A big thanks to all our donors!

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#flexforkal

KALEL'S FIGHT AGAINST DUCHENNE MUSCULAR DYSTROPHY

My buddy Dylan in the news fundraising for me!

Calling all Heroes

If you would like to contribute directly to Kal's Stem Cell Therapy, check out this great video or click here for more information:

Updates on Kal Stem Cell Treatment

Update after Kal's 1st Stem Cell Treatment back in February 25: 

All proceeds will go towards medical expenses & care for Kal

About Kalel

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Family

My name is Kal and I am 6 years old. I live with my mom, dad, and little sister, Livy, 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. 

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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, I am blessed to be receiving  stem cell treatment. 

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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, but ultimately for God's will to be done. 

Contribute

Your generous gift will help us fund medical care and equipment for Kalel. 

Pay with PayPal or a debit/credit card

 "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

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Contact Us

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Find out how you can help!

Contact us to find out more about Kalel, DMD, and fundraisers/donations.

Flex for Kal