Clickable: LUPUS INFORMATION & LUPUS RESOURCES.
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Thanks Hippi, I am just not sure what to do I can live with the pain and fatigue but this mouth thing really has me depressed. I just came to terms with having to slow down in life and that I need to nap daily and that I can't do a lot of things I used and now this I just can't come to terms with. Having sjogrens scares the heck out of me. When they told me I had UCTD/LUPUS I was sad and shocked but I have a lady I worked with who has it so adapting to that was hard but I did it. But sjogrens I can't understand how people can get deal with that. I did try to get the magic mouth was but I live in Canada and I went to 4 pharmacies and no one has a clue what I am talking about. So I have just been using salt water and it's better a bit but now the roof of my mouth is a mess too. I have a bad cold and cough every 30 second so that is likely not helping. I think I must be starting a flare...... I am going to cry now...
Anon you might try the malox too. I hope you feel better soon.
Post Edited (okie) : 12/30/2007 5:09:09 AM (GMT-7)