Fatal Familial Insomnia - a disease you may have heard of, as it's gained some notoriety on the internet despite its incredible rarity. I'm sure we've all felt insomnia before and know the frustration and the impact that just one or two bad nights of sleep can have on our functioning. Fatal Insomnia has two forms, sporadic and familial, although the very large majority of cases are familial. The genes for FFI have been identified in fewer than 80 families across the world.
Fatal Insomnia is thought to be the result of a prion disease which results in damage to the thalamus. Over time, a person with the disease develops chronic insomnia and deteriorating health over several months as disease onset progresses.
This video not only covers fatal insomnia, but a detailed case report of one patient - a doctor himself who had lost family to the disease - who embarked on a medical quest to stave off symptoms and maintain quality of life as long as possible. His case is notable today for having greatly exceeded expectations about the progression of disease symptoms, and perhaps having laid out a blueprint for treatments for the disease moving forward.
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- Published16 August 2021 at 00:39 UTC
- Length17 min
- RatingClean