My Hero 360

My Hero 360 is an online community dedicated to showing the human side of medicine. It is our deep desire and goal to honor, celebrate, and connect unsung heroes in medical communities worldwide. This initiative provides these extraordinary individuals with a platform to share their experiences and foster a ripple effect of inspiration. Together, we can empower each other and improve quality of life, one story at a time.

My Hero 360 is a society podcast hosted by Unknown Host, with 40 episodes on record and a Required Pod Score of 80. PitchCentric scores this show on Booking Probability, Listen Score, and live audience signals refreshed every 24 hours.

Unknown Host hosts My Hero 360, a society show with 40 episodes published.

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  My Hero 360

  2’10” and Ready to Conquer the World | Robert and Monica Quarles

  Jul 9, 202650 min

  In this episode, Kerri Fitzgerald sits down with Monica and Robert Quarles, who share their daughter’s journey with Alagille syndrome. Upon welcoming Miracle to the world following an IVF journey, Monica and Robert knew something wasn’t right. Six weeks later, they finally had an answer, but the journey was just getting started. Monica and Robert discuss the emotional, financial, and physical challenges that they and Miracle have faced. Their experience highlights the importance of trusting your gut, finding support, and never giving up. In the video, Miracle, now 3 years old, also makes an appearance, shyly showing the world her infectious smile. Developed in partnership with the Alagille Syndrome Alliance, this episode shines a light on the realities of parenting a child with a rare condition. Key Highlights: Hear how Monica and Robert Quarles navigated feelings of dismissal from the medical community before reaching a diagnosis for their daughter, Miracle. Be inspired by Monica and Robert’s determination to spread awareness and education for Alagille syndrome, while being a voice for their daughter’s story. Hear how Monica and Robert's fierce advocacy allowed Miracle to get the liver transplant she desperately needed. Learn about how community, such as the Alagille Syndrome Alliance, has made an impact on the family’s ability to navigate this chronic health journey. 00:00 Introduction & Background 02:08 A Mother’s Intuition 09:20 Meet Miracle! 10:15 Rare Conditions Impact the Whole Family 18:10 Finances and Faith 23:13 Miracle’s Life Now: Advocating for Her Life and Future 47:49 Advice to Younger Selves 48:57 Closing Remarks Connect with the Alagille Syndrome Alliance: https://alagille.org/ https://www.linkedin.com/company/alagille-syndrome-alliance https://www.instagram.com/algsalliance/ https://www.facebook.com/ALGSAlliance/ About My Hero 360: At My Hero 360, we honor, celebrate, and connect heroes worldwide. By sharing their stories, we aim to inspire and provide hope for humanity. Follow us to hear more incredible stories of unsung heroes who make a difference in the world. Support My Hero 360: https://myhero360.com/ https://www.instagram.com/myhero.360/ https://www.tiktok.com/@myhero.360 Listen to Our Heroes’ Stories: Apple Podcasts: https://podcasts.apple.com/us/podcast/my-hero-360/id1870681068 Spotify: https://open.spotify.com/show/1LnJ9ce28OkweYcopCZx2L?si=ae174fd84ef44334 Amazon Music: https://music.amazon.com/podcasts/aa426e78-fb79-4978-8851-d5aab25cf951/my-hero-360

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  My Hero 360

  Talking Rare Disease, But Make It Cute | Ashley Brooks

  Jun 25, 202619 min

  In this episode, Kerri Fitzgerald speaks with Ashley Brooks about her rare disease journey. Ashley first learned about generalized myasthenia gravis (gMG) during her studies in college and later learned she actually had the chronic autoimmune neuromuscular disorder. After getting diagnosed, she noticed an absence of people who looked like her—a young woman—featured in resources online linked to gMG, so she decided to start Ashley’s Anatomy as a way to shine a light on the condition and provide education and real-world insights on living with gMG. Key Highlights: Hear how Ashley came to understand that her symptoms were not the result of typical collegiate exhaustion, but rather a chronic condition. Be inspired by Ashley’s passion and success in creating a space for young people with invisible illnesses to better represent themselves. Hear why Ashley was determined to help people better understand rare conditions by framing the discussion in layman’s terms. Learn about her brand, Ashley's Anatomy, which seeks to validate the experiences of those living with a rare condition while educating those who may not understand the struggles faced. 00:00 Introduction & Background 00:44 Exhaustion? Or Something Worse... 03:05 Struggling to Reach a Diagnosis 06:39 Creating a Space for Young People With Rare Conditions 09:18 Advocating for a Treatment Plan 12:15 Creating a Community on Social Media 17:30 Advice to Younger Self 18:17 Closing Remarks Connect with Ashley: ⁠ https://ashleysanatomy.com/blog/ ⁠ ⁠ https://instagram.com/_ashleysanatomy ⁠ ⁠ https://www.tiktok.com/@_ashleysanatomy ⁠ ⁠ https://www.youtube.com/channel/UCXrzesB_OXb68gftMqms7iQ ⁠ ⁠ https://www.facebook.com/AshleysAnatomy/ ⁠ About My Hero 360: At My Hero 360, we honor, celebrate, and connect heroes worldwide. By sharing their stories, we aim to inspire and provide hope for humanity. Follow us to hear more incredible stories of unsung heroes who make a difference in the world. Support My Hero 360: ⁠ https://myhero360.com/ ⁠ ⁠ https://www.instagram.com/myhero.360/ ⁠ ⁠ https://www.tiktok.com/@myhero.360 ⁠

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  My Hero 360

  Our Missions Align – Why We Partnered With the HypoPARA Association | Hypopara Series: Part 7

  Jun 8, 20269 minS0

  <p>As part of this video series celebrating Hypoparathyroidism Awareness Day, Hero Philanthropy made a $2500 donation to the HypoPARAthyroidism Association. Patty and Michele, both advocates and heroes, sit down with My Hero 360’s Chris Ciraulo to discuss the ways in which the two outlets’ missions align. Both seek to spotlight the stories of individuals living with chronic rare health conditions, with the hoping of offering community and inspiration and to improve patient quality of life and outcomes. Connect with the HypoPARA Association: https://www.hypopara.org/ https://www.youtube.com/channel/UC8fpei7liF73LFflvU6zZHwhttps://www.instagram.com/hypoparaassoc/ http...

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  My Hero 360

  This Advocacy Group Is Changing Rare Disease Care | Hypopara Series: Part 6

  Jun 5, 20267 minS0

  <p>In this special episode, Kerri Fitzgerald sits down with Patty Keating and Michele Rayes, the leadership team behind the HypoPARAthryoidism Association, to discuss and define what it means to have hypoparathyroidism, giving listeners a glimpse into the daily struggles and symptoms of individuals with hypoparathyroidism. The two women share recent wins for the Association and share how listeners can get involved and support the Association. </p><p>Connect with the HypoPARA Association: https://www.hypopara.org/ </p><p>https://www.youtube.com/channel/UC8fpei7liF73LFflvU6zZHw </p><p>https://www.instagram.com/hypoparaassoc/</p><p>https://www...

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  My Hero 360

  Fighting to Fix the Broken Healthcare System | Hypopara Series: Part 5

  Jun 4, 202623 minS0

  <p>In part 2 of our conversation with Michele Rayes, she shares how legislative change is a critical part of supporting and protecting people living with a rare disease. She discusses legislative bills that the HypoPARAthyroidism Association supports and provides an educational lens into how to be a good patient advocate. Michele explains specific pieces of legislation she is fighting for, like responsible AI integration into insurance claim reviews and denials, and shares why she is so passionate about advocating for yourself and others. Watch part 1 of Michele's interview: https://youtu.be/Qzp6hyhC3_U Key Highlights: • Hear how the HypoPARA As...

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