Welcome to The Lucky Few Podcast where we are shifting the narrative by shouting the worth of people with Down syndrome.
Through heartfelt conversations, personal stories, and expert interviews, hosts Heather Avis, Micha Boyett, and Mercedes Lara explore parenting, disability advocacy, and shifting societal views. Since 2018, The Lucky Few Podcast has been a beacon of good news, practical advice, and infectious humor.
With over 300 episodes and more than 1 million downloads, we've spent seven years empowering listeners through topics like IEP navigation, parenting tips, healthcare, and legislative issues. Tune in to the leading podcast on Down syndrome — and join us as we work to create a world where differences are embraced, and everyone belongs.
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Shift the Narrative and Shout Their Worth in style with some new merch! We are so excited we have a brand new shop with so many new designs. Use promo code: podcast at checkout for 10% off!
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The Lucky Few Podcast officially launched on March 21, 2018 on World Down Syndrome Day.
We would love to notify you when the first episode posts. In addition, we will be offering events and other fun opportunities for you to participate with The Lucky Few in the future.
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Join us as a corporate sponsor and let audiences know that your brand is actively working to create a more inclusive world where everyone belongs. The Lucky Few Podcast was created in 2018 as a way to share relevant stories and helpful advice on topics ranging from IEPs, to parenting to hot topics, to other important issues such as health care and legislation in the Down syndrome community.
The Lucky Few Podcast has become a trusted source for an active and engaged audience. With a diverse audience of parents uniquely committed to inclusion and advocacy. The Lucky Podcast listeners are parents, teachers, students and advocates of people with Down syndrome who are committed to seeing a more inclusive world where Everyone Belongs.
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Leave us a voicemail or text and share some good news that you've experienced with you son, daughter, sister or brother with Down Syndrome. Or, about yourself and how you are finding worth amidst your journey among the lucky few. Each episode we read your submission on the show and we'd love to hear how you're doing!
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In this current political climate, one of our goals is to keep you all up to date on legislature that impacts our community. So friends, its time to talk about the “Big, Beautiful Bill” and how it will affect individuals with Down syndrome. We are SO grateful for an incredible guest to help us out. Sean Feely is the new Director of Advocacy and Policy at the National Down Syndrome Society and he’s here today to answer all of our questions.