← Return to Burning mouth syndrome (BMS)
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Autoimmune Diseases | Last Active: Nov 8 8:45am | Replies (78)
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Replies to "i had bms for many years with no diagnosis. finally tests determined sjogrens, no help but..."
Hi uncbball,
Just came across your posting.. Can you tell me the name(s) of any of the newer saliva increasers you've tried?
A rheumatologist gave me pilocarpine (salagen) and then civemeline- the first worked for a while then brought on a chalky taste, the 2nd actually made my mouth drier.
I appreciate it if you can get back to me.
Maggie45