A few weeks ago, the Pickerd family received news that changed everything.

Cliff — a 59-year-old husband, father, and one of the kindest people you will ever meet — was diagnosed with ALS.

If you know Cliff, you know this diagnosis does not define him. He’s the guy who would drop everything to help someone in need. The one who makes people laugh when they need it most. The kind of man who puts his family above everything else, no questions asked.

I remember the first time I met Cliff. I was nervous, thinking it would be the typical “dad talk” about dating his daughter. It was the complete opposite. He was welcoming, genuine, and immediately made me feel comfortable. He wanted to know who I was as a person and how I would treat his daughter—not in an intimidating way, but in a way that showed how deeply he cared.

When I asked him for permission to marry my now wife, he didn’t just give his blessing—he treated me like family. Like I was already a son to him.

That’s who Cliff is.

But ALS doesn’t care how good of a person you are.

In just a short time, we’ve already started to see the effects. His speech has begun to decline, and his motor skills are being impacted. Simple, everyday tasks — buttoning a jacket, pulling up socks, or even holding silverware — are becoming increasingly difficult. Things most of us never think twice about are slowly becoming daily challenges.

And the hardest part is standing by and watching someone you love go through something like this, knowing there’s only so much you can do.

As a family, we are heartbroken. His wife, his son, and my wife are facing something no one is ever prepared for — watching a strong, caring man go through an incredibly difficult battle. It’s emotional, overwhelming, and at times feels helpless.

But if there’s one thing we can do, it’s show up for him the same way he has always shown up for everyone else.

Cliff has always been a man of passion. He loves woodworking, spending time outdoors hunting, and anything involving race cars. He enjoys making wine and, more than anything, cherishes time with his family. That’s who he is at his core — someone who truly lives and loves deeply.

Now he needs support.

The financial burden of ALS is overwhelming. Medications like Radicava can cost between $145,000 and $171,000 per year just to help slow progression. On top of that, there are ongoing medical visits, physical and occupational therapy, and eventually the need for mobility equipment and home modifications to help maintain comfort and independence.

Funds raised will go directly toward:

• Medical treatments and medications

• Physical and occupational therapy

• Mobility and accessibility equipment

• Travel and lodging for medical care

• Home modifications as the disease progresses

We are setting this goal as high as possible because the reality is — the need will continue to grow.

If you’re able to donate, no matter the amount, it truly makes a difference. And if you can’t, sharing this page means just as much.

Cliff has spent his life helping others without hesitation. Now it’s our turn to stand behind him and do the same.

Thank you for your support, your prayers, and for being part of his fight.