Hello everyone,
im a new member here. I’ve just found out I have hearing loss on both ears and I’m so lost, confused and have so many questions at the same time. I’m so grateful to be able to run into this forum and understand more about hearing loss from all of you. I would like to share my story with everyone and if possible please educate me more on this. I’m a 28 years old woman. For as long as I can remember, I’ve always been having trouble understand television, movies, song lyrics, radio. I can hear the sound coming out but for some reasons I can’t understand them even though I know 90% of the words they’re saying when I look at the subtitles. I didn’t pay much attention at the time because English is my second language and I thought to myself that hmm maybe my listening skill is not good that’s why I can’t understand what the natives are saying. I also experienced difficulties understanding professors as well as group discussions in classroom setting when I was in college. I couldn’t understand up to 90%. Again, I thought to myself my English sucks that’s why, I also thought that voices are harder and more echo to listen to when they’re spoken in a big rooms anyway so I didn’t care much. Now that I think of it, I do have trouble understanding conversations in noisy places, and sometimes i don’t understand certain things when talking to people. for example, we can be talking normally but all of a sudden i cant understand what youre saying and i will have to ask you to repeat. it would sound like you were mumbling. There are also time I cant hear the rain drop outside, running water, doorbell, phone ringing. Life kept on going for me and I really never thought about it. It was til end of December 2022 that I decided to see a doctor for my hearing when I was on vacation out of the country. I don’t really recall why I decided to have it checked but anyway doctor ordered a hearing test ( there was no word recognition test) she told me that my hearing is weak and that I need to use electronic devices less, sleep early or else I’ll end up with hearing aid. She also diagnosed me with tinnitus and gave me some prescription to take. I think my tinnitus is very mild though. It doesn’t bother me at all. I can hear ringing or buzzing sounds if I pay attention to it or when the sorroundings is dead quiet but other than that it’s fine . So I looked up the prescription and they appeared to treat depression. I decided not take them and planned to have my hearing retested when I get back to the states. When she told me I have weak hearing I didn’t think much of it. I thought oh ok it’s just weak it’s not like I’m going to be deaf. I looked at the audiogram and just see some lines going up and down , had no idea how to read them. after I got back to the states, I scheduled my hearing test with an audiologist, and saw her last week. She said I have moderate hearing loss, my low frequency is good but high frequency is not and recommended HA. She said HA will make my life easier, I’m still young and it would benefit me. She wasn’t able to tell me why Im having the loss but we both thought maybe it’s genetic since my sister’s audiogram is very very similar to mine. She refers me to an ENT just to double check that’s everything is fine ( I will see an ENT in 5 weeks) . After I was told that I would need HA, I was shocked and worried. I came home and did more research on HL. The more I research the more scared I become . I have never thought that Hearing loss is so common and can happen so randomly . And it’s actually happening to me. I learn to read the audiogram and it’s starting to make sense . I was in denial and cried for a few days. But it got better as Im browsing this forum. I will share my audiogram here, with questions that I have. Please advise/ educate me so I can have a better understanding. Thank you so much .
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By looking at my audiogram , how bad do you think my hearing loss is in percentage? Does it look like I have lost 40-50% of my hearing ability? do you think HA is needed?
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Is HA painful / uncomfortable to wear? Will my ears always feel like they’re plugged even after the break in period ? I mean will I ever be able to feel like they’re not even there when I’m use to them?
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Will HA worsen my loss? This is what concerns me the most . My aunt told me it will make my hearing worse 🥹
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Will my hearing loss plateau or will it get worse with time? How likely is it that it will get so bad that I’ll loose 100% of my hearing? Says when I reach 50-70 years old 🥹🥹
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HA on airplane and through airport custom? Will there be any problems that I should be aware of? Do I have to take them off?
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my word recognition score is 76% and 72%. I understand that HA won’t restore 100% of my hearing but will it at least bring it my word recognition somewhat maybe up to 90%? I would love to be able to understand better because I’m looking for an office job and I’m so scared I won’t be able to follow instructions or participate in meetings
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Is it possible to have auditory process disorder at the same time as hearing loss . Maybe this applies to me since I don’t understand from time to time ?
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Why do people say it’s best to start wearing HA early / as earlier as you’re qualified for it? What are the cons and pros of starting HA early?
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For those that have servere and profound loss, will you still be able to have normal conversations without the aids or you will definitely need it ? Will severe and profound loss still be able to hear sounds or is it like Dead Sea with no sound at all?
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Is it better to have aids on both sides than one in term of performance? Money is not an issue I just want to get the best quality and treatment.
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What brands of HA are the best ?
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What styles are the best in term of performance (any style that you can recommend for my case) ? Is certain styles better than the others?
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How often does HA need to be adjusted?
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I was doing some research on HA and lots of people mentioned that bringing their HA to the audiologists to have them cleaned . Is it a must? Can’t we clean HA by ourselves? If that’s not an option then how often do they need to be cleaned?
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Right now my word recognition is 76 and 72 will they get worse as I get older with and without aids?
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I’m learning piano right now . If I get HA can I still learn piano?
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Why does HA need to be changed every 5-7 years? Why can’t we keep using the same one
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Why do we need to wear HA all the time and not just when we want to?
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Can I still use my aidpod with my HA on?
Thank you so so much everyone!! 🥹🥹