Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
An eye patch helps, but I don't like to wear it.
Kerry
Excuse me for rambling on again, to answer the question :-) any thing that helps one eye be dominant like wearing an eye patch or placing a film over one side of your glasses or sunglasses would probably help. I haven't tried using a clear patch of color, then you could drive in the clear lane or the blue (red, yellow or whatever) lane and ignore the other. Any of those things would help distinguish eye problems from neck problems like Ann's. b.
But, while I was going from one eye specialist to the next trying to figure out what was wrong with my eyes, I found one doctor that showed me I didn't have to completely patch one eye. (This only works for those of use that wear glasses. ) Place a single strip of scotch tape up and down in the middle of one of your glasses lenses. This will block out the double vision, but will allow you to still have all your peripheral vision.
Hope that this helps someone.
The more I use my eyes the worse they get sometimes
but resting in my room that has no windows is BORING
ann
I am happy to start by saying since PLEX my double vision and blurriness are much better. I don't say that out loud since I don't want to mess anything up, lol. I know exactly what you're talking about with the dizziness. I have the same thing. It really isn't what I would call true dizziness or vertigo but it seems to be my eyes not tracking well which makes me feel very dizzy. If I sit and stare at one thing I don't have it or if I close my eyes it goes away. It's also episodic so it comes along with all the other symptoms when they hit. It's almost like a warning. It's like the world becomes unstable. I wish I had a suggestion on how to get things to settle down. I agree, it is one of the symptoms that bothers me most, right up there with slurred speech.
Cathi
My speech also slurred just prior to the really scary drive home last night. Thanks for forewarning me that this may be a warning sign.
The mestinon helps with it for the most part (when it at it's peak) and it is not an issue when I close my eyes which makes me feel more comfortable that it is an MG thing and not a medication side effect.
Thanks Jen for the advice on the insurance! I called my advocate and they were able to find a provider and make me an appointment for the 16th... if it is still bad tomorrow I will try to move it up a bit at their other office. You just saved hundreds of dollars at least! :)
The bonus is they got me in to a Neuro Opthamologist ! (yeah Annette)!
Bless you all!!!
Love, Becca
hugs to all,
Annette
tv seems to make them owrse but resting in a void is boring
I have to say that out of all the things I have noticed improvement on since start of cellcept, my vision has been the most improved. After over eight months on cellcept, I at worst, have spotty double vision, and it is quickly correctable. I get an occasional droop upon great usage? for a period of time like when I went to see "Planet of the Apes" recently on the big screen, my one eye took a little while to stop being droopy. Of course I use my mestinon also.
At anytime I wish though, I can demonstrate what I call my "Igor from Frankenstein" look, and even that is at the point to getting to be almost unnoticeable.
Now, if I can just to get that to flow through the rest of my body parts. I have some improvement everywhere, just not as much as I have noticed in my eyes. Maybe because my eyes are so close to my brain it happens the quickest? LOL, I don't know...
GO BECCA and GO CELLCEPT!
Best wishes,
TJ