Giving Tuesday 2026
VirtualWhat moments mean the most to you? Birthdays, weddings, quiet evenings with loved ones? For families facing polycystic kidney disease, these moments are too often stolen by pain, hospital visits, and uncertainty.
12:00 am - 11:59 pm
6:30 pm - 7:30 pm
Join us for an educational webinar focused on helping patients and families understand the importance of PKD research participation.
Overview:
We’re planning an educational webinar focused on helping patients and families understand the importance of PKD research participation. The session will simplify the basics of clinical trials, outline what participation involves, and highlight how research drives new treatments and hope for the PKD community. It will also spotlight the role of the ADPKD Registry in connecting patients, data, and researchers to accelerate progress.
Learning Objectives:
Explain how clinical trials work and their role in developing PKD treatments
Describe the purpose and impact of the ADPKD Registry
Identify ways patients and families can get involved in research
Speakers:
Chris Chen, VP of Research Programs, PKD Foundation (Confirmed)
Stephen Seliger, MD, University of Maryland (Confirmed)
Tasha Vraspir, Patient Advocate (Pending)
What moments mean the most to you? Birthdays, weddings, quiet evenings with loved ones? For families facing polycystic kidney disease, these moments are too often stolen by pain, hospital visits, and uncertainty.
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