"Associations between Long #COVID and challenges related to housing stability and home accessibility highlight the need for systemic changes, financial support, and advocacy."
Looking to support a fellow Autist whilst navigating your own ASD journey?
I invite you to follow my Autistic Diaries Blog!
I share insight on my own personal experiences as a Chronically ill Autistic person. My life, my diagnosis, and some information about Autism and my chronic illnesses (Coeliac and Graves', as well as POTS, and other conditions)
I’ve tried every level of government and they simply won’t help. Ask people in real life if they have somewhere for me to go. Is anybody an #advocate? I need help.
"Getting tenure was so profoundly destructive to my health that it prepared my body for severe #LongCovid one Latina researcher in the humanities tells Nature. “I feel like my academic job demands my death.”
Question: Anyone who specializes in indoor air quality able to take a look at something? Used @cleanairstars tool to ask for filters for a classroom and was told it's not needed bc HVAC is ASHRAE 62.1. Thanks!
Parent or teacher interested in a Covid safe school?! Centered in disability justice. One is forming in MA/RI, location TBD. Email for more info or with questions!
My new paper on welfare reform politics and the risk of #longCovid following the trajectory of stigmatised conditions such as #MECFS. Includes health & disability White paper, macro-politics of the PACE trial, psy-corporate-state alliances etc.
Hunt outlines the history of the construct of "‘deserving’ and ‘undeserving’ impairment, ill-health and related disability" that causes problems for people with ME/CFS, and likely also for people with #LongCOVID.
Maybe you've heard that people can be nonverbal or nonspeaking. But did you know there are many ways to be semi-speaking? I'll list some I just learned about below. Sing out if any of these resonate with you! @autisticadvocacy
@autisticadvocacy Expensive speech is the newest term for me. It resonates so deeply as someone with energy-limiting illness. I imagine many people with #longcovid might resonate with this one as well.
My scooter doesn’t have a tight turning circle so using it on a bus is a lot harder than my powered wheelchair but after my lesson today I feel confident enough using it on buses 😀
Does anyone know what happened to the Hummingbird Foundation for ME website? They had a really nice symptom severity scale that I used to point people to, but the whole website is gone now.
Does anyone know whether it would be okay if I post the scale directly in the MEPedia, since the link is broken?