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Amanda ‘science fan girl’ Morris (she/her) 🤟🏻🌵
@AmandaMoMorris
Former disability reporter for The Washington Post & inaugural disability reporting fellow for The New York Times. Proud hard of hearing CODA. 🤟🏻
Posts
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    Woke up today to find that my partner was missing & got a note from a “concerned friend” asking me, an “esteemed detective” to meet them in New York to solve the case. There was also an enclosed train ticket. I love a good mystery. My weekend is about to get interesting.
    A black suitcase sitting in the middle of an apartment foyer with an envelope on top of it. The envelope has a handwritten scrawl that says “READ ME!!!”
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    One source who has an immunocompromised, high-risk daughter, whom I interviewed for a story, has just told me that her daughter caught Covid and was life flighted to the hospital in critical condition. This pandemic is still very real & still very, very scary for some.
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    A lot of disabled people have posted recently about how Twitter helped them pay their medical bills, find community, get diagnosed, or support their businesses, among many other things. For them, Twitter isn't just a social media platform. Many said it's a "lifeline."
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    !!!!!!!!!! My first A1 !!!!!!!!!!!!!! (& its above the fold)!! My brain is short circuiting because I still can’t believe my work is on the front page, but you can read the story here: nytimes.com/2022/01/03/us/…
    Amanda’s hand lays flat on the front page of the front page of the New York Times newspaper. This is the January 4th edition and it lays flat on a kitchen table. To the top right of her hand, Amanda’s story, titled “When 3 Shots Don’t Do the Trick, Some Try 4 or 5,” lies above the crease where the newspaper folds in half. The story is centered on the page and near the top.
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    I’m excited to finally announce my next step! I will be joining the New York Times to report on national disability issues: a dream job on a beat that carries so much personal significance. This one is for you mom & dad: thank you for everything. 💕
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    Replying to @AmandaMoMorris
    She's 8 years old, has an autoimmune disease and takes medications that suppress her immune system. She told me her favorite color was "Galaxy," which she described as "pink, purple and blue mixed together." When she grows up, she said she wants to help kids like herself.
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    After four years of dating, my mother finally gave my partner a name sign!!! (It’s a big deal)
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    Secret's out!!! 🥳🥳🥳 I'm so, so thrilled to announce that I'll be starting a dream role with the Washington Post next week, covering disability and health under a new team led by the amazing @taraparkerpope. Gratitude barely begins to describe how I feel.
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    MY FIRST STORY FOR THE WASHINGTON POST IS ALSO MY FIRST A1 !!!!!!!!!!!!!!!!!!!! 🥳🥳🥳
    The front page of the Saturday, Sept 17 edition of the Washington Post. In the middle left of the page, Amanda’s article titled “Uneven battery policies leave wheelchair users stranded” appears with a photo of Rep. Jim Langevin in his wheelchair and her byline.
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    As a CODA, I know firsthand how many in the deaf community feel compelled to watch any movie or show with deaf characters & almost always have mixed feelings afterward. It's a privilege to share a few thoughts from deaf & CODA people in my latest:
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    Replying to @AmandaMoMorris
    I wrote about the impact that current changes at Twitter could have on this community, which will likely be even more pronounced in an ongoing pandemic where some are still isolating in their homes, socializing mainly online: