u/Far-Ganache-9456

Apologies if anyone has talked about this before the search function seems to keep getting worse I can never tell haha

Like the title says, just looking to hear anyone's experience if they have had meta with Sjogrens. I have it myself and I'm planning (hoping) to get meta in the near future and there's just not a lot of information out there for me to go off especially not personal experience. I would be extra interested to hear if anyone with sjogrens has had UL, but any information at all is extremely appreciated. Just want to know if there's anything I should be thinking about/ asking surgeons as I get closer to meta. thanks and good luck to everyone else!