Emerge Australia
@emergeaus
Supporting Australians living with ME/CFS (mylagic encephalomyelitis / chronic fatigue syndrome). Education | Research | Advocacy | Support Services
ID: 102267014
https://www.emerge.org.au/campaigns/eofy-appeal-2023/ 06-01-2010 04:08:53
4,4K Tweet
2,2K Followers
517 Following
Tom Kindlon
@tomkindlon
With ME 36 years (30 yrs severe). 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 28 yrs
Anika Wells MP
@anikawells
Trying to be a good ancestor. Australian Minister for Aged Care and Minister for Sport. Member for Lilley on Brisbane’s Northside.
Kimberley Kitching🇦🇺🦘
@kimbakit
🔎Labor's Shadow Asst Minister for Government Services & NDIS 🌏Chair Senate Foreign Affairs References Committee 🏞Senator for 6.7 million Victorians #auspol
☔Jason Murphy
@jasemurphy
Journalist and economist. Author of the book Incentivology. amazon.com.au/Incentivology-…
Geoff 💙
@geoffers1967
Bit poorly. Campaigning for ME Research/Awareness. Music ⭐️ Films ⭐️ Sport ⭐️ Comedy ❤️ Nieces ❤️ Animals ⭐️ Spurs ⭐️ Thomas Dolby ❤️ Janey ❤️
@richardvallee.bsky.social
@richardvallee
I play language. Mostly irreverent. Debugger. AI. Global warming. Integrity. Healthcare. Science. We are actually in the pre-truth era. #MillionsMissing
Jennie Spotila
@jspotila
Writer/ME Activist. We are more than our disease.
Jac
@jac15_9
We are all in the gutter, but some of us are looking at the stars. - Oscar Wilde. 💙❤️💛@Adelaide_FC She/Her #eds #mecfs • Find me on bsky jac159.bsky.social
Solve ME/CFS Initiative
@plzsolvecfs
Making ME/CFS, Long Covid & associated conditions widely understood, diagnosable, & treatable. #SolveME #MECFS #LongCovid Donate @ ow.ly/jQji50Srbuv
Melissa Sweet
@melissasweetdr
Journalist sharing news re health equity, First Nations health, climate justice, health in all policies. See @CroakeyNews @WePublicHealth. She/her.
ME Association
@meassociation
We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RPs do not necessarily mean endorsement.
Australian Department of Health and Aged Care
@healthgovau
Updates, news & information from the Australian Dept of Health & Aged Care. Email questions: [email protected] Email media enquiries: [email protected]
ThinkGP
@think_gp
ThinkGP offers free content for busy healthcare professionals to keep their knowledge fresh and meet their CPD point requirements. @rxglobal_
Nick Rheinberger
@nickrheinberger
ABC radio presenter, podcaster, comedy sketch and song writer, professional sceptic who cries easily.
Bloom
@bloomstweet
SINGER • SONGWRITER • NATIONAL TOURING ARTIST
Dr Keith Geraghty
@keithgeraghty
Research Fellow | Primary Care, Medical & Health Psychology | People-focused, evidence-based researcher & chartered psychologist |@FBMH_UoM, @PrimaryCareMcr
Clara Valverde
@enfermarebelde
Sick anarchist. Rebel writer. Retired nursing professor #SevereMECFS #MillonsMissing #carnival4david #FridaysForFuture #MareaBlanca #MemoriaHistorica
Tracey Spicer AM GAICD
@traceyspicer
Global keynote speaker. Multiple Walkley Award winning journalist & author. Former TV news anchor. Buy my book about AI bias here: tinyurl.com/2b3wzh8c
CapitalHealthNetwork
@capitalhealthnw
Capital Health Network is the ACT’s primary health network. We advance how health care is delivered in Canberra.
Adj Prof Karen Price, 20-22 RACGP Past Prez
@brookmanknight
GPDU co-founder Monash Adj Professor. GP. President RACGP (2020-22) Melb Uni board Enterprise & Innovation, WONCA exec. AMA GP Chair, MBBS, FRACGP, PhD, GAICD
Anil van der Zee ©
@anilvanderzee
Former professional ballet dancer | Bed/sofa-bound M.E. patient | Using Twitter to raise awareness for #MyalgicE | #IACC #art2cureME #pwme #millionsmissing
Skedulo
@skedulo
Champions of the Deskless Workforce
Dan Wyke 🦠➡️🧠🔥
@dan_wyke
M.E. inactivist, person-centred counsellor (see link), recovering poet (Rack & Waterloo Press)
David F Marks
@david_f_marks
Author. Follow, follow back #science #wildlife #nature #photography #homeostasis #GeneralTheoryofBehaviour #psychology. Follows and RTs are not endorsements.
Juan Siôn Castillo-Glas
@inflammasean
Was mainly #MECFS, #PASC, chronic illness & science account. Any kind of nonsense now; just trying it out. Don't cry, laugh my sweet children 💔😅
Casey Stoner AM
@official_cs27
2x MotoGP World Champion, keen fisherman and proud dad
Jacob Teitelbaum, M.D.
@endfatigue
Best-selling author Jacob Teitelbaum, M.D. combines the best of natural & standard medical care for #pain, #chronicfatigue, #sleep, #fibromyalgia, & #longcovid.
davidtuller
@davidtuller1
Senior Fellow in Public Health and Journalism, Center for Global Public Health, UC Berkeley. My academic position is largely funded by donations from patients.
Open Medicine Foundation
@openmedf
OMF is fundraising to support open, collaborative research to find effective treatments and diagnostic markers for ME/CFS, Long COVID, and related diseases.
Katy B
@katybruce108
Myalgic Encephalomyelitis ME + POTS 38 years Donor to the @mecfsbiobank for 10 years & @DecodeMEstudy Please watch dialogues-mecfs.co.uk/videos/ #pwME
Dr Maria Alejandra Pinero de Plaza, PhD
@mariaapinero
A scientist committed to facilitating healthy living and better public health services through knowledge translation and health research. Research Fellow.
Michael VanElzakker
@mbvanelzakker
Neuroscience researcher @MGHMartinos / @HarvardMed and @PolyBioRF, researching #MEcfs, #LongCOVID, & #PTSD. (all opinions are my own)
Rivka
@rivkatweets
Activist/Organizer: ChronicIllness, disability, ME/CFS, Lyme, LongCovid, women | Writer: WashPost, MarieClaire, NPR, Ms, Newsweek | Playwright: Many productions
Hilary Harper
@hilarykharper
ABC RN Life Matters host, MC, YA and fantasy fan, food addict, Melburnian. Retweets: maybe outrage, fascination, confusion? Not endorsement.
Jacinta Parsons
@jacinta_parsons
ABC Radio Melbourne Afternoon host. Author of Unseen - the secret world of chronic illness. Any posts or likes do not reflect the views of the ABC.
PwME 4 bioMEdical research
@valebodi
Surviving #MyalgicE #AAG to tell the story, patient&advocate w/ a JD, into: MEdicine, Social justice & the Arts, Human neutrino/MEdical apolide/gnarled Pacer
#MEAction Network
@meactnet
A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing linktr.ee/meactnet
IMPACT
@impactdeakin
This account is currently not actively managed. You can find us on LinkedIn at @IMPACTDeakin.
Janet Dafoe
@janetdafoe
Caregiver for very severe ME/CFS son, advocate and fundraiser for End ME/CFS PROJECT at OMF and CFSRC at Stanford. The rest of my life is on hold...
Zoe Simmons | she/her
@itbeginswithz
Award-winning journalist. Editor. Copywriter. Author. Chronic pain warrior. Mental health & disability advocate. I write to make a difference. #AmQuerying
Monika Dryburgh (she/her, they/them)
@monika_dryburgh
#NEISVoid-dweller; recovering ex-PhD student. I ❤️ (teaching abt) words #ActuallyAutistic #EDS #hypermobility #POTS #autoimmune #IBD #arthritis #endo ?#MCAS
Chloe Strahan
@chloe_strahan
Producer at @abcmelbourne. Views are mine. [email protected]
Milli
@milliisonair
Love live but feeling trapped in my body due to ME. Follow ME (MilliOnAir) on Bluesky: @milliinmotion.bsky.social
Ken Walder
@ken_walder
Willow the seeker 🪐🌝🛸🌲
@owlsandtea
I am passionate about social justice and our planet. I am a survivor of child abuse,I love to do art and stand up for the voiceless. I live on Peramangk land.
ME/CFS News
@mecfsnews
News, interesting information and commentary on ME/CFS. Mostly inactive these days.
Tapanui 'Flu | @tapanuiflu.bsky.social
@tapanuiflu
Kiwi Grandmother | New Blogger 2024 | #MyalgicEncephalomyelitis since 1983 | #TapanuiFlu epidemic | Mostly housebound | On welfare | #LongCovid ally.
ME Foreningen
@meforeningen_dk
ME Foreningen er patientforening for sygdommen ME (Myalgisk Encephalomyelitis) #MECFS #sundpol. Kontakt [email protected]
Sherryn
@sherrynh12
ME/CFS Australia
@mecfsaustralia
ME/CFS Australia is the national peak body representing all people in Australia living with or affected by ME/CFS. Our members are several ME/CFS organisations.
Astrid Spoor
@astridspoor
Life on hold since 1995 due to ME, Myalgic Encephalomyelitis, a neurological multisystem disease... means living on the square centimeter (in time and place).
Daniel Missailidis, PhD
@danmissailidis
Researching the cell biology of PD, ME/CFS & Long COVID at La Trobe Uni in Melbourne, Aus. Papers: scholars.latrobe.edu.au/d2missailidi/p…
This Is Visibility
@thisvisibility
Raising awareness and sharing stories of #hiddendisability and #disabilities | Sign up below
ME Research UK - Science
@meresearchuksci
ME Research UK is a charity which funds biomedical research worldwide into ME/CFS. Account run by our Science & Engagement Director. Funding call info below!
Relevium Documentary
@releviumfilm
The story of one doctor and her understanding, treating, and acknowledging people with ME/CFS and FM.
YME
@yme15758406
Advocacy for Young People with ME Australia
Dr Heidi Nicholl
@drheidinicholl
PhD ethicist. President Humanists Victoria. Spent time at Yale and UCL. I've been CEO of a few things. Kindness enthusiast, humanist. No DMs thanks 🌱
ME Group Australia (Rachel)
@megroupaust
ME Group Australia is a registered Australian charity to advance health for Myalgic Encephalomyelitis (ME). Opinion is my own. “Like & RT” are not endorsement.
Elizabeth Watson-Brown
@ewatsonbrown
@QldGreens Member for Ryan. Living & working on Turrbal & Yuggera Land. She/her. Authorised by E. Watson-Brown, Brisbane
MikeMusker
@michael_musker
Norges ME-forening - Rogaland Fylkeslag
@me_rogaland
(The Norwegian ME Association - Rogaland) Our account is on pause.
Carole Bruce
@carolebruce17
💙Art, Nature, Books, Some Music. Severe ME 32 years. Daughter severe 38 years. Furious about treatment of ME. bsky.app/profile/cabruc…
Adam
@abrokenbattery
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos.
Sten Helmfrid 🇺🇦
@stenhelmfrid
Ph.D. in physics, also interested in mathematics and science theory. Loves to apply general knowledge of science to other fields, for example ME/CFS.
Anne Wilson
@annewil87285253
CEO, Managing Director, Director
Melbourne Disability Institute
@mdi_unimelb
The Melbourne Disability Institute is building a collaborative and inclusive interdisciplinary disability research agenda at the University of Melbourne.
Millions Missing France
@millionsmissgfr
Asso de patient·e·s Pour la prise en charge de l'#EncéphalomyéliteMyalgique en France & le développement de la recherche #EBM #handicap #AutodéfenseSanitaire
Lou Smith
@loulordsmith
primary languages, including Latin & ITT; tutor including Latin gcse; ex-secondary science teacher