Does anyone suffer from dry eyes and mouth who don’t take any medications? Already ruled out Sjogrens from blood work and lip biopsy. Have burning mouth syndrome as well which causes dry mouth. Just curious if others out there share my symptoms who don’t take prescription drugs for their fibro.
Yes sorry I realized that after I posted it. My eyes still feel dry so I use the drops I’m on the computer quite a bit. My insurance covers it so cost isn’t an issue.
I use Restasis at my last eye checkup my doc said my eyes look great no dry eyes, but they sure do feel dry still! My Schirmers test was neg.
@Tawnalnman believe it or not, chronic dry eye can make your eyes water. Watery eyes is the body's response to the irritation of dry eyes. That’s how I found out I had chronic dry eyes.
My insurance doesn’t cover much...if any. The last time I got it, it was $85 🙁
@A MyFibroTeam Member, my last post was for Tawnalnman. She said her eyes tear a lot, I was letting her know it could be dry eye. If your test for dry eye was negative and your doctor said your eyes were fine, why would you use RESTASIS? If I didn’t have to use those drops, I wouldn’t.....they are expensive 🙁