Before I was diagnosed in December but had been suffering with jaw/shoulder pain since Oct, my taste buds stopped working. Smell is still okay. Some days I think it is improving, then next day things taste sour/sweet/bitter. Just curious if others have experienced this. Think GCA was lurking but not diagnosed and I did lose vision in one eye.
Loss of Taste??: Before I was diagnosed in December... - PMRGCAuk
Loss of Taste??
I lost much of my sense of taste about a year ago after about 12 months on Prednisolone and about 6 months on Prednisolone & Methotrexate- prescribed for PMR. A horrible metallic cheese taste all the time, and unable to taste anything sweet. Can still smell everything.
Doctors have no idea why it has happened.
Good luck. I recommend chillies, fresh black pepper, raw onions, soy sauce.
😒 Tx for responding as my doctors have n0 answers either. Love your advice tho....do love the spicy bits
..and ginger! Makes stir fry vegetables much more amusing.
You are making me hungry now! HaHa Love ginger too & can actually taste some of it. I am a huge bread lover, and all tastes like sawdust now. Keep hoping!
Might I recommend Scottish gingerbread?
eg. google.com/search?q=mcvitie...
Hmmmmmmmm. Sounds wonderful. Will check out our local shops here in B.C. Thank you for that.
This is a key COVID symptom. Have you had a test?