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EP 131: “Three Hearts, One Journey: The Massie Family’s Journey with Alport Syndrome”
Manage episode 518934013 series 3351759
Title: EP 131: “Three Hearts, One Journey: The Massie Family’s Journey with Alport Syndrome”
🎙️ Episode Summary
In this episode of This Thing Called Life, we meet Kaitlin Massie, whose family’s story is one of strength, resilience, and hope. Kaitlin, her mother Amanda, and her brother Hunter all live with Alport Syndrome, a rare genetic condition that leads to kidney disease and, for many, the need for a transplant. Kaitlin shares how her family’s challenges have turned into a powerful story of advocacy, awareness, and gratitude for the gift of life.
Kaitlin has turned her personal challenges into purpose — pursuing a Master’s Degree in Bioengineering at the University of Washington and working on developing a portable dialysis device that could change the future for patients like her.
- Andi Johnson introduces Kaitlin Massie, the daughter of Amanda and sister of Hunter, who joins the podcast from Vanceburg, Kentucky, where she is currently receiving dialysis treatment.
- Kaitlin shares her background, including her Alport Syndrome diagnosis, her Master’s Degree in Bioengineering, and her innovative work on a portable dialysis device at the University of Washington — a project inspired by her own experience as a patient.
- Kaitlin addresses the widespread misconceptions surrounding organ donation, encouraging listeners to research thoroughly and rely on credible medical sources instead of fear-based narratives.
- She clarifies that being a registered organ donor does not affect the quality of medical care you receive — an important myth to dispel.
- Kaitlin emphasizes making informed decisions based on facts and personal conviction rather than hearsay or outdated assumptions.
- Andi inquires about the process of learning more about living kidney donation and how individuals can register as donors.
- Kaitlin highlights the UK Living Donor Clinic, sharing her positive experience and the inspiring number of people willing to get tested for potential matches.
- She mentions that her father was told he didn’t need to get tested because there were already so many individuals in the pipeline — a beautiful testament to generosity in action.
- Kaitlin encourages others to take initiative, reminding listeners that every potential donor adds hope for someone waiting.
- When asked about her daily life, Kaitlin opens up about her family’s shared journey, explaining the emotional and physical toll of living with kidney disease.
- She shares that she and her brother attend dialysis together, which helps them both find comfort and strength in shared understanding.
- Kaitlin recounts emergencies when her low hemoglobin levels required hospitalization — moments where her brother’s presence made all the difference.
- Andi expresses deep gratitude to Kaitlin for her courage and transparency, wishing her family continued strength and healing as they wait for transplants.
- The episode closes with a heartfelt reminder from Andi: over 100,000 people are currently waiting for a life-saving transplant — 90,000 of whom need kidneys.
- Listeners are encouraged to register as organ donors or consider living donation through trusted platforms such as RegisterMe.org and Network for Hope.
📝 Key Takeaways
- Knowledge Over Fear:
Kaitlin reminds listeners that misinformation is one of the biggest barriers to organ donation. By turning to medical and scholarly resources, individuals can make empowered, informed decisions rooted in truth rather than fear. - The Power of Family Support:
Facing dialysis alongside her brother Hunter, Kaitlin’s story highlights how shared strength and empathy within families can turn even the hardest challenges into moments of connection and resilience. - Innovation and Hope for the Future:
Through her studies in bioengineering and her work on a portable dialysis device, Kaitlin represents the next generation of changemakers — patients turned innovators who are redefining what’s possible for kidney health.
📢 Tweetable Quotes
“I think that there are a lot of misconceptions surrounding organ donation and that that gives people a lot of hesitation, but I would just encourage people to do your research and really look into it and look at it from scholarly sources, rather than, like, fear mongering.”
- Kaitlin Massie
“And I've actually had really great success with that, because UK has told me that they just have a massive list of people willing to get tested to the point where they haven't even, like they contacted my dad when he was willing to get tested and told him, like, we have plenty of people in the pipeline. We don't need you, and they haven't called him back to ask him to get tested.”
- Kaitlin Massie
“It's stressful for sure, because I'm worried about myself, but then I also have to worry about Hunter and mom as well.”
- Kaitlin Massie
“It gives me a lot of anxiety just worrying about them all the time, but at the same time, it's kind of nice to have people that understand what I'm going through and that I can relate to, like Hunter and I go to dialysis together.”
- Kaitlin Massie
Resources:
https://www.networkforhope.org/
https://www.networkforhope.org/about-us/
https://www.networkforhope.org/stories-of-hope/
https://www.facebook.com/NetworkForHopeOPO
100 episodes
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