I felt like maybe I should write a post about
Abi and her glasses. I'm sure most of you have noticed that she doesn't ever have them on...
We started this out with her wearing her glasses almost all of the time. She would complain that she couldn't see when she was doing things like reading, doing puzzles, watching
tv, being read to, etc. and would always ask for a 'break' from her glasses.
We went back to the specialist to ask her about this. I know I posted about that... about how the
dr. was telling
Abi "Oh you can too see this." when
Abi would say she couldn't. That really made my protective side come out. I tried to talk to her about vision therapy and was just shot down. I will never go back to that
dr. Even if she was right about everything having to do with
Abi's eyes, I really feel that doctors need to be open and willing to discuss concerns with patients/ parents so that everyone understands and is in agreement about things.
Doug's mom suggested that we try to get her into the Moran eye clinic in Utah when we were visiting because it is really well known and highly praised. I tried but they had no availability. I did, however, get some advice from the guy on the phone to look at their website.
It never stated whether they were for or against bi-
focals for children but it did have a little video to watch that showed what it is like for a child that wears bi-
focals.
Basically in the video it showed how things really close (like if
Abi was eating an ice cream cone or something) are in focus and it keeps her eyes from crossing when she looks at it. It showed that things far away looked fine. But then it showed how anything in between is super blurry. Basically the voice over said that anything in that middle range (books, computer,
tv, people, etc) will be blurry unless they back up or get up really close to it.
This realization really made me feel bad. I knew that this is why
Abi would say she couldn't see things.
I am just not sold on bi-
focals.
So, we got home and I started trying to figure out what I wanted to do about it. To go anywhere besides that one particular
dr, we have to have
Abi on our vision plan and we can't put her on it until late fall.
As I was thinking about this I began to notice that her eye wasn't doing it anymore. What?
In almost a month I never saw her eye cross. Not once.
I was beginning to think that it had gone away whether naturally or miraculously.
Then a couple weeks ago, one night when she was really tired, she looked at me up close and there it went.
Since then she has talked to us about sometimes seeing "two of things" and we've seen it happen again a few times a day.
It is the one eye. It goes inward. Sometimes.
Doug and I just don't know what the right thing to do is.
At this point I have decided that we will put her on the vision plan as soon as it opens and I will take her for a second opinion as well as try to get her into vision therapy. Until then, when I see that her eye is starting to cross or she says anything about her vision the glasses will go on.. chances are they won't be on too much because it really doesn't happen that often and she really doesn't like her glasses. And we all know how stubborn
Abi can be.
I feel guilty. Doug feels guilty. I don't know if we are doing the right thing. I don't know if the glasses make it worse or better. It seems like the more she wears them, the more her eye crosses.
ughh.
Anyway, now you all know the confusion and questions that are going through our mind continually and understand in a way why you never see
Abi in her glasses.