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I have had HFS for four years before having the surgery. The surgery completly cured the spasms but I've had a few side effects, hearing lost which I was aware could happen, but others that where not explained to me, high blood presure not easily controlled and my sense of taste has been altered, everything (even water tastes bitter). I been reading about the funtions of the cranial nerves and the facial nerve has to do with all my side effect, does anybody know if this is permanent or will that nerve go back to normal at some point.
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