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Old 06-11-2013, 12:46 AM #1
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Wink Greetings!!

tukats,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Click on the following forum. There will be a great deal of friends to help you out.

Myasthenia Gravis:
http://neurotalk.psychcentral.com/forum77.html

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.
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Old 06-11-2013, 07:05 AM #2
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Hi ~ I worked in the "eye" business for many years as an ophthalmic assistant, and I never heard of putting needles in the eyes! I'm sure things have changed a LITTLE -- but I still don't think they put needles in the eyes.

They use drops to dilate the eyes so the doctor can better see into the eye. That can make your vision blurry for a time after testing. It's nothing serious but it's blurrier than it was when you came in. It corrects itself after awhile.

Other testing includes optical pressure, visual fields, visual acuity, photos taken of the inside of the eye, keratometry which measures the curvature of the eye, and of course the doctor checks your prescription. There could be a couple of other tests that I've forgotten, but they are nothing to worry about.

But honestly, I have NEVER heard of putting needles into the muscles of the eyes. If it's something new, then I apologize -- I'd certainly tell you if I knew. But it just doesn't make sense to me.

I wish you the very best. Please let us know how you come out, will you? God bless and please take care. Hugs, Lee
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Old 06-11-2013, 03:37 PM #3
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Hi Lee! Thanks so much for putting my mind at ease...same as when I had a root canal, pl were full of horror stories about how painful it would be...I had no problems. I go for tesying July 3, won't know results til I see my neuro's nirse practitionet July 26. If positive results for ocular MG I neef to see another neuro to confirm. Worst thing about this is mot knowing for sure if I have MG, and if so how bad it cam gey and how fast it migjt prpgress. I'll definitely keep yoy posted!
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