Thank you, everyone, for your suggestions. I will try these out. Can you please tell me something about the RX toothpaste "Prevadent"? How much does it cost and how much hassle does your insurance co. give you to get it paid for- or do you have to pay for it out of pocket? My ins. co does not honor RX written by the dentist, so I will have to have my GP write it for me. Now I understand why I get this nasty metallic taste in my mouth. Thank you for pointing that out. I have tons of info on Sjogren's and I don't remember that being mentioned. I am in a severe IC flare right now and I have a wierd metallic "filling" taste. I now realize that I have actually had Sjogren's most likely beginning in 1970 when I was just a young thing of 16. However, I was unaware I had Sjogren's until very late in the "game," as were all the doctors, dentists, endodontists and periodontists that I saw in the 80's and 90's. Talk about clueless!!!In Phase I, Sjogren's first went through and destroyed my entire mouth and by 1979, all but my very front teeth now have either root canals, full crowns or are hollow shells filled with tons of fillings. In 1995 I even had two lower left molars pulled due to excruciating pain. There was actually nothing wrong with the teeth & all the specialists I saw said I had "excellent home care." You would think that because of all the rapid decay and gum erosion they would begin to investigate for the cause since it wasn't due to poor hygiene. Go figure. (I had tons of lab work done in the 80's- all positive for an Autoimmune Disease. These tests were ignored by my doctor. Again, go figure). In Phase II, I had and still do have, severe Trigeminal Neuralgia on the left side made worse the dental work done in the mid 90's. My left side of the face was actually paralyzed for awhile. Phase III, the Sjogren's began to destroy my corneas in 1999, and I had to have an emergency visit and treatment by my ophthalmologist so I wouldn't lose my eyesight. This is when I was officially diagnosed with Sjogren's. Thank goodness the eye doctor knew "his stuff." When this happened I had END STAGE IC,and the stress from IC caused the Sjogren's to progress very rapidly and Phase IV is when the severe dry skin appeared. At first I thought it was due to being middle aged. But I was wrong. Regarding diet: I was always very thin and never worried about my weight so I have NEVER EVER used artificial sweetners, I can't stand the bitter wierd taste. I am not a cola/soft drink person. I prefer natural fruit juices. (When I was finally diagnosed with the IC in 97 I was put on meds in 97 & 98 for a short time which I became violently allergic to which caused me to gain 35 lbs,and also caused dry mouth & eyes, etc. I can't get the weight off now!). My meds right now are: Elmiron, and round the clock opiate narcotics for the unbearable pain. I can't tolerate any "anticholinergics" which cause the severe dry mouth, eyes & skin. The severe dry mouth and skin I have now is due solely from Sjogren's. Drinking water or juice does not help, plus I don't like to pee. It hurts. I chew tons of Trident when my mouth become unbearable. That's about it for the Sjogren's saga. I will try all the suggestions everyone was kind enough to mention. Thanks!!
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Laura Hubbard

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Laura Hubbard
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