Well, this is what my GP told me last time I visited her. I'm sure it's the same with many of you!

I'm posting this to know your suggestions about "What do you think I should do next". It's almost been 1 year since I have Sjogren symptoms show up. I have had typical symptoms -- dry eyes, mouth, some brain fog, skin rashes etc--for about an year. Last month, had a painful "gout experience" as well!
Most annoying of all symptoms has been numbness in my anal region and constipation. My GP sent me to neuro who gave a "clean chit" for now after performing CT Scan of pelvis, blood work etc. He didn't do an MRI though (my insurance didn't accept it). Numbness and constipatoin have been around for 3 months now.
GP mentioned that next I might have to see a gastrologist/rheumatologist but she will leave it to me to decide. She seems a bit confused. Blood work for SjS is negative. I haven't done a lip biopsy and not planning for it at least as of now.
How do you think I should proceed. I'm not asking for medical opinions. Of course I can see gastrologist/rheumatologist for that. I'm just asking for general directions. Other than numbness, other symptoms are well taken care with drops/skin creans etc. I'm not worried about them, and I'm generally doing well.
I'm taking things one step at a time, and at this time wondering if I should simply wait, see a gastrologist or a rheumatologist or change my GP (she is very nice but I puzzle her - she admitted frankly! May be she doesn't have too much experience handling such patients; Having said that I like her.)
Any thoughts?
Maya