Lisa McCorkell
formerly a patient-led research collaborative co-lead, always a co-founder | MPP | she/her | natures 10 in 2022
@kdurquiza.bsky.social
Causing good trouble at the nexus of people, climate, public health, economic security and art. Co-founder @MarkedByCOVID. Goldman School. Lux et veritas always.
@jesslee.bsky.social
Human rights attorney working for equity in education and the workplace. Black, Muslim, feminist, disabled, queer, golden ear. The one who always makes it weird. (Formerly JessLeeEsq)
@publichealthaction.bsky.social
We're creating tools and resources for folks with COVID and Long COVID, and we advocate for clean air and prevention of airborne diseases. publichealthactionnetwork.org
@erictopol.bsky.social
physician-scientist, author, editor https://www.scripps.edu/faculty/topol/ Ground Truths https://erictopol.substack.com SUPER AGERS https://www.simonandschuster.com/books/Super-Agers/Eric-Topol/9781668067666
@weselymd.bsky.social
Husband & Dad. ICU Doc. Vanderbilt. @CIBScenter studies Covid & Long Covid, ICU Survivorship, Dementia, Delirium, PICS. Fighting misinformation. Posts my own. Still learning.
@mileswgriffis.bsky.social
Co-founder/editor @TheSickTimes.bsky.social Columnist @HighCountryNews.org miles@thesicktimes.org #LongCOVID
@yogafogie.bsky.social
DMV native. COVID long hauler. Patient-Led Research Collaborative.
@longcovidsos.bsky.social
UK based charity advocating for those impacted by #LongCovid Recognition - Research - Rehabilitation www.longcovidsos.org info@longcovidsos.org Charity reg no 1199120
@chromatowski.bsky.social
This account will prob be about biomed research—complex chronic illnesses and Covid—w/some material on disability justice and organizing. ME ‘05, LC ‘23, many of their friends along the way. Very severe (FUNCAP 0.8), thanks for your patience.
@leticiasaurus.bsky.social
Co-lead & patient-researcher @patientled.bsky.social. Biologist, PhD. Brasileira.
@ginaassaf.bsky.social
Participatory Design & Research/Strategy - Tech for Social & Global impact. Co-leading #longCovid @patientled research and Managing @obidigital
@julialmv.bsky.social
Long COVID patient-researcher @ Scripps Research & Patient-Led Research Collaborative
@protectdemocracy.org
We are a nonpartisan, nonprofit group working to prevent authoritarianism. This account is owned and operated by Protect Democracy United. Follow us on other platforms ➡️ https://protdem.org/m/stay-connected
@carlbergstrom.com
UW biology prof. I study how information flows in biology, science, and society. Book: *Calling Bullshit*, http://tinyurl.com/fdcuvd7b LLM course: https://thebullshitmachines.com Corvids: https://tinyurl.com/mr2n5ymk I don't like fascists. he/him
@realcatbrooks.bsky.social
Executive Director, Justice Teams Network and @aptpaction.bsky.social | Host, Law & Disorder on KPFA Radio | Organizer, Strategist, Columnist, Artivist, and Playwright, Director and Actress | catbrooks.org
@vashetc.bsky.social
ph.d. perpetually horizontal. writer, researcher. ✍🏽 v ash e t c [dot] com — vashetc.com profile ID: brown person poses in wheelchair in front of a wall of pink paperflowers. banner: lake & mntn @ sunset. There’s a silhouette of a family in the water
@janetdafoe.bsky.social
ME/CFS patient advocate and caregiver. Mom to Whitney. Spouse of Ron Davis. Child Psychologist.
@anamariecox.bsky.social
Writer, host of podcasts: sci-fi deep dive "Space the Nation" & mental health convos at "Another Day." Leading The Third Story Workshop. More at anamariecox.com
@thesicktimes.bsky.social
A nonprofit news site chronicling the #LongCOVID crisis. Founded by journalists @BetsyLadyzhets.bsky.social & @MilesWGriffis.bsky.social Website: thesicktimes.org Newsletter: thesicktimes.org/newsletter Donate: the-sick-times.fundjournalism.org
@emilyesfraser.bsky.social
Former doc filmmaker/cinematographer/teacher, current full-time sick person, occasional poet
@tinu.bsky.social
It is I, trouble maker Tinu, Empress of Twerk, Thirst of my Line. Take a pic it's me. I have a weird Leukemia and Long COVID. So forgive me for being MIA for days or months, it’s medical exhaustion.
@adamswendya.bsky.social
Scientific/Medical Innovation Formerly Research Grant Director, Bay Area Lyme Foundation
@taylorlorenz.bsky.social
Subscribe to my tech and online culture newsletter UserMag.co Listen/watch Power User podcast on all platforms!!
@jessieharney.bsky.social
AP Public Policy & Administration @ Colorado State, justice system reform, will favorite all dog GIFs
@filowenstein.bsky.social
writer + journalist covering health justice, wellness culture, LGBTQ+ stuff + more... https://www.fionalowenstein.com/ The Long COVID Survival Guide: https://theexperimentpublishing.com/catalogs/fall-2022/long-covid-survival-guide/ they/them
@kcoombs.bsky.social
Plants and mushrooms ❤️🌱☘️🍄, Lyme, ME, Peer Support #LongCovid, #LongCovidKids https://padlet.com/krcoombs/long-covid-associated-conditions-2eb2h1agyvdeyffh
@meactnet.bsky.social
A global network of people empowering one another to fight for equity for myalgic encephalomyelitis. Home of the #MillionsMissing linktr.ee/meactnet #pwME #MyalgicEncephalomyelitis #LongCovid #MECFS #ChronicIllness #DisabilityJustice
@patientled.bsky.social
Patient-Led Research for #LongCovid! http://patientledresearch.com
@jannamoen.bsky.social
Postdoctoral scientist studying the neurobiology of #longCOVID in the Iwasaki lab @ Yale. Patient, scientist, advocate. | ♿🏳️🌈 | she/her My long COVID research newsletter: lcbreakdown.substack.com
@rhyothemis.bsky.social
~fluttering from topic to topic~ MLIS, MSc (marine biology) interests: art & architecture, biology & medicine, nature & environment, natural product chemistry, gardening, permaculture, reading, cats
@dysautonomia.bsky.social
We are the leading non-profit advocating for over 70M people around the world living with autonomic nervous system disorders. Research, Clinician Education, Patient Empowerment, Public Awareness & Advocacy is what we do. DysautonomiaInternational.org
@shelleyjules.bsky.social
MECFS from the long before times but not diagnosed for 23 years…LC since 2020 - interested in advancing patient led research (Renegade Research & Remission Biome) & all avenues that lead to effective treatments for everyone. She/her. Love is my language. 💖
@naomidharvey.bsky.social
Zoologist & veterinary research. She/her. 22yrs with #MEcfs Pro-vax but vaccine injured. Life on pause due to moderate/severe ME/CFS ♿️ Patient Expert in ME/CFS, POTS and syndromic Long Covid. Please excuse my typos.
@richellesepulveda.bsky.social
Long Covid, MECFS, ADHD, etc. Patient-led research is my jam. A bit obsessed with GIP.
@lizhighleyman.bsky.social
Freelance medical journalist. Science editor for @pozmagazine.bsky.social, Hep & CancerHealth. Words for @slate.bsky.social, Bay Area Reporter. Research beagle adopter. Socialists think I'm a libertarian, libertarians think I'm a socialist.
@sabrinapoirier.bsky.social
#CommunityEngagement Expert. Life sidelined by #MECFS #MCAS #POTS #Fibro #Gastroparesis + #MECFS & #LongCovid #ResearchPartner & #Advocate • Chair of #MedicalEducation Group • #PwME #Disability (Unceded) #Canada https://linktr.ee/sabrinapoiriercanada
@carriemcginn.bsky.social
Infection-associated chronic illness advocate | Life sidelined by #LongCovid #MECFS #POTS | #PatientPartner | MSc | Mom | She/Her | 🇨🇦 #Canada #Quebec #CovidConscious #StillMasking #MyalgicEncephalomyelitis #pwME #EMSFC #CovidLongue #CovidLong #pwLC
@elizabethlinos.bsky.social
Assoc Prof of Public Policy & Management, Harvard Kennedy School Faculty Director, The People Lab ElizabethLinos.com peoplelab.hks.harvard.edu
@julierehmeyer.bsky.social
Author of Through the Shadowlands: A Science Writer's Odyssey into an Illness Science Doesn't Understand. I mostly write about complex chronic illness and math. Bylines in NYT, WashPost, Discover, Wired, Slate, Stat News, Science News, lots more. She/her.
@mildtin.bsky.social
Usually a lurker, Chronically Online for #LongCovid and other #IACC | Australia
@longcovidjustice.org
We are leading grassroots efforts to confront the Long COVID crisis, while centering racial, social, economic & disability justice. Our work is done by and for chronically ill & disabled people, our families and communities. linktr.ee/longcovidjustice