
Hot takes on everything from disability justice and chronic illness to reality TV and pop culture from a former journalist (and Gemini rising) with ME/CFS. I’ve got fun facts and lots of opinions and I’m not afraid to use them.
| Platform | Pricing | Only free issues | Publishes | Weekly | |
|---|---|---|---|---|---|
| Issues | 32 | Founded | 3 years ago | Last Issue | 2 months ago |
| Active | |||||

It’s Saturday, noon, one of those warm and windy days that feels a little bit romantic, like you should be barefoot in the grass wearing a Boho dress and falling in love.
I am not, however, falling in love. I’m sitting on my couch, looking...
It’s strange how chronic illness can both connect you to and isolate you from everything that’s going on in the world.
Connect you to, because all oppression is interconnected; because there are disabled people in every marginalized group,...
A few weeks ago, there was big news in the ME/CFS community.
Whitney Dafoe, a very well-known severely ill patient, spoke words out loud for the first time in twelve years.
Most of us were introduced to Whitney by the film Unrest, where...
I don’t think it’s fair to say that if people choose the thing that helps them function, it’s because there’s something wrong with their soul. Maybe it’s because there’s something wrong with a system that makes them choose.
Of all the various pacing techniques and disability workarounds I’ve learned over my nearly nine years of having severe ME/CFS, perhaps the most helpful and revolutionary has been this:
You don’t actually have to wash your hair.
Not that...
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