self-diagnosed adultRecently I decided to google around and see if I could find anything on the internet matching my problem of not being able to understand people in noisy places even though hearing tests say my ears are fine and everyone around me doesn't seem to have the same problem. I found a thread that mentioned CAPD and it sounded like the most likely culprit. This has been an issue my entire life, and now in middle age I find an explanation but it seems treatment is all for kids, which makes me wonder if there's anything that can be done for a middle-aged guy like me, or if I'm just stuck. Not that I have any money to look into treatment anyway, but I am wondering if that's even a possibility. |
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Re: self-diagnosed adultWelcome Cheroid. You might want to look into a book called "When the Brain Can't Hear" it's a book by a APD suffering audiologist. It's a pretty thorough book, it goes into detail about many different ages of people who have issues with APD. But nothing can be as conclusive as having testing, it's worth the investment. |
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Re: self-diagnosed adult Hi cherold
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Re: self-diagnosed adult
I wouldn't say there isn't treatment for adults, but you'd have to talk to a speech language pathologist that specifically works with CAPD about it. There are many programs out there that work with different aspects of CAPD, depending on what you're specific diagnosis would be. I happen to know that Earobics has 3 levels, the last one is meant to go up to adult teaching. For peace of mind, and to empower yourself, testing is the best thing. That way, you can get strategies on how to deal with the problems that come up in life. What can it hurt to get tested? At least you'd know what exactly you are dealing with, and how to overcome it. Diana |
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Re: self-diagnosed adult Hi cherold and Diana
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Re: self-diagnosed adultHi, I was diagnosed when I was in my mid-20s. I've found that while my diagnosis didn't particularly "do" much for me, it did help me come to terms with my disability. Also, once I had my diagnosis I developed more confidence in asking for the support I needed in work and at school. I was able to take a lip-reading class which was paid for by my health insurance as well. And just being able to put a name on my problem was especially helpful. |
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Re: self-diagnosed adult I can see getting validation that this is an actual thing is important to a lot of people here, but for me, if there's no treatment I don't much care why I have these problems. I have a lot of brain oddities - I appear to have both CAPD and a relatively mild case of prosopagnosia (a.k.a. face blindness - it can take me weeks or months of repeated contact to recognize someone's face, but that's a lot better than people who can't even recognize their own parents' faces), and while this is far less important, I also can't visualize things. It took me a long time to realize any of this was unusual (and the article on CAPD mentioned things I still never thought of as all that unusual, like my need to have people at work email what they want done so I don't forget it), and longer still to put a name to any of it, but knowing it's a thing serves no purpose beyond giving me a way to explain to people what's going on with me, and I think people are as likely to believe me with or without a doctor's verification.
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