The Rare Remix is a podcast for families navigating rare disease, disability, caregiving, accessibility, developmental differences, and life after a diagnosis changes the rhythm of everything. Hosted by Bryan and Lindsey, The Rare Remix features real conversations with parents, caregivers, advocates, experts, and anyone on a remixed journey. Together, we explore the everyday realities that families quietly learn to navigate, and discuss potential solutions based on first-hand experiences. This may not be the life you imagined. It’s a remix.
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Contact path
Verified email
Booking probability
28%
Guest openness
Selective
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Signup to Generate a PitchThe Rare Remix is a podcast for families navigating rare disease, disability, caregiving, accessibility, developmental differences, and life after a diagnosis changes the rhythm of everything. Hosted by Bryan and Lindsey, The Rare Remix features real conversations with parents, caregivers, advocates, experts, and anyone on a remixed journey.
Recent episodes include "Episode 10 - Finding a Way with Rett Syndrome: A Conversation with Sarah" (6 October 2026, 42 minutes), "Episode 09 - Down Syndrome Is the Least Interesting Thing About Her: Staci & Nate's Story" (16 September 2026, 46 minutes), and "Episode 08 - What Physical Therapists Want Caregivers to Know" (3 September 2026, 35 minutes).
The Rare Remix publishes roughly every two weeks, with episodes averaging 36 minutes across 10 episodes.
Booking probability for The Rare Remix is 28%, and the host is rated Selective on guests. The Rare Remix requires a Pod Score of 80 or higher. The Rare Remix's contact route on record: verified email.
The strongest fits for The Rare Remix are Family & Social Services. The Rare Remix has a society audience.
The Rare Remix is a society podcast with 10 episodes published.
Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.
Episode #10
In Episode 10, we talk with Sarah about her life with 9-year-old Aleah, who lives with Rett syndrome. We discuss the long search for a diagnosis, early intervention, choosing a care team that listens, and Sarah’s...
Episode #9
In Episode 09, The Rare Remix welcomes Staci and Nate for an honest conversation about raising their daughter Amelia, learning her Down syndrome diagnosis at birth, and discovering that a diagnosis can be life-changing...
Episode #8
Caregiving is physical work, but most families are never taught how to protect the body doing it. In Episode 08, The Rare Remix welcomes pediatric physical therapists Emily, Brittney, and Katelyn for a practical...
Episode #7
In this mini-episode, Declan and Liam join The Rare Remix to talk about their cousin Ava, who has Rett syndrome and uses a Tobii eye-gaze device. They explain what they have learned about communicating with someone who...
Episode #6
In Episode 6, The Rare Remix welcomes Tami and Donnie, who recently became caregivers and guardians for Tami's younger sister, Lori. Born in 1968, Lori spent most of her life at home with parents who built their family...
Episode #5
In Episode 5, The Rare Remix welcomes Allison and Brendan, parents to Anya and Clare. Clare was diagnosed with Rett syndrome in 2020, just as the world shut down, leaving their family to navigate life-changing news...
Episode #5
<p>In Episode 5, The Rare Remix welcomes Allison and Brendan, parents to Anya and Clare. Clare was diagnosed with Rett syndrome in 2020, just as the world shut down, leaving their family to navigate life-changing news...
Episode #4
<p>In Episode 4, we sit down with Susan Norwell and Kourtney Barnum from Rett University to explore the transformative world of Augmentative and Alternative Communication (AAC).</p><p>As internationally recognized...
Episode #4
In Episode 4, we sit down with Susan Norwell and Kourtney Barnum from Rett University to explore the transformative world of Augmentative and Alternative Communication (AAC). As internationally recognized specialists in...
Episode #3
<p>Episode 3 features Dianne, mom to 8-year-old Dru, who lives with Au-Kline syndrome. We discuss the challenges of an ultra-rare diagnosis, navigating life with AAC, and the value of asking for help along the way.</p>
Episode #3
Episode 3 features Dianne, mom to 8-year-old Dru, who lives with Au-Kline syndrome. We discuss the challenges of an ultra-rare diagnosis, navigating life with AAC, and the value of asking for help along the way.
Episode #2
Episode 2 features Karen, mom to 30-year-old Lynzie, who lives with Rett syndrome. We talk about the unique timing of Lynzie’s diagnosis, the challenges of making tough decisions in adulthood, and the importance of...
Episode #2
<p>Episode 2 features Karen, mom to 30-year-old Lynzie, who lives with Rett syndrome. We talk about the unique timing of Lynzie’s diagnosis, the challenges of making tough decisions in adulthood, and the importance of...
The Rare Remix
<p>Bryan and Lindsey introduce The Rare Remix, share the story behind the podcast, and explain why they’re creating a space for real conversations, practical insight, and solutions for families navigating life with a...
The Rare Remix
Bryan and Lindsey introduce The Rare Remix, share the story behind the podcast, and explain why they’re creating a space for real conversations, practical insight, and solutions for families navigating life with a new...
Recent guests on The Rare Remix. Study who booked and why before you pitch.
Rett University
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