My wife is currently being assessed for possible Sjögrens as she has most, if not all of the symptoms.
Before she was sent down the Sjögrens rabbit hole, however, she was diagnosed (eventually) with Lichen Planus. I say eventually because she was first misdiagnosed (during COVID) by a doctor who wouldn’t even examine her (despite only being in the next room) and relied on a mobile phone picture taken by a nurse before pronouncing that her skin rash was scabies (!). By the time a proper diagnosis was made, about 3 months later, the condition had spread to her mouth and tongue.
At around the same time, she had also noticed that she was starting to lose her sense of taste and smell (both of which have now disappeared completely) and increasing dryness in her mouth.
Could the loss of taste and smell be down to the OLP?