Cevilemine worries again

I began to respond after about 4 weeks..in mornings too much saliva, sometimes nausea. But oddly enough rarely respond with saliva, just profuse sweating and mot side effects listed. Frustrating, not sure what to do. If I can get Rheumatologist to talk to me, maybe suggestions from her. Heard the alternative pilocarpine, more intense shorter responses..similar profile of side effects ( possibly more ( but based on old research) .Are there any other alternatives? Saw on old article in a journal about some electr- stimulation tool, but no recent info. Might not have worked . Hard to speak, losing more weight, don’t want to eat. ANYWAY, .if anyone still taking “pilo” , please share your experiences. I know “hugs” are an attempt to be supportive, but please refrain. Looking for specific experiences or mainstream resources . Please only respond if you have experiences, or sources of reputable information. Appreciate everyone’s support, but hugs not necessary. Hope rheum will help , but unlikely .