I shudder to think about someone else with ME/CFS or Lyme being portrayed worse than me and, in turn, being used to marginalize a group of sick people. That's just not right.
You can’t dupe a person’s family into saying he’s a hypochondriac and expect him to just be happy that the film is “raising awareness.”
I feel like I should be thankful for every moment that I'm not too miserable to concentrate on my own thoughts. And I am! I'm incredibly grateful, but that mindfulness is hard to sustain when things don't get better.
A few years ago, when I was still on my feet walking the streets, I saw someone stop in the middle of the road and take a selfie. I remember giving a sardonic smile, shaking my head, and waiting for the sound of tires screeching on asphalt. This, of course, was before stopping traffic to... Continue Reading →
One evening a couple weeks ago I woke up from a nap and groggily checked my phone, then my email. Sitting in my inbox was a message from Daniel Jones, editor of the Modern Love column at The New York Times. Even if you haven't heard his name, it's likely you've read, or perhaps even... Continue Reading →
Mothers, especially single ones, are the epitome of strength. My mother is no exception. She raised me and my sister under difficult circumstances and though I was unaware of it until recently, my mom's tribulations as a single woman and mother influenced my outlook on being an adult. From my perspective, my mom had always... Continue Reading →
I realized, "Why the hell am I trying to do squats with a piece of driftwood on my back when I can't even go grocery shopping?"
If enough users agree to The Terms, maybe Lord Zuckerberg will finally put the doors back on the bathroom stalls and stop broadcasting our personal phone calls over the company PA system.