Tomorrow is Ella's hearing test....

**RedSoxMama** · March 2009

I feel like everything comes down to how she does tomorrow. All our questions are either going to be answered or multiplied and honestly it scares the crap out of me.

Mrs.JDD · March 2009

I haven't seen your posts, so I'm not sure what is going on, but I just wanted to say good luck!

xbrooklyngrl · March 2009

No, I think it will be fine! Based on what you've said, I think it'll be the answer to most of your questions. Don't worry, it's a good thing!

lizlemon77 · March 2009

I'll be keeping you in my thoughts tomorrow!

I was going to say that I hope they find out that everything is fine but I know that's not always the desired result. They may find something that's really easy to fix and she will be on her way to talking your ear off!

joseysbride · March 2009

Where have I been? I have no idea what is going on with her.

I hope it all goes well, and no matter what you find out, at least you will hopefully know what is wrong so it can be addressed. Good luck!

**RedSoxMama** · March 2009

We hope they find she has hearing loss due to ear infections/fluid. she will get tubes, be able to hear again and we will be done with EI because she will be talking and understanding when everyone is talking to her. that is our best case scenario.

surfergirl28 · March 2009

I hope everything turns out perfectly!

Yodajo · March 2009

I hope your best case scenario happens tomorrow. I can understand why you're anxious about it. Good luck!

Kapalua · March 2009

xbrooklyngrl:
No, I think it will be fine! Based on what you've said, I think it'll be the answer to most of your questions. Don't worry, it's a good thing!

ditto this, and ((hugs)). I know it's nervewracking (sp?)

wellfleet04 · March 2009

Good luck!

But I also wanted to say that even if she needs the EI/speech therapy, it is not the worst thing in the world. LOTS of kids get EI for all kinds of things (Kate was in it twice for gross motor delays) and the services are great and help them to catch up. You would never know now that Kate was gross motor delayed, and I don't think there was any "stigma" to her having EI. I'd rather she have EI services and catch up than have a true medical problem.