The Utah Parent Center’s mission is to help parents help their children, youth and young adults with all disabilities to live included, productive lives as members of the community. They strive to accomplish that by providing accurate information, empathetic peer support, valuable training and effective advocacy based on the concept of parents helping parents.

In this episode, we dig into the Individualized Education Program. We learn all kinds of new acronyms and get you ready for your first meeting. Jennie Dopp is a parent advocate at the Utah Parent Center. She gives us the basics in a very authentic way of understanding and utilizing the IEP.

“Working for a nonprofit, it’s about mission, none of us are in it for the money. We love what we do.”

The Utah Parent Center’s mission is to help parents help their children, youth and young adults with all disabilities to live included, productive lives as members of the community. They strive to accomplish that by providing accurate information, empathetic peer support, valuable training and effective advocacy based on the concept of parents helping parents.
In this episode, we dig into the Individualized Education Program. We learn all kinds of new acronyms and get you ready for your first meeting. Jennie Dopp is a parent advocate at the Utah Parent Center. She gives us the basics in a very authentic way of understanding and utilizing the IEP.
“Working for a nonprofit, it’s about mission, none of us are in it for the money. We love what we do.”

On "Celebrating the Spectrum," KSL's Debbie Worthen delights in the joy and happiness her son, a child with autism, has brought into her world. Each week Debbie consults the experts and connects with others who are also learning to navigate life with a child who has special needs. This is a place where we find hope, look for solutions and connect with those working to create a better world of inclusion.

On "Celebrating the Spectrum," KSL's Debbie Worthen delights in the joy and happiness her son, a child with autism, has brought into her world. Each week Debbie consults the experts and connects with others who are also learning to navigate life with a child who has special needs. This is a place where we find hope, look for solutions and connect with those working to create a better world of inclusion.

Celebrating the Spectrum

An Introduction to the IEP with The Utah Parent Center

Today we talk to Liv Gilbert, Debbie’s oldest daughter about what it’s like when a sibling gets an autism diagnosis. She recalls her emotions at the time and how she feels about her brother.

Today we talk to Liv Gilbert, Debbie’s oldest daughter about what it’s like when a sibling gets an autism diagnosis. She recalls her emotions at the time and how she feels about her brother.

I’m Just Living in the Moment!

This week we will revisit some of our favorite interviews. Don’t get us wrong, we have loved all our guests and we will likely do this more often because it was so much fun going back to some of our first interviews.

This week we will revisit some of our favorite interviews. Don’t get us wrong, we have loved all our guests and we will likely do this more often because it was so much fun going back to some of our first interviews.

Some of Favorite Moments So Far

Charlotte Deleste is a journalist in Wisconsin. Her son, Giovanni, was born with a rare genetic condition that caused him to have up to 80 seizures a day. Despite his disabilities, Gio was declared “not disabled enough” to get home nursing care. She couldn’t believe it. Instead of accepting a system that felt broken, she and her husband created what has turned into a non-profit helping hundreds of families with respite care, therapy, and family support. You will be inspired by her drive to get her son, and other families, the help they need.



“That’s all we want to do, just make a difference, make a positive difference and hope that it just keeps going and somebody else will do the same down the road.”

-Charlotte Deleste, Founder of Gio’s Garden

Charlotte Deleste is a journalist in Wisconsin. Her son, Giovanni, was born with a rare genetic condition that caused him to have up to 80 seizures a day. Despite his disabilities, Gio was declared “not disabled enough” to get home nursing care. She couldn’t believe it. Instead of accepting a system that felt broken, she and her husband created what has turned into a non-profit helping hundreds of families with respite care, therapy, and family support. You will be inspired by her drive to get her son, and other families, the help they need.
 
“That’s all we want to do, just make a difference, make a positive difference and hope that it just keeps going and somebody else will do the same down the road.”
-Charlotte Deleste, Founder of <a href="http://giosgarden.org/">Gio’s Garden</a>

An Introduction to the IEP with The Utah Parent Center

Celebrating the Spectrum

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Celebrating the Spectrum

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