In my 20 years with an MS dx, I have never dealt with what I'd call fatigue. But I'm PP, and very often Primary Progressive just doesn't mimic RR or SP symptoms.

I've had long, often eventually permanent, tiredness or weakness in my extremeties in the months prior to the eventual loss of the use of them. But I never felt overall fatigued with the necessity to actually go to bed or to sleep.

I'd love to hear from other PP folks to learn of their experiences regarding fatigue. For you others, how bad has your fatigue affected your daily activities?

MsBluIs