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Squawk Pod

The Path with Becky Quick: A Beast of a Journey 3/2/26

Squawk Pod

CNBC

Business News, News, Investing, Business

4.2543 Ratings

🗓️ 2 March 2026

⏱️ 45 minutes

🧾️ Download transcript

Summary

In 2024, Jeffrey Allen applied to the first season of “Beast Games,” a reality competition show on Amazon Prime Video that was inspired by the Netflix series “Squid Game” and created by YouTuber MrBeast. Why did this California Dad want to be on a game show? “Beast Games” offered the largest cash prize in history – and Allen wanted to make a difference in the search for a cure for his son Lucas’ rare disease. Lucas was diagnosed as a toddler with Creatine Transporter Deficiency, or CTD, a rare genetic mutation that blocks the transport of the natural source of energy from the brain and muscle. Symptoms can include difficulty growing and gaining weight, slowed development of motor skills, intellectual disabilities, autistic behaviors and seizures, according to the National Organization for Rare Disorders. There are, estimated, just a few hundred CTD patients worldwide. Known as Player 831, Jeffrey Allen won the first season of “Beast Games” and the massive $10 million prize. “It’s all a miracle,” he says about the serendipitous achievement and the gift of parenting Lucas. To follow “Ruck for Rare,” visit: https://creatineinfo.org/ruck4rare/ Join us in advancing awareness and understanding of rare diseases. Visit CNBC.com/Cures to access clips, resources, or to sign up for our weekly newsletter. Follow Becky Quick on X: @BeckyQuick Please share your thoughts or rare disease story in the comments, and join us on The Path.

Transcript

Click on a timestamp to play from that location

0:00.0

Lucas, his soul, chose this body, chose us as parents.

0:09.0

For the world to care about rare diseases, people's hearts need to be changed.

0:15.0

You know, we can't just have money be thrown to the problem.

0:19.0

831 is blindfolded and can no longer see what's going on.

0:22.6

Beast Games application, Mr. Beast.

0:24.6

I don't have a job right now.

0:26.6

Like, I think I can apply...

0:28.6

Ten million dollars!

0:30.6

It's all a miracle.

0:32.6

But it's also tragic to think that I have to go in the largest game show ever

0:35.6

for people to know about my son.

0:38.4

Keep going!

0:40.0

Good job. Great job, bear.

0:46.3

I'm Becky Quick. Welcome to The Path from CNBC Cures, a podcast series about the people, the struggles, the science, and sometimes, yes, the

0:56.3

miracles of rare disease.

0:58.9

Bye.

1:01.1

I'm a mom of a child with a genetic disease.

1:04.4

My nine-year-old daughter, Kaylee, has one of the thousands of rare genetic conditions,

1:09.3

diseases, disorders, illnesses that are lurking in the

1:12.8

basic code that makes us who we are. Kaylee's condition is called Syngap 1. She's part of a very

1:19.1

small patient group. There are only about 1,700 other people in the world with this diagnosis.

1:24.6

Essentially, she only produces about half of the CINGAP protein that's needed

...

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