A Little Something Extra (alittlesomethingextra)

After learning that 80% of people who receive a prenatal diagnosis of Down syndrome do not give birth, Ashley knew that it was her purpose to become a mother to Ever. On our newest episode of A Little Something Extra, we sit down with "Super Mom", Ashley Williams from EverandMom. Ashley is a Down syndrome advocate, influencer, and “Super Mom” to her daughter Ever. In this episode, Ashley and Nancy dive into why Ashley felt the need to share Ever's story to the world, her reaction to receiving the diagnosis, Ever's modeling career, and so much more!   Visit http://alittlesomethingextrapodcast.org/ to watch this and other episodes!

We are thrilled to welcome MLB player Jake Burger and his wife and entrepreneur Ashlyn Burger! This October, Ashlyn and Jake joyfully welcomed their baby girl, Penelope, who was born with Down syndrome. With this beautiful addition to their family, Jake became the only active MLB player with a child with Down syndrome. In this heartfelt episode, we hear about Penelope’s diagnosis journey, the story of how Ashlyn and Jake met, what they love to do in their free time, and their hopes and dreams for the future. In a moving, joyful, and deeply inspiring episode, you’re sure to feel moved and uplifted. 

On this episode of A Little Something Extra, we are joined by two really special guests to GiGi’s and the Down syndrome community! Our first guest is a former standup comedian, turned non-profit entrepreneur, who has used his expertise in the comedy industry to create an improved troupe called the Imporvaneers! This improv troupe is the first to ever solely consist of individuals with Down syndrome. Our second guest is one of many incredible self-advocates that GiGi’s is lucky enough to have as part of our network. Along with being a self-advocate, he is also a hilarious comedian and original member of the Improvaneer Method!

In our conversation, Rob talks about his inspiring life’s journey from starting as an aspiring comedian in Chicago, to running a non-profit that is changing the lives of individuals with Down syndrome. He also talks with us about the benefits that improv has on people with unique abilities.

Nick, the BIG DAWG himself, then joins the show to talk about his journey and how The Imporvaneer method has changed his life! We hope you enjoy this super fun and interesting episode of A Little Something Extra. Don’t forget to listen in for GiGi’s tips on “not taking yourself too seriously”!

Watch the video version here: https://youtu.be/R1kxdUEimyc

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.

 

This episode of A Little Something Extra tells a story of inspiration, determination, and love through the eyes of an incredible couple. Nancy and GiGi sit down with artist, Dan Keplinger and his wife Dena. Dan is a famed artist who channels his inspirations from life experiences. What makes his story so powerful is he’s achieved so much while carrying the weight of Cerebral Palsy. For those who don’t know, Cerebral Palsy is a congenital disorder that affects one’s muscle movements. While the limitation on his muscle control has been a barrier, Dan has spent his life courageously showing his strength and ability through his art. Another amazing part of Dan’s story is the story of him and his wife. A love story in its purest form, Dan and Dena shows us that nothing can get in the way of true love.

See the video version of this episode here: https://youtu.be/PfnXOxpCtso

A Little Something Extra is almost back! Next Thursday, June 17th, A Little Something Extra podcast returns, featuring an incredible guest!! Nancy Gianni and GiGi Gianni are joined by actor, comedian, and producer Nic Novicki. Along with his theatrical accolades, Nic is also a trailblazer! He is the founder of the Easterseals Disability Film Challenge, a challenge that gives filmmakers—with and without disabilities—the opportunity to collaborate to tell unique stories that showcase disability in its many forms. Check out this teaser then tune in next week to hear more about Nic and his amazing story! 

 

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

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.

Just in time for the 2021 Olympics, The Little Something Extra podcast is joined by an amazing guest, Olympic bobsledder, Elana Meyers Taylor!! This week’s episode is centered around hard work and determination. Elana perfectly encapsulated both of those attributes, to be one of the best in the world at being a bobsledder and a mother! Last year, Elana gave birth to her beautiful son Nico. After learning about his Down syndrome diagnosis, she immediately became an advocate and has begun using her son as motivation to work harder every day! Hear what fuels Elana’s determination and inspiration, her perspective about keeping a positive outlook on life, and much more on this episode of A Little Something Extra!! 

Check out the video version of this podcast here: https://www.youtube.com/c/gigisplayhouseinc

On this episode of A Little Something Extra, Nancy, GiGi and Franco interview Dr. Brian Chicoine of Adult Down Syndrome Center in Park Ridge IL. Dr. Chicoine is an expert on the Down syndrome diagnosis after working with Adults with DS early in his career, to then starting his own medical center in 1990. In this episode, Dr. Chicoine gives an extremely informative conversation on all things Down syndrome. We talk the growth of the diagnosis and how much has changed over the last 30 years. He provides expert advice to families and supporters of the diagnosis on maximizing potential. He talks about all the resources that his center has to offer for teens and adults with Down syndrome. Plus, we are also joined, at the end, by Linda and Mike Mussallem, who have been loyal supporters and friends of Brian’s since their brothers too visited his center. Lots to take in, on this amazing episode of A Little Something Extra!

Catch the video version of this podcast at: https://youtu.be/bvwC18x5wKM

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.

This episode of a little something extra features the rockstar father-son duo of Rick and Noah Smith! When Noah was born 10 years ago, Rick started a YouTube channel called Noah’s Dad and the sole purpose of the channel was to just highlight what it was like to raise Noah. Fast forward to now and Rick has amassed quite the following of over 300K followers across his social channels! Rick realized the need to share experiences and to provide hope for others in the same situation. This led to the creation of his non-profit, Hope Story. In this episode, hear all about how a dad with a vision to simply just share his experience with the world, turned into an organization that helps in providing hope and joy to families during the time that they need it most! This is what finding your something extra is all about!! Enjoy episode 17 of A Little Something Extra.

Watch the video version of this episode here: https://www.youtube.com/watch?v=Bd_B3J5sAW4

We are so thrilled to welcome Erin Merryn to the show! Erin is widely recognized for her activism and for pushing for legislative changes aimed at protecting children from abuse. As a survivor of childhood sexual abuse, she created Erin’s Law which requires that all public schools in each state implement a prevention-oriented child sexual abuse program. Not only is she making amazing changes in the world, but she is also related to one of GiGi’s Playhouse Hoffman families! In this episode, she shares her personal story, the surprising challenges she faces getting the law passed, how she overcame the doubts from her educators, and the impactful stories from kids and adults who found the courage to speak up. Beyond her advocacy, we get to know Erin as a person, including her hobbies, her cat, and what she hopes to share with the world! 

Watch the video version of this episode https://www.youtube.com/@alittlesomethingextra 

With the Super Bowl just around the corner, and our I Have a Voice Gala happening in nearly 2 weeks A little Something Extra is releasing a surprise episode today, as a little sneak peek of season 2! Nancy and GiGi were joined by former NFL wide receiver, Wendell Davis and Tom Serpento, Executive Director of the Retired Professional Football Players of Chicago

. Wendell and Tom, and the rest of the RPFPC have been HUGE supporters of GiGi’s Playhouse since 2015 and will continue to support at our 2022 I Have a Voice Gala!

Nancy, GiGi, Wendell and Tom discuss the importance of serving others, how to love, the impacts made by those most important and so many other important life lessons!

Visit the link in our bio to watch today’s episode on your favorite podcast platform, there you will also find more information on how to participate in this year's I Have a Voice Gala!

Learn more about the gala: https://gigisplayhouse.org/ihaveavoicegala/

Watch the video version of this episode: https://youtu.be/i5e5yHlwmHQ

#GenerationG #NFL #downsyndrome

Join us in a conversation with the creator of a nationwide beer collaboration benefiting people with Down Syndrome!!

Pat Craddock, a dad from a Detroit suburb, wanted to take his two passions: His son, Ian, and beer and create an opportunity to give back to the Down syndrome community. Luckly, Pat is the CFO of Griffin Claw Brewing Company, and he was able to launch the TRI-21 Project. TRI-21 Project is a worldwide, open-ended beer collaboration created to raise awareness for individuals with Down syndrome during World Down Syndrome Month (October) to World Down Syndrome Day (March 21st) and raise support for GiGi’s Playhouse.

In this episode, Pat tells us all about the inception of this amazing project and his dream to have it spread across the country! Pat is the man and someone we are extremely lucky to call a friend. So kick back, crack open a cold one, and enjoy!

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

In the third episode of our video podcast, A Little Something Extra, Nancy and GiGi Gianni of GiGi's Playhouse, interview actor, advocate, and dad John McGinley! John's son, Max, was born with Down syndrome. Initially riddled with fear of the uncertainty, John has been inspired by his son and has dedicated his life to advocating on behalf of Max, standing up for others and giving them a voice. He dives into tough topics like eliminating the R-word and dealing with a 24/7 diagnosis from birth to adulthood. John has starred in more than 60 films and 25 television shows. Becoming a father to Max, John re-evaluated the trajectory of his career so he could spend quality time with his son - and ended up the lead on the hit television show Scrubs. Watch out for a couple of special guests during the interview!

 

About the podcast: We all have a little something extra inside of us, and sometimes we don’t even know it’s there! Through A Little Something Extra, we hear about the forces in people’s lives that drive their passion in hopes that others will find theirs! We’ll get to hear what makes our guests so inspiring – their superpower – even if they do not feel it within themselves! Every episode will feature guests who have accomplished the impossible and have changed the world! Be prepared to find yourself motivated with every installment with insights from a wide range of guests from A-list celebrities to everyday people! Learn more at www.alittlesomethingextrapodcast.org.

With over 50 brick-and-mortar locations across the United States and Mexico and 200 inquiries to start new locations all over the world, GiGi’s Playhouse is the ONLY network of Down Syndrome Achievement Centers. GiGi's Playhouse is also currently serving families in more than 45 countries worldwide with GiGi's At Home. Learn more at gigisplayhouse.org.

This week’s episode is centered around siblings and the positive impact that a brother or sister with Down syndrome can have on your life! Nancy, GiGi and Franco sit down with siblings Mike Mussallem and his wife Linda. Mike is the CEO of Edwards Lifesciences, and organization that manufactures heart devices that quite literally have saved the lives of hundreds of thousands, while Linda is a leader in the California non-profit community! In this episode Mike and Linda talk about the impact that having older brothers made on their lives. From their brothers brining them together, to dedicating their lives to philanthropy, being siblings of Down syndrome made them both into the world changers they are today. Enjoy this touching episode of A Little Something Extra!

To watch the video version of this episode go to https://youtu.be/wuKLtXxRqEI

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.

Today, we’re talking with Chad Sorentino—a retired Army vet, GiGi’s Playhouse Ambassador, and fitness coach! After 21 years of service, Chad found his mission in empowering adaptive athletes, especially those with cognitive disabilities. He’s seen firsthand how fitness can overcome hurdles and break barriers. Growing up with a best friend who had disabilities, inclusion has always been Chad’s core value. Now, as the coach of the GiGiFIT Adult Program, he’s showing the world just how strong his athletes. In this episode, we dive into everything from keys to longevity to Chad’s hobbies outside the gym. Get ready for a high intensity conversation—we’re pumped to have him on the show! 

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

Hey Chicago what do you say, A Little Something Extra video podcast has a special guest today! CEO and Chairman of the Chicago Cubs, Tom Ricketts, joins Nancy, GiGi, and Franco for the 4th episode of A Little Something Extra! Tom and the Chicago Cubs have been a part of the GiGi’s Playhouse family for several years - in fact, GiGi’s Playhouse has been a recipient of Cubs Cares and GiGi impressed the fans at Wrigley Field by singing the National Anthem before a Cubs game! Tom and the crew talk about changes to the stadium atmosphere due to COVID, Tom’s focus on improving the typical “Day at the Ballpark” for Cubs fans, a few of Tom’s favorite Cubs players, and much more! GiGi petitions to be on the Cubs coaching staff by revealing her top life tips for being a good teammate. The show concludes with the crew singing a very familiar song!  

About the podcast: We all have a little something extra inside of us, and sometimes we don’t even know it’s there! Through A Little Something Extra, we hear about the forces in people’s lives that drive their passion in hopes that others will find theirs! We’ll get to hear what makes our guests so inspiring – their superpower – even if they do not feel it within themselves! Every episode will feature guests who have accomplished the impossible and have changed the world! Be prepared to find yourself motivated with every installment with insights from a wide range of guests from A-list celebrities to everyday people! Learn more at www.alittlesomethingextrapodcast.org.

With over 50 brick-and-mortar locations across the United States and Mexico and 200 inquiries to start new locations all over the world, GiGi’s Playhouse is the ONLY network of Down Syndrome Achievement Centers. Learn more at gigisplayhouse.org.

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

We are excited to be joined by Curtis Hargrove, a Canadian endurance athlete and philanthropist renowned for his long-distance fundraising efforts. From running the Chicago Marathon in 3-inch red high heels to completing 34 marathons in 34 days, Curtis exemplifies unwavering commitment to making a difference. On A Little Something Extra, he shares his story and his determination to make an impact, no matter what it takes. Throughout his fundraising journey for various causes, he has faced numerous challenges, including a medical pause during the Chicago Marathon, an unexpected arrest on the highway, and last-minute issues like losing access to an RV. Starting his philanthropic work at just 15 years old, Curtis has shown his superpower through extraordinary advocacy. So, kick off your shoes, relax, and enjoy! 

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

In this week’s episode, we have the privilege of speaking with the incredible Kennith Allen Thomas!! Known as Kenny Clutch on social media, Kenny is a motivational speaker, leadership coach, and dedicated family man. Kenny shares his inspiring journey, including the emotional story of his son Christian’s birth and the discovery of his cancer diagnosis. He talks about what it truly means to "show up and show out" in life, how he met his wife, and shares funny and heartwarming stories about his kids. Along the way, Kenny offers valuable motivational advice, discussing how to follow your calling and pursue a life of purpose. His passion, wisdom, and humor make this an unforgettable conversation. Don’t miss out on hearing Kenny’s powerful story and the lessons he’s learned along the way! 

Watch the video version of this episode https://www.youtube.com/@alittlesomethingextra 

With World Down Syndrome Day just around the corner, this week’s episode of A Little Something Extra feels a bit more special! To celebrate, we spoke with the founder of The Lucky Few, Heather Avis! Heather is a New York Times best-selling author, podcaster, and a Down syndrome advocate, working to create a more inclusive world where everyone belongs. The Lucky Few has grown from this concept of celebrating those lucky enough to be influenced by a Down syndrome diagnosis to a lifestyle brand and organization that is synonymous with the Down syndrome Diagnosis. The Lucky Few concept has now become a global storytelling movement, shifting narratives to create a more inclusive world where everyone belongs.  

In this episode, Heather talks with us about her incredible journey as a mother of 3 kids, 2 having Down syndrome, and the perspective it has given her when it comes to celebrating who we are. We then dive into the mission of The Lucky Few and the global impact it has made on the Down syndrome diagnosis and the members of its community. GiGi also shares some tips on living your best life, and of course, we learn the Little Something Extra of a world-class changemaker. A perfect episode for celebrating a perfect day of recognition! We hope you enjoy it!

You can also watch the video here:https://gigisplayhouse.org/alittlesomethingextra/

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.

This week’s episode of A Little Something Extra is all about differences and taking the time to recognize and acknowledge them because in doing so it will completely change perspectives. The guest who joined us was determined to show the world that differences aren’t so different after all. Meeka Caldwell is a mother, author and advocate who noticed a lack in representation of children with special needs, specifically black children, in kid’s books. Being the trailblazer she is, she decided to create her own, with her son, Anian, as the main character. Nancy, GiGi, Franco, and Meeka discuss many different topics regarding societies' viewpoints on differences and the changes that need to be made to create a more accepting world. GiGi also gives some of her famous TIPPPSS on accepting people for who they are!

Watch the video version of this podcast at: https://www.youtube.com/watch?v=GGkntZyrhis

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.

On today’s new episode of A Little Something Extra, we are joined by two incredible gentlemen all that way from Ireland! This father/son duo is paving the way for change on an international scale, traveling all around the world to show people the beauty of Down syndrome and all their unique abilities!

Fionn and Jonathan join the podcast to discuss their 26-year journey, navigating the complex work of living life with a unique ability. We hear about Fionn and Jonathan creating their production company, Fionnathan Production, and how they leverage Fionn’s diagnosis to make it all possible! Fionn also shows off some of his talents on the fiddle (and gives a little glimpse of how it works on the ladies). We also hear about their journey that has taken them all around the world in the pursuit of change from the start till now!

Fionn and Jonathan are a true testament to leveraging the hand life deals you into a life of learning, adventure, and love! Make sure to listen to the end to hear GiGi’s tips and some warm words about the beauty of life, specifically about sharing life with someone who makes you value each and every day. We hope you enjoy it as much as we do!

Check out the video version of the episode on our website: alittlesomethingextrapodcast.org

 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.

On this week's episode of A Little Something Extra, we are joined by the absolutely incredible Madison Tevlin! Staring in the upcoming movie, Champions, premiering Friday, March 10th. Madison is a 21-year-old with Down syndrome, but she likes to say her diagnosis is the least interesting thing about her. I think after listening, anyone would agree! You may remember Madison from her viral video back in 2012 of her singing “All of Me” by John Legend. Well, she didn’t stop there! Fast forward to today, and she is an actress, model, influencer, and advocate. She continues to show the world that no diagnosis should hold you back from following your dreams. We hope you love this one as much as we did!

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

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.

We’re back with our second episode of our video podcast, A Little Something Extra, the first podcast co-hosted by an individual with Down syndrome! In this episode, Nancy and GiGi Gianni of GiGi’s Playhouse are joined by Amanda Booth -- model, mom, and advocate. Amanda’s son, Micah, was born with Down syndrome and has followed in his mom’s footsteps in a big way – he’s been featured in numerous campaigns including Tommy Hilfiger and Amazon Fashion. Micah and his mom have also graced the cover of Vogue Living, and were featured in Parents and People magazine, among others! Amanda’s most important mission is ensuring that Micah has a voice and she aims to make sure that differently-abled people are in the media. Tune in to hear more about their story on A Little Something Extra!

About the podcast: We all have a little something extra inside of us, and sometimes we don’t even know it’s there! Through A Little Something Extra, we hear about the forces in people’s lives that drive their passion in hopes that others will find theirs! We’ll get to hear what makes our guests so inspiring – their superpower – even if they do not feel it within themselves! Every episode will feature guests who have accomplished the impossible and have changed the world! Be prepared to find yourself motivated with every installment with insights from a wide range of guests from A-list celebrities to everyday people! Learn more at www.alittlesomethingextrapodcast.org.

With over 50 brick-and-mortar locations across the United States and Mexico and 200 inquiries to start new locations all over the world, GiGi’s Playhouse is the ONLY network of Down Syndrome Achievement Centers. Learn more at gigisplayhouse.org.

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/

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!

This episode of A Little Something Extra goes out to the siblings! The theme is Standing Up for Your Siblings, and do we have a guest that has gone above and beyond to do just that. We are joined by Jeanhee Hoffman, a sibling of a brother with Down syndrome, who founded GiGi’s Playhouse Raleigh.

Jeanhee has an incredible story, that is filled with love and inspiration. Jeanhee and her brother, Sam, are second generation Korean Americans, and she shares with us her families’ experiences from a different cultural perspective. She talks on her and Sam’s experiences growing up in a less inclusive society and the challenges it posed as a sibling. It was not until 2015 when Jeanhee stumbled upon a place where her brother can grow and feel at home!

After seeing the impact that GiGi’s had on her brothers life, she vowed to make sure there was a place in her community for families like hers could have a place to call home. Listen now to hear how a sibling finding a place for her brother, sparked a flame within her to create a playhouse of her own community!

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.

We couldn’t let the conversation end just yet, so we’re back with the Valentine Brothers! In this extended version of episode 2, it’s the Zach show! We play all his favorite games, do his challenges, and learn all about the brothers! Tune in for a fun-filled ride. 

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

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

In this episode, we meet with Actress, dancer, model, and motivational speaker, Sarah Gordy! Sarah is best known for her in the British hit drama, The A Word, in a role written for her! As well as BBC shows, she has acted in short films, radio dramas, commercials, and many theatre productions. 

In 2018 she became the first woman with Down syndrome to be made an MBE (The Most Excellent Order of the British Empire is a British order of chivalry, rewarding contributions to the arts and sciences, work with charitable and welfare organizations, and public service outside the civil service.) and the first person with Down syndrome to receive an honorary degree from a UK university.

Sarah is one of the principal dancers for Culture Device Dance Project, an experimental dance company for professional dancers with Down syndrome. She has also given talks in schools and gave a talk called “Escape from labels. Be free, be different” at TedX in Hackney, London. Sarah embodies everything it means to be a trailblazer, as she shows the world that there is nothing she can't accomplish!

Watch the video version of this at: https://youtu.be/LJJgTtByUwU

This episode was the first podcast popup, recorded at the 2021 GiGi’s National Leadership Conference! This episode is so special and close to the GiGi’s heart because it focuses on the people of our organization. It features 18 interviews and 27 guests from the GiGi’s network. Nancy, GiGi and Franco talk with model and actor Amanda Booth. Author and influencer Kelle Hampton, Adult participants; Farzin, Michell, Samir, Brian Daniel and Harry, GiGi’s Playhouse Canton’s Nick Doyle, INC Board members Scott and Steve, Dan a GiGi’s Chicago Board member, Jason the board vice president of GiGi’s Syracuse, Andre an employee at GiGi’s Annapolis, Laura the founder of the third every GiGi in McHenry, Kim Hanna the CIO of GiGi’s Playhouse, Zayne a grandfather from GiGi’s Madison, 4 members of the Sacramento GiGi’s Team, founders of the GiGi’s National Youth Board, and Erin 2 time volunteer of the year winner from GiGi’s Cleveland!

Watch the video version of this podcast here: https://youtu.be/D-vOs316j8E

We are kicking off Down Syndrome Awareness Month a week early with a very special guest! In today’s new episode of A Little Something Extra we are joined by the fabulous Jaime Brewer. Jaime is an inspiration to all, showing the world that one little diagnosis isn’t going to hold her back from making her dreams come true! In our interview, Jaime talks about everything with us, from her life as an actress on her hit show American Horror story to her goals in life to be a fashion designer!   Catch the video version of this podcast here: https://youtu.be/P_c66v00s20

Join us as we hit it out of the park with Bill Leroy! Bill has been the catcher for the Savannah Bananas for the last 7 years. The Savannah Bananas are more than just a baseball team. In these games, the players break into dance and other antics in a baseball game to entertain the fans!! In this episode we learn all about Bananas Foster which is a non-profit organization committed to helping bring families together in the foster care community. Not only did we hear everything about the Bananas, but we also learned about Bill’s go-to way to impress others. Grab your peanuts and hotdog as we load the bases with Bill’s faith, baseball experience, favorite dance moves, and inspirations; a recipe for a homerun!

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

This week’s episode takes us back to earlier this year when Nancy GiGi and Franco were joined by Dr. Brian Skotko at the National Down Syndrome Conference! Dr. Skotko is a Board-certified medical geneticist, serving as the Emma Campbell Endowed Chair on Down Syndrome at Massachusetts General Hospital. As the Director of the hospital’s Down Syndrome Program, he has dedicated his professional energies to children with cognitive and developmental disabilities. It was because of his sister, (Kristin) who has Down syndrome, that he originally found his calling first as an advocate, then later as a doctor.

Through Brian’s passion and dedication towards serving individuals with Down syndrome, he has created many amazing resources both for them and their families! During his first year at Harvard Medical School, he co-authored a book titled Common Threads: Celebrating Life With Down Syndrome. A book that profiles the accomplishments of 59 different people with Down syndrome! Fast forward 8 years, where he then wrote another book dedicated to helping siblings better understand the Down syndrome diagnosis, titled: Fasten Your Seatbelt: A Crash Course on Down Syndrome for Brothers and sisters.

Now Brian joins the podcast to tell us about his journey to better the lives of all people affected by Down syndrome and his most recent endeavor, Down Syndrome Clinics 2 You (DSC2U)! A platform created to provide personalized care plans for families that do not have access to any specialized Down syndrome clinics. This episode is full of incredible insight into resources and information given by a leading industry expert! We hope you enjoy it as much as we did!

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.

This week, we had the privilege of speaking with Lauren Costabile, the Founder and Executive Director of Hearts of Joy International. This nonprofit organization provides life-saving heart surgeries for children with Down syndrome around the world, while also offering educational resources, counseling, and advocacy for their families. Prior to launching Hearts of Joy International, Lauren was a volunteer at GiGi's Playhouse in New York! In this episode, we dive into Lauren’s journey, from her background and the motivations that led to the creation of Hearts of Joy International, to the impactful work the organization is doing for children and families worldwide. Tune in today to hear more about Lauren, discussing her hobbies, hearing GiGi’s favorite karaoke go-to songs, and learning the many ways people can get involved with Hearts of Joy International! 

 

Watch the video version of this episode https://www.youtube.com/@alittlesomethingextra 

This week we are joined by the incredible Penny Tovar—a nurse, influencer, and new mom to a beautiful baby girl with Down syndrome. In this episode, Penny shares her emotional journey through the diagnosis, offering an authentic and raw glimpse into her worries, fears, and the deep love she has for her daughter, Amari. She opens up about the moment she received the diagnosis, the thoughtful approach she took in announcing it to family and friends, how her career as a nurse has shaped her life, and the immense importance of creating a supportive, loving environment from the very beginning. Grab your tissues to enjoy these heartfelt moments, laughs, and words of wisdom as we cap off season 3!  

Watch the video version of this episode at https://www.youtube.com/@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

We're thrilled to welcome The Valentine Brothers to A Little Something Extra! This episode is extra special, featuring both the brothers and a special guest appearance from their mom! We dive deep into the world of social media, explore what sparked the creation of The Valentine Brothers, and hear all about their #GenerationG Hero Award win at GiGi’s Playhouse National ‘i have a voice’ Gala. Don’t miss out on this heartwarming and exciting episode! This one goes out to all the amazing siblings out there helping make a better world for their brothers and sisters! We hope you love it as much as we do!! Stay tuned for part 2 of this episode, as Zach has much more to bring to the show! 

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

We’re excited to share the premiere episode of a new podcast called A Little Something Extra – the first video podcast hosted by an individual with Down syndrome! In the inaugural episode, co-hosts Nancy Gianni and The GiGi Gianni of GiGi’s Playhouse are joined by NBA player Justin Jackson and his wife Brooke. Justin and Brooke have been involved with GiGi’s Playhouse for several years, and were even compelled to help start up the Sacramento Playhouse! We’re so inspired by their dedication to each other, their careers, and helping others. We dive into their “little something extra,” and even jump into a dance-off!

Watch the episode here: https://gigisplayhouse.org/alittlesomethingextra/episode1/

About the podcast: We all have a little something extra inside of us, and sometimes we don’t even know it’s there! Through A Little Something Extra, we want to hear about the forces in people’s lives that drive their passion in hopes that others will be able to find theirs! We’ll get to hear of what makes our guests so inspiring – their superpower – even if they do not feel it within themselves! Every episode will feature guests who have accomplished the impossible and have changed the world! Be prepared to find yourself motivated with every installment from a wide range of guests including A-list celebrities to everyday people! Learn more at www.alittlesomethingextrapodcast.org.

 

With over 50+ brick and mortar locations across the United States and Mexico and 200 inquiries to start new locations all over the world, GiGi’s Playhouse is the ONLY network of Down Syndrome Achievement Centers. gigisplayhouse.org

GiGi’s Playhouse New Orleans very own, Craig Blackburn joins us on this episode of A Little Something Extra! Craig is an amazing man, who not only inspires those in his community but those around the world. Craig is a self-advocate, who has traveled all over the world to show that a Down syndrome diagnosis shouldn’t stop anyone from achieving their dreams! On top of being an advocate, Craig is also a team manager for the NBA team, New Orleans Pelicans! Craig Is also a loving husband to his wife Heather. Hear Craig talk about all these incredible pieces of his life, and more in this episode of A Little Something Extra!! 

Watch the video version of this podcast at: https://www.youtube.com/watch?v=UyukjLY9gn8

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.

We are finally back with a new episode of the A Little Something Extra podcast!! It has been a minute since we released a new episode, but we are kicking things off again with a great one! Nancy, GiGi, and Franco are joined by award-winning gospel/Christian rock artist Aaron Shust. Aaron is an award-winning talent in the music industry, a gifted writer, a profound minister, and most of all, a devoted husband and father to 3 boys, one of whom has Down syndrome.

The theme of this episode is, Never Loose Faith. This is a common theme in Nancy and GiGi’s journey, as well as so many others who have faced adversity in life. We walk with Aaron through his journey and some of the moments where God has challenged his faith, and WOW, are these moments profound and awe-inspiring. His stories of never losing faith in the wake of 2 sons facing life-threatening diagnoses will surely give you goosebumps.  We also talk about his creative process and his love for music. Then as we always do, GiGi shares her tips on staying faithful, as she has learned to do throughout her life. Make sure to pay attention to the stories and quotes from Aaron because each carries a special message that may help you see the world from a different perspective. Our favorite is his view on what Down syndrome means to him. We hope you enjoy it as much as we did!

 

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

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.

 

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.

Meet Brad Ludden! We are so excited Brad to introduce pro whitewater kayaker, philanthropist, and founder of First Descents onto our show!!! From kayaking in Madagascar and Africa to being the inspiration behind the naming of Nose Breaker Waterfall in Norway, Brad’s life is all about embracing the extremes. In overcoming fears, Brad shares the importance of enjoying what you do and having fun. Brad turned his passion for the outdoors combined with his Aunt’s battle with cancer into a mission of hope for others-- founding First Descents to provide adventures for young adults facing cancer when he was just 18 years old. Nearly 25 years later, Brad has given the gift of a life-changing adventure to thousands of people. Join us on our incredible adventure with Brad Ludden!

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

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.

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

This week we are so excited to introduce the Executive Director of CASA Kane County Jim Di Ciaula!! Recently honored with the 2024 William D Barth Community Service Award, Jim is an extremely active member in his community. In his role at CASA Kane County, he leads this volunteer driven nonprofit that is dedicated to giving children a voice in court and hope for a brighter future. Not only does Jim do this for his job, but for his life! As the founder of Random Acts Matter, he inspires individuals to foster compassion and kindness through acts of support and connection! In this episode we learn all about CASA and Random Acts Matter as well as reflect on our mentors in life, embrace the gift of serving others, and be grateful for the life we have. Don’t miss this uplifting episode, we hope you are inspired to spread kindness!  

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

In this episode of A Little Something Extra, we are joined by someone who not only goes above and beyond to make an impact but who also celebrates going above and beyond to change the world. Andrew Moses is the Vice President of Business Development & Marketing at MorganFranklin Consulting. Though if you ask him, he identifies himself as a super-connector and thought leader, sharing the stories and success tips from people in sports, business, and everyday life leading by example. In this episode we discuss his backstory, which led to the philosophy that inspired his podcast, Everybody Pulls the Tarp. Nancy, GiGi, Franco, and Andrew discuss the importance of being a team player and how it translates to all facets of life. We also discuss ways of handling life and being able to battle through the curveballs that get thrown at you. We hope this episode will inspire you to dig deep into the moments that challenge you and to know that no one is too important or too high on the totem pole where they shouldn’t help pull the tarp!

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

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/

 

Watch the video version here: https://youtu.be/BaN_iuPBusc

“In my eyes, you’re not supposed to mistreat nobody.” This is the mantra that special guest, Dennis Dixon, tries to live by every day. From facing a near-impossible childhood to overcoming the odds, Dennis is an inspiration who shows us that no matter the obstacles in our way, if we keep pushing, we can accomplish anything!  

He shares his amazing life journey and gives us a fresh perspective on how important it is to be accepting of people just as they are. We're proud to have Dennis be a member of the GiGi's Playhouse family and grateful for his role and support at our Little Rock Playhouse. This is a story you don't want to miss! 

About the podcast: We all have a little something extra inside of us, and sometimes we don’t even know it’s there! Through A Little Something Extra, we hear about the forces in people’s lives that drive their passion in hopes that others will find theirs! We’ll get to hear what makes our guests so inspiring – their superpower – even if they do not feel it within themselves! Every episode will feature guests who have accomplished the impossible and have changed the world! Be prepared to find yourself motivated with every installment with insights from a wide range of guests from A-list celebrities to everyday people! Learn more at www.alittlesomethingextrapodcast.org. 

With over 50 brick-and-mortar locations across the United States and Mexico and 200 inquiries to start new locations all over the world, GiGi’s Playhouse is the ONLY network of Down Syndrome Achievement Centers. GiGi’s Playhouse is also currently serving families in more than 50 countries worldwide with GiGi’s At Home. Learn more at gigisplayhouse.org. 

In this episode, we interview a guest who is a valuable member of the GiGi’s Playhouse family! Amy Smith is an adult ambassador at GiGi’s Playhouse Cleveland, a role that allows her to inspire people every day. The theme of this episode with Amy is Love & Respect. We discuss her life growing up in a time where individuals who were different, never received the love and respect that they so deserved. We also discuss the impact that GiGi’s Playhouse has had on her life, by having an entire community embrace her with love and respect! Amy’s sweet soul will surely touch your heart and leave you questioning how anyone can disrespect such a beautiful spirit. Enjoy episode 15 of a Little Something Extra with Amy Smith!

Watch the video version of this episode at: https://youtu.be/5rIjxFW-vrs 

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.

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

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.

This week on A Little Something Extra, we’re thrilled to welcome the amazing Nora Michaelis! In this episode, we dive into Nora’s journey as the founder of bEquals, explore her many hobbies, and hear about the impactful lessons she’s learned—all at just 17 years old! Get ready to learn about bEquals and the powerful impact it’s having, not only on those in the program but also on Nora herself. Tune in for a conversation filled with wisdom, passion, and insight into how Nora’s vision is creating lasting change. This episode is sure to leave you inspired and motivated to make a difference! 

Watch the video version of this episode https://www.youtube.com/@alittlesomethingextra

We are so excited to welcome some familiar faces to the podcast this week! You may know them from The GiGi’s social media and their viral 6-month anniversary video...welcome GiGi and Lukas! In the holiday spirit, this episode looks back on the relationship between these lovebirds as well as their hopes for the future. This episode will leave you laughing, smiling, and wanting more! Happy Holidays!  

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra

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.

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.

This week we are kicking off season 4 with some familiar faces! We welcome back Valeriia and Anya, but this time as #GenerationG Hero Award recipients! We will hear more about Valeriia and Anya’s incredible story coming to the US from Ukraine, the pivotal moment Anya showed her passion for working out, their passion to use their platform to make a difference, and all about their #GenerationG Hero Award at the GiGi’s Playhouse National ‘i have a voice’ Gala! Don’t miss this, these charming sisters will be some that you will want to share!  

Watch the video version of this episode at https://www.youtube.com/@alittlesomethingextra