference and support me by donating to my CF Climb fundraising campaign today! Donate an amount that is meaningful to you, anything you can give is appreciated! Thank you in advance!

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$477.16
raised of $500 goal
 

Achievements

Member of

Team Mary

$1,792.16
$3,500

Recent Donations

Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.