They put electrode type things on his forehead and behind his ears. Then they put a tool in his ear that makes different noises. I'm not sure what exactly is happening but I can hear a difference. We got pretty much the same results as we did at our last visit. It appears that Kelson's ear is working but his brain is not responding in a synchronized way. I asked the audiologist what exactly that meant and she compared it to a radio that wasn't quite set on the right station. You can understand part of what is being said, but there is a lot of static.
Apparently Auditory Nueropathy is not a real common thing (much like the other issues that Kelson has already proven he was too tough for, like they hydrops and they chylathorax). We visited with a lady at ECHO today that has worked with other patients with this diagnosis and she said she had worked with 8. All of them had different challenges associated with the auditory nueropathy and different things helped them to cope with it. Some have hearing aids, some have had cochlear implants, some use American Sign Language some use cued speech. Each child is different, and as much as I hate the idea of waiting, that's all we can do right now. Hopefully Kelson will mature out of some of these issues, and if not, we'll just have to figure out what works for him.
We also got a call from Early Intervention today (FINALLY). The coordinator will be coming Friday morning to meet with Trever and me. After that we will meet with a therapist to determine what types of therapy Kelson needs. We have been recommended for speech and hearing help as well as developmental help. They will work with Kelson on these things, but they will also help our family and friends to get the resources that we need to work with Kelson. If we need to learn sign language, they will help us get the resources we need. They will work with Claire for ways to play with Kelson to develop his communication.
This is just another hiccup that we'll overcome together.




