I am learning that getting any equipment for Abby is going to take a long time. Our insurance is notoriously slow. Add to that the fact that Abby's disability qualifies her for Medicaid, which is very helpful, but carries along with it a lot of additional red tape. Maybe the goal is to make the process of getting equipment so slow and painful that people will eventually give up? I'm not sure. In any case, it's ridiculous. We have been working on getting a trial for an eye gaze communication device since November-ish. I just got a confirmation last week that the company had all the necessary documentation to submit the claim to Medicaid. Finally. It had already been approved by our insurance, which is probably what took the first 7 months. Now we wait. And I know it will be worth the wait. I'm just SO anxious for her to have a talker! There are plenty of girls who haven't acquired a device until a much older age than Abby, and are doing well. I don't think there is a closing window of opportunity. But its just crazy that we know there is something out there that will allow her to communicate and its taking so long to get it. I am not ungrateful. It appears that our insurance is considering it a covered expense, which is a good sign, its just that it is taking SO LONG to get it!!! I think it could be much simpler.
The patient cannot talk. She cannot use her hands. She shows the required cognition to use such a device. Give it to her!
See? Pretty simple.
I hope I don't sound ungrateful. We have been so blessed. Whenever we really need something for Abby, we have been able to find a way to get it. Its just that I think this will be the closest thing to hearing Abby talk. We've already been waiting a long time to hear what Abby has to say and she's been waiting a long time to express herself in a way that others understand. Can you tell I'm a little anxious?!?
