Best Matthew Santoro Podcasts (2024)

1
268. First Responders and Teacher of Patience: A Lesson in Understanding 58:09

3h ago58:09

58:09

We’re thrilled to have Carmen Vincent and Tom and Tina Felter join us to discuss their powerful Emmy award-winning documentary, Teacher of Patience. This film showcases the incredible journey of the Felter family and their daughter, Emily (who makes a surprise appearance!), who has Down syndrome. Tom shares the story behind developing The Emily Tal…

1
267. What Is It Like To Have A Sibling With Down Syndrome? (Featuring Our Kids!) 59:08

1h ago59:08

59:08

Friends, the last two weeks we got to hear from some amazing siblings. Today we hope you’ll join us for a very special episode, we're sitting down with our kids to talk about what it's like to have a sibling with Down syndrome. Micha chats with Ace’s older brother Brooks (13), Mercedes sits down with Sunny’s younger brothers Rhodes (9) and Shepard …

1
266. From Sibling Love to Community Change (w/Taylor Gardner Chaney) 1:05:00

1h ago1:05:00

1:05:00

Today we’re chatting with another amazing sibling! Taylor Gardner Chaney is a passionate entrepreneur whose younger sister with Down syndrome has influenced her understanding of disabilities and guided her career choices. Taylor discusses viewing life as a series of seasons and how focusing on the "why" behind her work helps her push through challe…

1
265. Brotherly Love: From Childhood Adventures to Adult Dreams (w/Matthew & Thomas Von Der Ahe) 49:03

4d ago49:03

49:03

Today, we're thrilled to chat with Matthew Von Der Ahe, known for his roles in 'Champions' and other films. Joined by his brother Tommy, they reminisce about childhood, explore their evolving adult relationship, and discuss maintaining their strong bond despite living apart. Matthew, an actor recognized for his work in 'The Secret Lives of Dorks' a…

1
264. Healing and Hope: Navigating Down Syndrome Regression Disorder (w/ Dr. Santoro & Dr. Quinn) 59:52

23d ago59:52

59:52

Today, we're chatting about the mysterious and challenging world of Down Syndrome Regression Disorder (DSRD). This condition has left many parents searching for answers as they witness profound changes in their children. Joining us are two leading experts, Dr. Jonathan Santoro and Dr. Eileen Quinn, who will share their insights and experiences from…

1
263. Designs that Dance: A Tale of Friendship and Creativity (w/Dance Happy Designs) 55:59

21d ago55:59

55:59

Today, we’re chatting with the creative minds behind Dance Happy Designs! Emily Scott is here to chat with us about the power of inclusive entrepreneurship, friendship, and creativity and share some of co-founder Julia’s thoughts on their friendship and partnership, plus what her favorite design is! Emily shares their experiences creating high-qual…

1
262. 45 Years of Advocacy: A Conversation w/ NDSS President Kandi Pickard 57:31

25d ago57:31

57:31

We’ve been so grateful to have had the opportunity to collaborate with National Down Syndrome Society (NDSS) over the last few years. Today, we’re chatting with Kandi Pickard, the President & CEO of NDSS, and celebrating their 45th Anniversary coming up on June 20th! Kandi is sharing the organization's journey from a support group that has grown in…

1
261. Fearless Together: Lessons In Bravery, Hope, & Resilience (w/David and Andrew Olshine) 47:45

2M ago47:45

47:45

Join us for a special Father’s Day episode featuring the dynamic father-son duo, David and Andrew Olshine! They share their inspiring journey of writing and publishing the book Fearless As A Honey Badger, Brave Like A Wolverine. Learn about the lessons they've learned, the message of hope and resilience they aim to share with the world, and how And…

1
260. What Did We Learn From This School Year? 1:10:46

2M ago1:10:46

1:10:46

Cheers to making it through another school year! Join us as we share our experiences, celebrate the successes, and learn from the challenges of the 2023-2024 school year. Discussing everything from what types of supports and settings worked for our kids, to the injustices in our education system and the reality of our kids still leading the way in …

1
259. Home Is Our Classroom: Homeschooling A Child With Down Syndrome 1:00:38

2M ago1:00:38

1:00:38

Friends, we know there are so many ways to learn, join us today as Mercedes chats with fellow homeschool mama Rachel Prescott about what it's like to homeschool kiddos with (and without!) Down syndrome. Mercedes has homeschooled her daughter Sunflower who has Down syndrome and her three boys for over five years now, Rachel who has twin six-year-old…

1
258. Unlocking Potential: Strategies For Every Learner With Down Syndrome (w/Mrs. Brown) 56:55

2M ago56:55

56:55

Friends, we’re so excited to be joined by Mrs. Brown today, you’ve heard us mention her many times over the years! She has developed a successful and innovative program that teaches reading and other academic skills to learners ages three to adult. We learned about her passion and gift for teaching individuals with Down syndrome in 2018 and had her…

1
257. Brother Do You Love Me?: A Journey of Resilience and Repair (w/Manni & Reuben Coe) 1:12:42

3M ago1:12:42

1:12:42

Friends, today we have Manni and Reuben Coe, two remarkable brothers from the UK, who are here to share their deeply moving journey and new book, brother. do. you. love. me. Their story is one of extraordinary resilience, heartwarming repair, and the profound rediscovery of brotherly love. These magical brothers remind us of the power of love and r…

1
256. Celebrating Motherhood, Advocacy, & Community (w/Black Down Syndrome Association) 1:07:28

3M ago1:07:28

1:07:28

Friends, we put, “I’m A Really Good Mom” on a t-shirt because we know moms doubt this truth about themselves daily. Today in honor of Mother’s Day we’re celebrating the importance of community, friendship, and advocacy with our friends Kelli Caughman and Crystal Lotterberry! Kelli & Crystal are the founders of the Black Down Syndrome Association an…

1
255. A Haircut Beyond The Chair w/Vernon Jackson 57:21

3M ago57:21

57:21

Friends, we’re so excited to have barber Vernon Jackson on the show today! In his barbershop and salon in Ohio, haircuts are more than just a service—they're an act of love and understanding. Through his viral program, The Gifted Event, Vernon provides free haircuts to children with disabilities, offering them patience, empathy, and a sense of belo…

1
254. The Next Step: Navigating Healthcare Transitions for Individuals with Down Syndrome (w/ Dr. Emily Johnson) 51:34

3M ago51:34

51:34

254. The Next Step: Navigating Healthcare Transitions for Individuals with Down Syndrome (w/ Dr. Emily Johnson) Today, we’re chatting about navigating healthcare transitions with Dr. Emily Johnson, a dedicated advocate and physician specializing in the healthcare needs of individuals with Down syndrome. We discuss the importance of starting the tra…

1
253. What If You Don’t Feel “Lucky”? 1:03:25

4M ago1:03:25

1:03:25

What does it mean to feel “lucky” to have a child with Down syndrome? We’re having a candid conversation about the evolving meaning of “lucky” within our community and personal journeys. Through the challenges and the joys, we know that things like toxic positivity and social media can leave us struggling to feel “lucky.” We’re sharing our thoughts…

1
252. Planning For The Future: Involving Siblings In The Decision-Making Process 45:54

4M ago45:54

45:54

We’re so excited to have Phillip Clark back on the show, he’s the founder of ENABLE Special Needs Planning and is here to chat with us about involving siblings in the guardianship and decision-making process. Phillip shares the importance of having open conversations early on with siblings about guardianship and gives advice about getting the conve…

1
251. Rethinking What It Means To Be “Blessed” (w/AUTHOR Micha Boyett) 59:30

4M ago59:30

59:30

You know and love her as the bubbly blonde that breaks into song on nearly every episode, today our girl Micha Boyett isn’t just The Lucky Few Podcast host, she’s our guest!! Join us in celebrating her new book Blessed Are The Rest Of Us (available April 9th!)! We’re chatting about her journey of writing this book, and how she chose to write more t…

1
250. Who Has The Right To Use Down Syndrome Or Disability As A Punch Line? 55:47

4M ago55:47

55:47

Friends, we had another hot topic in our group text that we knew we needed to bring on the pod to have with all of you! Today we’re chatting about the February 25th episode of “Saturday Night Live” with a guest host who used his niece and her Down syndrome diagnosis as a punch line to his set. We’re talking about our reactions and the larger conver…

1
249. One Million Reasons To Celebrate….The Lucky Few Podcast LIVE! 1:04:50

4M ago1:04:50

1:04:50

For nearly 250 episodes we’ve had educational, encouraging, and meaningful conversations amplifying voices and shifting narratives for individuals with Down syndrome. Over the last 6 years, we’ve tackled topics on education, health & wellness, accessibility, stereotypes, legal rights, media representation, advocacy, and so much more! We were even r…

1
248. Everything No One Tells You About Parenting A Disabled Child (w/Kelley Coleman) 58:20

5M ago58:20

58:20

We’re so excited to welcome feature film executive turned author and disability advocate, Kelley Coleman to the show! Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Support releases TODAY!! Friends, this book is like gold, it provides the kind of support and confidence we al…

1
247. The Transition To Adulthood: Fostering Independence, Dignity Of Risk, & Supporting Decision-Making (w/ Amy Julia Becker) 1:08:29

5M ago1:08:29

1:08:29

Friends, we’re so excited to have award-winning writer, speaker, podcaster, disability advocate, and Mom of three, Amy Julia Becker, joining us for a third time today! She’s here to chat about what the journey with her daughter Penny has looked like after turning 18 and entering adulthood. She’s been in the process of making decisions about educati…

1
246. Heart Health & Navigating Heart Defects (w/Dr. Lorraine Schratz) 56:44

5M ago56:44

56:44

Friends, we know that seeing specialists and hearing your child could potentially have cardiac issues after receiving a prenatal diagnosis can all be overwhelming. We also know that while months of celebrating and advocating for awareness can be helpful, but also adds to those valid overwhelming feelings when you’re new to a diagnosis. While those …

1
245. Can An Advocate Get It Wrong Sometimes? 1:01:39

5M ago1:01:39

1:01:39

Friends, you know we don’t shy away from asking the hard questions; today we’re diving into a complex one: Can an advocate get it wrong sometimes? We discuss the balance of advocating and learning, the foundation of a good advocate, and how humility shapes our advocacy journey. We explore the responsibility and journey of advocating for those with …

1
244. Love, Advocacy, & A Viral Proposal (w/Matthew Schwab & Lucia Romano) 59:01

6M ago59:01

59:01

Friends, we’re celebrating Valentine’s Day with a couple that are sharing their enchanting love story! Their engagement was marked by a viral video and widespread media, Matthew Schwab and fiancé Lucia Romano share everything from their first date to their dreams for the future. This power couple is dedicated to shifting narratives for people with …

Podcasts Worth a Listen

Matthew Santoro Podcasts

Podcasts Worth a Listen

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The Matthew Santoro Podcast

Matthew Santoro

1
The Lucky Few

The Lucky Few Podcast

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Dear Teacher, Don't Give Up!

Make Them Master It

1
268. First Responders and Teacher of Patience: A Lesson in Understanding 58:09

1
267. What Is It Like To Have A Sibling With Down Syndrome? (Featuring Our Kids!) 59:08

1
266. From Sibling Love to Community Change (w/Taylor Gardner Chaney) 1:05:00

1
265. Brotherly Love: From Childhood Adventures to Adult Dreams (w/Matthew & Thomas Von Der Ahe) 49:03

1
264. Healing and Hope: Navigating Down Syndrome Regression Disorder (w/ Dr. Santoro & Dr. Quinn) 59:52

1
263. Designs that Dance: A Tale of Friendship and Creativity (w/Dance Happy Designs) 55:59

1
262. 45 Years of Advocacy: A Conversation w/ NDSS President Kandi Pickard 57:31

1
261. Fearless Together: Lessons In Bravery, Hope, & Resilience (w/David and Andrew Olshine) 47:45

1
260. What Did We Learn From This School Year? 1:10:46

1
259. Home Is Our Classroom: Homeschooling A Child With Down Syndrome 1:00:38

1
258. Unlocking Potential: Strategies For Every Learner With Down Syndrome (w/Mrs. Brown) 56:55

1
257. Brother Do You Love Me?: A Journey of Resilience and Repair (w/Manni & Reuben Coe) 1:12:42

1
256. Celebrating Motherhood, Advocacy, & Community (w/Black Down Syndrome Association) 1:07:28

1
255. A Haircut Beyond The Chair w/Vernon Jackson 57:21

1
254. The Next Step: Navigating Healthcare Transitions for Individuals with Down Syndrome (w/ Dr. Emily Johnson) 51:34

1
253. What If You Don’t Feel “Lucky”? 1:03:25

1
252. Planning For The Future: Involving Siblings In The Decision-Making Process 45:54

1
251. Rethinking What It Means To Be “Blessed” (w/AUTHOR Micha Boyett) 59:30

1
250. Who Has The Right To Use Down Syndrome Or Disability As A Punch Line? 55:47

1
249. One Million Reasons To Celebrate….The Lucky Few Podcast LIVE! 1:04:50

1
248. Everything No One Tells You About Parenting A Disabled Child (w/Kelley Coleman) 58:20

1
247. The Transition To Adulthood: Fostering Independence, Dignity Of Risk, & Supporting Decision-Making (w/ Amy Julia Becker) 1:08:29

1
246. Heart Health & Navigating Heart Defects (w/Dr. Lorraine Schratz) 56:44

1
245. Can An Advocate Get It Wrong Sometimes? 1:01:39

1
244. Love, Advocacy, & A Viral Proposal (w/Matthew Schwab & Lucia Romano) 59:01

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