For HNers with ME/CFS (or an interest in it) I can recommend last year's documentary Unrest by Jennifer Brea: https://www.unrest.film/. It's available on Netflix.

It's a confronting look at the human side of severe ME, and a call for greater recognition. If you've had people around you struggle to understand what you're dealing with, showing them Unrest could help a lot. Check it out.