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Functional Electro Stimulation?
Tingly badger was looking for help with her (?) crowd funding request for help with the cost of FES, given that she lives in an area where FES is not funded by the NHS. I too live somewhere where the CCG will not fund FES unless your circumstances are ‘exceptional’ and of course, no one with MS is exceptional.
I dare say the mods have had to remove the post because a link to the crowd funding app was included.
Tingly badger, I hope you get the last bit of money you need as for many people FES is the difference between independence and incapacity.