I only use my fes for walks over 400m because I walk not too badly under that distance.
The effect of my fes wears off quite a bit after about half a mile and my physio doesn’t understand it. I know I’m one of the lucky ones being able to walk that distance, but all my mild symptoms have been getting slightly worse over the past two years. I find the foot switch a bit of a pest going upstairs and pause it.
My MS centre gave me the fes two years ago and expect me to use it more often.
I’ve still got to think about lifting my left foot every step, but only tripped once with it on.