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My Great Strides Story

Gerald Brantner

Fundraising for Eau Claire Great Strides 2026

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Gerald Brantner

Hello family and friends! This is another milestone for our family. Our Cystic Fibrosis Walk is 4 1/2 months away. May 16, 2026. Our daughters are 40 and 37 currently. Please assist in making it the year that CF will stand for Cure Found for Cystic Fibrosis, Help us!
Please assist us in our dream of making a Cure for Cystic Fibrosis. We have many blessings and memories that our daughters have brought to us. Please make a donation and support us on behalf of Rachel-37 and Geralyn-40.

I am supporting CF to help raise money and awareness to find a cure for our 2 daughters that are living each day with cystic fibrosis which have many challenges but have been fighting strong through daily CF smartvest airway clearance system treatments and many medications.
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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$150
raised of $5,000 goal
 

Achievements

Member of

Team CF Cruisers

$250
$8,000

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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.