The last time i mentioned this, it didn't go down as i'd intended, it ended well in the end though [ :o) ] please dont slap me think educational and not my opinion of your circumstance! Its not actually that uncommon for medical students to experience what they are studying, they've even got a name for it 'medical student syndrome' but sometimes learning about a medical condition has actually ended up in a dx. http://www.cmaj.ca/content/178/7/820.full
My opinion: is that from my perspective and experience, what you are describing doesnt actually sound like double vision to me (diplopia), but that could simply be that you've not said anything other than "I get double vision" you haven't provided any details. What you have described, are different visual sx's to diplopia, and sounds more consistent with the light sensitivity (photophobia) and is common in people with out eye disease but do suffer from migraines.
http://www.rnib.org.uk/eyehealth/eyeconditions/eyeconditionsdn/Pages/photophobia.aspx
Think about it, isn't it possible that if loud sounds can affect your vision, that migraine may be the more likely explanation?
Cheers..........JJ
Hi everyone,
Thanks for getting back to me!!!
Ironically, as it turns out, I am a student doctor of optometry. I'm a second year. I've talked to some of my upper classmen and the doctors at my school about my intermittant diplopia and they seem kind of confounded, which is part of why I think this may be more neurological in origin. Since it occurs at distance and monocularly, it can't be a convergence insufficiency. I also got checked to see if this was caused by a refractive error, and that's a negative too. My optic disk is normal, which rules out optic neuritis. Basically, everything about my eyes themselves is normal. I'm sorry I didn't mention I've been checked out by optometrists....
Do people with MS get both monocular and binocular diplopia that is not related to optic neuritis?
I will definitely make a point of getting copies of all of my medical records for myself. And Sara, I will be sure to browse around those resources a little more as well!!
I'd be making an appt with your eye doctor as those are not normal signs
As for ms, what bothers me is you refer to bilateral problems. Ms normally starts with one side or the other.
Please feel free to browse our help sections listed on the right side which contain much good information.
Welcome and I hope you solve your puzzle but you still have more mimic diseases to rule out!
As Minnie says. Always request a disc copy and written copy for your records!
Oh, and I meant to mention something about your "normal" MRI. The first neurologist said mine was normal too. However, I got a copy of both the disc and written report. Most facilities will provide this for free if you just ask.
Anyway, the Radiologist identified one lesion and the second neurologist I saw identified another. The wise folks here advised me to start a health file and keep copies of all of my tests. That way you have everything together and if you go to a different doctor and the records aren't sent you will have them.
I hope this helps,
Minnie :)
Hi, I'm pretty new to all this too. I have a lot of the same visual symptoms you have, with the exception of the streaks. Mine began suddenly. My neurologist said I should see an Ophthalmologist, and I found that I have convergence insufficiency X (T) and refractive diplopia.
Convergence Insufficiency is common in children because their eyes are still developing. Adult onset with no prior history can be a sign of something neurological. The refractive diplopia has something to do with how your eyes receive light and apparently doesn't have anything to do with neurology. I am a bit confused by this because I never had double vision before. In my research, though, I have read of people who were originally thought to have refractive diplopia and it was really Optic Neuritis.
I am nowhere even close to an expert. Still learning myself. The Ophthalmologist I saw did request diagnostic results and evaluation of something (that part was at the bottom of the report and was cut off of my copy). So, short story long, it would be a good idea to get checked out by an Opthalmologist as it could help put pieces of the diagnostic puzzle together.
Best of luck,
Minnie :)
Hi there,
I am also new to this community, and in the same dilemma. So I feel your frustration.
It is so confusing to have these symptoms, yet no final dx. So many times my Neuro has told me that he cannot take MS "off the table".
He did all other rule out tests and treats it with monthly Sol-u-medrol and other meds for the spasticity, fatigue and what ever else I might need.
One test he did do was called a rule in, a blood test by Glycomids, I believe that is the name, you can google it. Anyway, it came back 95% positive that I would have it. However, that, the leisions, optic neuro, etc...still do not have the dx...
Hang in there