Adventures with Anaphylaxis
Every time I think I’ve run out of things to write about, life throws me a…
Brianna Albers (she/her) is a crip-cyborg storyteller living in Minneapolis-St. Paul. She was diagnosed with spinal muscular atrophy type 2 in 1996 and lives with co-occurring physical and mental health conditions. By day she works as an advocate, bridging disability and mental health awareness to empower people to live their best lives; by night, she dabbles in imagination, and is currently writing "Death and the Blade," an adult romantasy with #OwnVoices disability representation. Find her online at bhalbers.com and on social media @bhalbers.
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Every time I think I’ve run out of things to write about, life throws me a…
There comes a point in every SMA patient’s life when someone asks, “Why are you in a wheelchair?”…
There are, in my experience, two kinds of depressive episodes. The first leaves one lifeless and…
I’ve done some arguably ridiculous things over the past two decades in the name of health.
I’ve quoted my favorite poet, Ada Limón, several times throughout the history of this column. Her…
“For the most part, my solutions to human problems have been simple ones—get more rest, do…
It’s hard losing abilities you’ve had all your life. Of course, that’s just part of having…
It seems like everyone I know is getting married. People I went to high school with…
I was nervous about “Hamilton.” For one thing, I’d listened to the…
Classes started yesterday. My third semester of graduate school, which is a little weird to think…
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