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PODCAST

The Lucky Few

The Lucky Few Podcast

Hey friends! Welcome to the Lucky Few Podcast where we are shifting the narrative by shouting the worth of people with Down syndrome. With your hosts, Heather Avis, Micha Boyett, and Mercedes Lara.

kids & family

All Episodes

00:39:25

299. Reasonable Risks for Our Kids with Down Syndrome

The Lucky Few ·

2025/05/13

If you’re a parent, you’ve likely wondered.. Should I let my child use this public restroom on their own? Is my child able to handle these kitchen tools? Can I let my child attend this sleepover? And if you’re a parent to a child with a disability, you might have even more fears around these risky activities. It’s time for a conversation about reasonable risks for our kids with Down syndrome. Here’s what we’re chatting about today:What does “dignity of risk” mean? Is the risky activity an

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00:47:25

298. What’s going on with the Department of...

The Lucky Few ·

2025/05/06

Overwhelmed by all the news lately? Us too. That’s why Ashley Barlow (@thecollaborativeiep) is back on the show today to breakdown all of the changes to the Department of Education and the impact on students with disabilities. Here’s what we’re discussing today:Budget cuts and the impact on early learning for students with disabilities (no more Head Start program in 2026?!)Pros and cons of school choice and vouchers (What does “welfare for the rich” mean?)Action steps to make sure your child’s

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00:41:35

297. Extracurricular Activities and Inclusion: How to...

The Lucky Few ·

2025/04/29

Picture this: your child with Down syndrome tells you they want to play a sport. You sign them up for the local team, drop them off at practice, and pick them up without any difficulties. Everything goes smoothly… But that’s not always reality is it? Lets break down the complexities of extracurricular activities today:How to ask for accommodations that promote safety, respect, and inclusionSeparate programs designed for people with disabilities.. and what to do when they’re not as inclusive as they

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00:35:54

296. Planes, Trains & Presuming Competence

The Lucky Few ·

2025/04/22

The Avises are back from an 18-day European vacation with tips, tricks, and travel stories for all of us. So Heather and Josh are here today to answer all the questions: How do you “lean in” to surprising (and sometimes frustrating!) moments with your kids? What to do when your family vacation doesn’t look like other families? What are your major tips for traveling with kids/teens who have Down syndrome? There are so many travel resources out there.. disability discounts, wheelchairs, free

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00:41:27

295. How can I help my child with a disability sleep...

The Lucky Few ·

2025/04/15

How many nights per week would you say your child (with or without a diagnosis) sleeps well? We asked our audience and discovered that sleep is a struggle for a LOT of us! So if you’re feeling like you’ve already tried all the online hacks but your child still wakes you up at the same time each night, this episode might have a new tip for you! Here’s what we’re covering today: What’s the biggest sleep challenge for our kids with Down syndrome? And our kids with a dual diagnosis of DS and

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00:33:20

294. Why Down Syndrome Isn't Something to "Cure"

The Lucky Few ·

2025/04/08

When we saw this headline, “CRISPR Snips Away Extra Chromosomes, Offering New Hope for Down Syndrome Treatment,” we knew we had to discuss this article together. So that’s what we’re doing today. Here’s what we’re covering in this episode:The ethics of gene editing - What about other conditions with serious life-threatening effects? Why do some people assume that we need to “cure” Down syndrome? What would we do to alleviate some of the medical challenges in the DS community? The problem with not

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00:38:20

293. Potty Training with a Dual Diagnosis

The Lucky Few ·

2025/04/01

Raise your hand if the thought (or maybe even the memory) of potty training gives you anxiety! This parenting milestone sure brings up a lot of feelings, especially for those of us in the disability community. Here’s what we’re chatting about today:Micha’s potty training journey (including some behind-the-scenes voice notes and training tips!)The impact of a dual diagnosis (Down syndrome and autism) on potty trainingDealing with internalized ableismPLUS: WHY do we actually want certain things for

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00:36:34

292. What's going on with the Department of...

The Lucky Few ·

2025/03/25

If you’ve watched the news recently, you know that there are some HUGE changes happening in our government, especially with the Department of Education. We’re breaking it all down today with our guest host, Ashley Barlow! She’s a mother to a son with Down syndrome, special education attorney advocate, IEP expert, former teacher, current speaker and podcaster. We are so grateful she’s here to cover all these topics:Why did the administration take action so quickly?What exactly is the HR 899 bill and

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00:43:30

291. New Season, Same Us: Life Updates & What’s Coming!

The Lucky Few ·

2025/03/18

Here we are with a NEW season of The Lucky Few Podcast! Join us for this first episode back for some big life updates!From Mercedes: mother-daughter bonding with Sunny, braces, medical thingsFrom Micha: potty training for Ace, communication device debates, new therapiesFrom Heather: her mother’s health, extracurriculars.. dances, musical theater, basketballFrom the pod: BONUS episodes that you can access as a member of The Lucky Crew!Join THE LUCKY CREW for $4.99 a month for bonus episodes and

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00:55:49

Throwback: Is Inclusion A Privilege?

The Lucky Few ·

2025/01/21

UPDATE for 2025:First, we want to say how much this podcast community means to us. Over the past seven years, we’ve released 290 episodes, reaching millions of listeners worldwide. You’ve been with us through laughter, tears, challenges, growth, and friendships. This podcast exists because of you, and we’re deeply grateful for your support. To keep The Lucky Few Podcast thriving, we’ll be making some changes early this year. While we focus on restructuring and exploring new ideas, we invite you to

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00:57:53

Throwback: Everything No One Tells You About...

The Lucky Few ·

2025/01/08

UPDATE for 2025:First, we want to say how much this podcast community means to us. Over the past seven years, we’ve released 290 episodes, reaching millions of listeners worldwide. You’ve been with us through laughter, tears, challenges, growth, and friendships. This podcast exists because of you, and we’re deeply grateful for your support. To keep The Lucky Few Podcast thriving, we’ll be making some changes early this year. While we focus on restructuring and exploring new ideas, we invite you to

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00:54:43

290: Redefining Resolutions For Growth, Not...

The Lucky Few ·

2024/12/31

Happy New Year friends! Join us as we welcome back Amy Julia Becker and her daughter Penny for an inspiring conversation on redefining resolutions for growth instead of perfection. We’re talking about the power of celebrating small wins, how caregivers and families can support loved ones with Down syndrome in setting and achieving goals, and the transformative lessons we’ve learned from goal-setting with our children. Penny also offers her perspective on staying motivated, what success looks like to

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00:51:08

289. It's time for Good News! The Holiday Edition.

The Lucky Few ·

2024/12/24

It’s Christmas Eve, and whether you’re wrapping up last-minute gifts, squeezing in a classic Christmas movie, or running errands around town, we’re thrilled to be keeping you company! Today, we’re diving into something extra special to celebrate the season—a deeper look at the good news in our lives. In the Christmas tradition, there’s a powerful moment when the angel declares the arrival of Jesus as good news. Inspired by this, we’re dedicating today’s episode to celebrating all kinds of good news:

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00:32:01

288 A Christmas Movie for all: with Mia Armstrong and...

The Lucky Few ·

2024/12/17

Today, we’re bringing you some Holiday cheer as we head to the fictional and festive town of New Hope, TX. I have the honor and thrill of speaking with Julia Barnett, the writer and director of the new holiday movie A Christmas in New Hope, and Mia Armstrong, one of the lead actors who plays Charlie, the daughter of a single mom fighting to save her home before Christmas. Mia, who has Down syndrome, shines in a role where her diagnosis takes a back seat, showcasing her as a fully realized

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00:53:41

287. Embracing “Good Enough” Holidays

The Lucky Few ·

2024/12/10

How do you handle the grief that comes with unmet holiday expectations? As we dive into the holiday season, many of us wrestle with the dream of a “perfect” celebration that doesn’t match reality. In this episode, we’re having an honest conversation about releasing those high expectations, navigating the challenges and grief that come with letting go of the idealized holiday image, and discovering joy in what is rather than what could have been. From coping with unplanned moments to redefining

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00:43:06

286. Beyond The Gift: Celebrating Non-Profits This...

The Lucky Few ·

2024/12/03

Today is Giving Tuesday! This year we’ve decided to switch up our traditional gift guide and bring you some of our favorite non-profit organizations doing incredible things for our community. In the spirit of Giving Tuesday, we encourage you to consider supporting their work with your time, resources, or donations. From advocacy to education to direct support, these organizations are transforming lives, and Giving Tuesday is a powerful opportunity to join them in making a lasting change. We hope you

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00:49:21

BONUS. Dreaming Big and Showing Up From The NDSS...

The Lucky Few ·

2024/11/28

That’s right friends, we’ve got a BONUS episode for you this week! Today, we’re bringing you our closing keynote from the NDSS Adult Summit, we’re sharing our takeaways from the weekend, practical tips, and tools for building a future that people with Down syndrome deserve. From dreaming about employment and supporting Down syndrome-owned businesses to creating transition plans and embracing independence, this episode is packed with inspiration and actionable steps. You’ll also hear from incredible

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01:06:27

285. The World We Deserve: LIVE From The NDSS Adult...

The Lucky Few ·

2024/11/26

Friends, we had an epic time at the National Down Syndrome Adult Summit in Costa Mesa, CA! It’s a weekend of connection and educational sessions on a variety of topics that address adulthood and aging for the disability community. We had the honor of helping to launch the NDSS Town 21 PSA and spoke with Town 21 news anchor Jessica Kishner about her role in the video, her passion for music, and her dreams. We also got the chance to talk with NDSS President Kandi Pickard and the creator of the NDSS

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01:17:02

284. Why Does Inclusion for People with Down Syndrome...

The Lucky Few ·

2024/11/19

We’ve talked about impactful PSAs that the Down syndrome community has put out over the years. Today we’re talking about the most recent PSA from our friends over at the National Down Syndrome Society, if you haven’t seen it already follow the link in our show notes and go watch their powerful, important, and impactful message and listen to some behind-the-scenes interviews on this weeks episode! We’re chatting with the president of NDSS Kandi Pickard, an amazing couple Jeremy and Audrey featured in

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00:36:40

283. Navigating Tube Feeding With Down Syndrome...

The Lucky Few ·

2024/11/12

Nutrition is key to a child's development, but for some children with Down syndrome, feeding challenges make it difficult to get the nutrition they need. That’s where tube feeding comes in. Today, we’re chatting with Dr. Lauren Fiechtner, Director of Nutrition at Mass General for Children, to talk about the different types of feeding tubes, why they are sometimes necessary, and the unique feeding challenges that children with Down syndrome may face. We’re chatting about when tube feeding is

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353 results

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