Just a quick note to say that I’ve started writing articles for the wonderful ME support and advocacy network #MEAction!

As some of you may know, I suffer from myalgic encephalomyelitis (ME/CFS) so I’m pleased to be writing about my and other people’s experiences with the illness, as well as working closely with some of the awesome people involved with #MEAction. You can read my first article “Toxic Masculinity Made My ME Much More Punishing” here and there is more to come!

I first became aware of #MEAction after going to a screening of Jen Brea’s amazing documentary Unrest. You can read my thoughts on the film here, and you can follow #MEAction UK on Twitter here.

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