Jun 8, 2026 · 50 min · 11 segments
For more than two decades, Simon Dyson has been a caregiver, advocate, father, and unwavering source of support for his son Billy, who has cerebral palsy. In this powerful episode, Simon shares the…
Simon DysonGuest
Daryl PerryHostChad WilliamsHost
I sat with Billy and I said, what are we going to do now? And I enjoyed what I did, but I didn't really enjoy what I did because I didn't actually feel that we actually made any impact on people's lives.

We cared about premiums, but I didn't think we actually cared about the individuals.

It was about educating people so they can make informed decisions for themselves and their families.

we started our little business together and uh then i uh my friend in the uk um matt gallagher was diagnosed with motor neuron disease which is very sim which is not very similar is the same as als and he'd been given two years to live and uh he formed uh he formed a foundation called the matt gallagher foundation to raise money and awareness but not for himself but for all others suffering with motor neurone disease, to help them, to get them the things they needed when they needed it, because it's a very, very aggressive disease.

I sat with Billy and I said, what are we going to do now? And I enjoyed what I did, but I didn't really enjoy what I did because I didn't actually feel that we actually made any impact on people's lives.

We cared about premiums, but I didn't think we actually cared about the individuals.

It was about educating people so they can make informed decisions for themselves and their families.

we started our little business together and uh then i uh my friend in the uk um matt gallagher was diagnosed with motor neuron disease which is very sim which is not very similar is the same as als and he'd been given two years to live and uh he formed uh he formed a foundation called the matt gallagher foundation to raise money and awareness but not for himself but for all others suffering with motor neurone disease, to help them, to get them the things they needed when they needed it, because it's a very, very aggressive disease.
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