I have had several episodes of not being able to make it to the bathroom and have also wet the bed several times. My doctor gave me Enablex and the episodes stopped. I stopped taking Enablex and the bedwetting and not making it to the bathroom happened again. The doctor started me on Vesicore and again the episodes stopped. Have you ever heard of this happening after TUMT? I had the TUMT so that I could stop taking Flomax.
I'm not sure how to describe what I'm feeling or even if it's real or imagined from nervousness. My left side only...leg from about knee down, not feet and my left lower arm/hand feels "weird"...mostly at night when I get in bed and lay to watch t.v. I think my left hand feels weird when I'm typing, not fingers. I have no "pain" , numbness, tingling...just a weird, mild feeling. Sometimes a small shakiness.
In short, I was referred to an eye specialist because I was having horrible eye pain/pressure, double vision, and bright flashes of lights that looked like tiny flies were all over my vision. The 1st eye doc said there were no problems with my eyes and eluded that I was making the symptoms up! A year later another eye doc diagnosed strabismus. Obviously, I was pretty happy that at least one of my symptoms could be observed!
I have serious vision issues, pain, fatigue and lately cement legs that I am not sure what the heck is going on. Complicated migraines or migraines in general can and do cause certain vision problems. I am not a doctor but I know today my vision is more then migraines.
We won't even get into my cognitive issues with brain fog! ;-)
Found this thread and now I can see both this one and MS.
Oh gosh did I answer the question?
I went to the ER on Friday because I was having vision problems. An MRI found that I had brain lesions. They kept me in the hospital for a few days to discover what was going on. On my third day of my hospital visit I was called with results for an STD check. They said that I tested positive for gonorrhea. I was treated in the hospital but I am so afraid that I caused this damage to my brain. Did I ruin my vision and damage my brain? Is there anyone I can call to get help?
I would try first to see an experienced refractionist to see if they could get you at your best vision with contact left eye plus glasses for reading in both and see how you do. There is a chance that your problems with vision are due to the right eye's retina and cataract surgery won't fix all your concerns. You may want to get a second opinion too while you're at it.
what happens is i will see double, but i can feel my right eye jumping(for lack of better word) if i cover my left eye i literally see everything going up and down as if i were jumping up and down when i was perfectly still. when this happens i cant focus, its harder for me to look around and i cant make it stop it starts and stops by its self ive tryed closing my eyes for a minute or looking at something different but there nothing specific that starts it.
My Rheumatologist asked me to stop taking my daily cymbalta for a week before my Brain MRI appointment. So, its been 7 days and since then my vision has changed and I feel disoriented..spacey like. When I stare at something and then turn to look away I get dizzy and feel like I am NEO in the Matrix movies..everything moves slowly. Even there are times while walking I get that wierd matrix like feeling. I guess I really cannot explain the feeling correctly..but thats what I think it feels like.
Hello im new to this and i wanted to ask about my vision and see what i can do for it? I have blurry vision in both eyes and i some times see spots of light and i see weird when i look down it seems like if the floor is not flat and not straight and it makes me feel dizzy. When i walk my eyes cant stay focus they kinda jump as i walk. I want to know what can it be? What can i do for my symptoms.
t know why but I got flashes in my centre or near center vision too but I got tiny flashes in center vision and big flashes in peripheral vision I read on internet that pvd flashes doesn't last long for like 5 years and also pvd flashes comes in only peripheral vision I also read that you get flashes if your rod and cone are damaged I don't know why I am getting this flashes
3) black spots I have them in peripheral vision they will come as one the I got second one and then I got third
She is now having problems seeing things clearly and reading. The nurse has told us this is a common reaction and her vision may take up to six weeks to normalize. I haven't been able to find any info about this online. As she is in high school taking advanced classes, this presents a real problem... any suggestions?
I would see a neurologist. Be sure to tell them about the blurred vision, shimmering vision and swirling vision. The exam you had by the ophthalmologist does not mean that you do not have a problem, it just may not be in the eye but in the brain or blood supply to the eye.
I do not think stress is a cause.
I think it important to keep looking.
hello my son is 12yrs old and for the past few weeks out of no where he has been experiencing symptoms where his eyes will start hurting then right after everything goes black and he says he can't see anything. It only last a few seconds and then his vision is clear. He has alwayas been a healthy kid and there has been no change in his diet and when it happens he is not doing anything active besides walking into a room, taking out the garbage, or taking a shower.
I too have been experiencing Kaleidoscopic vision accompanied by a daze feeling 24/7 for about five years now and my doctors aren't sure what is causing it.
t get the new glasses until just recently, as I felt my vision was still changing, and I was almost finished tx, so I was going to wait it out. I have my new glasses, and still can't see well. my left eye is totally blurred close up, and distance is not much better with the glasses.
I will make another appt to see my optometrist, but not sure if My vision will recover post tx, if I should wait a bit. Seems to me, a previous treater mentioned something aboutvision problems.
When I fell ill i started having foggy vision and floaters, since then 2 years ago I still sufer with foggy vision at times and floaters- they really bother me! Sometimes i have flashes of lights and I am very sensitive to bright lights. I have had my eyes tested and all is ok, I am also over the Postnatal Depression but I still have the visio problems/distrubanaces- can you advise me of what this might be and how I might be able to have my old normal vision back ?
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