My Great Strides Story
Andi Horstkotte
Fundraising for East Tennessee Great Strides
Andi Horstkotte
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.
Here's a little note from Jadzia - The Princess Warrior herself!
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Hi!
I am Jadzia. I am 11 years old. I like to sing, dance, and paint! Those are my favorite things to do. I also LOVE pancakes. I have a sister and one brother. I like that they play games with me. I also have three dogs and I love them...ALOT.
I want to raise money for the Cystic Fibrosis Foundation because, I want to find a cure. God made me and He is wonderful. I hope that you will know about Jesus!
Here is a video when I was 4 years old that shows what a day in a life with CF looks like for me....
https://youtu.be/cpa_kSvRnMQ
(copy and paste this to your URL to watch the video)
The things that are different now is that I take Trikafta and Hypertonic Saline daily and lots of other good supplements!
Goodbye!
Jadzia
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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.
Grab your purple and cameo clothes, join our Team Princess Warrior and let's go raise awareness!
Saturday, May 2, 2025
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.
Here's a little note from Jadzia - The Princess Warrior herself!
-------------
Hi!
I am Jadzia. I am 11 years old. I like to sing, dance, and paint! Those are my favorite things to do. I also LOVE pancakes. I have a sister and one brother. I like that they play games with me. I also have three dogs and I love them...ALOT.
I want to raise money for the Cystic Fibrosis Foundation because, I want to find a cure. God made me and He is wonderful. I hope that you will know about Jesus!
Here is a video when I was 4 years old that shows what a day in a life with CF looks like for me....
https://youtu.be/cpa_kSvRnMQ
(copy and paste this to your URL to watch the video)
The things that are different now is that I take Trikafta and Hypertonic Saline daily and lots of other good supplements!
Goodbye!
Jadzia
--------------------------
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.
Grab your purple and cameo clothes, join our Team Princess Warrior and let's go raise awareness!
Saturday, May 2, 2025
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