SF
Science for ME online forum
@scienceforme.bsky.social
We are an independent, patient-led, international discussion forum (www.s4me.info) for people with ME/CFS and the carers, clinicians, scientists and advocates who support us.
61 followers6 following99 posts
Impact of COVID-19 on myalgic encephalomyelitis/chronic fatigue syndrome-like illness prevalence: A cross-sectional survey - Wood et al. www.s4me.info/threads/impa... 2/14
Impact of COVID-19 on myalgic encephalomyelitis/chronic fatigue syndrome-like illness prevalence: A cross-sectional survey, 2024, Wood, Unger+
Impact of COVID-19 on myalgic encephalomyelitis/chronic fatigue syndrome-like illness prevalence: A cross-sectional survey Mariah S. Wood; Nicole...
A Network Medicine Approach to Investigating ME/CFS Pathogenesis in Severely Ill Patients: A Pilot Study - Hung et al. www.s4me.info/threads/a-ne... 3/14
Preprint - A Network Medicine Approach to Investigating ME/CFS Pathogenesis in Severely Ill Patients: A Pilot Study, 2024, Hung/Davis/Xiao
https://www.medrxiv.org/content/10.1101/2024.09.26.24314417v1 A Network Medicine Approach to Investigating ME/CFS Pathogenesis in Severely Ill...
SF
Science for ME online forum
@scienceforme.bsky.social
We are an independent, patient-led, international discussion forum (www.s4me.info) for people with ME/CFS and the carers, clinicians, scientists and advocates who support us.
61 followers6 following99 posts