A Little Something Extra

Kim and Jen, Co-Founders of the new dating platform for adults with Autism, join the show! The Mix is a new platform for helping adults with autism find love or friendships in a safe and fun community! Kim and Jen have been working in the Autism community for a long time. Kim is a school psychologist and Jen is a social worker and BCBA. In their experience, they both noticed the lack of resources available to people with disabilities after high school, especially the lack of resources that help develop social skills and relationship building. So, they created a platform to help people with autism meet new people, build relationships and just socialize in a safe environment! In this episode we talk all about; the inception of this idea, the current environment for people with autism and other disabilities, how the platform works and the importance of love and relationships in the lives of everyone! This episode is so important because it sheds light on a new resource that so many desperately need. To learn more about The Mix, check them out on social media @TheMixDating or visit their website at www.themixdating.com See the video version of the episode here.

We are joined on this episode by Courtney and Thomas Hawthorne III, or T3! You may have seen him on social media when a video of him hitting a home run went MEGA viral! We saw the clip and knew we had to get them on to share their story! Thomas is your everyday 9-year-old kid, but also has a condition called Osteogenesis Imperfecta, or brittle bone disease, which is a genetic bone disease that causes fragile bones that easily break. Though T3 has this diagnosis, he still loves sports, playing with friends, playing video games and exploring the world! His mom, Courtney, created his platform to share his story and show the world that even when diagnoses can cause limitations, life should still be lived to the fullest! In the episode, we hear the story of his diagnosis from his mom’s perspective. She talks about how she never expected to be on this turbulent journey and how the family has fully embraced it. We also discuss the impact that sharing milestones in life can have on people’s perceptions. T3 then tells us a bit about his joys, dreams, and aspirations in life! This heart-filled episode shows us that, regardless of what life throws at us, we can all hit it out of the park! See the video version of this episode here

This episode features an amazing mother! Katrina Placzek and her daughter, Dallas, can be seen all over social media spreading awareness about the importance of understanding and inclusion! Dallas was diagnosed at 2 years old with Cerebral Palsey, but her diagnosis sure hasn’t stopped her from living her best life! Katrina, Dallas’ mom has been an amazing advocate for her daughter, sharing her journey and helping spread the importance of inclusion! This has led her to creating a non-profit called The Recess Project! In this episode, we hear all about Dallas and Katrina’s story. Starting with Dallas’ diagnosis and the fear it brought to her young mother. We then dive into how amazing Dallas’s life has been along with some of the limitations that inspired her mom to step in! Katrina then shares her journey starting The Recess Project, a non-profit that helps in creating more inclusive playgrounds for kids with disabilities. It is an amazingly humble episode, that will touch anyone’s heart! We hope you enjoy it! See the video version of this episode here.

Advocate and non-profit entrepreneur, Reilly Cate Ferguson, joins the Show!! At just 13 years old Reilly walked into GiGi’s Nashville to volunteer her time, having no connection to disabilities. The experience was so impactful on her that at just 15, she started her own non-profit serving people with Down syndrome! As founder and president of Brushfield International, she is on a mission to enhance the global Down syndrome story by providing community, hope, and support to people impacted by Down syndrome! In this episode, Reilly tells us the story of her journey, starting with her time volunteering at GiGi’s Nashville, her inspiration to start Brushfield International, and how she has been able to balance life as only a freshman in college! She shares what she has learned so far, how her connection to Down syndrome was formed, a beautiful message to the world, what the future holds for her, and of course her inspirational ‘something extra’! This episode is all about being a change-maker and how it doesn’t matter your background, the key is just finding your purpose! With this one, we hope to inspire more people to live like Reilly! See the video version of this episode here

On this episode we are joined by Valeriia and Anya, known on social media as VallitFit and Anyundik . They are sisters, fitness influencers, and advocates showcasing their amazing relationship and fitness journey all across social media. What is even more incredible is Anya has done all of this while having an extra 21st chromosome! She isn’t letting that little something extra stop her from showing the world her strength. In this episode we hear all about their journey, from growing up in Ukraine, then being separated and finally reunited in the United States! Valeriia tells us all about how this fitness journey began, where it has taken them and how her sister quickly stole the spotlight. Anya shows us some of her favorite workouts, her incredible art skills and we learn a lot about their healthy diets. This episode is filled with lots of heart, laughs, plus some important lessons about staying healthy and loving family. A perfect episode for anyone to see! We hope you enjoy it as much as we did. Watch the video version of this here.

Listen to a tasty new episode of the podcast as Shawn Askinosie of Askinosie Chocolate joins the show! An author and chocolatier, Shawn shares his inspirational journey of how he left the courtroom (practicing law for twenty years!) to follow his true passion in life. Shawn swaps stories with us about what it means to run an ethical chocolate company, how he found his passion, and how he helps others find their passion. Shawn even explains how all of us doing “a little something extra” every day has the power to change the world. It’s a fun, inspiring episode. Grab your favorite sweet treat and give it a listen! Watch the video version of this episode here.

Dive into our latest episode of the podcast with Mary Borman, aka “Mermaid Mary”! Back by popular demand, Mary brings a wave of fresh stories that’ll leave you hooked! Catch up with Mary as she talks about her life both in and out of the water. A competitive swimmer, model, public speaker, and self-advocate, Mary wears many hats (or fins)! Mary sits down with Nancy, GiGi, and Franco to discuss her triathlon training, the importance of nutrition, and she even shares some model-worthy tips! This episode is a boatload of fun! Don’t miss out, tune in now! See the video version of this podcast here.

NEW EPISODE OUT NOW!! In this special episode of the podcast, Franco takes the solo hosting reins, but he’s far from alone. Multiple members of the GiGi’s Playhouse Hillsborough Youth Board join the show! Comprised entirely of teenagers, the Hillsborough #GenerationG Youth Board is leading the way on inclusion and acceptance for the next generation. They sit down with Franco to discuss how their initial involvement as volunteers sparked a greater passion, and how they’re working to promote inclusion, understanding, and plenty of fun and lively events in their community! They even share how something as simple as (so-so) face painting can help promote kindness and acceptance! This episode is both entertaining and inspiring -- you won’t want to miss it! Watch the video version of this episode here.

A close friend of the podcast, Matthew Schwab, joins the show!! OMG, we are so excited about this episode. Matthew Schwab is a public speaker, self-advocate, founder of Matthew Schwab Speaks AND a fiancé! If you have never had the pleasure of meeting Matt, you have likely seen his viral engagement video on social media. He is seriously one of the most incredible individuals anyone can ever meet. This episode is just GiGi and Franco hosting! Franco and Matt go way back, so it’s a typical buddy-buddy conversation. We kick things off by talking about his recent engagement with his beautiful Lucia, surprising his mom with the news, walking us through the whole proposal experience, his life living independently, and all of his amazing accomplishments, including starting a self-advocacy company! He drops some knowledge on us about what it means to be “typical” and the importance of seeing past a diagnosis. We love this episode because it’s all about the importance of having friends from different areas of life and the value it can bring! We hope you enjoy it as much as we did!! “We are all typical in our own right because we have the same strengths, the same weaknesses, and the same emotions about the life we want to live. So even though a disability is something we have inside of us, and it may affect us more than others but ultimately we are typical people.” - Matthew Schwab. Watch the video version of this episode on our website.

Father and son authors Andrew and David Olshine join the show! Andrew and his father, David, join us to talk all about their journey which ultimately led to the creation of their brand-new book, Fearless as a Honey Badger, Brave Like a Wolverine. In this episode, David, an established Author of 16 books, tells us about his experience as a father of a son with Down syndrome and how he embraced the diagnosis to create the best life possible for his son. Andrew (who we would all want as a best friend) is a miracle in his own right! He shares his story of overcoming Gulliane Barre Syndrome and how his bravery and strength helped him overcome the virus. After recovering, his dad helped him channel that bravery and his love for animals into their latest book! We then dive into some fun conversations about our greatest fears, our favorite animals, the experience of co-writing a book together, some inspirational words to live by, and of course some great ‘Little Something Extras’! It is a super fun episode with a really amazing father/son duo. We hope you enjoy it as much as we did! To purchase their new book, visit: Home | Fearless Brave Book Watch the video version of this episode here

Connor Tomlinson, breakout star from Love on the Spectrum season 2, joins the show!! Joining Connor are his mom, Lise, and brother, Ben. Love on the Spectrum did such an amazing job capturing the dynamic of this amazing family, and we wanted to bring that same energy to the podcast! If you have not seen Love on the Spectrum, it will surely be your next binge. For those who have, you saw Connor steal the show by being his most authentic self. From being a one-liner machine (which you can find all over his new merch) to his love for movies and lore, how could you not want to hang with this guy? In this episode we talk about his experience on the show and how it has transformed his life overnight. He tells us about his perspective on autism and its “the next step in human evolution.” We walk through his experience being on the show and his plans for dating in the future. Lise and Ben give us some interesting insight into the family growing up with a brother/son with autism. Connor tells us about his interests and, of course, some perspective on the Game of Thrones vs Lord of the Rings debate. It’s a perfect episode for celebrating Autism Awareness Month and the amazing people blessed by it! We hope you enjoy it! Watch the video version of this episode on our website.

The great John O’Hurley and his golden voice join the podcast in the studio!! John O’Hurley is an incredibly talented actor, comedian, author, television personality, and even a singer! You may know him as the eccentric J. Peterman in the hit sitcom Seinfeld. He also hosts the National Dog show, voices King Neptune in SpongeBob along with hundreds of other voice acting roles! He joined us just hosting the GiGi’s “I Have a Voice Gala” This one is a Seinfeld lover dream! In this episode, we touch on it all! John tells us about his journey into acting, voice acting, the theatre, and more! We talk about his experience landing Seinfeld and how he brought this character to life. We recap some of his favorite moments from his time on the show and hear some of his most famous quotes (literally Franco’s dream conversation)! We touch on his career in the theatre, his greatest passion. We also discuss his role in hosting the National Dog Show and his life as a dog lover! He talks about his role in hosting our gala and how eye-opening the experience was in learning about the Down syndrome diagnosis and how it changed his perspective on life. This episode is filled with big laughs, wise words of wisdom, fascinating insights into the entertainment industry, and some great tips for public speaking! “Then In the distance, I heard The bulls. I began running as fast as I could. Fortunately, I was wearing my Italian Cap Toe Oxfords." - J.Peterman. Watch the video version of this episode on our website.

Tampa Bay Bucs defensive back Dee Delaney, and wide receiver Deven Thompkins join the podcast in studio!! Dee and DT(Deven) have really inspiring stories to tell. While being NFL players and teammates, both Dee and Deven are also parents to kids with Down syndrome! Deven’s story begins at just 19 years old, he talks about his experience having a son with Down syndrome in college and how he embraced the responsibility to create an amazing life for his children. Dee talks about his family’s experience having a beautiful daughter with Down syndrome at the age of 25, balancing that with an NFL career and embracing the diagnosis from the beginning. Earlier this year, both Dee and Deven participated in NFL’s My Cause My Cleats campaign, rockin’ GiGi’s Playhouse on their cleats! In the episode we discuss the campaign and the opportunities that came with it. We then dive into the impacts these young men are making and will continue to make for the Down syndrome community and beyond in promoting and creating acceptance for all! It’s a really special episode in the way you can see the realization in both these men regarding the impact they can make in this world. We absolutely loved hanging out with them and hope you enjoy it as much as we did! Watch the video version of this episode here

In honor of World Down Syndrome Day, the extremely talented Kevin Iannucci and James Keith join the podcast!! Kevin and James are both actors who starred in the 2023 comedy Champions, A Bobby Farrelly comedy centered around a college basketball coach who was ordered to coach a special needs basketball team. Both Kevin and James KILLED IT in their roles, so they joined us to talk about it! Kevin and James are both really impressive guys. Kevin is an experienced actor who has Down syndrome. He was featured in multiple roles leading up to Champions, with this being his breakthrough role! James’s path is a bit different, being a Special Olympics athlete who took this on as his first acting role, but you would never have known! In the episode, we discussed their experience on set with the big stars, their acting methods behind the scenes, and their interests and hobbies outside of acting; we did some podcast karaoke to a certified classic, learned their ‘Little Something Extra’ and of course heard some of GiGi’s TIPPSS! It is a super fun episode filled with a lot of laughs and a lot of heart. Like us, you’ll surely want to be best friends with these dudes when it's over! Enjoy!! See the video version of the episode here.

On this week’s episode of A Little Something Extra, we are joined by Love on the Spectrum star Tanner Smith and his amazing mom, Nicci! Love on the Spectrum is a show that follows various individuals on the autism spectrum on their search for love. Tanner was a breakout star in season 2, no doubt due to his upbeat personality and his incredibly positive outlook on life. In his own words, Tanner is polite, he has a good personality, and he is a kind young man! His mom, Nicci, is equally as amazing. Only seeing a few short snippets of her on the show, this podcast takes a deeper dive into her experience raising Tanner, Tanner’s transition into adulthood, and his newfound fame. She is legit a super mom, whose story and words of wisdom need to be heard! In this episode, we talk with Tanner and Nicci about his experiences dating, his life at Clemson Life, the experience of growing up with Autism, parenting advice, some words of inspiration, and, of course, some…TIPPSSSSSSS on spreading joy! We hope you enjoy this conversation as much as we did! See the video version of this episode here.

Season 3 of A Little Something Extra is starting off with a bang, featuring John and Mark Cronin the father/son duo behind John’s Crazy Socks! If you are not familiar with their story, this is the perfect place to learn it. Mark (father) tells us about his journey, both as a professional and as a father of a son with Down syndrome. John then tells us the story behind his crazy sock empire! Their story takes us from their humble beginnings of hand-delivering socks, door to door, to them becoming one of the largest sock companies in the world! This story, fueled by a lack of opportunity and value seen by the world, leads us to a greater discussion about the importance of developing careers for those with Intellectual disabilities. Finally, it wouldn’t be A Little Something Extra without some laughs, moments of inspiration and dare I say…TIPPSSSS! We hope you enjoy it as much as we did!

Jennifer McCormick joins the show!! On this week’s episode, we are celebrating the beauty of motherhood by featuring parent blogger and influencer, Jennifer McCormick. Jennifer has a three-year-old with Down syndrome, named Riley. Riley falls right in the middle of, soon to be, 5 kids! Making all her siblings her biggest fan and advocates in the world. We talk about the impacts that a child with Down syndrome can have on their siblings and the people they turn out to be. As well as all the funny and odd circumstances that come along with the journey of raising a family with a child with Down syndrome! Jennifer talks about how social media and her life as a blogger have impacted her life. She started her social media because of the lack of guidance and understanding she was exposed to when Riley was born. She is now a part of an amazing community of social media moms helping break the stigmas behind Down syndrome and helping other parents realize there is nothing to fear! We of course then hear some amazing words of inspiration from Jennifer, including her “One Message to the World” and her “Little Something Extra”. This is an amazing episode for all the moms out there looking for some guidance and peace of mind or for those looking to see the impact that someone with Down syndrome can have on your life! Watch the video version here.

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/

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

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.