Janers, at least you were on the right track when you were taking care of
the dry eyes waiting to see the doc!  Sorry that it is another Lupus thing
and hopefully after being on the meds it will clear up and not be bothering
you as much!  It just never ends does it?

Merry Christmas to you and yours!  Hope the New Year brings better health to
all of you.

Hugs,
Sherry

Well tis the season to be "jolly"?

I had to see that opthamologist and he did check my eyes and believe me the
pain had not let up. Did the Schirmer's test, the one for "dry eyes" .
almost had to peel that sucker out of my eyes.  Ever have one done?
Make a long story short, it is the lupus, sjogren's he says is JUST a fancy
word for "dry eyes"  LOL.  So that is what it is.  Pain is from the eyeball
not being able to make the tears and drying.  I am now on natural tears
hourly. Then a cortisone drop for inflammation for 2 weeks, and ointment at
night,  PLUS the new drug restasis twice a day.  I told him well looks like
I know what I will be doing the rest of my life, dropping drops in my eyes.
He didn't think that was funny LOL. But I have to go this route and it is
not a good route because this apparantly can get worse.  LIKE it is
getting.

SO I was doing the right thing by the natural tears.  He did say humidifier
at bedtime is a must and I have to use one due to my sinus junk and such.
So that was already being done.
The restasis takes about 6weeks to be really noticible and see a
difference.
Right now any eye drop burns but sun glasses help too.  Man this is no fun,
I can't set here too long either.  Let's hope it clears up but he didn't
look like he was promising me zip.
There ya got it.  Another round of something or other and My vision is my
life saver, because I am hard of hearing wear aide and need that for lip
reading...
good thing there is something to try and fix it..

hugs to all and to all a good night.

me again janers