The Frosty Fight Blog

Welcome to The Frosty Fight Blog

This is where I share the real, unfiltered journey of living with ALS — the challenges, the victories, and everything in between. Here, you’ll see what it’s like day-to-day, how we push back, and the moments that keep us moving forward. No fluff, no filters — just the fight, told honestly.

The Sales Year No One Knew About

When I look back at early 2021, it feels like a lifetime ago. On January 2, 2021, I started a new job. It was right in the heart of COVID. Every interview had been done over Zoom. I hadn’t met a single person from the company in person, even though

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Game On: Facing ALS One Adjustment at a Time

When I was diagnosed with ALS, it was hard to fully explain what that moment felt like. As you can imagine, it was a combination of sadness, weirdness, oddness, and almost incomprehensible to tell friends and family. How do you even begin that conversation? How do you put into words

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The Day the Mouse Stopped Clicking

Looking back, it’s strange how something so small can quietly change the direction of your life. In 2020, I was selling software for a living. A big part of my job was running remote product demonstrations — 7 to 8 hours a day, five days a week — constantly clicking,

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5 years

Five years ago today, I was diagnosed with ALS. I don’t know if that’s something you’re supposed to celebrate. ALS isn’t exactly a milestone-friendly disease. From the moment you hear the words, the clock starts ticking, and the so-called experts tell you to expect two to five years. That’s the

Read More »

The Sales Year No One Knew About

When I look back at early 2021, it feels like a lifetime ago. On January 2, 2021, I started a new job. It was right in the heart of COVID. Every interview had been done over Zoom. I hadn’t met a single person from the company in person, even though

Read More »

Game On: Facing ALS One Adjustment at a Time

When I was diagnosed with ALS, it was hard to fully explain what that moment felt like. As you can imagine, it was a combination of sadness, weirdness, oddness, and almost incomprehensible to tell friends and family. How do you even begin that conversation? How do you put into words

Read More »

The Day the Mouse Stopped Clicking

Looking back, it’s strange how something so small can quietly change the direction of your life. In 2020, I was selling software for a living. A big part of my job was running remote product demonstrations — 7 to 8 hours a day, five days a week — constantly clicking,

Read More »

5 years

Five years ago today, I was diagnosed with ALS. I don’t know if that’s something you’re supposed to celebrate. ALS isn’t exactly a milestone-friendly disease. From the moment you hear the words, the clock starts ticking, and the so-called experts tell you to expect two to five years. That’s the

Read More »
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