A big thanks to all our donors!
Flex for CRD!
Please help us help our friends at Cure Rare Disease (CRD) reach a historic moment in the fight against Duchenne Muscular Dystrophy. CRD is set to deliver a custom therapeutic using a CRISPR drug to a young man with Duchenne. To help make this happen, please visit our online store to purchase Flex for Kal gear. Half of the proceeds for the month of July will go to CRD to help raise the remaining $100,000 needed to deliver the first custom therapeutic. Find out more about the great things CRD is doing by following them on Facebook, Instagram, Twitter, LinkedIn, or visiting their website! 💚
About Kalel
Family
My name is Kal and I am 7 years old. I live with my mom, dad, and little sister, Livvy, in California. I love helping my dad on the farm where we raise organic pastured pork and sometimes chicken. I also help my grandma on the weekends with her garden where we have all kinds of delicious organic veggies.
Diagnosis
I was officially diagnosed with Duchenne Muscular Dystrophy (DMD) on December 30th, 2018 through a genetic test. Although I don't really understand what it all means, I am glad that I finally know why I couldn't keep up with the other kids at school and why I kept falling. There is currently no cure for DMD, but there are some potential ones on the horizon. In the mean time, we are pursuing treatments not covered by insurance in hopes of preserving my muscles.
Faith
Despite this diagnosis, we remain optimistic and trusting in God. We believe in the power of prayer, and ask that you continue praying with us and for us, especially for a miracle..
Contribute
Your generous gift will help us fund medical care and equipment not covered by insurance for Kalel.
"We rejoice in our sufferings, because we know that suffering produces perseverance; perseverance, character; & character, hope. And hope does not put us to shame because God's love has been poured out into our hearts through the Holy Spirit" -Romans 5:3-5