I've Had MG For Over 5 Years. I Was Taking A Beta Blocker. That's A No No For Most People With MG. My Eyes Are A Mess. Any Suggestions?
I have prisms in my eyeglasses which helps my double vision greatly.
Do you have any neuro opthamologists near you? They would be most familiar with impact of MG on eyes. The problem is this is a rare disease. Docs may not see this illness much in their practice. You might need to ask if you specialist has had experience. Neurology and Rheumatology would be typical specialists.
My eye doctor put me on areds (eye vitamins). I have noticed an improvement most of the time in the blurriness, except when I am exhausted. I've only been diagnosed for 15 months. I haven't heard back from my neurologist re: areds.
I also am having issues with my eyes. Mestinon, prednisone, and IVIG have not helped this particular problem. Wish I could have been more helpful and hope you get some relief. It's awful.
I'll be asking fir a referral tomorrow.
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