Seal Wives and Fae Women: A Parable of Lost Girls

John Bauer, The Princess and the Trolls, public domain image

I wrote this poem back in January, which feels like a thousand years ago now. I held off posting it because I know how hard a year it’s been for doctors and how many of them have also succumb to an illness not yet understood, abandoned and devalued like so many of us chronically ill folks were long before Covid-19. But, given the attitudes towards disabled and chronically ill people in the US and the UK especially (“Just stay home!” or “Hurry up and die and decrease the surplus population!”), the people in retirement homes and other institutions left to die, the all too familiar plight of those with “Long Haul Covid”, and the continual dismissal of disabled and chronically ill voices in a time when we have real wisdom to offer–be it about finding yourself to still be ill when doctors can’t explain it or won’t believe it, coping with a reality that isn’t any less real just because we don’t want it to be or find it too hard to bear, or making due in isolation without adequate support systems–make this poem’s message all the more necessary. It’s my story and millions of others’; now, last year, and a thousand years before me. But I sincerely hope not a thousand years hence.

Six Hours to Go!

WE DID IT! 6 hrs left to go and the Nothing Without Us anthology and all its stretch goals, including an audiobook, an illustrated version, and enhanced author pay, have all been funded! Thanks so much for supporting this own voices project and the disabled authors and publishers trying to change the literary landscape one accurate depiction at a time. If you want to hear more about why this kind of project is so important, check out my author interview where I discuss disability rep, chronic illness narratives, why they both matter, how they impact the real world on a micro and macro level, and why I had to ragequit watching The Flash.

It’s the Last Midnight

Hey, all. For those of you who aren’t already aware from the constant reblogged author interviews, I have a short story in an upcoming own voices disability themed anthology called Nothing Without Us. What does own voices mean, you ask? In this case it means that all the stories in the anthology feature disabled, deaf, neurodiverse, mentally ill, and/or chronically ill main characters written by actual disabled, deaf, neurodiverse, mentally ill, and/or chronically ill authors! And this anthology is extra special in that it also has disabled publishers, so everyone involved in this project from beginning to end has the lived experience these stories are trying to accurately represent and explore. And not a bit of inspiration porn in sight!