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In this episode of PKD Chronicles, we’re exploring how participation fuels progress in research and treatment development.

Nephrologist and PKD researcher, Neera Dahl, M.D., joins us to help you discover:

  • Why clinical trials and registries are critical to advancing PKD research
  • Common myths and concerns about participation
  • How informed decisions can empower patients and caregivers
  • The PKD Foundation’s ADPKD Registry and its role in connecting patients with research opportunities

Listen today to learn how you can play a pivotal role in shaping the future of PKD treatment and research.