May is ME/CFS Awareness Month!
ME/CFS stands for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
Chronic Fatigue (CF), a symptom of many chronic illnesses, is not the same as Chronic Fatigue Syndrome (CFS). There is a push for ME/CFS to be exclusively known as Myalgic Encephalomyelitis (ME) in the future
ME/CFS is a complex, fluctuating, chronic medical condition affecting multiple body systems and symptoms can change unpredictably
Post-exertional malaise (PEM) is the hallmark of ME/CFS
More on symptoms: Symptoms of ME/CFS
ME/CFS affects an estimated 836,000 to 2.5 million Americans, the majority of those diagnosed being AFAB
An estimated 90% of people with ME/CFS are undiagnosed
About 25% of people with ME/CFS are bedbound or housebound for long periods
Most of those diagnosed never regain their pre-disease level of functioning
The root cause of ME/CFS is unknown
Possible triggers include: viral infections (such as mono, the flu, or COVID-19), bacterial infections, physical or psychological stress, and immune system changes. There may also be a genetic component
There is no cure or approved treatment for ME/CFS
However, some symptoms can be treated. For example, PEM is treated by pacing. More on treatments: Treatment of ME/CFS
ME/CFS costs the US economy about $17 to $24 billion annually in medical bills and lost incomes
The ME Association and the CDC have more in-depth articles on ME/CFS for more information















