Scared,

I would make an appointment with an ophthalmologist as soon as possible. This type of doctor is a specialist in diseases of the eyes.

As far as having to start on steroids within 24 hours, that is the first time I have heard of that. When I had ON, there was a definite lag of a week or so before I could even get in to see an ophthalmologist, at which point I was put on steroids.

My eye cleared up in approximately 4 months and I have not had eye problems since then. That was in 1972.

As far as I know, a cyst in the brain is not the same thing as a MS lesion. There are medically knowledgeable people on this board that will correct me if I am wrong about this.

gmi

I have had MS since 2002, one of my major symptoms was that I lost my eye sight in my left eye, I had no vision what so ever. Along with that I had a few other problems as well as numbness and such but the most serious was my eye sight. This happen in Feb of 02 and went on till Aug of 02. At the time I had no clue that I even had MS, I put it off to working to much and laying in the tanning bed. When I finally got in and got dx with MS and ON I was put on steroid treatments right away for a week. Not only did it clear up my symptoms but I got my eye sight back. I have not lost my eye sight completely like before but I do know that when I start going into a flare up the way to tell is by my ON. MY eye's start getting blurry or double visioned and after getting the steroids it clears up. Hope this helps and that I didn't shoot over the point. Take care.

I have heard the eye problems frequently occur in the early stages of MS and resolve as time goes on, but total loss of sight is new to me. Good luck to you guys.

http://www.nationalmssociety.org/Sou...ual%20Loss.asp

Take care.

Scared,
Every time I see this thread, I shudder. Please repost and give me an update, I am sure others are curious too.

I have crps and im having problems with my optic nerve my left eye is blind now happened last night still don't have any vision

Hello reneemommy
Sorry you are dealing with this.
As you posted on an old thread on our MS forum, I want to give you the link to our CRPS forum so that you can post there to get specific input from others
http://neurotalk.psychcentral.com/forum21.html