My vision has just been weirdly different at times. After the last 3 SGB's, within a couple days experienced ocular migraines (scintillating scotomas and loss of central vision) which my PM doc says are related, the opthamologist thinks they may be but is really moot at this point. They last about 1/2 hour. Strange...

If you go to RSDhope, the founder got RSD in his eyes first so it can be in the eyes. I notice some medications give me blurred vision. I also sometimes get stinging in my eyes which i believe is this beautiful RSD!

I have had my RSD for almost two years now, and last friday my vision was extemely decreased for more than 24 + hours. It finally seemed more like normal yesterday. It was like looking through a glass of water. Has anyone had any visual disturbances from RSD. I am also concerned that it may have been effected by one or more of the meds I take.

jclg[/QUOTE]

I had rsd in knees for 10 years and in a wheel chair after a trama of eye surgery my I could walk again now I am having problems with my eyes and was told I be the first in medical history to have this in my eye can anyone tell me what specialist helps with this

Hi. I may have rsd in my eyes. I have severe eye pain,pressure,raw,dry I could go on. Over the past 3 years I have seen I would say 10 eye specialists 45 apts many meds,neuros,rheumatologist I could go on. Anyhow I have rsd in my legs. It is hard to find a doctor even ones that deal with rsd a lot to believe it can impact other areas but I feel from others I met it can. I hope that with proper treatment for the limbs it will also help the eyes. Of course I feel it is important to rule out other conditions. Some meds though impact sight but I would get into the eye doctor and just get them checked as a starting point. Hope you feel better

I had rsd for ten years and I had trouble walking my huband had to push me in a wheel chair and became a recluse. After a bad cater. surgery in my left eye the lense had dropped. No one would believe I couldn't see afterwards when I went to Wills Eye Director he sent me for a test a it showed right away he sent me to the Best Cater. Surgery and he fix it I could see right away. After laying in bed all summer I thought it was over. I then realize my left eye had a lot of pain I could walk stopped talking all my pain pills and zanc. Been to ever type of specialist the doctor me if my rsd to eye my eye I would be the first. To embassed to ask them this QUESTION

YES RSD can effect the eyes when i have a bad days i have the same problem the reason i know is that when I get a nerve block in my neck for my rsd in my ams it effects my eyes my doctor also told me this. good luck

I have been very recently diagnosed with RSD (haven't even seen pain mgt dr yet) so this is all VERY new to me. I have noticed vision problems lately and was going to ask my doctor the next time I go in. However, I do suffer from migraines (sudden onset - might be related to RSD as well) so the vision problems could be from them.

I have read a lot of testimonials from people on here and other places and I also am affected by it. I, just last week saw my eye Doctor who said because of my blurry eyes - "because of your RSD, no glasses will help. There's nothing I can do for you! I, however, looked on the net. I.found that if you get PINHOLE GLASSES it helps blurriness tremdously! I'm right now buying some for $1.65 on Amozon. I really hope this helps even one person! Good luck everyone.

I am one of the ones who has it in the eyes. My thread is on here somewhere. My eyes are getting worse, but I hope they'll slow down eventually,

TK

I am so thankful for this post. I have been having vision issues for several years now but never, ever considered it could be connected in any way with my RSD/CRPS. I "see" research in my future today.