Hi, my name is Laura, and I’m asking for your help for my husband, Shawn, who has been bravely battling ALS (Amyotrophic Lateral Sclerosis) since December 2024.

ALS is a cruel and devastating disease that is slowly taking everything from him—his strength, his independence, and now even his voice. Watching the person you love fade in this way is something I wouldn’t wish on anyone.

We have two sons, and seeing their dad go through this has been incredibly painful for all of us.

Shawn was never one to sit still. He lived for the outdoors—kayaking, fishing, hunting—anything that kept him moving and living life to the fullest. That was who he was. But it’s now been over a year since he’s been able to do any of the things he loved. Piece by piece, ALS has taken that away.

Today, Shawn is in a wheelchair and beginning to lose his ability to speak. The progression feels relentless, and time feels incredibly precious.

But we are not ready to give up.

We’ve found a clinic in Miami—BodyScience Hospital—that offers specialized treatment for ALS patients using advanced testing and personalized therapies. While it’s not a cure, some patients have seen improvements or a slowing of progression. For us, even a little more time… a few more memories… would mean everything.

The reality is, we cannot do this alone.

The cost of treatment, travel, and staying in Miami is overwhelming, and we are reaching out for help during the hardest time of our lives.

If you can donate, no matter the amount, you are helping us fight for more time with Shawn.

If you can’t donate, please share this—because sharing could reach someone who can.

I will continue to update you along this journey, holding onto hope with everything we have.

More than anything, I just want more time with my husband. More time for our sons to have their dad. More moments, more memories—before this disease takes any more from us.

Thank you for standing with us, for your kindness, your prayers, and your support.

With all our hearts,

Laura, Travis, and Colby