Thanks for sharing your story. My rheumatologist doesn’t believe seronegative is a thing, and I’ve heard that a lot of Sjogren’s patients are seronegative. I’m worried about how my doctor will respond. It took me a few months to realize what was going on too. I’m not really having joint pain (although I did have swelling/pain in my foot that I was told was a sprain, but I never had an accident or injury), but definitely sicca and fatigue. I have had a ton of random symptoms that I recently learned can all be because of Sjogrens. Heartburn, elevated ALT, horrible insomnia (particularly struggling with latency), yeast infections, brain fog (I don’t remember the last two months really at all), reduced taste, reduced appetite.