Eleanor Lewis
@eleanorlewis.bsky.social
Phonetics PhD. Life on hiatus with ME/CFS. Cats, music and excessive screen time. Naarm/Melbourne. (she/her)
Reposted by Eleanor Lewis
Quite disheartening to return from 10 days working with some of the most important and relevant #MECFS and #LongCOVID researchers in the world and to read this drivel being allowed through from @bmj_latest. Let's be unambiguous about this: BMJ has
www.bmj.com/content/389/...
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www.bmj.com/content/389/...
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Patients with severe ME/CFS need hope and expert multidisciplinary care
Reframing beliefs about illness, along with specialist rehabilitation, can help recovery in people with severe ME/CFS, write Alastair Miller, Fiona Symington, Paul Garner, and Maria Pedersen
Myalgic...
www.bmj.com
May 15, 2025 at 8:34 AM
Quite disheartening to return from 10 days working with some of the most important and relevant #MECFS and #LongCOVID researchers in the world and to read this drivel being allowed through from @bmj_latest. Let's be unambiguous about this: BMJ has
www.bmj.com/content/389/...
1/
www.bmj.com/content/389/...
1/
Reposted by Eleanor Lewis
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 D.Missailidis@latrobe.edu.au
April 9, 2025 at 5:35 AM
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 D.Missailidis@latrobe.edu.au
Reposted by Eleanor Lewis
A heartfelt thanks on Long Covid Awareness Day to the incredible myalgic encephalomyelitis community who've used their precious energy to provide crucial information and validation to desperate Long Covid sufferers like myself. Five years ago, you were the only ones who understood.
March 15, 2025 at 6:40 AM
A heartfelt thanks on Long Covid Awareness Day to the incredible myalgic encephalomyelitis community who've used their precious energy to provide crucial information and validation to desperate Long Covid sufferers like myself. Five years ago, you were the only ones who understood.