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I have been managing the effects of facial palsy for over a year now. Initially I lost my sense of taste early on, but then it gradually returned. Since March though , I have lost most of my sense of taste and now smell too. Has anyone else experienced this yo yoing of senses? Does it come back?
my GP has referred me to ENT for further checks and my FP physio has suggested I should have a contrast MRI of nerves in my head to check out any other more serious problems. I am grateful that it’s being checked , but wanted to hear any advice / feedback from fellow sufferers.
its all a bit frustrating, but it seems the recovery goes like that!!
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