Did you wake up with a craving for a new ME/CFS book with dozens of chapters about research methods? Well, it’s your lucky day link.springer.com/book/10.1007...

Finished just in time for Easter! Looking forward to starting experiments!

85/100 samples in the freezer! We now need to round out our control cohort. If you know anyone who is apparently healthy who might be interested in giving a sample to the project (with $20 reimbursement of time and expenses) please refer them to [email protected]

Very important research - please register via the QR below

We’re running a day of blood draws for ME, LC, and recovered post-C19 / healthy ppl on campus at La Trobe. This Wednesday April 2nd, all day 8am - 6pm. Details in signup link below.

Pleased to share this research from my PhD in @graemecowan.bsky.social's lab! We replicated existing evidence of moderately increased IGHV3-30 usage in B cells of patients with mild/moderate, but not severe ME. www.frontiersin.org/journals/imm...

Looking for a handful of people with ME/CFS in VIC to round out a large study of immune and metabolic function and gut microorganisms. I do home visits where helpful and provide reimbursement to all participants. ❤️ If you’re interested please get in touch at [email protected]

PhD scholarship + project available - ME/CFS & Long COVID related. If interested please get in touch with Dr Sarah Annesley at [email protected]

Let’s goooooo (tomorrow!) #SpendChristmasWithME

Our new Long COVID pilot study found two genes whose mRNAs separated a small cohort of Long COVID from recovered post COVID blood samples with 100% accuracy: www.frontiersin.org/journals/imm...

Bring together #pwME and/or #pwLC this Christmas 🎄 Share a photo of your Xmas with #MECFS or #LongCovid and enjoy suggested movies knowing that you are not alone and others are watching with you. See my pinned post to see how you can get involved. #SpendChristmasWithME

Amazing work, Tina. Your passion for this field really comes through.

How is everybody faring today?

I just laughed in public to this

It’s amazing how I tweeted this on the other site and got a fraction of the support and weird conspiracy stuff and insults. Thanks for the love here on bluesky. Love you all.

Aussies with #mecfs! The next Parliamentary Friends of ME/CFS meeting will be held in Canberra on Monday (11am-1pm AEDT). The focus of the meeting will be: clinical guidelines and education, access to the NDIS, research funding, and chronic illness items under Medicare. Register to watch via Zoom

First Long COVID paper accepted for publication!

Nearly 20 home visits to people with ME done in the last two weeks (and a few with Long COVID as well). Many more to come. Thank you for your generosity. #MECFS #LongCOVID

This is such a nicer place than Twitter…

Anybody in Australia, with ME, with a suspected viral origin interested in helping to review a project proposal with Dr Sarah Annesley on a grant she is preparing? Pls email me at [email protected] (We’re looking to have an advisory team representing diverse perspectives)

Hello everybody, I am now on this website. #MECFS #LongCOVID #pwME