This is an automated archive made by the Lemmit Bot.
The original was posted on /r/cfs by /u/fugapku on 2025-01-29 09:02:36+00:00.
Despite affecting millions, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) remains poorly understood. EU Lawmakers stress the urgent need for research funding and better diagnostics to support patients. Will this finally lead to action?
You must log in or register to comment.