Robyn -
I don't know if I'd be "lost" without it. There are others who are SSD and they adjust very well.
But I was not one of those who adjusted well. I hated being SSD from the very beginning. I was asking my neurotologist about the BAHA within days of my AN surgery.
I can tell you that personally I find it's made a huge difference in my life. As I told me neurotologist about 6 weeks ago, I feel "whole" again.
Just this morning I was at the driveup window of the bank and I had forgotten to put my processor on. Being deaf on my left side it was very difficult to understand what the teller was saying to me. I had to ask her to repeat herself not once, but twice. If I would have been wearing my processor, I would have heard her clearly the first time.
I also find that it helps me a lot in both social and business situations. For example, when sitting in a meeting at a large table with my colleagues, I no longer have to seek out the seat where I will be able to hear everyone. I also don't have to turn my body and sit sideways - with my "good" ear pointed towards the conversation - like I used to do. Now I can hear people regardless of whether they are on my "good" side or my "bad" side.
Jan