RSD for 12 yrs for 2 yrs my eyes are getting worse
Does any one know about this
Thank you
Galway

I too have rsd in my eyes mine got so bad at one point they were so swollan that 3 blood vessels hemoraged. One thing I found that helps is some eye drops with prednisolone in it which numbs it so the burning and stinging pain helps alot

Sam

Thank you Sam. I don't have redness. I have blurred vision. I go to Boston where the major hospitals are June 28. You have to wait so long to see the dr. I tryed eye drops and they burned my eyes. Do you have RSD any place else.
I have it on my rt side arm and neck, now left leg and arm...hands too.
Thanks
Galway

I had severe eye problems that set in within about six months of diagnosis. I was convinced that my vision problems could be addressed by new glasses but after a visit to the eye doctor I was told that that new glasses would not help. Both my neuro and PM docs agreed the symptoms were CRPS related. The problems only became worse as did my other symptoms until I was treated with tDCS. My improvements were slight during the first course of treatment. Now that I am treating on a regular basis I have seen dramatic improvements in my vision, including elimination of dry eyes.

Hi I am new on this site so not sure how to move around and make friends. I don't belong to Any RSD group. What are the treatments you got....tDCS. I see the Nuoro eye dr June 28 as the regual eye dr and my Nuoro can't find out what is wrong with my eyes. Thanks for the good news. Do you have RSD in our parts of your body.. I do
Your friend
Galway

There is a tDCS thread that you can review. It has experiences from different people.

Hope this helps.

Ya I have rsd other places I have it full body and internal. The dropps Iam talking about arent normal drops they didnt hurt my eyes as the numb it on contact. I have had blurred vision and double vision that comes and goes which I havent found anything that helps it so have to put up with it until it goes away.

Did u get my email?
Galway