@victoriani. Thank you for reviving this thread.
There are many members on MR with hearing loss but few posts.
I, like many others, have no Insurance that covers hearing. All is cash out of pocket.
Most full hearing people view other folks hearing loss as an aggravation... And it is, without a doubt.
We talk too loud, misunderstand others communication attempts, and are just plain a PIA.
My years of dealing with the hearing industry, including the docs, have shown their main interest is in selling disgracefully over-priced hearing aids.
I have found a couple of work-arounds that have helped over the years, including lower cost hearing devices. If there is interest here I will post more later. a2
Hello All. a2jack, your post says so many truths about us who suffer hearing loss. I just joined this forum and read all the most enlightening comments from everyone. Some names of the hearing conditions and other terminology were unknown to me so tried googling some. But I hesitated to post here as I haven’t yet gotten my most needed aids so without this experience I couldn’t be of help (maybe this is why others aren’t posting?). Reason I haven’t is I find it too difficult to find the right ones AND invisible ones despite my being a very old senior! Ah vanity thou follow me to the grave! lol Also like you a2, I distrust the doctors AND the hearing aids from the “scentists” to manufacturers to distributors to dispensers and so on.
However, I’ve surpassed the degree of tolerance of my friends and now I’m urging myself to get up, update my testing and definitely start trying some aids to find the right ones once and for all. Even though I can’t help others with hearing aids experience, may I express my problem here and ask for your help?
It’s been mentioned that’s better to see an ENT first? I went to a
Doctor of Audiology at Audio Health Hearing Centers near me in NYC. He tested and gave me the report, and after diagrams and other hieroglyphics, the Summary:
“Pure tone testing indicates moderate to moderately severe sensorineural hearing loss bilaterally. Word recognition is fair bilaterally. Tympanograms are within normal limits bilaterally.
I understand there‘s not much to discuss once we know we are hearing deficient, but nevertheless I expected him to explain a little the meanings of those signs and widgets, as to which types would fit my case, etc. He was polite but uninterested and gave me their brochure with only 2 types of aids with prices and some promotional offers. I had gone to him with renewed hope of fixing my audio and show my friends how I can stop irritating them with my
“whats?”…but came out depressed and again lost interest in the struggle to fix my problem.
Does anyone think testing at Hunter’s College, Center for Communication Disorders, School of Health Sciences, is a good idea? I was tested there about 3 years or so ago. Their testing was very thorough also testing some areas on my head, forehead, etc. And gave me a 3-page report where besides the diagrams they explained under these titles:
Otoscopy; Pure Tone Testing; Speech Audiometry; Acoustic Immittance Testing; Otoacoustic Emissions; Speech-Language-Voice. And then a “Diagnostic Summary”. I know they’re probably students, but closely supervised, and I see my Report was signed by 3 persons two of whom were doctors showing next to their names:
“AuD, CCC-A Center Director”, another:
“AuD, CCC-A Supervising Audiologist.” and the third one: BS ED Student Clinician.
They also wrote they’re giving me a list of hearing aid dispensers, I don’t know what relationship there is between this Hunter College Dept. and the dispensers, but I seem to have lost the list. Please forgive the lengthy of this post… :d
Will appreciate very much any ideas so I can get started on the right foot this time? ? Rosedala
P.S.
“I have found a couple of work-arounds that have helped over the years, including lower cost hearing devices. If there is interest here I will post more later. a2.” I’m interested and look forward to reading it. Thank you.