How do you support your family, keep working, and keep looking for answers without losing yourself along the way?

In Episode 11, Jamie shares her experiences as a sibling, a parent in a neurodivergent family, and the publisher of Uniquely You. She talks about watching her mother advocate for her brother and creating a magazine that connects the disability community with personal stories and useful resources.

We explore the everyday realities of supporting her nonspeaking autistic son, the communication approaches their family has tried, sensory needs, and changes in school and therapy. Jamie also shares how block scheduling, faith, support groups, and personal growth help her navigate caregiving and work.

For educators, relatives, caregivers, and families across diagnoses, this is a conversation about asking questions, finding your people, and taking the next manageable step.

Note: Guests share personal experiences, including health and nutrition approaches. The episode is not medical advice or a treatment guide.

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 experience appealing Medicaid waiver denials. She reflects on the work that can be overlooked when caregiving becomes your everyday routine, and why asking for support can feel so difficult.

Sarah also opens up about navigating much of Aleah’s care on her own, and accepting help during her own cancer treatment. Alongside those challenges are triumphs like wheelchair adapted costumes from May We Help, a custom stroller solution with help from a robotics team, adapted water skiing, and the immense sense of belonging at Rett U camp at The Center for Courageous Kids. Aleah’s humor, personality, and love of being around people stay at the heart of the conversation.

This episode is a reminder to see the person beyond the paperwork, make room for joy, and build a community that shows up. Sarah’s first lesson for listeners: whatever the diagnosis, your child is still your child. Meet them where they are. You will find a way.

#TheRareRemix #RettSyndrome #CaregiverSupport #DisabilityInclusion

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 while still being only a small part of who a person is.

They share the emotional shift from fear and uncertainty to knowing Amelia as a spunky, opinionated, deeply empathetic child. They also discuss the realities behind a family life that may look easy from the outside: speech that is not always easy to understand, elopement and safety concerns, constant supervision, and the pressure of trying to understand a need that cannot always be expressed clearly.

The conversation explores public reactions, sibling and family dynamics, marriage, and why children often approach disability with more natural curiosity and acceptance than adults. Staci and Nate also talk about navigating insurance, Medicaid, medical paperwork, and the life-changing value of finding GiGi's Playhouse, community resources, and other families who can offer both practical help and a fuller picture of the future.

This episode reaches far beyond one diagnosis. It is for newly diagnosed families, parents, educators, and anyone who wants to move past assumptions, make inclusion more ordinary, and see the whole person.

#TheRareRemix #DownSyndrome #DownSyndromeAwareness #DisabilityInclusion #DownSyndromeFamily