Cure for Cade

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

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.

04/17/2026

POV: You’re a medical mom watching a moment you weren’t promised 🤍

Special needs parenting means living in the unknown—especially when it comes to mobility. Walkers, therapies, long appointments, and questions no one can fully answer. Raising a medically complex child teaches you to celebrate progress that the world might not even notice.

For the medical moms, the special needs parents, the families navigating mobility challenges—you know what this moment means.

Address

Juneau, AK

Website

https://gofund.me/d348d19d

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