r/deaf • • 4h ago

Daily life Self-isolating

8 Upvotes

I’m HoH and have been for about 20 years. My hearing is bad enough that even with my hearing aides if I can’t see someone’s face I can’t understand I them. I just sent my husband off to a social event without me. I don’t know any of the people and standing around making small talk is exhausting. So basically, I self-isolated but now I wish I had gone. Although, I know the reality is it would have been exhausting and depressing. I have 1 friend in town. My main social network were work colleagues but I retired and they are all in DC. I am very isolated and wondering why I didn’t just go even though I doubted it would have been much fun.

I guess, I’m just posting to put this out where others will understand. My husband is compassionate and supportive, but let’s face it, he doesn’t “get it”. How many of you self-isolate, or how have you moved past it?


r/deaf • • 9h ago

Hearing with questions How do I tell my deaf neighbor that his smoke alarms have been chirping since we moved in?

22 Upvotes

We’ve only said hello in passing but we did get their phone number at that time.


r/deaf • • 13h ago

Technology reducing background noise…how?

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2 Upvotes

Question for everyone who uses CIs and the Nucleus Smart app:

I'm currently facing the following problem: I can't open the app anymore. I need IO18, but I can't install it.

I really rely on the app, especially the “reduce background noise” feature (in noisy environments).

Does anyone have any ideas on how to activate the background noise feature some other way? Does anyone know of other apps that can be used instead?

For the other settings, I use the iPhone’s built-in settings anyway, but that feature for background noise isn’t available there…

It’s frustrating how much social participation depends on the smartphone’s current operating system…

I’m grateful for any tips <3


r/deaf • • 1d ago

Daily life My take on Deaf/Hearing relationships

13 Upvotes

🤟Recently, there’s been lots of conversations about deaf dating hearing.

It’s my turn to talk about this.

Not all deaf / hearing relationships are bad.

Yes, we have up and downs but it doesn’t meant that our relationship will fail because each of us came from different world.

We always have wonderful time introducing each others to new things.

How you can find somebody special if you only limits people from your own community and world?🤟


r/deaf • • 1d ago

Hearing with questions Movies about the Deaf experience?

8 Upvotes

Hi! I’m hearing, and I’ve long been interested in ASL and the Deaf culture. I was wondering if there are any movies that are filmed from the Deaf experience. I know there’s quite a few good ones about Deaf folks, but are there any that are filmed to be from a Deaf perspective, ie. little or muffled sound, or maybe sounds that change with the presence or absence of cochlear implants? Or maybe something directed/written/filmed by a Deaf person. Anything of the sort would be really cool! I know there’s a lot of bad portrayals out there, so I’m just curious what yall would recommend.


r/deaf • • 1d ago

Technology 'Frozen' animator launches an interactive ASL learning app and vows to keep it free forever

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58 Upvotes

"Josh Staub created the app as a labor of love alongside Deaf animators, engineers, and other collaborators."

“I want it to be very clear that learning from a Deaf ASL teacher is by far the best way to learn the language,” Staub told Upworthy.


r/deaf • • 1d ago

Deaf/HoH with questions Request interpreters for social/network events

4 Upvotes

Just a random thought I've been mulling over lately. I've noticed that almost all the Deaf and HoH people I know tend not to request interpreters for informal social or networking events (and as a result, end up skipping them altogether).

I'm really curious about the main reasons behind this. Building relationships with peers, colleagues, and supervisors is so critical for career development, and simply knowing the people around you better makes the day-to-day work environment way more comfortable. From a career standpoint, being there definitely seems beneficial.

Part of why this is on my mind is because I try to go, and sometimes literally have to fight with the accessibility coordinator just to get an interpreter approved for these kinds of events. It makes me wonder if people are just burned out from the administrative pushback (since social events are rarely treated as a priority), feel like these events aren't worth the trouble, or if there simply isn't a common norm yet around bringing interpreters into mostly hearing social spaces. Or maybe there are other factors I'm completely missing.

For those of you in school or the workforce: do you request interpreters for professional social/ networking events? If not, what's the main reason you skip them?


r/deaf • • 1d ago

Deaf/HoH with questions Provider dropped me

28 Upvotes

So today, a provider responded to my paperwork and had her assistant schedule me for an appointment after months of waiting. We talked about the time, location, got things squared away. Before we ended I made sure to request an interpreter. The assistan got cagey and said she would have to talk to the Doctor about that decision, and the call got wrapped up pretty quick. 20 minutes later I got an email saying they were dropping me as a client. The only things different between going ahead and being scheduled and being dropped was an interpreter request that the assistant framed as 'something the doctor would need to weigh in on.'

Do I have any recourse at all? I called and demanded why, no real reason was given.


r/deaf • • 2d ago

Hearing with questions For my fiancé

0 Upvotes

Hello, I was hoping I could gain some insight into learning ASL and potentially Spanish sign language if the dialects are different enough. Are there any good apps or websites I should turn to that are budget friendly? I'm not in a great spot to drop a ton of money. Any and all advice is appreciated!


r/deaf • • 2d ago

Question on behalf of Deaf/HoH Based off a true story

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32 Upvotes

r/deaf • • 2d ago

Hearing with questions NYC's top art cinemas still treat open captions as a special event

19 Upvotes

I'm hearing, and English isn't my first language, so I'm posting here as an ally, not speaking for Deaf viewers — please tell me if my wording is off.

At NYFF and MoMA, open captions are only on select screenings. For most English-language films, the alternative is a borrowed cup-holder device. I'm asking them to start with Q&A screenings, especially for films that only screen once or twice a year, because there's no second chance to catch them.

Petition here, happy to hear feedback: https://www.change.org/p/make-open-captions-the-standard-for-english-language-films-at-nyff-and-moma


r/deaf • • 2d ago

News After Godzilla star Kaylee Hottle died aged 18, her deaf sister is taking over her role in a disability-led superhero film

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82 Upvotes

Kaylee Hottle sadly died in July. Her final role was set to be in the upcoming film What Doesn't Kill Us alongside Marvel star Alaqua Cox. Now her sister has taken over, the producer/writer says he wanted to maintain the representation both on and off screen


r/deaf • • 2d ago

Deaf/HoH with questions vrs? virtual interpreters????? convo app???????????

0 Upvotes

hi! im HoH. ive recently started accepting and requesting accommodations that make my life less difficult

im a community organizer, im try to find an interpreter for this sunday for an organizing meeting because the last one i did without an interpreter hurt (metaphorically) MUCH. much much short notice so im looking into virtual interpreters who you dont need to book far in advance for. there seems to be many different services that might offer this in this context but it seems like a lot of them are for companies and like stores and stuff, which i am not. i am also relatively poor and cant afford to pay a whole bunch. my girlfriend sometimes interprets for me but they are not available. i saw a Deafie on instagram recently posting about using the convo app and how it was helpful for her. has anyone experience this service??? how do i use virtual interpreters, how do they work? help 🥲

thank you in advance <3 sorry if this question has gotten asked a lot, thank you for your patience!


r/deaf • • 3d ago

Vent Increase in hearing fatigue

11 Upvotes

Twice now in 2 weeks I’ve had migraine inducing hearing fatigue, and I’m starting to get to the point where it’s pissing me off. I wear my hearing aids all day every day and I’m in a mostly quiet environment most of the day.

What’s worse is that emotionally and mentally I feel okay until the physical symptoms start to appear, and then I have to excuse myself to put my hearing aids away and tell everyone that I need some alone time (with peace, quiet, and 1000mg Tylenol)

I’m so over it 🫩


r/deaf • • 3d ago Heartwarming

Deaf/HoH with questions Every Deaf/HoH Person Should Learn Sign Language

63 Upvotes

I grew up in a hearing family, was "diagnosed" with a "mild, cookie bite hearing loss" when I was 4 years old. The audiologist recommended hearing aids, so my parents bought a pair of CICs and I refused to wear them. The fact that you could still see them in my ears was mortifying to me. I was 5.

The "hearing loss" progressed throughout my life. We revisited hearing aids when I was 11. Got another pair of CICs. I wore them in class a few times, but then this girl I liked saw them and asked, "What's in your ear?" And I was, again, mortified. I never wore them again. I was always socially clumsy, shy, and pretty enraged growing up. I felt like I was constantly left out and it infuriated me. I never dated anyone throughout all of grade/high school. And I NEVER told anyone about my "hearing loss."

In college, I really noticed the impact because I was always around people. In grade school, you go to school and then you come home and I would isolate when I was at home. But in college, you have roommates, there is a lot more social activity, etc. Plus with the "progressive" nature, I perhaps felt its impact more strongly. I started to tell people about my "hearing loss," mostly because I was in such close contact. I told my closest friends and my roommate, etc.

I was so depressed in college. I found drugs (weed, mostly) and got super into that. (Didn't love drinking.) I would skip class and play video games alone or stay up until 6am smoking weed, binge watching shows (before streaming, I was OG binging), etc. I did exceptionally well in grade school and high school and my test scores were really high, I took a lot of AP classes and basically tested out of my Freshman year of college. In college, as an engineering major, I got Cs, Ds, and Fs the first year or so. Part of it was I was in a lot of sophomore classes so I had no real "on ramp" introduction of how to "be in college." Sophomore year I did better, I think because at the very least I was accustomed to college life a bit more. Junior year, I went on anti-depressants and I decided to get hearing aids, another pair of CICs, but I only wore them for class, never socially. I lost my virginity Junior year but still never had a girlfriend. I dropped out second semester Junior year. Senior year, I re-enrolled but then dropped out again and left school after first semester, moved back home.

Back home, I got a job waiting tables and met my first girlfriend. I was wearing my CICs more often now -- I literally had to as I waited tables for a living lol -- and I was dating this person I predictably fell utterly in love with. We broke up after 6 months and it shattered me. I started a series of very unhealthy patterns re: relationships in which I would become obsessive and try to get back together, only for it to go the same way again. It is a really dark part of my life that I regret. It's not an excuse, but I was so miserable and mired in such unfathomable darkness, it all feels like a blur.

I started performing stand-up comedy. I think it was a way for me to express myself in a world where I felt like I couldn't. It was also nice because I got to talk and the audience listened. (Most of the time.) They came out with a new hearing aid called the Lyric (from Insound, later bought by Phonak). What made the Lyric special was that it was 24/7 wearable and it was fully invisible. Literally. It sat inside the ear canal so deeply that nobody could see it. And the battery was housed inside the unit, so you wore them until the battery died and then your AuD replaced them. It was a subscription model. I got those pretty early, around 2008, and sort of never looked back. They allowed me to hear well enough (I thought) and called zero attention to themselves. There were some rough edges with them, but it was by far the best "solution" I had ever seen. The underlying darkness, depression, anxiety didn't go away, but I felt like I had resolved something.

Over the next 15 years, I continued to wear the Lyrics. My "hearing loss" "progressed" and probably took me out of range for Lyrics, but I kept using them anyway. I couldn't fathom a world in which I switched to a different, visible hearing aid. I didn't even let myself think about the prospect of my hearing changing, I pushed it out of mind as much as I could.

In my late 20s, early 30s, I started to be a bit more open about it. I talked about it on stage, I would tell people I wear hearing aids, I would allow myself to say "what?" more often. (I used to not let myself say it. Ever.)

Around 37, I got an ear infection which meant I couldn't use one of the hearing aids. I noticed that with only one, I could barely function in the world. I felt isolated. This also coincided with a bout of tinnitus that nearly ruined my life. As dark as life got, and as depressed as I was throughout it, I was never suicidal. Tinnitus was the closest I had ever come to suicidal ideation. I didn't want to kill myself, but I couldn't imagine living this way for the rest of my life. I was so depressed and alone. I wasn't sleeping, I wasn't going outside. I just sat in my apartment (this was post-Covid, so it was like a reprise!). I went to an ENT for both the infection and the tinnitus. The infection eventually cleared up, but the tinnitus remained. The ENT asked me to send him all my hearing tests throughout my life, so I went to gather them. Seeing them all at the same time, looking at the progression, it was a bit shocking. I sent them in and he said, "Your hearing loss is severe." Which is a word I hadn't heard before. He said I was a candidate for a cochlear implant, which was a jaw-dropping thing to hear. He also said that he had no idea it was so severe because of how well I interpolate. I didn't know what he meant, but he explained that I must be figuring out what people are saying in my head. And on some level I knew I did this, but nobody had ever named it before or given it contour. He said, "You must be working really hard."

And I broke. I don't even remember the rest of the appointment. My whole life flashed before my eyes. I was sobbing on the train on the way home. I FaceTimed my best friend's mother (who is a HoH hearing aid user and an AuD herself) and just sobbed 37 years of life out into a phone. Every single moment of my life was suddenly made clear to me. The LABOR it all required, was suddenly laid bare. This thing I denied was suddenly staring at me in the face. I just needed to say it. The thing that I had not wanted to say my entire life. That I had tried so hard to prevent people from knowing...

I am Deaf.

And with that came so much grief and anger, so much crying... but also so much clarity. Oh. I'm deaf! Like if I stopped fighting it, all of this energy got freed up. It was liberating. I felt lighter.

The first thing I did was go to my audiologist and tell him I wanted new hearing aids, the right hearing aids for me. He fit me with a RIC from Phonak and it was night and day. I of course did not realize how much I was missing. I was like a poster child for a hearing aid company... "And then I go hearing aids, and I could hear everything!" Of course it doesn't work like that. But it was a significant improvement. The world sounded so different. I went to lunch with my cousin and I thought we were talking way too loudly lol. Also they helped manage the tinnitus, which never went away but eventually habituated.

I went on like that for about a year. One surprising side effect of these hearing aids was that they were more traditional. Where the Lyrics stayed in your ear 24/7, these hearing aids went on and off. You could wear Lyrics in the shower, to sleep, etc. But these new ones, I had to take them off to shower, to sleep, to charge, etc. I was more often in touch with my Deafness. My body, without hearing aids, was something I experienced more often. And it started to change how I viewed myself, and hearing aids. Hearing aids started to feel like a costume I had to wear in order to matter. In order to be considered valid. In order to be worthy of my friend's or family's time. If I didn't put these on, then what? Who is going to meet me here? Do I just cease to exist? Do these relationships disappear? It was confusing. And it made me sad.

A year after the ENT appointment that rocked my life, I started to think more about the "progressive" nature of my "hearing loss." And I thought, in the future, what if it gets to the point where hearing aids don't allow me to function the way I'm used to. Maybe one day I will "need ASL." So I thought, maybe I'll start learning it now, might as well get a head start.

I signed up for a class, 6 weeks, low commitment. I knew zero ASL beforehand. (Maybe I knew half the letters?) I was so Deaf-ignorant, I even emailed the school and said, "Your website says there is no voicing in class. How will people who don't know any sign language be able to learn?" They emailed me back, very nicely, and said, "Don't worry, we use slides and everyone comes in with little to zero knowledge!" I felt more comfortable.

I showed up for the class and it was a bit strange to see a purely Deaf space. Chairs in circles. Multiple classes in the same room. A flashing light doorbell. I had ZERO Deaf friends and had never really met a Deaf person before.

From minute one, from the first sign... I was completely transformed. Within 10 minutes, I thought to myself, "I think this is going to change my life." And that was an understatement. I fell so utterly in love with this language. It was all I talked about. All I wanted to do. I studied as much as I could online. I started going to Deaf/ASL events. ASL museum tours. ASL happy hours. ASL interpreted shows. I was in way over my head, but the more I went, the more I improved. I started taking multiple classes at the same time. I signed to myself as I walked around town. As I sat on the couch and watched TV. I met Deaf and HoH people. I met hearing signers, interpreters, CoDA, etc. After 6 months or so, the school asked ME to teach Level 1. I was rapidly improving and I couldn't get enough.

To be in a space where I didn't have to work to be there... I can't explain what that did to me. At ASL social events, it was the first time I never noticed time passing. I wasn't scanning the room or noticing things around me; I was so locked in on the conversation, the person I was chatting with. I was a fundamentally different person. I didn't even know this was possible. I never dreamed something like this could exist.

The class also included bits about Deaf history, Deaf culture, Deaf identity, Deaf awareness, etc. One slide said, "Deaf children who grow up without access to sign language or the Deaf community can feel depressed or have low self esteem." All the hearing students were like, "Oh interesting." And I was like... sobbing.

It fundamentally reshaped how I saw myself. My identity. I feel like myself in ASL even though I'm so new to it. I didn't realize how MUCH I was carrying in order to function in hearing spaces, and how much that was interfering with my ability to connect. To relate. To exist.

I've spent the last 2.5 years immersing myself as much as I can in ASL. I still lead a bit of a "split life." Because I am so adept at "passing" I have a lot of tension around it. I have friends, family, work... relationships that are all built on my "passing." But I don't want to pass hardly ever anymore. So the inertia of my life is in conflict with the momentum of my identity. This is something I am trying to resolve, but my goodness, I am so glad to be here rather than the darkness I was in for so long.

My point is not that everyone has to go "full Deaf" or "hate the hearing world!" My point is that without sign language, without knowing other Deaf/HoH folks, I could never understand myself. Without giving myself the exposure to what life is like when you DON'T have to work, or pass, or carry the burden of interpolation... I would never know how much it was costing me. I would never be able to CHOOSE how I want to show up in the world. And I think it is a birth right for every Deaf or Hard of Hearing person, at any age, to be able to CHOOSE. And sign language is the key that makes that choice possible. To be denied it or to be without it is to be denied choice, to be denied agency, to be denied IDENTITY. And I don't care who you are, nobody on earth deserves the pain of that level of denial. You deserve to decide what it means to be YOU.

TL;DR -- Sign language is the most beautiful thing on the planet.


r/deaf • • 3d ago

Other I created a Discord community for Deaf/HoH and trans people! 💜

34 Upvotes

Hey everyone! 💜🏳️‍⚧️🤟

I recently created a Discord server for Deaf/Hard of Hearing and trans people!

I got the idea after seeing a discussion on here and realizing how difficult it can be to find a community where these experiences overlap.

It's a brand new server, and I'm hoping to create a welcoming space to connect, share experiences, support each other, or just hang out and make friends!

The server is mainly aimed at adults, but younger people who meet Discord's age requirements are welcome too. Allies are also welcome! 🌈

Feel free to join or share with anyone who might be interested!

🔗 https://discord.gg/D4zUFe6Zg

PS: Sorry if this post isn't allowed!


r/deaf • • 3d ago

Vent Just got hearing aids. Feeling extremely down and hopeless. I need some Deaf pride to help me feel better about the fact that they didn’t magically turn me into a hearing person

34 Upvotes

I know there is no “hearing loss,” only “Deaf gain!” I have an amazing Deaf community where I live. But I work only with hearing people and I’m feeling so isolated.

Today is my first day wearing them at work. They’re super helpful, but not perfect. Even with them on and turned all the way up, I still only understand a fraction of what is said in conversation. If someone mumbles something across the room, I don’t hear it but my hearing colleagues know exactly what they said and can respond to it.

Even with these devices in my ears that cost an entire month’s paycheck out of pocket, I STILL need to deal with the obstacles that come with being a non-hearing person. I knew going in that they won’t make me hearing, but I still feel completely hopeless. My one way out from all the challenges and frustrations of Deafness wasn’t a way out, I’m still very much in it.

I guess I’m just having an existential crisis. I will be Deaf for the rest of my existence. This is as good as my hearing will ever get. I know Deafness should be celebrated. But deep down, it’s a horribly depressing feeling that I am living without one of the senses that is necessary to function in society.

Anyone else ever get these feelings? How did you deal with them?


r/deaf • • 3d ago Heartwarming

Deaf/HoH with questions Any trans Deaf/HoH people?

51 Upvotes

I feel kinda lonely in both my identities (HoH + ftm) - I have few trans friends and only one hoh friend (but she's not a SL user) but none who are both and it just feels kinda isolating :/

Anyone trans and Deaf/HoH?

Please tell me about your experiences and something positive please?

I just kinda want some hope :')


r/deaf • • 3d ago

Question on behalf of Deaf/HoH Where does everyone place their captions for Youtube and other video players?

5 Upvotes

is it easier to follow if captions are able to be placed anywhere in the screen you want?


r/deaf • • 3d ago

Technology Halliday's new glasses finally let me keep eye contact while reading captions.

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5 Upvotes

I review smart glasses and AI wearables every week for a show called Proof Cases. I'm Deaf.
Halliday sent me their second gen, the G2, to test. The thing that actually matters: on the first gen, the caption light sat off to the side, so I had to look away to read it. You'd think I'd stopped listening. On the G2, the words sit on the lens, both eyes. I can hold eye contact and read at the same time. That's the first time any pair of glasses has done that for me.

Then I hit the part that still isn't fixed. Captions run on a credit system. Translation is completely free. I timed both: captions took about nine seconds to catch up, translation took about ten, doing twice the work. So the piece that actually helps Deaf users costs money, and the piece that doesn't is free.

Disclosure: review unit provided by Halliday. They didn't ask for this episode and had no editorial input.


r/deaf • • 3d ago

Hearing with questions Classical Music for Deaf Audiences?

0 Upvotes

Hello! I am a hearing classical musician currently learning Auslan for fun. As a beginner Auslan student and professional classical musician, I have been wondering how music is experienced by d/Deaf audiences, especially acoustic music that might not have the same bass levels as EDM/club music.

I would like to learn about how classical music is enjoyed by the d/Deaf community currently, and how my concerts could be made accessible. Any resources, personal experiences and advice are appreciated!


r/deaf • • 3d ago Bravo

Other Gallaudet and International Students

5 Upvotes

I find it bizarre that many Deaf American students at Gallaudet University are not exactly welcoming to international students who come to study at the university unless they are from Canada, Europe, or those already familiar with ASL and American culture and they are usually White. American students at other colleges and universities in the United States have no problem interacting with international students so with Gallaudet University being the only university for the Deaf and HoH in the world, I find this behaviour of Deaf American students to be astounding even to hearing Americans that I often wonder what exactly Gallaudet is supposed to be other than it being a party college. They seem to not mind meeting Deaf people in other countries and learn their language and culture, but at Gallaudet University? Most of them are not interested in getting to know international students and are choosy about it. I wonder if they behave that way due to Gallaudet's social hierarchy mentioned on Deaf U.


r/deaf • • 3d ago

Deaf/HoH with questions Newly deaf Dad. Struggling with my kids. Could use some encouragement or kind words.

130 Upvotes

Hey all. I could really use some kind words.

36yo Dad to two toddlers. I recently became completely deaf (4 weeks ago) due to an illness, and I'm just struggling. I have a great counselor/therapist, my family and Wife are SUPER supportive, honestly I'm amazingly blessed by how people have been coming together for me.

But I'm just battling not being able to talk well with my kids and missing out on what we bonded over most (music).

Due to the speed at which I lost my hearing (over the course of only 3 days) we were not able to really prepare anything. We are diving into ASL but it's just not possible to be fast enough for many things. My wife and I have learned enough to do very basic talking and I'm really good at reading lips. So with her, things have gotten much better for her and I.

But with my kids, they mumble and the younger one is just starting to form talking sentences, let alone now adding ASL to his list of things to learn. I can't read their lips and they still struggle to grasp that they can't get my attention verbally. They have been so amazing at wanting to learn ASL, but this interim "gap" before they learn more is just so hard on all of us.

They throw sad tantrums they can't communicate with me, that I dont know what they need. And it just hurts my heart. They are taking on a huge new mental burden on my behalf.

I KNOW it will get better. But I guess I just needed to write this out and maybe seek some encouragement that things will work out. I've come to terms with loosing my hearing. But seeing other people (my wife and kids) struggle hurts me.


r/deaf • • 3d ago

Deaf/HoH with questions Deaf colleges

7 Upvotes

Have any of you gone to deaf colleges, if so what was your experience? I’ve been losing more and more of my hearing and know no other deaf people in my life. It’s really lonely and I sometimes consider transferring to a deaf college where I could know more people like me who have the same struggles


r/deaf • • 4d ago

Hearing with questions everyone thinks im deaf, i am not deaf

2 Upvotes

hi i am look for advice because i have a issue where everyone thinks i am deaf but i am not deaf. why thi shappened is so i do have higher needsautism i can type well but not talk on the phone and issue talking in person but can do it to diff abikities depending and sereve mental illnesses so i use to never be able to make phone calls even if i t was a emergency and i had to ring emergency services i cannot do phone calls.

so then i found out about a relay service and ever since then i have used that for my phone calls basically. and it is great because now i make lots of phone calls when before i couldnot ever make one even in emergency.

something i find though like today i had contacted the building person and told htem my electricity issue and but htey kept having electricity people just show up to my door unanncouned and ring me and i cannot anse phone calls so they kept cancelling the job so it been broken for over 1 month. so i rang the bukldiing thing again and i told them they need to tell me before they come (i cannot answer door with no notice unprepared) and they cannot ring me they have to text.

and they told me they would write a note saying that which they did but it is clear they also wrote a note saying i am deaf because the people came and didnt knock sent me a text and when i open the door they just be talking very loudly and doing hand gestures for things which is fine but i just know they said i am deaf.

and it ok ish in this instance but i find alot of the time when people find out i am not deaf then they told me to just call them normally now or accuse me on malcious intent. like i gone to the dentist the other day i had to ring for appointment and i speicifically even told them on phone (i do this sometimes to save the awkwardness of them thinking i am deaf) i told them i am not deaf i have autism also told htme this because they kept saying i will need a intreper for the appointment or they wouldnt book it and i had to keep saying i dont need a interper but they wouldnt let me book then so i told them its just because i have autism that i ring on this so they agreed to book it. but ive other times where ive been literally refused appointments like by a pyschaitrist because they told me i forogt exactly how it was read but basically beause that pyschaitrist didnt know auslan

and i was upfront and i was like okay i dont even know auslan and i said i just have autism and dont need a intreper or anything and this was after i had already booked and PAID for the appointment online i just rang to aska question and because i rang ont he deaf service then they kept saying they are going to cancel that appointment now because that pyschaitrist doesnt speak auslan even though i told them so many times even i dont know auslan (australian sign lanaguge) and said i can talk in person and hear and stuff.

when i went to the dentsit for that appointment then after the appointment she said to just ring her normally in future for appointments. and i find this happens alot. when people find i am not deaf then they will start just like basically bullying me for ringing on the deaf service and not answer my calls on it anymore.

even the public housing govermetn too i use to ring them on the relay service and a few times was answered and they were rude and tellnig me i am not deaf ring normally (they know i have autism and sereve mental illnesses they have my whole files and i have speicic workers there) and they accuse me of ringing them on the relay service saying i am doing it because the calls are recorded (implying im going to use it against them which is never something i have done) then they refuse to answer my calls on that now and they ring me normally and refuse to talk to me over text even though i tell them answering the phone call is never going to happen.

people often act weirded out when they find out i am not deaf like if i book a appointment then go in then they are like why did you ring ont he deaf srevice and what i always say is i say either i am scared oof phone calls or i say because i have autism and am scared of phone calls. and apparently people are not happy with that answer. or sometimes i told them its because i have a speechdisorder which i actually have/ use to have childhood apraxia of speech it use to be very sereve when i was younger so people couldnt understand me i am older now so i still have it but sometimes it is not noticable or too noticable but sometimes it is?

like ive told people before i have it and they tell me no i dont and then tehre is other times i am just talking and then people will literalyl tell me i hav ea speech disorder or lots of trouble understanding me??

one time i was fed up and i did try to lie about being deaf i only did it once it is cause i rang to book a appointment and i went in and the lady was saying like she thought the call was a scam because it was a 1300 number (business number) and i was like oh okay it wasnt and she kept asking me questions like repeatedl like so accusetory she was why did you ring on that and she said it so accusetory to me and i felt so bad so i just said i am half deaf and i like to ring on that service bcecause it is easier. and hten she said to me i dont look deaf.

and then kept asking me again and pressing me like making me feel like i did something wrong. and she told me in future to just ring myself the normal way.

something else too when ive had to ring emermegecy services so i ring them and i tell them too i said i cannot answer phoen calsl and when i get off the emergency phone the police will ring me before coming out for the job and if i dont answer there is a high chance they dont show up?? and ive texted the number sand said i cannot answer phone calls due to disbailtiies and they will keep ringing only ??

i am looking for advice please i know i am not deaf but i like to use the relay service or i might just have to go bac k to not being able to do any calls or call in emergency