Go Shout Love Podcast

Meet Nathaniel from St. Louis, Missouri. A Happy and resilient personality who reminds us of how many ways people can have a voice beyond audible speech, and how important it is for everyone to have that right.

At Go Shout Love we do amazing things for amazing families with kids on rare medical journeys.

Each month we shout love for families through the sale of creative apparel inspired by kiddos like Nathaniel.

Every purchase in March will be used to help purchase a bike trailer to allow Nathaniel to go biking with his family.

Visit our website at goshout.love to support Nathaniel through the purchase of a t-shirt, sweater, hoodie, tumbler, or other items

Josh and Jessica talk with Stephanie and Rodney, the parents of Sofia, a beautiful 6 year old who has Leukodystrophy and Epilepsy, and is our feature kiddo for this month.

At Go Shout Love we do amazing things for amazing families with kids on rare medical journeys. Each month we shout love for families through the sale of creative apparel inspired by the kiddos.

This month’s “Known & Loved” t-shirt design is inspired by Sofia, whose loving, warm, and silly personality allowed her to connect deeply with people at a very young age. Every purchase in February will be used to help remodel Sofia’s bedroom and bathroom to be adaptable and accessible. Visit our website at www.goshout.love to support Sofia through the purchase of a t-shirt, sweater, hoodie, tumbler, or other items.

At Go Shout Love we do amazing things for these amazing families with kids on rare medical journeys then check out this month’s “Same Storm, Different Boat” design that is inspired by Maddy and Mady.

Separated by only 80 miles, these sweet girls are navigating their own unique medical journeys, but have many experiences and battles they share with each other and other kiddos on rare medical journeys.
 
Every purchase in January will be used to help cover the costs of medical and mobility equipment for Maddy and Mady not covered by insurance.

Visit our website at goshout.love to support Maddy and Mady through the purchase of a t-shirt, sweater, hoodie, tumbler, or other items.

Our next episode will focus on another amazing family and an incredible kiddo. Stay tuned and Go Shout Love.

Go Shout Love is doing amazing things for amazing families with kids on rare medical journeys then check out this month’s “Same Storm, Different Boat” design that is inspired by Maddy and Mady.

Separated by only 80 miles, these sweet girls are navigating their own unique medical journeys, but have many experiences and battles they share with each other and other kiddos on rare medical journeys.
 
This episode surrounds Maddy M from Wamego, KS. We talk with her parents Megan and Joe about their journey, their family and everything in between.

Welcome back everyone today we are continuing our conversation with Cassie and Taylor the parents to Jensen lee, an 8 year old boy from Ava Missouri who has leukemia.

By the time we are posting this episode they will have only known about the diagnosis for about 40 days, so this family is still in the newness of it all with a long journey ahead. This is part 2, so if you haven’t listened to part one, pause this and head back to that.

Today we get to hear about how Jensen lee himself is doing, how he is handling his treatments and more about his wonderful personality. But it doesn’t stop there, both Cassie and Taylor are processing a lot of details and emotions and they are very generous to share that with us today.


Connect with Cassie and Taylor
https://www.facebook.com/cassie.f.wallace
https://www.facebook.com/taylor.wallace.750


Connect with Go Shout Love:
https://goshout.love
https://www.instagram.com/goshoutlove/
https://www.facebook.com/goshoutlove/

Get ready to shout love for Jensen Lee!

Jensen is a kind, compassionate, and loving 8-year-old boy who loves dirt bikes, animals, and baseball. He lives in Missouri with his parents, Cassie and Taylor, his older brother, Jack, and younger sister, Charlie.
This month’s “Brave” t-shirt design is inspired by Jensen and his journey with B-Cell Acute Lymphoblastic Leukemia. Every purchase in November will be used to help cover the costs of travel and housing expenses for Jensen Lee’s treatments.
We invite you to watch his video, read his story and subscribe to our podcast to listen to a couple conversations with his parents.
Get ready to shout love for Jensen Lee!

Jensen is a kind, compassionate, and loving 8-year-old boy who loves dirt bikes, animals, and baseball. He lives in Missouri with his parents, Cassie and Taylor, his older brother, Jack, and younger sister, Charlie.
This month’s “Brave” t-shirt design is inspired by Jensen and his journey with B-Cell Acute Lymphoblastic Leukemia. Every purchase in November will be used to help cover the costs of travel and housing expenses for Jensen Lee’s treatments.
We invite you to watch his video, read his story and subscribe to our podcast to listen to a couple conversations with his parents.


Connect with Cassie and Taylor
https://www.facebook.com/cassie.f.wallace
https://www.facebook.com/taylor.wallace.750


Connect with Go Shout Love:
https://goshout.love
https://www.instagram.com/goshoutlove/
https://www.facebook.com/goshoutlove/

This is part 2 of the conversation surrounding our feature kiddo Gabriel. We are talking with Stephanie and Scott, Gabriels parents. If you haven’t listened to part 1 yet, pause this episode and go back. There is a lot of context surrounding Gabriel and his background that will play a lot into this episode as well.

Today’s episode includes a lot of what is important for this family, including experiences. Living life to its fullest. We really didn’t touch on the medical side in part 1, but this episode includes a lot of that journey as well. Gabriel has been through a lot of procedures and is shown how much of a fighter he is.

Connect with Stephanie and Scott
https://www.facebook.com/stephanie.santomango
https://www.instagram.com/gabriels_gains/


Connect with Go Shout Love:
https://goshout.love
https://www.instagram.com/goshoutlove/
https://www.facebook.com/goshoutlove/

This month we are talking to Scott and Stephanie who are the parents to the always smiling, music loving 5 year old Gabriel.
Gabriel has been diagnosed with cerebral palsy and has a number of challenges and therapies that come with that diagnosis. Stephanie and Scot are going to fill us in on all of that. But what they also talk about is how Gabriel initially came into their lives and how the dynamic of their family is forever changed by this incredible little boy’s journey through foster placement and how that has lead to including another very important family member, Gabriels foster sister. There are many levels of inclusion layered throughout this entire conversation and we are excited to share that with you.


Connect with Stephanie and Scott
https://www.facebook.com/stephanie.santomango
https://www.instagram.com/gabriels_gains/


Connect with Go Shout Love:
https://goshout.love
https://www.instagram.com/goshoutlove/
https://www.facebook.com/goshoutlove/

Cece is our feature kiddo for the month of September 2021 and she has Pitt Hopkins Syndrome. This diagnosis comes with its challenges and that is how this episode starts off, with some of the difficulties and how this family is overcoming some of those. But the journey doesn’t begin and end with challenges and difficulties, those are elements involved. But other elements that are also very present are the joys…the positives…the love.

Thats what this episode is, it is a great insight to the life of a beautiful little girl like cece. Someone who will brighten your day. This episode also tackles a very big topic of “belonging” and what that really means to families like cece’s, but it doesn’t stop there. Belonging is for everyone and is something everyone deserves and how we can all have an impact on that.

Welcome to September 2021 as we feature a new family and a new kiddo. This month we are introducing you to Cecily…or Cece as her family affectionally calls her. Cece is a joyful and social 4 yr old who has been diagnosed with Pitt Hopkins syndrome. Today we are talking with Louie and Lizzy who are Cece’s parents.

There is a lot covered in this first episode, including getting to know the family through two great personalities in Louis and Lizzy. They talk about the journey of discovering the diagnosis and the various kinds of interactions with medical professionals. Some diagnosis are discovered before birth, Pitt-Hopkins is not one of those. Neither are easy, but this what Lizzy and Louie will walk us through.

Connect with Louie and Lizzy
https://www.facebook.com/ElizabethLucyDiNuzzo
https://www.instagram.com/lizzydinuzzo/
https://pitthopkins.org/cecilys-smile-squad/

Connect with Go Shout Love:
https://goshout.love
https://www.instagram.com/goshoutlove/
https://www.facebook.com/goshoutlove/