Empowered by Hope

By: Emily K. Whiting and Ashlyn Thompson
  • Summary

  • 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 CharlottesHopeFoundation.org.
    © 2024 Empowered by Hope
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Episodes
  • Transforming Fear into Courage: Empowering Children Through Medical Procedures
    Oct 1 2024

    Finding it hard to imagine your child transforming their fear of medical appointments into proud moments of bravery? This episode of Empowered by Hope illuminates that journey through the inspiring story of Charlotte, Emily’s daughter, who recently earned a bravery award for her courage.

    Navigating the complexities of medical procedures with your child is never easy, but preparation and self-care can make a world of difference. Ashlyn opens up about her own experiences with Emery, sharing pivotal moments that taught her the importance of being a calming presence. From the significance of clear communication with healthcare providers to the simple yet profound act of staying in the room during traumatic procedures, discover strategies that can help alleviate both your child's and your own anxiety during these challenging times.

    Empowering children in medical settings is crucial, and proactive steps such as creating a "poke plan" can turn anxiety into confidence. Learn how involving child life specialists and practicing at home can transform a child’s experience, as illustrated by Ashlyn who made ultrasounds enjoyable for Emery, by incorporating her love for animals and superheroes. Celebrate the small victories and the strength that comes from supportive connections, and remember, you are not alone on this journey. Subscribe for more insights and share your own stories to help sustain this empowering community.

    We kindly ask that you share this podcast with other families who might benefit from our insights and support. Additionally, please consider leaving a review on your preferred podcast platform. Our goal is 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: CharlottesHopeFoundation.org
    Email: Contact@CharlottesHopeFoundation.org
    Facebook: Charlotte's Hope Foundation
    Instagram: CharlottesHopeFoundationInc
    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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    35 mins
  • Uniting Families, Advancing Research: How Hardikar Syndrome Brought Us Together
    Sep 24 2024

    Receiving a life-altering diagnosis for your child reshapes everything. In this episode, Emily shares the emotional journey of discovering Charlotte’s rare condition—Hardikar Syndrome, a diagnosis with only nine documented cases worldwide at the time. We reflect on those heart-wrenching days and how hope and support helped Emily & Dan navigate the unknown. A key figure in our story is Dr. Alanna Strong, whose expertise and care have been invaluable.

    We explore how using #hardikar on social media led us to a global network of 21 families affected by Hardikar Syndrome. What began as a few online connections has grown into a strong community. Together, we’ve deepened our understanding of the syndrome and doubled the patient population for research initiatives led by Dr. Strong. This episode highlights the power of genetic research and community-driven support.

    Navigating a rare medical condition can be isolating, but it also brings moments of hope. We discuss how a diagnosis provides clarity, connection, and access to essential resources. No family should face this journey alone, and we invite listeners to share their stories and connect with us. Together, we can find strength in unity and spread a message of hope and resilience for families facing rare medical challenges.


    Hardikar Resources:
    1. "Novel Insights into the Phenotypic Spectrum and Pathogenesis of Hardikar Syndrome"

    2. Contact Dr. Alanna Strong

    3. Private Hardikar Syndrome Support Group - click here to join this group if you are the parent of a child with Hardikar or you have Hardikar

    4. 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



    We kindly ask that you share this podcast with other families who might benefit from our insights and support. Additionally, please consider leaving a review on your preferred podcast platform. Our goal is 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: CharlottesHopeFoundation.org
    Email: Contact@CharlottesHopeFoundation.org
    Facebook: Charlotte's Hope Foundation
    Instagram: CharlottesHopeFoundationInc
    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
    23 mins
  • Bringing Hope Home: A Mother's Journey to Secure Life-Changing Surgery for Her Child & Bring It to America for More Families
    Sep 17 2024

    Imagine discovering that the best medical treatment for your child's rare condition is halfway across the globe. Join us, Ashlyn and Emily, as we recount the incredible journey of Ashlyn's daughter, Emery, who was born with bladder exstrophy. Ashlyn's advocacy journey for Emery led them to a life-changing procedure at Great Ormond Street Hospital in the UK, making Emery the first American to undergo the 20+ year old surgery. This episode of Empowered by Hope underscores the importance of global medical options and the pivotal role of empowered parenting and relentless advocacy in finding the best care for our children.

    We detail our efforts to bring the revolutionary Kelly Continence procedure to the US, highlighting Charlotte's Hope collaboration with top surgeons Dr. Imran Mushtaq from London, Dr. Marc LeClair from France, and Dr. PJ Lopez at Rainbow Babies and Children's Hospital in Cleveland, Ohio. Learn about the collective quest to make this life-changing surgery accessible to more families, sparing them the daunting task of traveling abroad. We share highlights from a recent webinar where parents engaged with these world-leading experts, showcasing the power of advocacy in expanding medical horizons.

    Navigating the journey of advocating for your child can be overwhelming, but you're not alone. We provide practical advice on trusting your instincts, seeking multiple opinions, and staying informed about new treatments. Our episode emphasizes the strength found in unity and the importance of connecting with others for support. We invite you to subscribe, share your personal journeys, and remember that even on the toughest days, you are doing an exceptional job. Share your story with us at contact@charlotteshopefoundation.org and join our community of empowered parents.

    Additional Episode Resources:
    Link to Bladder Exstrophy-Kelly Continence Procedure Webinar: https://www.uhhospitals.org/health-talks/articles/2024/09/care-for-children-with-bladder-exstrophy


    We kindly ask that you share this podcast with other families who might benefit from our insights and support. Additionally, please consider leaving a review on your preferred podcast platform. Our goal is 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: CharlottesHopeFoundation.org
    Email: Contact@CharlottesHopeFoundation.org
    Facebook: Charlotte's Hope Foundation
    Instagram: CharlottesHopeFoundationInc
    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
    28 mins

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