Cooler but still well above normal this week

MPR News helps you turn down the noise and build shared understanding. Turn up your support for this public resource and keep trusted journalism accessible to all. 

Turn Up Your Support

When Jade Ochu was just a baby, she was diagnosed with systemic mastocytosis, a rare, painful and incurable blood condition. She was close to giving up on her treatments a couple of years ago.

 stepped in with the chance of a lifetime: 

 to the Country Music Association Awards. 

Jade, now 18, and her mom, Shonna Gacke, talked about the life-changing experience.

Make-A-Wish Minnesota

Thrifty Traveler collecting donations for Make-A-Wish Minnesota

Use the audio player above to listen to the program.

Subscribe to the MPR News with Angela Davis podcast on:

Arts and Culture

Music

Shows

MPR News with Angela Davis

Host

Author

When Jade Ochu was just a baby, she was diagnosed with systemic mastocytosis — a rare, painful and incurable blood condition. She was close to giving up on her treatments a couple of years ago. That’s when Make-A-Wish Minnesota stepped in with the chance of a lifetime: a trip to the Country Music Association Awards.

MPR News with Angela Davis - When Jade Ochu was just a baby, she was diagnosed with systemic mastocytosis, a rare, painful and incurable blood condition. She was close to giving  up on her treatments a couple of years ago. That’s when Make-A-Wish Minnesota stepped in with the chance of a lifetime: a trip to the Country Music Association Awards. Jade, now 18, and her mom, Shonna Gacke, talked about the life-changing experience.

MPR News with Angela Davis - A trip to the CMAs gave this Minnesota teen a reason to keep living

Make-A-Wish Minnesota sent Jade Ochu to the CMA Awards.

A trip to the CMAs gave this Minnesota teen a reason to keep living

Go Deeper.

Like this?

News you can use in your inbox