I dont know if this helps, but I have an eye disease of my cornea that disenegrates it and I see double vision and have sensitive eyes majorly and just weird symptoms... its called kerataconus. On top of that when I look straight one of my eyes is looking a little up and one is looking down, so all day my eyes have been fighting to focus on one spot and they put prisms in my lenses.... I dont know if this might help? But I have eye pain 24-7 for 10 years now and I am only 21... so I definately feel your pain... I dont know what single vision even is. Double vision is the way I live my life. I tend to not go out during the day as much as I could because of the sun, and in the house my tv is dimmed and computer is dimmed, and all the lights are off.

Try turning lights off, and keeping everything dark, turn down the tv contrast so its not as bright, turn down pitch on the volume... too much sensory overload makes everything worse. When I got RSD all the sensitivity got alot worse. Hang in there....

Teen I am sorry you ended up in the hospital. When is your neuro apt? I would keep calling for a cancelation to get squeezed in. I agree it is important to rule out other conditions. I always fear I will brush something off as rsd and it be something different. Did they discuss maybe a med that is used for migraines? Hope you feel better

Hannah I can so relate as I tend to not go out in the sun much from my eyes too. I made my bedroom into a dark room with the black out shades. Now my ears seem to be similar to my eyes

My eyes seem to be getting worse with the progression of RSD. The eye on my left side ( worst side) twitches constantly now also. When I had my SCS implanted it made it much worse, had a hard time even watching TV. For other reasons I have had to leave the stimulator off, but my vision still remains shaky and strenuous.
I also find sensory overload to make my pain worse. Dark quiet rooms, focusing on breathing, is where I find my most relief right now.
Wish you all the best.

I have recently started having a more difficult seeing. Problems with double vision and a sense of vibrations behind my eyes. I did not realize that others with RSD were having the same issues. Who is it better to address the issue through, your pain doc or eye doc? Hope you are getting so relief!

I have seen many pain doctors who deal with rsd and also many eye doctors. Many eye specialists have no clue what rsd even is. I think though it is always important to rule out other conditions so I would see an eye doctor and the pain doctor. Some pain doctors who deal with rsd even are not good with treating the eyes because they are more focused on the limbs. For myself I am hoping if I get rsd relief in my limbs from a treatment or meds etc it will help the eyes too

Hi Michelle here, I have CRPS in my lower limb but spreads around. I have found over the last few months my eyes have got worse, soreness, foggy vision, eye strain, now I don't know if it is to the CRPS but my pharmacist told me that one of my meds I'm on Lrycia causes I damage so will be seeing Pain Specialist soon so will mention this to him.

Might want to do a google search for neuro-ophthalmologists in your area. Is it RSD or myasthenia gravis or any number of other things.