Does anyone else get frustrated at people thinking we have Myalgic Encephalomyelitis (ME)?
When I say MS, people I think don’t realize MS is very different from ME (Myalgic Encephalomyelitis, commonly known as Chronic Fatigue Syndrome, or CFS). They treat me like I am making it up and just a bit lethargic. MS is neurological and autoimmune, is this correct? I feel like people don’t take me seriously so often I don’t even bother to tell people.