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TALK Down Syndrome
Chantele
60 episodes
3 days ago
TALK Down Syndrome is a podcast created to show the world how Down Syndrome is truly amazing. My goal is to inspire and support through YOUR life stories! Each episode is a unique interview that provides real life experiences about our loved ones, shared by you. Together we can create a new definition of Down syndrome! We are here to TALK (Teach, Advocate, Listen, and Kindness)
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All content for TALK Down Syndrome is the property of Chantele and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
TALK Down Syndrome is a podcast created to show the world how Down Syndrome is truly amazing. My goal is to inspire and support through YOUR life stories! Each episode is a unique interview that provides real life experiences about our loved ones, shared by you. Together we can create a new definition of Down syndrome! We are here to TALK (Teach, Advocate, Listen, and Kindness)
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Society & Culture
Episodes (20/60)
TALK Down Syndrome
TALK 40: Advocating Never Ends; Debbie Miller author of "Raising Ricky"

Debbie Miller is the author of "Raising Ricky," a memoir she wrote describing her journey advocating for her brother Ricky who not only has Down Syndrome but was recently diagnosed with Alzheimer's. Ricky was born in the 60's, in which Debbie gives us insight on how people with special needs were treated in the past and although support and aid for those with special needs has increased since then, we still have so much advocating to keep doing. Debbie now fights for new studies that highlights the importance of early detection of Alzheimer's Disease, especially for our older loved ones with Down Syndrome. Debbie is the perfect example of how advocating never stops.

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7 months ago
35 minutes 48 seconds

TALK Down Syndrome
TALK 39: The Counseling Couples; Petra Rojas

We always have episodes discussing our journeys with our loved ones with special needs, but why don't we ever ask ourselves "how is our marriage or relationship going after having a child with special needs?" Often times the struggles and obstacles parents face having a child with special needs draws them further apart than closer. Today we dive into just that with Petra Rojas from The Counseling Couple. Her and her husband Alex run a faith based couples counseling and this topic has been widely seen in their sessions. How to navigate through marriage (with base of Christianity) on parenting a child that has special needs. More importantly how to come together as a team and strengthen your relationship. We are happy to have you listen to this episode today. May it give you perspective and gratitude and comfort in whatever you have going on in your life.

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8 months ago
51 minutes 44 seconds

TALK Down Syndrome
TALK 38: Author Talia Frayre Martinez

Not only is Talia one of my newest friends, but she is an amazing author who just released her first book called The Adventures of Sammy and Rosie Conquering Thunder Hill, which is book number one of her series. Her main characters Sammy and Rosie are created after her children and Rosie has Autism just like her daughter in real life. Join us on this episode as we get into deep discussion about why she wrote this book, parenting and navigating in today’s society as a special needs mother, and how Christ is the foundation of her passion and daily commitment to changing todays norms on disabilities, prayer, and children’s readings. This episode holds dear to my heart and I hope it gives you listeners a sense of ease and empowerment in whatever struggles you may be conquering yourself, such as Sammy and Rosie do in Talia’s book.

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11 months ago
1 hour 26 minutes 26 seconds

TALK Down Syndrome
TALK: 37 The Upside of Down- Golf & Down Syndrome

This TALK episode we have guests, Phillip and Ramona Gallegos from The Upside of Down Foundation. Phillip and Ramona created a fun way to advocate for their son, Zachary, through Golf Tournaments. Today we speak to them about their journey with Zachary and how golfing and awareness have come together. This one is a good one, you don't want to miss it.

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1 year ago
38 minutes 8 seconds

TALK Down Syndrome
TALK 35: Discussion with Brady Murray, founder of RODS Hero’s
Today we get to talk to Brady Murray, owner and founder of RODS Hero's. Becoming a parent to a child with special needs is not only by chance but can also be by choice. We at TALK Down Syndrome absolutely love those who are first to raise their hand to the task of taking on such a special duty to parent a child with special needs and RODS Hero's agree. That is why Brady Murray and his family created this organization to help individuals that want to step into parenting our little special ones who need family and love. Talk a moment to listen to this beautiful calling of love and community on today's episode.
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1 year ago
32 minutes 46 seconds

TALK Down Syndrome
Episode 35: John’s Crazy Socks

Today we are kicking off World Down Syndrome Day, I would say SUPER early but only because when I think of WDSD I think of John's Crazy Socks. Today's episode features father and son duo, Mark and John Cronin owners and creators of John's Crazy Socks. When I first entered this community, I remember seeing John's Crazy Socks marketed everywhere online and it has finally come full circle where they are now on my podcast! It was such a joy to discuss how their business started as well getting to know more about John as an individual and I can tell you now, him and his dad have one heck of a relationship. What they have created is what all of us parents dream about, a successful business full of happiness, love, travel, and advocacy with our children. These two are quite a pair so take a listen to today's short but sweet episode of the journey of Mark and John Cronin of none other than the best socks in town, John's Crazy Socks.


If you would like to see more of John and Mark visit these links:


https://www.youtube.com/watch?v=dzPvxz1oUEA&feature=youtu.be

John's Crazy Socks (johnscrazysocks.com) Hiring Those w/ Differing Abilities Is Good Business | John & Mark X. Cronin | TEDxLakeSuccessStudio (youtube.com)


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1 year ago
40 minutes 25 seconds

TALK Down Syndrome
Episode 34: Making hometown changes, an Interview with Evelyn Acevedo
Evelyn Acevedo is not only an amazing mom to her son Lincoln, but she has one empowered and determined woman. This lady found a problem with her and her city, and took the steps to make changes and to bring awareness for our down syndrome community. Take some time to listen to this episode. I guarantee you will be rushing to the computer to find ways that you can advocate in your hometown. You don’t want to miss this one as Evelyn will not only inspire me, but I’m sure she will inspire you as well.
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2 years ago
54 minutes 40 seconds

TALK Down Syndrome
TALK 33: Courtney Sebastiano
Today I am introducing you guys to Courtney Sebastiano. Interestingly, Courtney’s first child Jaxon has Down syndrome. Courtney walks us through how courageous and resilient her newborn baby was as he faced aspiration issues, along with heart failure, and his first few months. Now a healthy, almost 3 years old little boy, alongside his brother, are just the most amazing and inspirational kids Courtney never knew she would be blessed with.
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2 years ago
53 minutes 1 second

TALK Down Syndrome
TALK 31: Brandy Duggan- Becoming a new mom to a child with DS while also learning about herself.
It took 7 months for Brandy to respond to my message on Facebook when I reached out to her to be a guest. Little did I know during that time, Brandy was embarking on her own journey of being a brand new mother to Brayden (who is diagnosed with Down Syndrome) but also learning about her own neurodiversity. Brandy shares with us how she maneuvers through social media taking down “trolls” and shining her own light of advocating for her two children.
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2 years ago
57 minutes 10 seconds

TALK Down Syndrome
TALK 30: Celebrating WDSD. Learning more about Autism & those that have a dual diagnosis.
This episode we do have just one special guest but TWO :) Dey, a mother to Adam who has Autism and Seleste, a mother to Genesis who has a dual diagnosis of Autism and Down Syndrome. Us three moms collaborate on what our diagnosis’ mean, how we maneuver through the struggles and triumphs in motherhood, and share our personal experiences of being super moms to our babies, and we learn something more about one another’s special child. It’s so wonderful to be able to share World Down Syndrome Day with the Autistic community. Because at the end of the day, no matter what diagnosis (or no diagnosis) we are all moms just trying to do our best and we can’t be our best without this kind of support, right? (This episode is dedicated to Everett Molino (15) who passed 3/15/23. Everett has Autism & we want to sincerely send our condolences to his family during this tragic time. 💙 May his beautiful soul rest peacefully.)
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2 years ago
1 hour 27 minutes 17 seconds

TALK Down Syndrome
TALK 29: Its not always a fight.
No special guest but just your host Chantele discussing certain instances in her journey that made her have a change in mind set. One, being told that as a parent of a child with Down syndrome we must always “fight” the school system. That is not always the case. Sometimes as parents we stand in the way of our own child’s happiness and growth. It’s important to see the whole picture. What a beautiful thing it is to know the truth, speak the truth, and grow from these experiences.
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2 years ago
51 minutes 16 seconds

TALK Down Syndrome
TALK 28: Azaiah "God is my strength" a Miracle journey just in time for the holidays.
Azaiah, only 5 months old, has much to say to the world and much to poop! Come listen to Janelle's story of her son, Azaiah, and his struggles he had with Hirschsprung's disease which effects the baby passing stool, and just overcame surgery. Azaiah, born at 3 pounds 5 ounces brings inspiration to any other families out there that may be experiencing this disease or other struggles. This tiny baby has such a huge fight and I can’t wait for you to listen to his journey.
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2 years ago
32 minutes 1 second

TALK Down Syndrome
TALK 27: "Lulu and Maya"
We kick off Down Syndrome awareness month by interviewing Lulu who is a mom to a fun energetic girl named Maya. Lulu spends time talking to us about her journey as Maya’s mother and helps us out on ways we can navigate through the IEP process & things she did that can make your educational plan better :)
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3 years ago
52 minutes 31 seconds

TALK Down Syndrome
TALK 26: Lets TALK Autism. Interview with Vanessa Gonzales
Today we TALK Autism! We are switching it up a bit with today's episode. It is important to not only raise awareness on Down syndrome but to be aware of other special needs diagnosis, such as Autism. This is why I invited a friend of mine, Vanessa Gonzales (who's daughter Chloe is Autistic) to be a special guest on this episode. Vanessa shares a bit of insight on what it is like to have a child with Autism and the importance of listening to your inner mommy hunch by investigating signs that you may suspect your child may be different than other children. 
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3 years ago
36 minutes 14 seconds

TALK Down Syndrome
TALK 25 : Katie Gresko VP of GiGi's Playhouse, Orange County

Who doesn't love GiGi's Playhouse? Well guess what? We have a new location opening in the beautiful Southern California and today we get to have on our episode Katie Gresko, Vice President (what what!!) of GiGi's Playhouse ORANGE COUNTY! Katie discusses how she got involved with GiGi''s Playhouse and how it has changed her life raising her first born Jack, who has Down syndrome. Take listen and hear Katie's backstory along with how you can start up your own GiGi's Playhouse or be apart of a team.  

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3 years ago
36 minutes 52 seconds

TALK Down Syndrome
TALK 24 with Vanessa Delagarza
This episode we have the beautiful, the strong, the boss babe herself Vanessa Delagarza of Amorcita Clothing. Vanessa joins us today to discuss her journey with her daughter, Amor, who has Down syndrome and shares how Amor gave her the inspiration to create her own clothing line. Amorcita Clothing not only gives an edgy look to our every day attire but contains words of strength and encouragement to parents and loved ones in the special needs community.  To find Vanessa and Amorcita Clothing go to: Instagram: Amorcitaofficial Website: www.amorcitaclothing.com 
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3 years ago
53 minutes 21 seconds

TALK Down Syndrome
TALK 23- Tabia Kocks "Tabia the Model" Interview
On this episode we are celebrating World Down Syndrome Day 2022 with Tabia Kocks. Many of you know her as "Tabia the Model." Tabia (28 years old) has been interested in modeling since she was in High School and has turned herself in a full-time professional model. Tabia has been named Miss Washington from 2019-2021, been featured in British Vogue, and recently had her own story published by the National Down Syndrome Society. Tabia is all over social media making her mark in the fashion industry and today she joins us in a mini-interview about her life and send her message to the world that "She's Got This!"  You can find Tabia at: Website: https://www.tabiathemodel.com/ Instagram: TabiatheModel Facebook: https://www.facebook.com/TabiaTheModel Subscribe to her Youtube Channel: https://www.youtube.com/channel/UCYanF5ErtmLUpNZLo0nLJVQ
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3 years ago
22 minutes 58 seconds

TALK Down Syndrome
TALK 22- Heather Avis from "The Lucky Few," and "The Lucky Few Podcast"
Today is Saint Patrick's Day (2022) and there is no more LUCKIER way than to celebrate with HEATHER AVIS from "The Lucky Few," and " The Lucky Few Podcast." We welcome you to get to know more about Heather and how (along side Micha Boyett and Mercedes Lara) the Lucky Few was created. We also touch on her New York Times Best Seller; "Different - A Great Thing to Be!" which is a children's book she wrote in homage to her daughter Macyn that promotes diversity and inclusion.  You can find Heather and the Lucky Few Podcast at:  Website: https://www.theluckyfewpodcast.com/ Instagram: theluckyfewpod Facebook: https://www.facebook.com/theluckyfewpod/ Apple Podcast: https://podcasts.apple.com/us/podcast/the-lucky-few/id1349646917 Spotify: https://open.spotify.com/show/2vyYBz3vcnJrdQleuZLuxE You can find out more about her book at: https://www.heatheravis.com/different
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3 years ago
42 minutes 36 seconds

TALK Down Syndrome
TALK 21- Jesse Norell "Aorta Borealis"
TALK 21: Jesse Norell is a musician and dad from Minneapolis, Minnesota who just released his album “Aorta Borealis,” which is centered around his daughter, Alyssa, 6 years old, who has Down syndrome and a rare heart condition called Atrioventricular Septal Defect (AVSD) Join us in this interview with Jesse as he describes the tough and happy times since Alyssa’s birth and medical issues they have overcome and how that has inspired him to create this full album telling Alyssa’s story. To stream this amazing album (trust me you want to!) go to jessenorell.com/music 
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3 years ago
38 minutes 52 seconds

TALK Down Syndrome
TALK 20- Melissa Steele Part 2
We welcome back Melissa Steele from episode #2. This episode we get to catch up on how Melissa's journey has been so far since she gave birth to her beautiful baby girl Joey and her current views of what life is like being a mommy to a child with Down syndrome. (Spoiler Alert!- Remember last time she was nervous and a little scared of what her journey would be like, well ladies and gents, SHE IS DOING GREAT and Joey is growing just fabulously!) Take a listen as we go back in time to reflect Melissa's experience. 
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3 years ago
46 minutes 7 seconds

TALK Down Syndrome
TALK Down Syndrome is a podcast created to show the world how Down Syndrome is truly amazing. My goal is to inspire and support through YOUR life stories! Each episode is a unique interview that provides real life experiences about our loved ones, shared by you. Together we can create a new definition of Down syndrome! We are here to TALK (Teach, Advocate, Listen, and Kindness)