Cure for Cade

Cure for Cade Cade was diagnosed with hereditary spastic paraplegia. Follow his story as we work to defy all odds!

06/30/2026

Coming up with creative ways to encourage movement is a nonnegotiable, because the strength that he’s building leads to an increase in his quality of life.

06/29/2026

There were days we didn’t know if this would ever be possible. Today, Cade is out on the trail, and every step feels like a gift. If you’re parenting a child with a disability or mobility disorder, don’t underestimate how much hope can carry you through the impossible. ❤️

06/23/2026

This trip to Dallas did not go as planned…

06/12/2026

10 weeks post gene therapy. We are seeing progress in compression.

06/08/2026

Thank you .adventures for inspiring our adventures

06/03/2026

It’s been two months since cade received gene therapy. And while he is walking better than he ever has, he also falls at regular intervals during our walks. I tend to film when he’s doing really well, but I know there’s a lot of rare disease parents out there following our story and I wanted full transparency of the progress he is making.

05/18/2026

Cade is filing a formal complaint…

05/15/2026

Thank you for being on this journey with us

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Juneau, AK

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