FAQ/Help |
Calendar |
Search |
Today's Posts |
|
Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
Reply |
|
Thread Tools | Display Modes |
04-26-2020, 08:24 PM | #1 | ||
|
|||
Newly Joined
|
Been on Mestinon for 4 months. Starting to not work........by 1200 noon, I struggle to see one image. My double vision begins. This has gotten worse over the last 6 weeks. Any ideas what’s next? Many thanks!
|
||
Reply With Quote |
04-26-2020, 09:58 PM | #2 | ||
|
|||
Junior Member
|
How much Mestinon are you on? Mestinon doesn’t always work for eye issues. Ask your neurologist or optho-neurologist. I don’t have eye issues so I’m not much help. Jim
|
||
Reply With Quote |
04-27-2020, 12:37 AM | #3 | |||
|
||||
Senior Member
|
I don't have MG but do have MS and can sympathize with vision problems like double vision.
I found this about ocular MG but the only suggestion here is wearing an eye patch over one eye. It might be worth a try if you haven't already done that: https://www.brighamandwomens.org/neu...sthenia-gravis
__________________
Repeal the law of gravity! MS diagnosed 1980. Type 2 diabetes, osteoarthritis, osteopenia. Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Currently: Glatopa (generic Copaxone), 40mg 3 times/week, 12/16/20 - 3/16/24 |
|||
Reply With Quote |
Reply |
|
|