Rare Mamas Rising: A Rare Disease Mom Podcast cover art

Rare Mamas Rising: A Rare Disease Mom Podcast

Rare Mamas Rising: A Rare Disease Mom Podcast

Written by: Nikki McIntosh
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Rare Mamas Rising is a podcast for mothers of children with rare diseases to find strategies, strength, support, and sisterhood! Hosted by Nikki McIntosh, founder of Rare Mamas, author of the book Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease, and a rare mom herself, each episode offers heartfelt reflections, practical tools, and empowering strategies to help you rise to the call of rare disease parenting. Catch an episode of Rare Mamas Rising and walk away encouraged, uplifted, and empowered. We rise stronger when we rise together—let's rise!2021 Hygiene & Healthy Living Parenting Psychology Psychology & Mental Health Relationships
Episodes
  • Learning to Mother Ourselves
    May 6 2026

    RARE MAMAS RISING- EPISODE 56

    Learning to Mother Ourselves

    In this Mother's Day episode of Rare Mamas Rising, Nikki explores what it means for rare moms to mother themselves with the same tenderness, attention, and care they so freely give their children. From noticing our needs before they become emergencies, to honoring our limits, speaking to ourselves with kindness, advocating for our own well-being, creating a soft place to land, and making room for joy and delight, this episode is a gentle reminder that rare mamas are worthy of good care too. Because we are not only the ones who comfort, protect, and hold everyone else—we are human beings with hearts that need holding, bodies that need rest, and spirits that need tending. Happy Mother's Day, rare mamas!

    For more support and sisterhood, check out Nikki's new book, Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease. Order the book today at the links below:

    Amazon

    Apple Books

    Barnes & Noble

    Bookshop.org

    Books-A-Million

    IndieBound

    Indigo

    Kobo

    Porchlight

    Book Info: www.raremamas.com/book

    CONNECT WITH NIKKI

    Facebook

    https://www.facebook.com/RareMamas1/

    Instagram

    https://www.instagram.com/Rare_Mamas/

    Website

    https://raremamas.com/

    Email

    info@raremamas.com

    PODCAST INFO

    podcast@raremamas.com

    Show More Show Less
    18 mins
  • Plugging Into the Rare Community
    Feb 23 2026

    RARE MAMAS RISING- EPISODE 55

    Plugging Into the Rare Community

    In this special Rare Disease Day episode of Rare Mamas Rising, Nikki McIntosh reads the chapter "Plugging Into the Rare Community" from her book Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease and reflects on what Rare Disease Day has taught her as a rare disease mom. This heartfelt episode explores the power of the rare disease community, the importance of caregiver support, and why connection among rare moms can change the way we carry even the hardest seasons of rare disease parenting. Whether you are newly navigating a diagnosis or years into your caregiving journey, this episode offers encouragement, validation, and a reminder that no rare mama was meant to do this alone.

    Links & Resources Mentioned:

    For more info on Rare Disease Day, check out:

    https://www.rarediseaseday.org

    https://rarediseases.org

    For more support and sisterhood, check out Nikki's new book, Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease. Order the book today at the links below:

    Amazon

    Apple Books

    Barnes & Noble

    Bookshop.org

    Books-A-Million

    IndieBound

    Indigo

    Kobo

    Porchlight

    Book Info: www.raremamas.com/book

    CONNECT WITH NIKKI

    Facebook

    https://www.facebook.com/RareMamas1/

    Instagram

    https://www.instagram.com/Rare_Mamas/

    Website

    https://raremamas.com/

    Email

    info@raremamas.com

    PODCAST INFO

    podcast@raremamas.com

    Show More Show Less
    14 mins
  • Hoping Through the Holidays
    Dec 8 2025

    RARE MAMAS RISING- EPISODE 54

    Hoping Through the Holidays

    Christmas is the season of hope. But hope can be complicated for rare disease parents navigating exhaustion, medical uncertainty, chronic stress, and the ache of unanswered prayers. In this episode of Rare Mamas Rising, we explore what hope really looks like for rare disease parents and caregivers during a season that can feel both beautiful and painfully complicated. This episode gently unpacks the realities of hoping in the hard: hope in the waiting, hope after disappointment, hope when you're exhausted, and hope when you're scared to try again. It offers reflections on why hope is an action we choose, how it keeps us moving in the world of medical parenting, and the surprising ways hope can transform us even before our circumstances change. For every rare caregiver navigating uncertainty or heaviness this time of year, this conversation creates space to reconnect with hope.

    Links & Resources Mentioned:

    For more thoughts on Hope, check out Nikki's new book, Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease. Order the book today at the links below:

    • Amazon
    • Apple Books
    • Barnes & Noble
    • Bookshop.org
    • Books-A-Million
    • IndieBound
    • Indigo
    • Kobo
    • Porchlight

    Book Info: www.raremamas.com/book

    CONNECT WITH NIKKI

    Facebook

    https://www.facebook.com/RareMamas1/

    Instagram

    https://www.instagram.com/Rare_Mamas/

    Website

    https://raremamas.com/

    Email

    info@raremamas.com

    Show More Show Less
    18 mins
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