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I'm a 28 year old female just diagnosed with Sjogrens I am wondering two things- anyone ever had Ranulas/ or oral surgery due to Sjogrens?
Know any good oral surg. in CT? Any Sjogren support groups in CT?

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Hi there, rebekkhaz, I'm really sorry to hear that you were diagnosed with Sjogrens because it's quite rare and it sounds like it's a pretty bad disease. I don't have it, but a good friend of my family does and she's doing fine so I hope that you realize that it is a disease that you can cope with. IN addition to posting here. there is an actual website for Sjogrens sufferers that you can do a google search for to find to talk to someone about this. Please keep us posted on how you're doing!