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内容由Emily K. Whiting and Ashlyn Thompson, Emily K. Whiting, and Ashlyn Thompson提供。所有播客内容(包括剧集、图形和播客描述)均由 Emily K. Whiting and Ashlyn Thompson, Emily K. Whiting, and Ashlyn Thompson 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal
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Uniting Families, Advancing Research: How Hardikar Syndrome Brought Us Together

23:08
 
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Manage episode 441612604 series 3423931
内容由Emily K. Whiting and Ashlyn Thompson, Emily K. Whiting, and Ashlyn Thompson提供。所有播客内容(包括剧集、图形和播客描述)均由 Emily K. Whiting and Ashlyn Thompson, Emily K. Whiting, and Ashlyn Thompson 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal

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. "Charlotte has a Diagnosis!"
2. "Novel Insights into the Phenotypic Spectrum and Pathogenesis of Hardikar Syndrome"
3. Contact Dr. Alanna Strong
4. 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
5. 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

  continue reading

章节

1. Uniting Families, Advancing Research: How Hardikar Syndrome Brought Us Together (00:00:00)

2. Empowered by Hope - Journey Together (00:00:13)

3. Discovering Hope Through Genetic Research (00:07:04)

4. Navigating Medical Challenges With a Diagnosis (00:14:45)

5. United in Support for Families (00:22:02)

63集单集

Artwork
icon分享
 
Manage episode 441612604 series 3423931
内容由Emily K. Whiting and Ashlyn Thompson, Emily K. Whiting, and Ashlyn Thompson提供。所有播客内容(包括剧集、图形和播客描述)均由 Emily K. Whiting and Ashlyn Thompson, Emily K. Whiting, and Ashlyn Thompson 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal

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. "Charlotte has a Diagnosis!"
2. "Novel Insights into the Phenotypic Spectrum and Pathogenesis of Hardikar Syndrome"
3. Contact Dr. Alanna Strong
4. 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
5. 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

  continue reading

章节

1. Uniting Families, Advancing Research: How Hardikar Syndrome Brought Us Together (00:00:00)

2. Empowered by Hope - Journey Together (00:00:13)

3. Discovering Hope Through Genetic Research (00:07:04)

4. Navigating Medical Challenges With a Diagnosis (00:14:45)

5. United in Support for Families (00:22:02)

63集单集

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