TALK Down Syndrome

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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)

  1. 26.03.2025

    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.

    36 Min.

  2. 01.03.2025

    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.

    52 Min.

  3. 03.12.2024

    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.

    1 Std. 26 Min.

  4. 04.10.2024

    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.

    38 Min.

  5. 13.05.2024

    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.

    33 Min.

  6. 08.02.2024

    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)

    40 Min.

  7. 24.07.2023

    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.

    55 Min.

  8. 06.07.2023

    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.

    53 Min.
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Info

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)

Informationen

  • Erstellt von
    Chantele
  • Jahre aktiv
    2020 - 2025
  • Folgen
    60
  • Bewertung
    Unbedenklich
  • Copyright
    © Chantele
  • Sendungswebsite
    TALK Down Syndrome