TALK Down Syndrome Chantele

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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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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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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Behind this podcast, behind every life event I have ever had (including the birth our children) is my main support, my husband, Michael Holm. This podcast has now been running for a little over 3 years, and guess what, my husband has never been featured on it. So for this episode we decided to drop the kids off at the grandparents, grab a drink, and record his viewpoint of parenting both our children, being a special needs parent from a father's perspective, and how he see's the future of our family raising a child like Cheyenne and Jade. This episode is extra special to me because I hardly get to have conversations from a man's perspective on special needs parenting. We ever so often hear journeys from women. So grab a drink with us and take a listen to our shenanigan's about what is was like having Cheyenne and Jade


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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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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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Support this podcast: https://podcasters.spotify.com/pod/show/talkdownsyndrome/support