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Freelance science & medical journalist | Bylines in Nature, Medscape, C&EN, Veritasium, ScienceAlert, The Guardian, ABC News, The Sick Times | http://frogsandstars.com (she/her)
Journalist, mom of three, and dog-lover.
Economics editor at The Bulwark. MS NOW (formerly MSNBC) anchor.
Previously WaPo op-ed columnist and NYT reporter.
Econ, politics, immigration, tax, etc. + occasional theater nerdery.
Equitable, accessible & affordable treatment for all. The Long COVID Campaign advocates for accelerated research & expanded support programs in U.S. & globally.
We are a progressive grassroots political party building a multiracial, feminist movement of working people. Text WFP to 30403 to join us.
linktr.ee/workingfamilies
Climate journalist, author, AT HOME ON AN UNRULY PLANET
http://madelineostrander.com
KSJ at MIT Fellow 2023-2024
Mastodon: @madelineostrander@journa.host,
@madelinevo on Insta
Journalist. Working on a book about grass.
Unofficial account exploring the intersection of biology, molecules, science, AI and protein folding with AlphaFold.
Globe-trotting, award-winning independent science writer in China | Words in @nature.com, @sciam.bsky.social, National Geographic and more | Writing a book on emerging diseases for @scribnerbooks.bsky.social | Ex: @ksjatmit.bsky.social, @nature.com
Retired writer of science who still does some freelance. Lover of science, dogs, long walks at the beach and mountains, all things nature, reading science-related books and mysteries and well-written novels. SCONC and NASW member.
Weβre a community of Covid longhaulers who have been brought together by this illness. We share the stories of folks who have been through it, who are going through it, and how theyβre surviving it. #LongCovid #CovidIsntOver #CovidIsAirborne #CovidSky
Science News from Academic Journals etc.
News and information about interventional trials for Long Covid, ME/CFS, POTS, and other post-viral illnesses. Message or tag me if youβre in a trial or otherwise have information to share.
staff writer @newrepublic.com / author A WOMAN IS AGAINST THE LAW (@littlebrown.bsky.social, 2KTK) + PLAYING THE WHORE (Verso)
// melissagiragrant.com
Β» melissa@melissagira.com
Β» tips (encrypted): melissagira.01 on Signal
@nyguild.bsky.social member
Once a lawyer, then a travel writer. Now disabled, writing about curiosity & health.
Travel writing & celiac translation cards: legalnomads.com
Best things I read each month: jodiettenberg.substack.com
MCAS, meditation, & health: jodiettenberg.com
PhD MICROBIOLOGIST
AMR, Biofilms, Phage Therapy, Drug Design and some other similar topics π€«π
@remissionbiome.bsky.social team
@renegaderesearch.bsky.social volunteer
DEFEND SCIENCE, RESIST IGNORANCE π«
#SonKale06
Ankara
Coming in early 2026: KEYWORDS/KEYIMAGES IN GRAPHIC MEDICINE
Current projects: #IllnessPolitics, chronic forms, & multi-modal pedagogies in action. Author of ILLNESS POLITICS & HASHTAG ACTIVISM, TREATMENTS, & INDIRECT ACTION.
Blogging at: lisadiedrich.org
Parisienne Buffalonian linguist spoonie mom. http://bcopley.com "The line separating good and evil passes...right through every human heart." -Solzhenitsyn
Professor of Communication and Psychology at BI Norwegian Business School and the University of Oslo
Past Yale, Harvard, UiB. Editor-in-Chief at Advances.in
Father. Views are my own.
creator of longcovidstudies.net, member of the Patient-Led Research Collaborative, and freelancer.
Policy. Advocacy. Public Health.
Health Equity. SRHRJ. COVID-19.
New Yorker. Midwesterner.
She/her.
Theater/film/music/book lover. Lipstick hoarder. Ukrainian-American. Life on pause due to #LongCOVID of the #MECFS / #POTS / #MCAS variety. Left-ish libertarian-ish. Suffering NY Rangers fan. Audiobook connoisseuse.
#MECFS #MILLIONSMISSING #MEAwareness
#PEM #POTS #MCAS
#PostCovid #LongCovid
#TeamWissenschaft #GdB
https://www.mecfs.de/was-ist-me-cfs/
My #LongCovid is mainly #PEM + #POTS + #MCAS
Facilitator | Researcher | Advocate
Author of The Long Covid Symptom Diary, now available in EN, FR, DE, NL & ES! - www.ddxpublishing.com
Here for the latest research + advocacy for Long Covid, ME/CFS, dysautonomia, connective tissue disorders, etc + disability justice community. Former HCP.
Chronically ill, autistic, demi/greyace
(mostly in bed, mostly homebound)
ME/CFS and probable LC
π·π·π·
Interests: climate, COVID, disability justice, parenting
Ltd cog energy, don't tend to follow back.
Toronto, Canada
She/her/they
Sustainability science studies on hold because of POTS + Long covid / suspected ME. Previously interesting, now mostly into resting.
Here to connect with other sick people and for science stuff.
#MEActionMaryland
Maryland chapter of the #MEAction Network: advocacy, education & support for people with Myalgic Encephalomyelitis #MECFS & complex chronic illnesses in MD/DMV
https://youtube.com/@meactmaryland
https://linktr.ee/meactmd
Postdoctoral scientist studying the neurobiology of #longCOVID in the Iwasaki lab @ Yale. Patient, scientist, advocate. | βΏπ³οΈβπ | she/her
My long COVID research newsletter: lcbreakdown.substack.com
#MyalgicEncephalomyelitis #pwME #SevereME #HyperPOTS #MCAS #PEM #PostExertionalNeuroImmuneExhaustion #PostExertionalSymptomExacerbation π·
My body has given up but I haven't...
Bed-tethered disabled Advocate on hiatus (but RESISTing) due to severe ME & LC & comorbids. Co-founder #MEAction Maryland.
Orioles/Ravens/Caps fan. She/her
Long Covid, ME/CFS, POTSβ¦. For now
#AssociateProf #CompBio #Omics #WomenInScience #LGBTQ+Ally #Scottish #PrecisionMedicine #HealthCare #MDx #ME/CFS #RareDisease #Informatics #SciFiNerd #LongCovidAffected
sites.uab.edu/cgds/ she/her
ME/CFS San Diego, a 501c3 public charity, is working locally to raise awareness of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), to help educate healthcare workers and researchers, to increase access and support for ME/CFS patients.
Reformed journo/editor, now working in health comms. Fighter of injustice in all its forms. Advocate for better research & support for ppl w uninvited friends POTS, ME/CFS, MCAS, LC, EDS, SjD, AnkSp plus other misunderstood AI conditions.
DMV native. COVID long hauler. Patient-Led Research Collaborative.
Long COVID, mild, since Apr 2022
ME / Long COVID diagnosed May 2024
Long COVID patient-researcher
@ Scripps Research & Patient-Led Research Collaborative
I'll "tweet" here about the things I don't like if the other app goes down
One of the #MillionsMissing with #LongCovid #MECFS JohnVsJon.com // Once a radio and podcast producer, always a Transom alum
π· Long covid is common π·
Wife/Mother, Science Writer, PT, HC Admin, Disease Detective, Voracious Reader, Connoisseur of Coffee, Graduate CSUN, Olive Farmer, HHS 2019-2022 Tick-Borne Disease Working Group, CDC Fdn ICUE patient advocate.
she/her | βοΈ | copywriter & π©΅ @ctpublic.bsky.social social media editor π©΅ Anime & Cartoons | ζ₯ζ¬θͺOK | Long Covid Mar 2022 | I complain often β¨πΊπ§‘ #CovidCompetent
ME patient, art appreciator, advocate, mother.
Author of IN GOOD HEALTH: Uncomplicated, Allergen-Aware Recipes For a Nourished Life
instagram.com/the.rachel.riggs
#EDS #MECFS #Food
#paleo #glutenfree #dairyfree
Writer / editor / photographer / full-time sick person. Cinema lover, cat-and-dog person, mostly horizontal. π
#MECFS #hEDS #HSD #POTS #MCAS #CCI #CSFleak
@wandering on Instagram βπ»
Disabled with Long Covid 51+ months
Long COVID Researcher @sfu-fhs.bsky.social
Masterβs Student @sfucmns.bsky.social writing on biopolitics & Long COVID
kaylijamieson.notion.site/research
Assistant professor of economics on medical leave from Northeastern University; macroeconomics, growth and development. Severely ill with MCAS/POTS/EDS/ME. Catholic convert who loves the balance of faith and reason. Native Oregonian.
In LongCOVID/M.E. hell looking for a way out! First wave Longhauler.
Trying to get my personality back from the disease.
Very cute dog.
MECFS from the long before times but not diagnosed for 23 yearsβ¦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. π
β doktora | research+policy | perpetually horizontal
IDβs: Brown skin woman w/ curly hair, wearing a brown tube top, smiles. Banner - Sepia picture of a couple getting married w/ family around them.
vashetc.com | restandmecfs.com | survivorsandallies.com
Salty | #LongCovid,#POTS & #ME | Books, Music, Food, Art #ATXRE | Excuse my typos
We are living in a choose-your-own dystopian novel
Silly Chicago girl, marketing professional, long covid patient. No DMs unless you donate to the mutual aid I repost. π
Novel coronavirus looking for friends. Always evolving. Pronouns it/its.
Molecular biologist and science educator putting science in your hands as President of @TheScienceHaven. All views are my own. Also known as Dr. Raven the Science Maven :)
Virologist at UNC, travel and food lover.
#JohnVsJonVsME campaign to get John Oliver or Jon Stewart to bring the awful history of #MyalgicEncephelomyelitis #GreatestMEdicalScandal to light
JohnVsJon.com
Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.
COVID-19 Longhauler Advocacy Project is a patient-led #LongCOVID 501(c)(3).
Visit longhauler-advocacy.org/lcamonth26 to learn more and take action this #LongCOVIDAwarenessMonth.
#LongCOVIDAwareness #OneInfectionAway
US ME patient advocate. Mother of a son and his wife who have ME and Long COVID. My other focus is on US politics and what's coming
π΅ Founder & Pres. @C19LAP https://www.longhauler-advocacy.org
π΅ Pw/ #LongCOVID, #IACCS, #Disability
π΅ Fmr. Firefighter/Paramedic
π΅ Fmr. Educator, Coach, & Dir. of Athletics
π΅ B.S. (ex science & health promotion)
π΅ #StillCOVIDING #COVIDConscious #Mask
Participatory Design & Research/Strategy - Tech for Social & Global impact. Co-leading #longCovid @patientled research and Managing @obidigital
indie journalist
Signal: Lygia.65
(editor, producer, en ES & EN)
cover: Latine, LGBTQ+, health stories +more #DisabilityJustice.
disabled. queer. #LongCovid + #ME.
lygianavarro.com
contributing writer @discojourno.bsky.social & @thesicktimes.bsky.social
Founder @ CrunchME | Creating the evidence & insight base to crunch infection-associated chronic conditions π
#MECFS #LongCovid #IACC #PAIS
π https://crunchme.org/
https://renesugar.substack.com/
~ Life stolen by MEcfs-hEDS-fibro-POTS-&c; FT sick since 12/2014
~ #LiveInBedButIAintDead
~ When brain & body behave: Chronic Illness Advocate
~ Discworldian, Browncoat
~π±(x3)π’ππ»π·πΈππΌοΈ
~ she / her ~ Love Is Love β€οΈππ§‘ππ©΅πππ€π€π©Άπ€π©·
https://linktr.ee/thedsavannah
Cherokee writer and journalist, check out my substack: https://gohini.substack.com/
Author of BY THE FIRE WE CARRY out now https://www.harpercollins.com/products/by-the-fire-we-carry-rebecca-nagle?variant=41322925359138
http://heymp.com.au/sickandtired
http://change.org/LongCOVIDInquiry
http://www.instagram.com/sickandtiredaus
https://x.com/JordanCrane2?t=qsba4zmDGLFUas_tcP_pnw&s=09
https://www.facebook.com/share/19nSvtGPNz/
501(c)3 transforming how #LongCovid, #ME/CFS & Lyme+ are studied, diagnosed, and treated. Leading the #LongCovid Research Consortium.
Calling for an NHS that's there for Long Covid & Myalgic Encephalomyelitis (ME) | www.thereforme.uk
Senior Fellow in Public Health and Journalism, Center for Global Public Health at the University of California, Berkeley. I blog at Virology Blog (virology.ws). My academic position is largely funded by donations from patients. davetuller@berkeley.edu
Living with ME/CFS since 1991. Here for the long haul. I am one of the #MillionsMissing.
#MEActionNetwork health activist. Patient, project manager, translator & polyglot. βπΎ #Stoic #WoC @NLizaki & @SaveLizNevra on Twitter. #MyalgicEncephalomyelitis since 6. 28 now. #PMDD #hEDS #POTS #MCAS #LongCovid
CrunchME is a patient-led organisation, creating the evidence and insight base needed to crunch infection-associated chronic conditions (IACCs), including #MECFS and #LongCovid.
π https://crunchme.org/
Riverside, CA
Equine History Collective
Renegade Research
https://katboniface.wordpress.com/the-glutamate-boss/
Physician/Internist focused on complex illness including Long Covid, ME/CFS, dysautonomia/POTS, MCAS, connective tissue disorder, and of course SIBO/Leaky Gut.
And sadly, the ongoing coup.
Neurologist and more. https://www.atria.org/doctors/dr-ilene-ruhoy/
Research: Ultrahigh-energy cosmic rays with #machinelearning at #TelescopeArray. Past: Science editor and #ScienceWriting faculty at Johns Hopkins. Essays: The Atlantic, Orion, Aeon, etc. Book: #SubatomicWriting (JHU Press). I worship MacGyver and Picard.
health journalist. Focus on aging, caregiving, policy, and more. Grandma. Dog mom. Partial to strong coffee, dark chocolate, red wine. AHCJ, ASJA, JAWS.
Director, CIDRAP
New episodes of our podcast on the latest infectious disease threats: https://www.cidrap.umn.edu/osterholm-update
Health journalist (AARP; Prevention; US News; WSJ), SELF survivor, mom of 20-something, amateur genealogist.
Worker-owned, community-oriented intersectional feminist journalism to unfuck your algorithm.
π theflytrapmedia.com
Men Yell at Me. I write books.
Physicist, airburst specialist, planetary defender, & CSI Fellow. I'm critical of the Younger Dryas impact hypothesis (YDIH) which has strong links to global warming denial, creationism, & pseudoarchaeology. It relies on misinformation & fake peer review.
Science writer. Communications director #WSUVetMed. NW Public Broadcasting voice. Yoga teacher. Opinions mine.
vetmed.wsu.edu
nasw.org/users/mgossard
Super nerd here to spread the joy of learning.
π Publisher @quantabooks.orgβ¬ at @simonsfoundation.org
βοΈ Founding EIC @quantamagazine.bsky.social
πΌ Prev @nytimes.com, CASW, CUNY J-School
π Books https://mitpress.mit.edu/author/thomas-lin-2820/
π΄πΌπΎβοΈ
Reporter at The Transmitter | PhD, Neuroscience from UPenn π§ | Prev: Science, The Open Notebook & β21 AAAS Mass Media Fellow at STAT News | Boricua π΅π·
Solve M.E. is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid, and other infection-associated chronic conditions.
The Long COVID Resource is dedicated to providing information and resources on Long COVID and summaries of studies.
Long COVID Resource: https://longcovidresource.com
