Kidney disease is often called a “silent illness”—but for those living with it, the reality is anything but quiet.In this powerful episode of Amplify: Elevating Patient Voices, Ursula Mann joined by Christine Pisapia and special guest Susan McKenzie, a kidney transplant recipient and leading patient advocate. Sue shares her deeply personal journey—from delayed diagnosis and emergency dialysis to receiving a life-changing transplant from her sister-in-law.Together, they unpack the hidden challenges within the healthcare system, including missed early detection, long donor testing timelines, and the emotional toll of dialysis. The conversation also shines a light on the transformative impact of peer support through the Transplant Ambassador Program, and why a “transplant-first” approach could improve both patient outcomes and healthcare costs.This episode is a candid, eye-opening look at the realities of kidney disease—and a hopeful call to action for better awareness, advocacy, and patient-centered care.🎧 Why You Should ListenGain a real-life perspective on kidney disease, dialysis, and transplantUnderstand the gaps in early diagnosis and healthcare systemsLearn why living donor transplants are often the best optionDiscover the emotional and mental health impact of dialysisBe inspired by powerful patient advocacy and peer support initiatives⏱️ Episode Highlights[00:00:00] – Introduction to Kidney Transplant Conversations Ursula and Brent introduce the episode and welcome Christine Pia and guest Susan McKenzie.[00:02:00] – Sue’s Personal Journey with Kidney Disease Family history, early warning signs, and the long road to diagnosis.[00:04:30] – Delayed Diagnosis and Missed Opportunities How lack of early intervention led to disease progression.[00:06:00] – Finding a Living Donor Challenges of genetic conditions and the emotional journey of donor matching.[00:08:30] – What Donor Testing Really Involves A deep dive into the extensive and often lengthy donor evaluation process.[00:12:00] – Why Preemptive Transplant Matters The missed opportunity to avoid dialysis and why timing is critical.[00:14:30] – The Reality of Dialysis Breaking the myth: why dialysis is physically and emotionally exhausting.[00:17:00] – The Hidden Struggles Patients Face Living with illness while trying to maintain a “normal” life.[00:18:30] – The Power of Peer Support How the Transplant Ambassador Program is changing patient experiences.[00:24:00] – Advocacy and the ‘Transplant First’ Movement Why systemic change is needed to prioritize transplants over dialysis.[00:26:00] – The Cost of Dialysis vs. Transplant A compelling case for better healthcare investment decisions.[00:29:00] – Barriers to Living Donation Why willing donors sometimes don’t make it through the system.[00:32:00] – Debunking Myths About Donor Risk Understanding the real (and minimal) risks of kidney donation.[00:33:30] – What People Don’t Know About Kidney Disease Why awareness and education are still lacking.[00:34:00] – A New Podcast to Amplify Kidney Patient Voices Sue shares her upcoming initiative to educate and support patients.[00:35:00] – A Heartwarming Ending Sue reflects on life after transplant—and time with her twin granddaughters.Want to Share Your Voice?If you’re a patient or caregiver, you can join Patient Voice Connect to share your experiences and help shape healthcare here.Join our email list to get new episode updates

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