PRESS & NEWS
CurePSP Community Conversations Webinar February 2, 2023
CurePSP is hosting a Community Conversations webinar about “The Powerful Role of Grandchildren Caring for PSP, CBD, and MSA” on Thursday, February 2
CurePSP is hosting a Community Conversations webinar about “The Powerful Role of Grandchildren Caring for PSP, CBD, and MSA” on Thursday, February 2, 2023, beginning at 6:00 p.m. Eastern Time (3:00 p.m. Pacific).
In this one-hour conversation-style webinar, Emma Wodwaski and Sanjay Geevarghese will share stories as grandchildren of persons diagnosed with progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD), respectively.
They will discuss how they continue to draw inspiration from their relationships with their grandparents and impart their advice to people living with PSP, CBD, and multiple system atrophy (MSA) and people who care for and about them. At the end of the webinar, they will answer questions from viewers.
Submit your questions when you register or send an email to events@curepsp.org.
Watch the replay:
This webinar will be moderated by Jessica Shurer, MSW, LCSW, CurePSP’s Director of Clinical Affairs and Advocacy.
A recording will be available on the CurePSP YouTube channel after the event. Registrants will be emailed a link when it's ready.
CurePSP’s mission is to raise awareness, build community, improve care, and find a cure for PSP, CBD, and MSA. CurePSP provides advocacy and support for patients, families, and caregivers; education for physicians and allied healthcare professionals; and funding for research.
Emma and Sanjay connected through CurePSP and started a virtual support group for grandchildren and young adult children of persons diagnosed with PSP, CBD, and MSA.
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