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Empowered by Hope

Empowered by Hope

Written by: Emily K. Whiting and Ashlyn Thompson
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About this listen

You want the best possible quality of life for your child regardless of diagnosis or prognosis. Raising a child with medical complexities is often lonely, scary and overwhelming. Join two parents of amazing children with rare medical complexities, Emily K. Whiting and Ashlyn Thompson, to get help and grow with them into empowered advocates for our kids. Here you’ll find a community of support, encouragement, education and resources, equipping you to navigate your child’s medical complexities with hope. To get more personal support, connect with us directly at www.ParentEmpowermentNetwork.org.

© 2026 Empowered by Hope
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Episodes
  • Emily K. Whiting: Love, Impact, and the Work that Continues
    Jan 19 2026

    Send us a text, we want to hear from you!

    January on Empowered by Hope is dedicated to something we talk about often but live out imperfectly: self-care. Or, as we prefer to name it in medical-parent reality, self-preservation — the small, necessary choices that allow us to be the parent advocates we want and need to be.

    This episode opens with a deeply personal conversation as we honor Emily K. Whiting, our incredible co-founder of Parent Empowerment Network and co-host of Empowered by Hope. Emily shares her decision to pause her formal role with the organization and the podcast in order to focus fully on her family and the ongoing complex medical needs that first inspired both PEN and this podcast.

    This is not an ending. It’s a season.

    We name a hard truth with compassion: when hospital days, surgeries, advocacy, and parenting stack up, something has to give. Choosing family does not mean abandoning a mission — sometimes it means protecting it in a different way. Emily’s decision reflects the very values PEN was built on: discernment, courage, faith, and honoring what each season requires.

    From there, we zoom out to the larger story you helped build. What began as a kitchen-table idea has grown into a global community across 18 countries. We revisit why being diagnosis-agnostic matters, why undiagnosed families must always feel fully included, and how that commitment led to one of our proudest outcomes: connecting Hardikar families worldwide, supporting expanded research cohorts, published guidance, and a first-ever family gathering. It’s one powerful example of what happens when determined moms, loving families, caregivers, and clinicians move together — faster answers, clearer direction, and a quieter kind of hope that lasts.

    In true Emily & Ashlyn fashion, this episode offers listeners powerful takeaways as we get practical. If “self-care” feels like another impossible task, we rename it self-preservation: being honest with ourselves about what must be prioritized right now and what might need to be paused or tabled for a season. The mission continues with open hands.

    Expect more empowering and honest conversations with medical parents who truly understand, trusted subject-matter experts and credible voices diving into the topics you’ve asked for, shared resources that make the journey a little lighter, and plenty of love, laughter, and support — the same steady presence this community is built on.

    We kindly ask that you share this podcast with other families who might benefit from our insights and support. Additionally, please take a brief moment to leave a review on your preferred podcast platform, which helps us to reach as many families as possible who are navigating this challenging journey, so they can find our support circle and access the assistance they rightfully deserve. No one should walk this journey alone.

    To get more personal support, connect with us directly at:
    https://parentempowermentnetwork.org

    Facebook: Parent Empowerment Network
    Instagram: ParentEmpowermentNetwork
    Join the Parent Empowerment Network Community of Hope
    Get your copy of She is Charlotte: A Mother’s Physical, Emotional, and Spiritual Journey with Her Child with Medical Complexities by Emily K Whiting on Amazon

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    32 mins
  • Smash A Plate, Not Your Nervous System
    Jan 12 2026

    Send us a text, we want to hear from you!

    New year energy can feel fraudulent when you’re parenting through hospital stays, procedures, and constant logistics. We’re trading perfection for something truer: a simple ritual to release what hurts and a short list of keepers that actually help us breathe, love, and carry on. No grand resolutions, no reinvention—just small, honest choices that hold up under real life.

    We start with a plate-smashing ritual—yes, really—to mark what we’re done carrying: self-depletion, people-pleasing, and the belief that unconditional love demands self-abandonment. Then we move to what stays. Laughter on purpose, curated so it finds us even on hard days. Childlike wonder that turns clouds, stars, and tiny flowers into quick routes back to calm. Ten minutes of morning prayer for alignment when the schedule is anything but predictable. Deep breathing to reset a nervous system trained by years of fight-or-flight. A phone in the “peace and presence” basket so feeding, rocking, and bedtime become connection instead of multitasking. And self-advocacy—asking for what we need from care teams and our circle without apology.

    Along the way we reframe mistakes with grace. You can name a misstep and still honor your heart. Own it, repair, and try again. That stance—gentle and steady—makes space for gratitude to grow, even in grief. We talk practical tools for caregivers of medically complex kids, from boundary-setting to micro-rest, and how to build a more regulated baseline without pretending life is easy. This is trauma-aware, faith-rooted, and deeply human.

    If this conversation gave you breath or language for your own reset, follow and share it with another caregiver who needs hope. Subscribe, leave a review, and email us your “leave behind” and “keepers”—we’d love to hear what goes on your plate and what you’ll carry forward.

    We kindly ask that you share this podcast with other families who might benefit from our insights and support. Additionally, please take a brief moment to leave a review on your preferred podcast platform, which helps us to reach as many families as possible who are navigating this challenging journey, so they can find our support circle and access the assistance they rightfully deserve. No one should walk this journey alone.

    To get more personal support, connect with us directly at:
    https://parentempowermentnetwork.org

    Facebook: Parent Empowerment Network
    Instagram: ParentEmpowermentNetwork
    Join the Parent Empowerment Network Community of Hope
    Get your copy of She is Charlotte: A Mother’s Physical, Emotional, and Spiritual Journey with Her Child with Medical Complexities by Emily K Whiting on Amazon

    Show More Show Less
    49 mins
  • Caring for the Caregiver: Nurturing You, Nurtures Your Child
    Oct 6 2025

    Send us a text, we want to hear from you!

    This open conversation between co-hosts, Emily & Ashlyn, offers clear language, practical insight, and zero judgment for parents, caregivers, and anyone walking the tightrope of medical advocacy and family life.

    What changes when the caregiver’s well-being becomes the foundation of the family—not an afterthought squeezed into the margins? We dig into the real-world difference between mental well-being (clear thinking, decision-making, stress management) and emotional well-being (awareness, regulation, expression), and show how both systems work together when you’re navigating complex care, hospital stays, and the relentless logistics of raising a medically complex child.

    We share a raw, honest arc—from coasting on grit to running on fumes—and the moment a therapist reframed anxiety through the lens of modeling. Kids don’t just hear our words; they absorb our state. When we pause to name feelings, set a 20-minute boundary for a solo walk, or ask for help before we explode, we’re teaching emotional regulation in real time. That’s not selfish; it’s skill transmission that lifts the whole household. You’ll hear why survival mode makes “take care of yourself” feel impossible, how delayed processing can hit when the fires calm, and how grace—not guilt—creates the space to refuel without apology.

    We connect the dots between caregiver health, fewer blow-ups, better decisions, calmer hospital interactions, and a higher quality of life for every member of the family. We also point you to a companion blog with expanded reasons and resources, plus a preview of our next chapter on the “how” of making change stick in a busy, unpredictable reality.

    If this resonated, subscribe, share it with a friend who needs it, and leave a quick review to help other caregivers find these tools. Tell us: what’s one small refuel you can commit to this week?

    We kindly ask that you share this podcast with other families who might benefit from our insights and support. Additionally, please take a brief moment to leave a review on your preferred podcast platform, which helps us to reach as many families as possible who are navigating this challenging journey, so they can find our support circle and access the assistance they rightfully deserve. No one should walk this journey alone.

    To get more personal support, connect with us directly at:
    https://parentempowermentnetwork.org

    Facebook: Parent Empowerment Network
    Instagram: ParentEmpowermentNetwork
    Join the Parent Empowerment Network Community of Hope
    Get your copy of She is Charlotte: A Mother’s Physical, Emotional, and Spiritual Journey with Her Child with Medical Complexities by Emily K Whiting on Amazon

    Show More Show Less
    27 mins
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