The Pressing On Podcast

At PressingOn.org, our mission is to uplift, resource and coach hospitalized families. The purpose behind the PRESSING ON PODCAST is very similar - to amplify voices of perseverance and highlight the amazing journey of hospitalized families, so that everyone who listens will be encouraged to “press on” through tough times holistically!

The Pressing On Podcast is a business podcast hosted by Pressing On, with 17 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.

Pressing On hosts The Pressing On Podcast, a business show with 17 episodes published.

Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.

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  Episode #16

  Episode 16: REGAN REEDER | “Celebrating the Holidays with a Medically-Fragile Child”

  Nov 26, 202448 minS2

  <p>In this holiday-themed episode 16, we welcome Regan Reeder back to the podcast to discuss the complexities of celebrating the holidays with a medically fragile child. She recounts their many holiday experiences with her daughter, Myka, and covers practical tips for traveling with special medical needs while emphasizing the significance of emergency preparedness. Richie and Regan discuss family challenges, essential packing tips, dietary restrictions, and the importance of support from family and friends. The discussion touches on empathy, understanding, and the significance of creating joyful memories despite the challenges. If your goal is to be present and supportive with your...

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  Episode #15

  Episode 15: GARRET & TARA WELSH | “Navigating a Congenital Diaphragmatic Hernia (CDH) Diagnosis during Covid”

  Nov 19, 202455 minS2

  <p>In Episode 15, Garret and Tara Welsh share about their journey of resilience as they faced the challenges of their son Theo's diagnosis of congenital diaphragmatic hernia (CDH) during the Covid-19 pandemic in 2020. The conversation delves into their personal backgrounds, the emotional impact of the diagnosis, the logistical challenges posed by the pandemic, and the invaluable support they received from family and friends during this difficult time.</p> <p><br /></p> <p>In this heartfelt conversation filled with faith, Garret and Tara share their journey through the challenges of their son Theo's birth and subsequent medical issues. They discuss the...

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  Episode #14

  Episode 14: MIKE & CHARITY MCKINNEY | “Embracing the Challenges of Propionic Acidemia”

  Nov 12, 202459 minS2

  <p>In Episode 14, Charity and Mike McKinney share their heartfelt journey as parents navigating the challenges of pediatric transplant for their daughter Annabelle, who was born with propionic acidemia. They discuss their early struggles with infertility, the shock of Annabelle's diagnosis, and the emotional rollercoaster of hospital stays and medical decisions. You'll enjoy listening to the McKinneys celebrate Annabelle's growth and development post-transplant, emphasizing the importance of focusing on her strengths and embracing their unique family dynamics.  They emphasize the importance of their faith throughout the conversation and the need for active involvement in their child's care. Mike and Charity d...

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  Episode #13

  Episode 13: JEN LAU | “Finding Grace in the Challenges of Biliary Atresia”

  Nov 5, 20241 hourS2

  <p>In Episode 13 we welcome Jen Lau, a dedicated advocate and mother who shares her journey navigating the complexities of her son Nathan's diagnosis of biliary atresia.  After Nathan's diagnosis, he underwent a life-saving liver transplant at nine months from a living donor.  Jen recounts the logistical challenges her family faced, the emotional toll of the diagnosis and the critical role of community support.  You’ll enjoy listening to Jen’s openness about the need for parental grace and she talks about their unique journey towards finding a living donor for Nathan's liver transplant.</p> <p><br /></p> <p>This transforma...

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  Episode #12

  Episode 12: SARAH VARGAS | “Moving Across the Country for a 2nd Pediatric Liver Transplant”

  Oct 29, 202447 minS2

  <p>In Episode 12, we chat with transplant parent Sarah Vargas, whose daughter Rosie was born with a rare metabolic condition called Maple Syrup Urine Disease, a sometimes fatal condition in which the body is unable to process certain proteins. Sarah and her husband Tony have navigated two pediatric liver transplants for Rosie, relocating to Pittsburgh in 2015 for specialized care at Children’s Hospital.</p> <p><br /></p> <p>Originally from California, Sarah holds a bachelor’s in marketing and an MBA. She’s also a former board member of Transplant Families, an organization that supports families on the transplant journey by pro...

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