The BAHA

Today, we had an unexpected blessing. Eleven days ago, Lily had the second of two surgeries for her BAHA sound processing system and for a last surgical attempt to get a prosthetic ear that works for her. We saw her surgeon this morning for her post-op check and he gave the go ahead for her to get the BAHA fitted today. We went to the audiologist's room and the BAHA was immediately put on Lily's head, allowing her to hear from both sides of her head. Up until now, the only time she's ever been able to do that is during a bone-conduction hearing test. Below, the audiologist is running a few hearing tests through the BAHA to adjust it for Lily's needs and preferences. She thinks things are kind of loud now, but the audiologist assured her that she would get used to it - that her brain needs to learn how to hear on that side. They said the hearing part of her brain will actually re-structure itself over the next few weeks to adjust to the change.
Afterwards, we were given instructions on how to use it and care for it at home. On the way home, we listened as she talked to her aunt and cousin on the phone; hearing her say "I can hear things I've never heard before!" brought tears to my eyes. We take so much for granted!

This is a picture of what the BAHA actually looks like on her head.

It's very, very tiny and will completely hide beneath her hair. The other two posts that you see will be used for a prosthetic ear.

Another cool thing is that the BAHA comes with a special "Share the experience" plastic post. We connect her BAHA to this post, plug our ears, hold the post to our head, and we can hear through it just like she can! It's meant to help the parents be able to trouble-shoot any problems, but it also gave her a chance to share her experience with her family.