Julie Hughes (@juliehughes2013) 's Twitter Profile
Julie Hughes

@juliehughes2013

Occupational Therapy Lecturer at Australian Catholic University. Returned from UK interested in #MECFS #PWME #mentalhealth,#OTeducation

ID: 1133481656

calendar_today30-01-2013 09:11:53

10,10K Tweet

1,1K Followers

932 Following

ME Group Australia (Rachel) (@megroupaust) 's Twitter Profile Photo

We are united for #FairGoForME! Marginal seats in #AusVotes2025 matters for #MyalgicEncephalomyelitis, #MEcfs, and #LongCovid! See details of the campaign here: [emerge.org.au/2025-federal-e…] Emerge Australia ME/CFS Australia ME Advocacy Network Australia (MEANA)

We are united for #FairGoForME! 
Marginal seats in #AusVotes2025 matters for #MyalgicEncephalomyelitis, #MEcfs, and #LongCovid! 

See details of the campaign here: [emerge.org.au/2025-federal-e…] 

<a href="/EmergeAus/">Emerge Australia</a>  <a href="/mecfsaustralia/">ME/CFS Australia</a> <a href="/MEAdvNetAu/">ME Advocacy Network Australia (MEANA)</a>
Emerge Australia (@emergeaus) 's Twitter Profile Photo

We’ve launched our #FairGoForME election campaign, and we need your help! We’ll post twice a week from now until the election—each post will spotlight a key theme or priority for #MECFS and #longCOVID. Like, tag, & share our posts & spread the word! #AusPol

We’ve launched our #FairGoForME election campaign, and we need your help! We’ll post twice a week from now until the election—each post will spotlight a key theme or priority for #MECFS and #longCOVID. Like, tag, &amp; share our posts &amp; spread the word! #AusPol
ME Association (@meassociation) 's Twitter Profile Photo

BBC: Trial seeks treatment for long Covid sufferers    Researchers at Plymouth University are working on an anti-viral drug trial alongside the University of Derby to treat the symptoms of Long Covid.    Project Leader, Mark Faghy, said "Five years on from the start of the

Emerge Australia (@emergeaus) 's Twitter Profile Photo

Many people with ME/CFS and long COVID struggle to access the NDIS and DSP. This must change! Visit your candidates' page today and tell them you will vote for the candidate who will give people with #MECFS and #longCOVD a #FairGoForME #AusVotes2025 #AusPol

Many people with ME/CFS and long COVID struggle to access the NDIS and DSP. This must change! Visit your candidates' page today and tell them you will vote for the candidate who will give people with #MECFS and #longCOVD a #FairGoForME #AusVotes2025 #AusPol
Renuka Dhinakaran (@renudhinakaran) 's Twitter Profile Photo

Women are susceptible to medical gaslighting more than men, with a lot of their symptoms being attributed to hormones, emotions or anxiety, a prejudice that dates back centuries. A thread. #LongCovid #women #MedTwitter

Emerge Australia (@emergeaus) 's Twitter Profile Photo

Don't miss Emerge Australia's ME/CFS Awareness Week Symposium on May 7th! Register and join us online to connect, learn, and offer support. Secure your spot: vist.ly/3m2xmu5

Don't miss Emerge Australia's ME/CFS Awareness Week Symposium on May 7th! Register and join us online to connect, learn, and offer support. Secure your spot: vist.ly/3m2xmu5
Eliza Charley | Actress on Pause (@elizacharley) 's Twitter Profile Photo

ME Awareness Month 2025 has begun! Here’s a collated list of activities to join - Opportunities to Learn, Connect, Raise Awareness, Fundraise and Play! 🧵 Share. Add. Join in when able ✨ #MyalgicEncephalomyelitis #MECFS #GreatestMedicalScandal #MillionsMissing #IACC

Emerge Australia (@emergeaus) 's Twitter Profile Photo

Emerge Ambassador • Actor • Writer “I’ve spent over 15 years navigating ME - through hospitals, clinics, film sets and advocacy forums.” From her home in Florence, Eliza Charley shares how her diagnosis shaped not only her career - but her mission to elevate unheard voices.

Emerge Australia (@emergeaus) 's Twitter Profile Photo

📣 ME/CFS Media Award Finalist #2 - Prof. Chris Ponting His article highlights prolonged medical neglect of ME/CFS, advocating for patients with fearless, top-notch journalism. 🔗 Read here: bit.ly/3iGnwsD Congratulate Chris with a 👏 for his impactful contribution.

📣 ME/CFS Media Award Finalist #2 - Prof. Chris Ponting His article highlights prolonged medical neglect of ME/CFS, advocating for patients with fearless, top-notch journalism. 

đź”— Read here: bit.ly/3iGnwsD

Congratulate Chris with a 👏 for his impactful contribution.
ME Group Australia (Rachel) (@megroupaust) 's Twitter Profile Photo

Eliza Charley | Actress on Pause Julie Hughes We are currently madly preparing with severe ME capacity… Could you reach out to potential #pwME and #pwLC panels for Lived Experience Forum? The forum will be hosted by Nicole like last year. 🙏 megroupaustralia.org.au/awareness/me-a…

Oonagh Cousins (@oonagh_cousins) 's Twitter Profile Photo

I've written a new blog for Linda Hughes.uk about rest - something I feel deeply about. I talk about how, as an athlete, rest was respected - a sign of discipline and strength. But living with ME/Long Covid, rest became something judged and misunderstood. Link in next tweet👇🏻

I've written a new blog for <a href="/thereforme/">Linda Hughes</a>.uk about rest - something I feel deeply about.

I talk about how, as an athlete, rest was respected - a sign of discipline and strength. But living with ME/Long Covid, rest became something judged and misunderstood.

Link in next tweet👇🏻
Emerge Australia (@emergeaus) 's Twitter Profile Photo

Join a study at The Baker Institute/University of Melbourne if you're 18+, live with ME/CFS or orthostatic intolerance, & can visit our clinic twice. Reimbursement available. More info here: vist.ly/3n6jcqr

Join a study at The Baker Institute/University of Melbourne if you're 18+, live with ME/CFS or orthostatic intolerance, &amp; can visit our clinic twice. Reimbursement available. More info here: vist.ly/3n6jcqr