The psychological cost of rare disease

Originally aired: Thursday, 23 September 2021

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Overview

It has been well established that mental health goes hand in hand with physical health. Living with a chronic condition places a daily emotional strain on both patients and caregivers. For those with a rare disease, the situation is exacerbated by unique challenges, including longer time to diagnosis; more frequent misdiagnoses; few, if any, available treatments; and often complex care. This greater mental load, accompanied by the physical challenges that come with a rare disease, has profound psychological implications. In addition, there are intractable well-being issues around genetic testing that need to be addressed, in concert with the real possibility of genetic therapies in the near future. How can these realities be compassionately and sensitively discussed, and how might they impact the way patients think about their medical condition? In this webinar, we examine these issues and address how physicians and the medical community can better support those living with a rare disease as well as their caregivers.

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Presenters

Presenter
Speaker: Kathleen Bogart, Ph.D.
Oregon State University
Corvallis, Oregon
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Presenter
Speaker: Debra Regier, M.D., Ph.D.
Children's National Hospital
Washington, DC
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Presenter
Speaker: Amy Hunter, Ph.D.
Genetic Alliance UK
London, UK
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Presenter
Speaker: Kym Winter
Rareminds
St. Albans, UK
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Presenter
Moderator: Sean Sanders, Ph.D.
Science/AAAS
Washington, DC
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