I APOLOGIZE IN ADVANCE FOR THE LONG POST I NEED ADVICE AND AM STRESSING. THANK U!! <3
i am, as well, aware the difference isn’t huge, but i don’t feel the test from today does accurately reflect my hearing. the audio and the way i was tested felt rushed and just overall icky to me
i (f19) just found out about 3 weeks ago that i have moderate bilateral cookie bite hearing loss and that it was recommended i get hearing aids. i was worried about it but came to terms with it quickly. i told my mom after getting the initial test done and she did not believe me so she scheduled an appointment with the ent at her work to confirm. i had that test today and i feel really weird about it. the initial test was in the ear and the one today was over the ear.
when i got to my appointment today i was nervous, of course, but excited to meet the doctor my mom talked to me about who had also diagnosed my grandpa with hearing loss (not bio grandpa so not genetic from him). he came in and he asked what had brought me in and that i had been experiencing hearing loss? and i told him yes i had and for about a year or so its been worse. he looked in my ears, said they were clean, and then said they’d do a hearing test. i went for that at the front of the office. when she took me back i was nervous still but the audiologist seemed nice so i felt a bit reassured. she put the over the ear headphones on me but the right ear was not sealed. we started with spoken word where a man would say words and i’d repeat as it got quieter. on my right ear (which my initial test said was worse) i missed maybe 2/3 of the words and on my left it was a little less than that but still i didn’t get them all (like i either couldn’t hear anything or i would say “i don’t know”)… the audio said at the end i got them all right and my results were perfect??? then we did the spoken at 55 dB and she said i got 100% for my right ear which, again, there were at least 2 words i didn’t understand so there’s no way i got 100%… my left ear she said i got 92%… then was the pure tones. my initial test was much more thorough consisting of the guy asking me my symptoms first, going pure tones, word recognition at different volumes, word recognition at 70 dB, bone conduction, and then some new test that they do with static sound and a siren.
long story short, she told me i have mild hearing loss instead and that my left ear is worse (which i avidly do not believe is true as i DO have more issues with my right ear…) and asked me if i thought i needed hearing aids. i said i thought it would be helpful as i can’t hear my classmates like my lab partner or my boyfriend or family when they are talking to me and she made some weird joke about “wow… i see people with much worse hearing than urs and they don’t want to get hearing aids” of course i don’t want hearing aids at 19 but i’m really struggling socially to hear and it has caused a lot of frustration between me, my family, and my boyfriend. she then made a comment about how hearing aids won’t help me at all with how minor my hearing loss is since mild hearing loss impairs hearing in group settings or when someone is not close and that i shouldn’t be surprised when the ha’s don’t help at all. i was like ??? she sent me back to a room to wait for the doctor to come review and when he did, all he did was look at the referral form, sign it, and tell me that i could benefit from hearing aids… but i was not told who to make an appointment with to do so and we just had to leave after he signed it…
no one the entire time asked me about my experience with my hearing loss other than the tinnitus. i don’t believe the mild diagnosis even matches the experience i’ve had (which i did post on this forum before my initial test but will also attach here):
“i’ve been really struggling to understand people speaking to me and it has progressively gotten worse. it is at a point where i am becoming extremely anxious talking to people as almost 50% of what they say, i can’t understand at all. with my partner and some family members its less anxiety inducing (mostly my partner) as i can just keep asking them to repeat but i get very anxious when asking people in my classes to repeat or people at restaurants, drive throughs, appointments, etc. i often will just nod or say “ahh yeah i guess” or “maybe” when i can’t hear someone because i get nervous to tell them i didn’t hear it but if they look at me weird i will then ask them to repeat it. it has gotten worse though. i get frustrated when talking with my partner as i have to have them repeat things over and over or i have to be facing them and looking at their lips to understand them. i get frustrated when i’m showing them something with my airpods and they tell me it’s too loud but it feels too quiet to me. its becoming stressful and since i am a musician, i am scared about losing my hearing. i do get overwhelmed when there’s a lot of sounds going on around me and i was looking into getting loop earplugs but remembered that it would only make understanding people harder. thats what led me to think more about the actual issue”
i believe the moderate hearing loss diagnosis more accurately reflects my symptoms WHICH NO ONE HAD EVEN ASKED ME ABOUT TODAY AT THE APPOINTMENT . i was extremely worried something like this would happen today and of course, it did. my mom, though, now believes me and we are going to work towards getting hearing aids for me before the new year (insurance reasons lol) but this all just felt so wrong to me? (also the test from today does not have the AC PTA listed anywhere)