I have a hearing disability, so talking on the phone is a struggle. I have to concentrate on every word the other person is saying, but I still end up missing a good bit of the conversation. It’s extremely frustrating for me to have a phone conversation.
However, texting is a breeze. The words are right there for me to read and with the use of emojis the context and emotions behind those words is understandable.
Which do you prefer, texting or talking on the phone?
I’ve worn the BAHA (Bone Anchored Hearing Aid) implant for a couple of months now, so I thought I would write an updated review.
On the plus side, I am hearing a lot better with the implant. The other day, I was listening to crickets. I thought it was so funny that they sound like birds. I also find it easier to communicate with people. A few times, I even understood what someone behind me said. That was cool.
On the negative side, the outer processor is very delicate. I can’t wear it when I am engaging in any physical activity. I also can’t wear a hat with the outer processor. That has been frustrating for me, since it limits my ability to use the BAHA implant.
I would still recommend the BAHA implant to anyone that needs it. It is a great device and I enjoy having it.
I finally got the outer processor for my BAHA (Bone Anchored Hearing Aid) implant this week. I am not really sure how I feel about it yet.
I am hearing better, which is great. However, it sounds a lot different from a typical hearing aid. I struggle to understand what people are saying, but I guess that will get better as I get used to the device.
The outer processor has a magnet, which attaches to the magnet under my skin, and sends the sound vibrations to the titanium screw in my skull, which then vibrates to send the sound directly to my inner ear. The two parts are working great together and putting on the outer piece is really simple. I just hold it up to my head, so the magnets can pull toward each other, and it pops into place.
The downside of the magnet system is the outer processor can be knocked off my head. It’s a delicate and expensive device, so dropping it is not recommended.
The audiologist did give me a clip with a plastic wire that can attach to the outer processor and then it can be clipped to my shirt. I am not a fan of this device. I feel like a preschooler, whose parents clipped stuff to their shirt to prevent them from losing it.
In about a week or so, I am going to write another blog post about the implant. By then I will be used to it, so some of these problems should be solved.
I had to take my laptop to Mac Resource Store, because I accidentally got droplets of glue from a spray can on the keyboard. When I picked up my laptop, I was still wearing my bandages from the surgery.
The employee that helped me checkout is named Eric and he asked about the bandages. That’s how we got to talking about ear surgeries. Turns out, Eric also has hearing loss and he got a BAHA implant a few years ago. We talked a little bit about the surgery and other surgeries. We both had mastoidectomies done and we have even seen some of the same doctors.
I had a great time talking with Eric, because I don’t know anyone who has undergone similar surgeries as me. When I get the outer processor for the BAHA, I am going to visit Eric again, so we can compare thoughts on the device.
It may sound funny, but I am kind of glad I messed up my keyboard. I got to meet a great person that I can relate to in a way I have never done before.
I’m at Huntsville Hospital waiting for my BAHA (bone anchored hearing aid) implant surgery. I am a bit excited, because this should significantly improve my hearing and my ability to understand what people are saying.
I often repeat things or rephrase what I just said and say it again. If I have something important to say, the likelihood of repeating the statement goes up drastically.
Why is that?
It’s a subconscious behavior. I am not really thinking about it at the time. It comes from a lifetime of misunderstandings due to my own hearing disability.
I automatically assume the person may have trouble hearing me or understanding my statements, so I feel the need to clarify.
There are some disabilities which are invisible, meaning you can’t tell the person has the disability just by looking at them.
Hearing impairment is an invisible disability and that can lead to all sorts of misunderstandings.
- If someone greets you and you don’t respond, they usually assume you are rude. They may never consider you are hearing impaired.
- Failure at school or difficulties following directions may be viewed as an intellectual problem, if the hearing disability is not addressed properly.
Family and friends will shrug off my failure to respond, my problems with understanding, and even answers that make no sense. They know about my hearing disability and they understand how it causes problems in my daily life.
Strangers or even people that don’t know me very well, may assume I am rude or stupid. They may allow their assumptions to stop them from getting to know me, which I think is sad.