Hi Trish;

 

Thanks for taking the time to email me. I guess this must be some sort of support group.  I received a few emails from other sufferers.  I am so totally technologically impaired with computers that basically I can only open emails.  I got someone to research & find me some info. on here & he must of put me in touch with some sort of support group. I'm new at this Adie's thing too. I actually thought I was going blind all of a sudden.  I take pilocarpine to reduce the pupil & prevent the migraines but it also distorts my vision.  I work with small instruments & it's at the level where my vision is impaired.  The florecent lights bug me and I can't work with dark glasses inside. A patch would only force my other eye to work harder & put alot of strain on it.  Everyone that I have heard from up to you has had it in both eyes so I question that this disease is not progressive.  I will start on vitamin B complex as it 's suppose to be good for neurological problems, guess it can't hurt.  In the meantime I'm just coping as best as I can.  Please let me know if any discoveries or any new info. on the disease comes up.  Thanks again for writing.

Mimi

Trisha Marie <qcgirl63@...> wrote:

Everyone suffers differently but yet the same. Mine gets blurred but then I have days when I have no side effects.

Trish.

"Zamirowski, Jody" <Zamirows@...> wrote:

I'm constantly surprised by how my Adie's eye seems to freeze up in a blurred position. I'll go along fine not thinking a lot about it and then it will just stop focusing, especially when I'm reading. I was diagnosed in January and am still adapting to it. I did go to get new glasses. My doctor had recommened I wait a few months after diagnosis to see if my eye improved. Strangely, both eyes were quite a bit worse than when I had last gotten new glasses in December (pre-Adies). Does anyone know if it will progressively get blurrier, or should this now be the extent of it?

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