What is ME/CFS?
Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is not just “being tired.” It’s a long-term, fluctuating neurological disease that causes symptoms affecting many body systems, especially the nervous and immune systems.
ME/CFS can be severely debilitating: About 25% of people with ME/CFS are housebound or bed-bound as a result of their illness. 70% are unable to work.
Like Long Covid, ME/CFS is often triggered by a viral infection, but can also occur after physical trauma (e.g. surgery, a car accident), periods of intense emotional stress, or, rarely, vaccination. Its onset can be sudden or gradual.
ME/CFS is two to four times more likely to develop in women than in men.
The persistent psychologization of ME/CFS leaves many patients without care or financial support.
Notable symptoms
Comorbidities (POTS, MCAS, etc.)
Extreme physical & mental exhaustion, post-exertional malaise (PEM, a disproportionate worsening of symptoms after physical or mental activity)
Cognitive difficulties
Gastrointestinal issues
Heart palpitations, irregular heartbeat
Sleep disturbances
Flu-like symptoms, sore throat, or swollen glands
Muscle & joint pain
Headaches & migraines
Hypersensitivity to stimuli (light, sound, etc.)
Little-to-no improvement with rest
“ME/CFS is an inflammatory autoimmune disorder that progresses to a complex multi-system neuro-endocrine-immuno-microvascular disorder with cardiac involvement.”
—Professor Malcolm Hooper, addressing the UK Parliament in 2007