Polycystic kidney disease, or PKD, is a tough journey for patients. But what if their voices could shape the research that aims to help them? That's exactly what the EMPOWER PKD project set out to do. This project didn't just involve patients; it put them at the heart of the research. The goal was clear: find out what matters most to PKD patients and discuss how this disease affects their lives.

Imagine a world where research focuses on what patients truly need. That's what EMPOWER PKD was all about. Patients, caregivers, and researchers came together to identify the most important outcomes from a patient's perspective. This isn't just about fixing the disease; it's about understanding how it impacts daily life.

But why is this so important? Because research that aligns with patient needs is more likely to make a real difference. It's not just about finding a cure; it's about improving quality of life. PKD affects more than just the body; it touches every aspect of a person's life.

The project didn't stop at just identifying priorities. It also aimed to discuss the broader impact of PKD. This disease isn't just about physical health; it's about mental health, social life, and overall wellbeing. By understanding these aspects, researchers can create studies that truly make a difference.

So, what's the takeaway? Involving patients in research is more than just a nice idea. It's crucial for creating evidence that truly matters. It's about giving patients a voice and using that voice to shape the future of PKD research.

PKD Patients and Researchers: Together We Explore Priorities

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