Sjogren's affects each patient differently, so it's impossible to guess how your glands will be affected. It really depends on the severity of your disease and the effectiveness of your treatment.
Glands can be larger due to disease activity, not just from "plain old" inflammation. It might be best to ask your Dr how your situation compares to other patients that s/he treats.
I'm afraid this isn't the most active forum, so I'm not sure others will be along to tell you about
their experiences, and I don't have glandular involvement, so I'm not much use!
One place that really has a wealth of information on Sjogren's is the Sjogren's Syndrome Foundation at www.sjogrens.com
. Symptoms, diagnosis, treatment, etc. Check it out if you get a chance.
Lynnwood, Lupus & Sjogren's Moderator, Dx: 2000DIAGNOSING LUPUS & HW's LUPUS 101
"Life is far too important to be taken seriously." - Oscar Wilde