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My Great Strides Story

Hudson Dockry

Fundraising for Minneapolis Great Strides

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Hudson Dockry

Hello! 
Sweet little Hudson was diagnosed with CF at 2 weeks old, after a positive newborn screening, positive sweat test and confirmation through genetic testing. 
Rob and I were devastated, as we had no clue we were carriers and didn't know anything about the disease or how it would affect him. 
CF today, looks much different than it did years ago. Specialized medication and treatments have come a long way. However, there is still no cure at this time. 
We will continue to raise awareness and be advocates for him and Cystic Fibrosis.
Please consider donating to help find a cure! 
One day CF will no longer stand for Cystic Fibrosis. One day CF will stand for CURE FOUND! 
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There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.  

Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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$1,375
raised of $1,000 goal
 

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Team Hudson’s Heroes

$3,025
$5,000

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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.