Cure for Cade

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

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

05/01/2026

So happy to finally be home

04/27/2026

I’m not crying, you’re crying

04/23/2026

We get to go home one week from today!!!

04/21/2026

For two weeks, we have worked every day on walking to the top of the switch back. Today, he did it. Not many will understand what a massive accomplishment this was. Those with rare diseases, or with mobility challenges, you’ll get it.

04/19/2026

Sometimes the secret is… just being too stubborn to quit.

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Juneau, AK

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