So floored to see so many new followers! I'm @Nicole_Lee_Sch and I (for now) run the social media acct for the DAC. Collectively, our membership provides support to disabled individuals of higher ed. If you'd like a link to our server feel free to DM 1/7
Also check out our website where we have basic resources on accessibility and guest blog posts written by our membership. If you'd like to write something about disability and higher ed feel free to reach out! 2/7
Hopefully our membership will continue to grow throughout 2021. As the founder of the DAC I am so excited to see all that we have done, and to imagine all that we might do. Our members have supported one another in so many ways! 3/7
We have daily work accountability buddies and we've hosted mock job talks and conference talks. We have a disability studies discussion group and hopefully we'll be offering some skill sharing workshops this spring. 4/7
It was my goal to build a space for disabled academics to unabashedly be themselves and discuss the struggles and successes of navigating the academy. I'm constantly floored by the kindness, ingenuity, and helpfulness of our members. 5/7
The DAC has been the most successful creation of my graduate school career, and now it's grown far beyond me and its original small circle. Every member has been so incredibly giving of their time, empathy, and experiences. 6/7
The academy will doubtlessly throw us challenges in 2021, as it always does, but I feel ready to take them on with the DAC membership by my side. I'm excited to see what barriers we might tear down this year, and what ways well grow together. To 2021. 7/7
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This year is a good reminder that some students don't return to spring semester "refreshed" or ready to go. For students with complex chronic illnesses and disabilities, winter break is often a time to play catch up with their medical team or a time to try to secure a dx. 1/9
Students need those dx to get accommodations, but it's incredibly hard to get them. The costs for testing and appts can be excessive, specialists may be far away, and getting the right Dr is hard. These extended hospital closures are creating new barriers as well. 2/9
Over break so far I have 1. Fainted during bloodwork 2. Found I have double the inflammatory markers of an average person (Drs still not totally sure why) 3. Been dx with small fiber neuropathy 4. Undergone a punch biopsy 5. Been given a preliminary RA dx. 3/9
I'm not celebrating #DisabilityDay today. I'm not going to post stats again or raise awareness about inequality in higher ed. I'm not going to write again and again about how every disabled student faces discriminatory processes in higher ed and the job market. 1/4
Quite frankly I'm tired of awareness days. I'm tired of proving my humanity. I'm tired of compiling evidence of my oppression to try to convince you to care. As a disabled person, I deal with ableism every single day. I don't want to partake in a day of awareness. 2/4
Because for me awareness needs to happen every single day. Because for me awareness doesn't better my life. I need allies to take action. I need allies who recognize my oppression before it happens and call it out when it happens. 3/4
Boosting so all our members can answer! I have #EhlersDanlos so I have a really hard time hand writing. I try to limit my writing tasks because my hands cramp a lot. Investing in silver ring splints made it so so so much easier for me to type comfortably without dislocating.
I also was incredibly lucky to have a friend offer to help build me a desktop! Throughout grad school I had a $150 acer chromebook that I'd take to class with me. I loved it - it could be switched to tablet mode, it was fine for attendance and class discussion when teaching.
And it was lightweight. Made such a huge difference when traversing my campus. Then I have a nice desktop at home that's built to run with my access needs in mind. My friend recommended decent screens, and I set it up as a dual monitor.