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CRISPR, Sickle Cell Disease & Society: A VR Explainer & Ethics Discussion

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What is sickle cell disease and how can CRISPR help? How can DNA editing be used ethically? How do we reckon with the history of medical racism towards this patient community? Watch our two-part event on CRISPR, Sickle Cell Disease, and Society: A VR Explainer & Ethics Discussion, hosted by the IGI and the Bay Area Science Festival in October 2020, to explore these questions and more!

In the first part of the event, a CRISPR scientist explains what causes sickle cell disease and how CRISPR genome editing may be used to repair the sickle mutation (0:00–12:26). You’ll be taken on a virtual tour to see how sickle cell affects the body and watch CRISPR in action (12:26–19:26)! Following the tour, a set of panelists have a candid conversation on science and society, including topics like health disparities in the U.S., race and racism in medicine, access to emerging therapies, the ethics of CRISPR, and more (25:29–end). Watch the video below or scroll past it to learn more about the participants and see our recommended follow-up reading.


Expert panel

Megan Hochstrasser, Ph.D. | Education Program Manager, Innovative Genomics Institute

Marilyn Baffoe‐Bonnie | Doctoral Student, Rutgers University Department of Sociology

Cassandra Trimnell | Founder and Executive Director, Sickle Cell 101

Mónica Feliú-Mójer, Ph.D. | Associate Director of Diversity and Communication Training, iBiology; Director of Communications and Science Outreach, Ciencia Puerto Rico

Moderator

Kevin Doxzen, Ph.D. | Former Science Communications Specialist, Innovative Genomics Institute


Learn more!

Intrigued? Dig into the suggested articles below to dive deeper into the issues discussed during this event.

Resources from our panelists:

Other media:


CRISPR, Sickle Cell Disease & Society: A VR Explainer & Ethics Discussion
Innovative Genomics Institute & Bay Area Science Festival | October 23, 2020