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?
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