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Thursday, December 3, 2009

Lazy Eye

So yesterday Natalie had her 6 month check up with her eye Dr. The only reason we ever took her to the eye Dr in the first place was because she had such a hard time walking with out falling off edges. We thought she had a depth perception problem. The Dr gave her glasses 6 months ago and Natalie wore them, but then she wouldent keep them on. The Dr told us it wasn't a strong prescription and if we felt like she didn't need them then she didn't have to wear them.

Well yesterday when we went in for our check-up I told the Dr everything was fine with her vision as far as I could tell and she wasn't wearing her glasses and she was doing well. The Dr started looking at her eyes and she told us that Natalie has a lazy eye, she needs to wear her glasses and we have to put eye drops in her good eye everyday so she is forced to use her bad eye to strengthen it. If it doesn't get better in three months then she may need surgery.

So not what I was expecting for our check-up at all. I am really not looking forward to holding her down every morning and putting stingy eye drops in her eye.

She has an appointment to see her neurologist on the 10th. Hopefully her test results come back before we see him. It would be nice to finally know if she has Episodic Ataxia Type 2.

Natalie is doing much better with her speech. The other day we were driving in the car and she called my name from the back seat to say 'Hove you' which means 'Love you'. I almost cried. Then while we were in the Dr office Ben was joking around with Nat, he asked her if she could say opthamologist, and then Natalie proceeded to say 'Optamommy'.....We both just stared at each other in shock.


You can see in the pic below how her left eye is crossed. The pic was taken the past summer. My mother in law AND my mom both said they thought she had a cross eye then.

2 comments:

Sarah-Jane said...

Hi there...I do not know if you will get this but I was googling episodic ataxia 2 and your blog came up...There is a possibility that my 15 month old may have this. please let me know if you get this email...my email is:
Sarah-Jane.Ploof@ahs.state.vt.us

I would love to talk!

shashank said...

Here is a link to more information about the genetics of Episodic Ataxia that was prepared by our genetic counselor and which has links to some useful resources for those dealing with this condition: http://www.accessdna.com/condition/Episodic_Ataxia/680. There is also a phone number listed if you need to speak to a genetic counselor by phone. I hope it helps. Thanks, AccessDNA