Functional Electrical Stimulation

Has anyone had experience of FES for drop foot

I have had one for almost 25 years and the best solution to drop foot I have found. Your GP can refer you for an assessment.
Is there anything more specific you would like to know?

Functional electrical stimulation (FES) | MS Trust

Hi Ericladdy40(?)
I’m in total agreement with Whammel, I’ve only been diagnosed PPMS a couple of years and my issue started in 2020 with what I now know is foot drop. My Neurologist put me forward at my first face to face appointment to try out a FES…. It’s given me more confidence when walking outside and helps enormously to lift my foot rather than dragging it. Go for it I’d say!!
Good luck whatever you decide