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My Xtreme Hike Story

Shaun Cramer

Fundraising for North Carolina Spring Xtreme Hike

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Shaun Cramer

Max is my 8 year old son and was diagnosed with Cystic Fibrosis shortly after birth.  He is my motivation to be better every day.  To watch him do his daily breathing and pulmonary treatments along with his medication regimen without complaint is inspiring.  Max refuses to let CF define him!  Together lets do this for Max and all the CF'ers out there!!

My first CF Xtreme Hike was with the STL Gateway Chapter in 2017.  Max was 8 months old at that time and the experience was a physical and emotional rollercoaster.  Since then I have hiked with the Wisconsin Chapter and this year I'm joining the North Carolina Chapter, where the Xtreme Hike concept began. 


Hike 30 Miles in a day.......no big deal when you look through the eyes of someone living with Cystic Fibrosis.

Shaun - Proud CF Dad


The Foundation's employees, volunteers, and sponsors are an amazing Team of people that have true compassion for our CF community. 

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.
APR
8

2017 Gateway

2024 Wisconsin

2023 Wisconsin

2022 Wisconsin

2021 Wisconsin

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$3,006.25
raised of $3,000 goal
 

Achievements

Leader

Team MAXpedition

$3,006.25
$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.