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#1 | ||
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Junior Member
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Finally had my appointment with an ophthalmologist regarding my vision. Have had problems due to the optic neuritis in both eyes on different occasions that haven't really subsided 100% since the attacks. The answer I got was my vision was fine... Quite frustrated with this because I know first hand it is not. I asked if it can be permanent damage to the nerve they can't see. They said it was possible, but can't know for sure because it was my first time seeing them. Told me to contact them if I have another attack.
Anyone ever run into this problem? I'm thinking of asking for a referral to an neuro-ophthalmologist to further investigate. Thanks for reading, have a good weekend! |
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#2 | ||
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Senior Member
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used2party,
Yes, I would see a neuro-opthalmologist -certainly if it happens again and soon to get baseline before another problem. Best to you, ANN |
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"Thanks for this!" says: | SallyC (06-07-2013) |
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#3 | |||
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Member
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My eyesight has been going south for years but the eye docs have been telling me my eyes haven't changed at all. Well, my eyes tell ME different. Just because they cant see it, doesnt make it not real.
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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"Thanks for this!" says: | SallyC (06-08-2013) |
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#4 | ||
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Senior Member
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ditto here
At least I finallly got decent answer. My neuro laughed and said "Not surprising as they can only see the first part of the optic nerve by looking into your eyes. There coud be a lesion or an area of inflammation further along the optic nerve. It doesn't really matter what they say, as you are the one who 'sees' - not the optician/opthamologist" While it didn't "fix" my vision, at least I felt recognized/validated.
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Jane Cleverly disguised as a responsible adult! |
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#5 | ||
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Junior Member
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Thanks for all the replies everyone. Jane & Kitty you have described exactly how I feel. I kinda figured they could only see the front part of the optic nerve. When i tried explaining to the eye doc that my eyes are "out of sync" if that makes any sense, they kinda just looked at me like, "Oh"... Tried telling them that I've had optic neuritis at different times in both eyes with different amounts of visual loss each time. All they said was if another attack occurs come back in. Rather frustrating!
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#6 | |||
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In Remembrance
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An ophthalmologist should have done a more thorough test.
![]() Find a new one and feel better soon. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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