TALK Down Syndrome

TALK Down Syndrome

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TALK Down Syndrome episodes

  • 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.
    58 min
  • 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.)
    1 hr 28 min
  • 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.
    52 min
  • 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.
    33 min
  • 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 :)
    53 min
  • 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.
    37 min
  • 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.  

    37 min
  • 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
    54 min
  • 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
    23 min
  • 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
    43 min

About TALK Down Syndrome

From the publisher's feed

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…