Six myths and facts everyone should know about Myalgic Encephalomyelitis (ME)
Myalgic encephalomyelitis (ME), also known as ME/CFS, is a debilitating illness that affects millions of people worldwide. However, persistent myths and misunderstandings hinder its recognition and treatment.
For World ME day on May 12th 2025 WAMES is joining with the World ME Alliance (WMEA) and countries around the world to debunk six of the most common myths about ME and share the medical facts everyone should know.
Challenge the myths, champion the facts!
In the run up to World ME Day we will be releasing images to share
Myth: ME is a mental health condition
Fact: ME is a biological illness that disrupts the metabolism and impairs the brain, immune system and autonomic nervous system
Myth: ME is just about feeling tired
Fact: The defining symptom of ME is Post-Exertional Malaise (PEM)
– an extreme worsening of symptoms after even minor physical or mental exertion. While there is no cure for ME, there are compassionate ways to help patients manage their symptoms, in addition to pacing to prevent PEM.
Myth: You can exercise your way to recovery from ME
Fact: Exercise can be dangerous for people with ME
Unlike other chronic conditions where exercise can help, structured exercise programs often make ME symptoms worse as patients end up pushing themselves too far.
Myth: Only certain groups of people can develop ME
Fact: ME affects people of all races, genders, ages, and socioeconomic backgrounds
Myth: Doctors cannot help people with ME
Fact: Doctors can help people manage ME symptoms
While there is no cure for ME, there are compassionate ways to help patients manage their symptoms, in addition to pacing, to prevent PEM.
Myth: Long COVID is entirely different from ME
Fact: Many Long COVID patients have symptoms that match ME
More information
Myth: ME is just about feeling tired
Myth: Mae ME yn ymwneud â theimlo’n flinedig
Myth: ME is a mental health condition
Myth: Mae ME yn gyflwr iechyd meddwl
Myth: You can exercise your way to recovery from ME
Myth: Gallwch ymarfer eich ffordd i wella o ME
Myth: Only certain groups of people can develop ME
Myth: Dim ond rhai grwpiau o bobl all ddatblygu ME
Myth: Doctors cannot help people with ME
Myth: Ni all meddygon helpu pobl ag ME
Myth: Long COVID is entirely different to ME
Myth: Mae COVID Hir yn hollol wahanol i ME
#WorldMEDay #MyalgicE #MEAwareness
This is a great idea to spread correct information about ME and raising awareness on what a debilitating illness it is.
I really appreciate this informative approach regarding ME/CFS as I battle judgement from presumptive, people some being in positions of regularly assessing you & making a difficult life even harder as you battle their narrow mindedness based on ignorance, it only takes one person to negatively impact your life when you are constantly searching for positiveness to sustain you.