A Little Something Extra

S2 E18: A Little Something Extra with Joanne and Nathan

Britain’s Got Talent Semi-Finalists Nathan and Joanne join the podcast to talk about their amazing journey! Joanne and Nathan are a dancing duo who won over the hearts of Great Britain on the latest season of Britain’s Got Talent. This incredible journey began back in 2019 in one of Joanne’s dance classes. Nathan is an adult with Down Syndrome who has always been interested in dance and performing. Well, after taking classes with Joanne, he knew he had found his passion! Joanne did not go into this as an advocate looking to spread awareness for Down syndrome, nor did she see this as a charity case. Nathan and her merely formed a connection with one another on the dance floor that she believed the world should see! After years of practice and growth, Joanne secretly submitted an inquiry about performing with Nathan on BGT, and the rest was history!

Tune in now to hear their heartwarming story, some amazing British accents, see some of GiGi and Nathans's dance moves, hear GiGi’s Tipppsss on dancing your heart out, and much more fun!

Watch the video version at https://gigisplayhouse.org/alittlesomethingextra/

 

S2 E17: A Little Something Extra with Jennifer Hogan Jones

Jennifer Hogan Jones, known on social media as My Beautiful DS Journey, joins the show! Jennifer is a super mom who has been sharing her Down syndrome journey on social media. When she received her prenatal diagnosis that her son, Hudson, had Down syndrome, she thought her world would fall apart. Being a mom of 3 other daughters, she didn’t know how the family would take it. Well fast forward 4 years and those dark moments are a thing of the past. Jennifer talks with us about the reason behind sharing her story and the light that is spreading across the lives of so many. Tune into the episode to hear all about how Jennifer is changing the way the world views Down syndrome by celebrating Hudson’s life and showing people the beauty of the DS diagnosis.

See the video episode at, https://gigisplayhouse.org/alittlesomethingextra

S2 E16: A Little Something Extra with Houston and Katie Vandergriff

Houston and Katie Vandergriff join the show!! Houston is an adult with Down syndrome who is a professional photographer and world traveler. His mother, Katie, and him run the platform “Downs and Towns”, where people can view his beautiful photography and see his life journey! This episode is so important because it shows the power of following one’s passion. No one should be held back from following their passions, especially because of a measly extra chromosome, and Houston channels that energy! In this episode, we talk about Houston’s travels (most recently to Egypt), how he found his passion, and what he did to pursue it. We, of course, hear some incredible words of inspiration from his mother and some really beautiful “Something Extras”! We hope you enjoy it!

To watch the video version of this episode, click here.

S2 E15: A Little Something Extra with Grace and Carrie Key

The mother-daughter duo behind Candidly Kind, Grace, and Carrie Key join the show! Grace is a 22-year-old entrepreneur who so happens to have Down syndrome. Grace has a passion for art, fashion, and cosmetology so, like any great entrepreneur, she is channeled that passion into her business! Candidly Kind’s message is to spread light, love and acceptance through Grace’s original art. Then a percentage of proceeds go to various non-profits that support that same mission of spreading love and acceptance!

In the episode, we talk with Grace and her mom Carrie about their journey, from Grace’s birth and the mindset Carrie had in that moment through today and the incredible woman she has become! We get some amazing words of inspiration from both Carrie and Grace, of course, we dive into each of their “something extra’s,” and we finish off with GiGi’s Tips on being creative. We hope you enjoy it!!

Watch the full episode here: https://gigisplayhouse.org/alittlesomethingextra/s2-e14-a-little-something-extra-with-grace-and-carrie-key/

S2 E14: A Little Something Extra with Erin Johnson

Author, influencer, sister, and sibling advocate; Erin Johnson joins the show this week alongside her brother, Matt! This episode goes out to all the amazing sibling advocates out there. Erin is the older sister of her brother, Matt, who has Down syndrome. Erin and Matt share a story that a lot of people can relate to. Just a brother and sister who share lots of love, laughs, and appreciation for each other. Erin wanted to share her sibling story with the world to show the beauty of having a brother with Down syndrome and how amazing the journey is as an adult. Matt is now the uncle to a niece and nephew, and he could not handle the job any better!

In the episode, Erin and Matt share their sibling journey, giving us some valuable life lessons that any of us can learn from! We also talk about the impact that Matt has had on Erin outside of their relationship, such as her career, her experience as an author, even her decision to adopt a child with Down syndrome with her husband. Of course, we learn Matt and Erin’s Little Something Extra, and GiGi finishes things off with some tips on “loving your family”. We hope this one gives a little perspective on the importance of family!

You can find Erin and Matt on social media @Erinadvocates

Watch the video version of this epsoide here.

S2 E13: A Little Something Extra with Heather & Bill from our Syracuse location

Heather Rodriguez and Bill Alsid from GiGi’s Playhouse Syracuse join the show! Heather has been a friend of GiGi’s Playhouse and a die-hard advocate for Down syndrome for 10 years. Bill is a participant at GiGi’s Syracuse but is better known for his beautiful personality and his ability to make anyone smile.

This episode is for those who are looking for a way to give back without knowing where to start. Heather breaks down her story as an advocate, not having any connections to disabilities prior to her time volunteering and working at GiGi’s Syracuse. Heather did not know much about people with disabilities, specifically Down syndrome, and even more so, she didn’t know much she needed the diagnosis in her life. She just wanted to go out there and find a place to go, where she could serve and learn more about those with Down syndrome. Now, 10 years later, she doesn’t know how she can ever live in a world without DS.

We also hear a beautiful story of friendship blossoming from the fear of the unknown. Heather was unsure of how to befriend Bill, a grown man living with Down syndrome. Little did she know she was finding a best friend. Bill talks with us about his appreciation for Nancy and GiGi and how they have impacted his life through love and friendship. We then hear some wise words of wisdom regarding through Bill and Heather's message to the world, and of course, GiGi Gives us some tips on “how to have fun”! We hope that you enjoy this fun-filled episode of A Little Something Extra!

Check out the video version of this episode here.

S2 E12: A Little Something Extra with Sophia and Jennifer Sanchez

Actor and model, Sophia Sanchez and her mom Jennifer join the show! This week's episode is a super special one, because we are joined by an incredible mother-daughter duo. Sophia Sanchez is a 14-year-old with Down syndrome who is paving the way for others in her work as an actress and model. Sophia is starring in the upcoming film, Hunger Games: The Ballad of Songbirds and Snakes. A role she received not because of her diagnosis but for her talent! Sophia is also the inspiration behind the new book You Are Enough: A Book About Inclusion. Jennifer Sanchez begins their story detailing her family's journey in adopting Sophia from a Ukranian orphanage after she gave birth to a son with Down syndrome. Then walks us through Sophia’s amazing rise into the beautiful inspiration she is. The theme of this episode is The Power of Family and boy do the Sanchez’s know all about that! Catch their amazing story, some beautiful words of wisdom, a couple “something extra’s” and GiGi’s famous TIPSSSS on this fun-filled episode! We hope you enjoy!!

Watch the video version of this episode here.

S2 E11: A Little Something Extra with Lizz Maxwell and Missy Gibelj

GiGi’s Playhouse Cleveland’s very own Lizz Maxwell and Missy Gibel join the show!

We are back highlighting playhouses in celebration of 20 Years of Believing at GiGi’s Playhouse!! These 2 have pretty amazing stories to share, it was hard to fit them both in! Missy was on the team that started the 3rd playhouse to ever open back in 2006 in Chicago! She is a strong momma bear that just wanted to create a place for her daughter and other families that didn’t have a place to feel welcomed. Her family then moved to Cleveland, so she had to bring a playhouse with her! She then took it upon herself to open GiGi’s Playhouse Cleveland with the help of an incredible team. This introduces Lizz Maxwell, who does not have a child with Down syndrome but does have a heart large enough to support an entire city of people with Down syndrome. Lizz is the Site Director of GiGi’s Playhouse Cleveland and has helped in building up GiGi’s Playhouse to be a staple of the Cleveland community! This episode sheds some light on the heart and soul that goes into bringing a GiGi’s Playhouse into existence and the impacts it makes. Each and every one of us has a fire deep within ourselves that burns on passion. All it takes is the right outlet to further fuel that flame. We hope this episode and all our episodes help you in finding that fuel, or what we call your “Little Something Extra”.

 

See the video version of this episode here: https://gigisplayhouse.org/alittlesomethingextra

S2 E10: A Little Something Extra with Ellen Boyer

Ellen Boyer, founder and president of The Brett Boyer Foundation, joins the show! This episode is a bit heavier than others, but so beautiful, inspirational, and important. Ellen talks with us about her journey of turning tragedy into inspiration. At just 7 months old, Ellen and her husband lost their beloved Brett to complications due to congenital heart disease. Ellen and her family turned the tragedy into their life mission to celebrate Brett and others with Down syndrome while also raising awareness and funding to research solutions for congenital heart disease. This episode is a beautiful testament to her daughter and a testament to everyone who has faced tragedy/adversity in life. As we can learn from Ellen, it’s not the adversity that defines who you are, it’s how you respond to it.

Watch the video version of this episode here.

S2 E9: A Little Something Extra with Jennifer Gage

Throughout 2023, GiGi’s Playhouse is celebrating 20 Years of Believing, with an emphasis on highlighting the incredible people that have helped change the face of the Down syndrome diagnosis. On this week’s episode of A Little Something Extra, we are highlighting the founder of our Phoenix location! Jennifer Gage joins us to talk about what inspired her to help in bringing a GiGi’s Playhouse location to her community. Jen is a mother of 4 kids, including an amazing daughter with Down syndrome. Along with being a mother, she is an advocate and entrepreneur. Jen G embodies the Generation G mindset in all she does, with the goal of spreading Acceptance, Generosity, and Kindness to everyone she meets. We featured Jen to share her amazing story to show viewers like you that anyone has the ability to go out and change the world as long as you have the passion for doing so. Stay tuned throughout the rest of the year as we continue to pull in the founders and MVPs of GiGi’s Playhouses from around the country in hopes of inspiring others to go out and follow their “Little Something Extra’s” and make this world a better place.

Watch the video version of this episode here.