Posts in General
102. "More Than A Moment," w/Kelli Caughman
102. "More Than A Moment," w/Kelli Caughman

Kelli Caughman is a mother, wife, and a leading Black advocate in the Down syndrome community. Not only is she the Black Families Director for the Down Syndrome Diagnosis Network, she created the Black Family Village in Indiana and serves on the board of Gigi’s Playhouse in Indiana. We’re so thankful for everything Kelli brings to our DS community and we’re especially grateful she’s joining us for another important conversation during Black History Month. Today, we’re exploring the reasons behind the lack of diversity on social media, the mental strain on Black advocates over the past year, and tangible steps to take towards becoming anti-racist.

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GeneralValerie SchliederDown Syndrome, Advocacy, RaceComment
101. Jalondra Davis on Race, Disability, & Advocacy
101. Jalondra Davis on Race, Disability, & Advocacy

Have you ever thought about what enables you to ignore certain injustices in the world but not others? Do you feel safer advocating in certain spaces as opposed to others? Is privilege allowing you to pick and choose what and who you advocate for? There’s a lot to unpack here, friends.. that’s why we are so grateful that Jalondra Davis has joined us once again to discuss all things race and disability. Today, we’re covering everything from the aftermath of last year’s Black Lives Matters protests, to racial inequity in the disability community, and what Jalondra is realizing about her son’s identity as he grows up. We hope you join us for this important conversation, friends! Enjoy.

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GeneralValerie SchliederDown Syndrome, Advocacy, RaceComment
100. How did we get here?
100. How did we get here?

It all started when Micha tried to find a Down syndrome podcast that could help her get her son Ace to brush his teeth. When she couldn’t find one, she called Heather, who called Mercedes, and you know the rest of the story. Here we are 100 episodes later sharing our most memorable moments from the last 3 years and some special updates from former guests! We’re so glad that what started with us running around in shiny skirts with bright lipstick has turned into such a special community with you all. Thanks for sticking around for the last 100 episodes. Here’s to many, many more.

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GeneralValerie SchliederDown Syndrome, AdvocacyComment
99. Our Response to "The Last Children of Down Syndrome" by Sarah Zhang
99. Our Response to "The Last Children of Down Syndrome" by Sarah Zhang

Only 18 children with Down syndrome were born in Denmark in the year of 2019. The article “The Last Children of Down Syndrome” by Sarah Zhang is exploring all the reasons why.. starting with prenatal testing. Zhang says, “Prenatal testing is changing who gets born and who doesn’t. This is only the beginning.” Today, we’re taking time to respond to this article and sharing our own thoughts on prenatal testing, eugenics, the idea of “risk aversion,” the hopes we have for our children, and so much more. This is a heavy one, friends. But we hope you stick with us for this important conversation.

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GeneralValerie SchliederDown Syndrome, AdvocacyComment
98. Looking Back on 2020 & Moving Forward in 2021
98. Looking Back on 2020 & Moving Forward in 2021

Happy New Year, friends! We mustered up the courage to look back on our 2020 resolutions from last January.. and let’s just say, we didn’t quite meet all our goals for the year. But that’s okay. We’re moving forward with opportunities for growth in 2021 and we invite you to come alongside us! But first, join us for a chat about what we did over the holidays, health updates, 2021 goals (including T-swift and Beyonce aspirations) and so much more. We’ve missed you and we are so excited to release new episodes this year!

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GeneralValerie SchliederDown Syndrome, AdvocacyComment
Throwback: (Un)learning the Advocacy Language
Throwback: (Un)learning the Advocacy Language

We’re re-releasing one of our favorite episodes all about advocacy and language. This conversation never gets old! Enjoy.. When it comes to finding the right language to use in this advocacy space, it can be tricky.. to say the least! Do we go with person-first or identity-first language? Should we say disabled or differently abled? And how can we use language to empower our kiddos with Down Syndrome? We’ve done a lot of learning (and unlearning!) to try and figure this all out. And as women who do not have any disabilities or diagnoses, we know we still have a long way to go!

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GeneralValerie SchliederDown Syndrome, Advocacy, LanguageComment
Throwback: Is Inclusion Always The Best Option?
Throwback: Is Inclusion Always The Best Option?

We’re starting this year off strong with an important conversation all about school and inclusion. If you’re parenting a child with a disability, we think you’ll relate! Enjoy.. When Micha and her family moved across the country this summer, she realized it might be time to shift her son’s classroom setting as well. In this week’s episode, Micha’s discussing her decision to place Ace in a more restrictive classroom environment and we’re answering lots of hard questions about school for our kiddos with Down Syndrome.. Is inclusion really always the best option? Are you no longer an advocate if you choose a non-inclusive setting for your child?

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GeneralValerie SchliederDown Syndrome, Inclusion, EducationComment
Throwback: Unpacking Privilege & Understanding Intersectionality w/Jalondra Davis
Throwback: Unpacking Privilege & Understanding Intersectionality w/Jalondra Davis

As we head into the new year, we invite you to confront your privilege and pursue justice alongside us. Start by listening (or listening again) to this interview with Jalondra Davis. Enjoy.. We know that Down Syndrome does not affect one more race more than another so why is the advocacy space not more diverse? We have Jalondra Davis - author, scholar, feminist, and mother, on to address this topic and more. We’re chatting about everything from her son’s diagnosis story to the many systems that impact our children with Down Syndrome and the intersections between different types of injustice. Get ready to take notes, friends. We have so much to learn from Jalondra.

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GeneralValerie SchliederDown Syndrome, Advocacy, Inclusion, RaceComment
Throwback: Public Speaking & Self Advocacy w/Matthew Schwab
Throwback: Public Speaking & Self Advocacy w/Matthew Schwab

We’re back with another one of our favorite interviews! Join us for a fun and insightful conversation with an extraordinary self-advocate! Enjoy.. At 22 years old, Matthew Schwab is a public speaker, employee, volunteer, ambassador, intern, campaign manager, and so much more. You may have even seen him advocating for employing people with disabilities on his TedX Talk! When he’s not writing speeches or selling merchandise, he’s sending emails or hanging out with his girlfriend. We’re so happy he took the time to sit down with us and chat all about his busy life, his future goals, and his journey from being sad about his Down Syndrome diagnosis to embracing it!

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GeneralValerie SchliederDown Syndrome, Advocacy, Inclusion, SpeakingComment
Throwback: Shelley Gottsagen On Her Son Zack Gottsagen's Fame, The Oscars, + More!
Throwback: Shelley Gottsagen On Her Son Zack Gottsagen's Fame, The Oscars, + More!

Who remembers this awesome episode from earlier this year?! Listen (or listen again) for an amazing interview about an amazing self-advocate/celebrity! Enjoy.. You’ve seen Zack Gottsagen on the big screen during his hit movie, The Peanut Butter Falcon, and you’ve seen him onstage at the Oscars, but have you ever wondered about the woman who’s supported him since the beginning? In this VERY special interview, we’re talking to Zack’s mom, Shelley Gottsagen, who’s been shouting his worth boldly for 34 years. Tune in to hear more about a lifetime of self-advocacy, fighting systems, Zack’s relationship with Shia Lebeouf, The Oscars, Peanut Butter Falcon, what’s next for Zack, and so much more.

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GeneralValerie SchliederDown Syndrome, Advocacy, Story, MarriageComment
97. Our 2020 Holiday Gift Guide!
97. Our 2020 Holiday Gift Guide!

Looking for the perfect gift (that’s actually meaningful) to give your friends and family this year? We’ve got you covered! Our 2020 Holiday Gift Guide is here and we are so excited to tell you about all these wonderful, narrative-shifting, and worth-shouting businesses! Shop for bow ties and books, soaps and sweatshirts, and even jams, art, and coffee too! We have something for everyone on your list, including your furry, four-legged, friends! But don’t pay full price, use our discount codes!

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GeneralValerie SchliederDown Syndrome, Holidays, Christmas, GiftsComment
96. Handling Holiday Expectations
96. Handling Holiday Expectations

Covid-19 may have wiped out our December calendars, but let’s talk about the magic of a quieter holiday season.. Kids waking up in their own beds, playing in the snow without a care in the world, and actually making the gingerbread cookies you always said you would! Sounds a little bit better than going to a zoom holiday party doesn’t it? This week we’re chatting all about the good and the hard of this holiday season. We’re also giving some advice (or trying to) about dealing with difficult family members and what to do when your child just isn’t having it.

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GeneralValerie SchliederDown Syndrome, Holidays, ChristmasComment
95. What Are You Thankful For?
95. What Are You Thankful For?

As we head into the holidays and the end of 2020 (we made it!), we’re giving thanks for all the lessons learned this year. Let’s face it, 2020 hasn’t been easy and socially-distant holidays hold challenges of their own..But for now, we invite you to practice gratitude with us as we reflect on all the hard parts of this year that have opened our eyes to what we do have. We’re also chatting about why we’re thankful for Down syndrome, including the everyday moments with our kiddos that allow us (or force us) to pause and be grateful. And as always, we are thankful for all of you who listen and cheer us on. We love you, listeners!

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GeneralValerie SchliederDown Syndrome, Holidays, ThankfulComment
94. IEPs during Covid-19, ft. IEP Lawyers Vickie Brett & Amanda Selogie
94. IEPs during Covid-19, ft. IEP Lawyers Vickie Brett & Amanda Selogie

“There’s no way to make virtual learning fair for everyone…” Micha said it best but we’re all thinking it right?! Getting your child’s IEP needs met during virtual learning seems nearly impossible. And no one understands the legal battle behind a student’s disability rights quite like Vickie Brett and Amanda Selogie, two special education lawyers who created one of our favorite nonprofits: The Inclusive Education Project. We’re so grateful to have Vickie and Amanda on for an important conversation about IEP anxiety, disability education rights, virtual learning success stories (yes, they do exist!) and when to have your kiddo’s next distance learning IEP (the sooner, the better). Cheering you on, friends!

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GeneralValerie SchliederDown Syndrome, Education, InclusionComment
93. The (Older) Sibling Perspective, ft. Pat Ramirez
93. The (Older) Sibling Perspective, ft. Pat Ramirez

You may have been one of the 5 million people (no big deal right?) to see Zach & Pat’s viral videos on tik tok. This brother duo has taken social media by storm with their Down syndrome advocacy, positivity, and of course - dancing! So naturally, we needed to meet them.. which is why we sat down to chat with Pat all about growing up with a younger brother who has Down syndrome, navigating social media, and watching Zach find his passion!

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GeneralValerie SchliederDown Syndrome, SiblingsComment