A couple of notes before we begin:
I live in Minneapolis, which is still heavily occupied by ICE & Border Patrol due to
Operation Metro Surge.. To lend aid directly to those most affected, visit the
Stand With Minnesota website.
I have had this post written for weeks, and I kept saying to myself that I would post when everything "calmed down." It doesn't look like this is happening any time soon; however, dealing with the reality of living in an occupied city has both
materially worsened by symptoms of both suspected ME/CFS and c-PTSD; and has caused me to have to
cancel medical appointments due to safety concerns for myself & my wife/caregiver, who is a trans woman of color.
I'm posting now for two reasons:
1) The information is still actively relevant to my life, even while other crises occur, and
2)
Abolishing ICE, CBP, and all incarceration is a disability justice issue.
Immigrants and BIPOC in Minneapolis have been avoiding medical care because of the risks of kidnapping, detainment, or other state-sponsored violence.
Disabled people, especially BUT NOT EXCLUSIVELY immigrants and BIPOC, are also dealing with this threat. I cannot seek care because of Operation Metro Surge; I also cannot seek certain types of care or sometimes care at all because of the
unmitigated airborne pandemic still rampaging through the public.
My lack of care access is part of why my condition has declined since 2019. It's also why I feel like documenting honestly what's happening in my life and my body is the only choice I have, despite the fact that it often takes effort than makes me sicker for days or weeks.
Why write a whole post about your health & disability?
I often
don't have the physical energy or cognitive ability to sit and discuss the progression, next steps, and current concerns of my health, even if people are well-meaning, concerned, or wanting to help. It's also difficult to remember or keep track of
who I spoke to about what developments & when.
I've also always considered myself someone who uses my own experiences as information, advocacy, and a catalyst for change. In that spirit, I've decided to set down some things to (digital) paper so I can do the digital equivalent of handing people this business card when they ask,
"Hey Crash, what's wrong with you...?" no matter what the tone is behind that question.
If you're curious, you can read more about my disabilities, unexplained symptoms, and some FAQ in this post. This is by no means exhaustive (I reserve the right to some privacy!) but I try to be transparent. I learned about disability, access, and intersectionality reading peoples' blogs online; I see no reason not to continue that free flow of information for others.
The Short Version
( Read more... )Physical Health Stuff
Stuff We Know for Sure
( Read more... )Stuff We're Unsure About
( Read more... )Mental & Neurological Stuff
Stuff We Know
( Read more... )Stuff We Don't Know For Sure
( Read more... )Frequently Asked Questions
( Read more... )As always, if you have questions: comment here, message me wherever you find me, or send archaic messenger birds!