deaf topics

Deaf + Mental Health Access

September is Deaf Awareness month. It also is Suicide Prevention Awareness Month.

I’m going to talk about an important topic that combines of those two themes… Deaf and Counseling. Many of Deaf/Hard of Hearing people are still struggling to this day to find appropriate help. The issue is… accessibility. 

Let’s go back to my childhood. I grew up in a rural Upstate New York community. I struggled a lot being the only Deaf student in my mainstreamed school. From Kindergarten to Grade 4, I was in special education with other Deaf students that also had more disabilities. When I was going into Grade 5, I transferred to the local elementary school. I was the only Deaf student. I wanted to go to same school as my brother and my neighbors. To this day, I don’t regret that decision but it was a very isolated life for me as a Deaf student.

That was a big change in my life so my parents took me to see a counselor. There had been no Deaf counselors available in my area. The counselor I was taken to see was hearing with no background/experience in the deaf world. So a second person, an interpreter, was brought in. Which again, happens to be the same interpreter that was with me at school daily. I lived in a small town, it was impossible to find more interpreters. Imagine the awkwardness of having someone you see daily at your counseling appointments. My interpreter and I had a very close relationship, it was like having a family member sitting in the sessions with me. I recall only talking about the typical drama with my friends, never really opened up about deeper feelings related to my challenges/frustration with being deaf. It also wasn’t only because of my interpreter being there, but why would a hearing person understand my life as a Deaf person? 

My parents tried to find a Deaf counselor. My dad even wrote a letter to someone. It didn’t work out because back then, without computers and video conferencing, it wasn’t feasible. I didn’t continue with the counselor for too long. I didn’t have a counselor during my middle school years. In my high school years, the isolation got even worse. I was still the only Deaf student. I no longer had the same friends. It was tough for me to make new friends. The closest Deaf kids that I knew of were at least an hour away. I struggled a LOT during high school. I definitely felt depressed. I didn’t feel like I had a normal high school experience like everyone else. I felt lonely. All I thought about was getting through high school to that light at the end of the tunnel.

That light was Rochester Institute of Technology (RIT). I had attended a summer camp in Rochester the summer before my senior year in high school. The camp was for Deaf kids my age so I left there with MANY new friends. During senior year in high school, I came home and spent a lot time online talking to those Deaf friends. All I thought about that year was my future life in Rochester. Once I was in Rochester, I felt like I belonged. I was finally home.

Despite “being home”, it didn’t take long for the depression to kick in again. It was challenging for me to figure out my Deaf identity, accepting who I am on top of academic goals. I had spend 18 years of my life in the hearing world so switching to the deaf world wasn’t as quick as flipping a switch. It got overwhelming.  I had hit a low point in my life during second year. Luckily, RIT offered counselors, a few were Deaf and Hard of Hearing (HOH)! I scheduled my first appointment with a Deaf counselor. I was so nervous about seeing a counselor that also saw many other Deaf students including some of my friends. I didn’t want to run into them in the waiting room. I knew it was necessary for me to talk to someone. I ended up seeing that counselor for rest of my college years until graduation. It was the best decision I made. It was amazing to communicate to her in my native language. She understood the challenges we go through as a Deaf person. She also had grew up mainstreamed and mostly in the hearing world until she came to Rochester too. We could relate a LOT. I quickly opened up to her! She helped me so much. It was extremely hard to leave her when I graduated. 

When I moved to Connecticut, I had fun exploring a new area. This also was the further I’ve ever been from my family (Rochester was only 2 hours from my hometown so I could visit on the weekends). It was whirlwind of emotions and changes which unfortunately stirred up depression again. Especially when I wasn’t finding a job after a year and a half of trying. I had missed the deaf community in Rochester terribly,  it was all I talked about… going back there someday. With that distraction, it was hard to fully be in the present and enjoy my new life in Connecticut.  

The hunt began for a Deaf/HOH counselor… again. I found a counselor who was a CODA (Child Of Deaf Adult[s]) in a town a hour away. We took turns with driving to each other. I only had 4 sessions with her. She found out that I worked at the deaf institute up in Hartford, CT as mentioned in this blog. We had an awful experience working at the school so she ranted about it during EVERY session. I stopped scheduling appointments with her. 

It took another few years before I found another one. I even tried to reach out to the college counselor and see if it was possible that she could still have me as a client. I contacted the college, begging them to allow alumni to be able to access counseling services. 

Four years later, I finally found a Deaf counselor 20 minutes away! I couldn’t believe my luck. When I met her, I found out that she had worked at the same deaf institute and also had an awful experience. My fears from the previous counselor stirred up again but luckily she didn’t rant about that in our sessions. Still, I found myself not being able to fully open up to her. Why? I have finally found a good Deaf counselor. At this point, I had gone so long with no interactions with a Deaf person. I was lonely. I missed having Deaf friends. I found that we had a lot in common with hobbies and our mainstreamed background. I enjoyed going to counseling only because of our interactions. I wanted to be friends with her outside of the office. I didn’t open up because I didn’t want her to be turned her off from being friends with me in the future. Eventually one day, I told her I was ready to move on. 

I went a year until my grandpa passed away. It was first close family death that I had to deal with. I tried to go as long as possible to handle it on my own. I knew I had to reach out to her. I felt sad because I felt that the chance of being friends with her was getting low. I started seeing her again until the pandemic hit. The pandemic forced us to do the sessions virtually. I disliked that so much! The sessions would freeze a lot and prior to the pandemic, I’ve found it difficult to really open up over video-conferencing. I fell out of touch with her. 

It’s interesting to compare the experiences with all of the counselors I’ve seen. My life as a Deaf person has a LOT to do with my identity, the experiences in my daily life, the way I think, the way I do things and the challenges. I was so frustrated that I should feel lucky to find a Deaf counselor but I realized it didn’t work because I didn’t grow. I didn’t vent. I didn’t get what I needed. I was so lonely that I ruined it with the last counselor, I should have not been limited to only her. I should have many options like hearing people do. There needs to be more Deaf counselors available for all Deaf people, not just me. My experience is just one example of what other Deaf people go through in finding the help that they need. 

I live in Connecticut which is more congested and busier than the rural community I grew up in Upstate New York. I do have access to a lot more here. I STILL don’t have what I need. I can’t imagine how much hard this would be on me if I remained in Upstate New York. Mental Health shouldn’t be a low priority for the Deaf community. Mental Health isn’t something to mess with. 

I am also surprised (and also not) by the lack of counselors available online after the pandemic. All counselors had been forced to go virtual. This should’ve allowed more accessibility for Deaf/HOH people! It always was difficult even before the pandemic for us to find that help but you would’ve thought with everyone being remote, it would give us even MORE options!  

What’s next for me? I don’t know. I still have my bad days, but I have found ways to cope with the support of my immediate family. Sometimes that isn’t enough but I find the strength to fight through those bad days. But… that is ME. Not every Deaf person has that. 

Due to the lack of resources for the Deaf community, many of them don’t seek help. Self-medicating and self-help is common. Ironically the counseling center at RIT shares the building with the Substance and Addiction Intervention Services for the Deaf center. I was always embarrassed about that, wondered if the hearing people thought the majority of us had addiction issues. I quickly learned about the issues of providing care for the Deaf community, then I understood how important it was to have that center.  

I hope my experiences of the difficulty of finding help shows how important this topic is… Mental Health within the deaf community. We need more work on providing resources and accessibility. Deaf people deserves better care!

How to learn American Sign Language

If you’re one of the people who have said “I’ve always wanted to learn American Sign Language but I never know how to start!”, you’re in the right place!

As a deaf person, I love to help people find the right resources to learn about deaf culture and/or community. Learning American Sign Language may feel overwhelming to you but if you find some time, you can do it!

It’s HIGHLY recommended to learn from Deaf teachers. You can’t get more authenticity from someone directly from the community. It’s no different for any other languages - you would want to learn Spanish from a Spanish speaking person, right?

There are many ways to learn ASL. You can find them on YouTube, Instagram, websites or in person. I’ll share some recommendations:

ONLINE CLASSES

BOOK

“Learn to Sign with Your Baby: 50 Essential ASL Signs To Help Your Child Communicate Their Needs, Wants, and Feelings” by Cecilia S. Grugan

INTERNET

APP

  • The ASL App

  • Lingvano app

I will be continuing to keep this list updated as possible. Don’t hesitant to reach out if you need more help in finding resources to learn American Sign Language!

Happy Deaf Awareness Month!

September is Deaf Awareness Month. The reason why we have that is to bring awareness of deaf community, including communication needs, accessibility, etc. There’s so many topics within the deaf culture! Many do not realize that deaf people are highly diverse with a wide spectrum. There is a range of communication preferences, background experiences and identities.

Did you know that there are 70 million deaf people worldwide? Yet, there is no two deaf people who are alike. Some may prefer to talk, some prefer to sign. Each of us have different level of hearing loss.

That’s why it can be nerve-wrecking for hearing people to be approached by or interact with deaf people. How do you know what to do with them?

Patience.

That’s the most important. Be patient. The communication may be different from what you’re used to and may require some effort.

Eye contact.

Deaf people rely on eye contact. A lot. Make sure that you always face them. Some are able to lip-read, so they’ll need to see your mouth.

Don’t assume.

Not all deaf people can lip-read through, so do not assume that they can. Don’t put the burden of communication on them. Ask what their preferred method of communication is. It may be paper and pencil, using some kind of phone app, or whatever.

Don’t give up.

Do not give up if it’s challenging or struggling. The important thing is that the deaf people have the information. It doesn’t matter how it’s relayed, we just want to be understood. We’re humans too.

Don’t treat us differently.

We aren’t different from anyone else you interact with, just our hearing loss. We don’t want to be treated like a child or be made to feel incapable.

As a deaf person, I know I have to be patient too. I’m very willing to work with anyone to have effective communication. I won’t judge people for any mistakes because I understand that you don’t interact with deaf people regularly. I don’t want anyone to ever feel nervous. I would think many deaf people would have same understanding as we DO interact with hearing people on a daily basis.

Read more awareness blogs under DEAF tab on www.knotsoloud.com. I appreciate you being here to take the time to learn and be an ally for the deaf community!

Accommodations

This week kept many of us indoors due to the unhealthy air quality and smoke from the Canada wildfires. On Wednesday I decided to do a question and answer session via Instagram in the stories (it has since expired because stories are only visible for 24 hours).

One of the questions I received sparked a conversation with many people through private messages. What was the question?

Have you ever arranged a meet with anyone from here? How did you communicate?

Now, I’m sure you’re thinking… um why? I had a long winded answer where I explained my feelings. In summary, I said that normally I would never meet anyone in person because often they would act different (due to nervousness of interacting with me). I didn’t want to lose any of the online friendships I’ve made. It is hard enough that I’m isolated from the deaf community and it’s hard to make friends with people who don’t know how to communicate. Social media really helps with that.

Although, it’s been bothering me more and more lately. Some of those online friendships have lasted 5+ years. Wouldn’t you want to meet them in person? I started reaching out to some who shared that they had an upcoming trip to Mystic (where I am). I tell them I will bring someone who can help to interpret. In hopes of easing their nervous about meeting me.

I’ve had people apologize to me for not knowing American Sign Language. While I’m a huge advocate of learning ASL, I don’t expect everyone to know ASL. I went on to demonstrate via video (on Instagram stories) the app I use on my phone called Cardzilla. It is a FREE app that allows you to type out anything you want to say and the text is enlarged. It’s similar to the Notes app, but it doesn’t allow the feature of enlarging the text so that can be difficult for people to read.

Its not just my online friends, I also see many photographers have meet ups. They drive to a central location or explore a new town together. When I go out photographing, I’m often alone. Meeting up with more photographers is something I really want to do. But at the same time, I don’t want them to be stressed out about hanging out with me.

There has been unplanned encounters where I bump into people. So far, it always has happened when I was with someone or my family (who could help to communicate). Naturally those meets have been good. This is the reason why I think it’d help to tell those people online that I’ll bring someone to interpret.

This is where the messages started flying in my inbox:

Bringing someone is still making accommodations to make others feel comfortable, not for you!

I hope we can meet someday! I’m not nervous about meeting you but am I nervous about the communication. Yes. I don’t want you to feel the need to bring someone tho! I will try!

But why! People aren’t gonna authentically know you if you have another voice for you. It’s their problem not yours.

There are more messages that I didn’t share. People were upset that I feel the need to accommodate others. It is something I struggle with, all of my life I always wanted to make others feel comfortable around me. I’m only human, I want that interaction with people and I don’t want my deafness to drive them away.

I’ve recently stopped using my voice when I go to stores. When I used my voice, it seemed like people immediately thought I could lip read. Stopping the use of my voice helped to offload the burden of the communication onto them, not all on me. So the fact that I’m still accommodating others by bringing my ‘personal interpreter’ is still making it easier for others. I don’t know if that will ever go away - the feeling of need to make everyone else but me comfortable with communication.

I prefer that people be honest with me about if they’d be fine to communicate with me alone or with an interpreter. I care more about the interaction than the fact I’m still accommodating others. The interaction is more important. I enjoy the conversations with people I’ve met. I love to talk everything Mystic or anything they see from following me. I want to stress that if you ever see me out or want to arrange a meet in Mystic, I will be very understanding and flexible with our communication. I will make sure we understand each other. I will be patient, knowing that you may not know sign language.

Every time someone approached me in public, it does makes me feel great! It always leaves me smiling for the day. I still smile big to this day about that random shout out ‘Knot So Loud!’ from Abbott’s Lobster in the Rough when I passed by in my boat last summer!

National ASL Day

On April 15th every year, we celebrate American Sign Language (ASL)!

Today is also when American School for the Deaf (ASD) in West Hartford, CT was founded, in the year 1817. Formerly named Connecticut Asylum for the Deaf and Dumb is the first permanent school for the deaf in the United States. There was originally another school for the deaf that opened in Virginia but that was short-lived.

At ASD, there were many signs being used - French Sign Language, Martha’s Vineyard Sign Language and Native American Signs. The combination of all three became American Sign Language!

I’m very fortunate that ASL was created so that I could have access to information and have the ability to communicate. I grew up learning how to speak and lipread first which is known as the oralism method. Alexander Graham Bell (yes, the same guy who invented telephone) was the one who encouraged oralism and tried to dissolve sign language. I wrote a whole blog about the nonfiction book which explains the history of AGB and the deaf community here.

Almost 4 years old, I learned ASL when my family relocated from New Jersey to New York. My parents couldn’t find a program that focused on oralism so I was introduced to total communication (talk, lipread AND sign language).

To this day, sign language will always be the primary language which I feel the most confident using and I feel able to express more this way. I’m grateful that we’re celebrating the beautiful American Sign Language today on April 15th!

I love seeing ASL getting more recognition in the media. Many commercials have sign language! It’s a huge difference from my childhood years when seeing sign language was a rare opportunity. If you are interested in learning ASL, please seek out a deaf educator. It is highly recommended that you learn from someone within the deaf community, from someone who has the best knowledge of the culture. You can find more information here.

Happy signing!

Deaf Owned Businesses

During the holidays season in 2021, I originally shared a list of deaf owned businesses and have been sent more recommendations. I decided it was time to update the list! It’s amazing how many businesses there are, and it’s so easy to support them as you can do all the shopping online! As always, I tried to list as many but still missed a lot other businesses! If you are a business owner or have a favorite deaf owned business that you don’t see listed here, please feel free to contact me.

CLOTHING

By Mara - https://www.bymara.com/

Language Priority -  https://changing-the-narrative-language-first.myshopify.com/

Ivy’s Haven Boutique - https://www.ivyshaven.com

Erry B Shop - https://erryb.myspreadshop.com/

Girl & Creativity - https://www.girlandcreativity.com/

deafloveILY - https://www.deafloveily.com/

Lila & Pip - https://www.lilapip.com/

Love Ashlee Rose -https://www.loveashleerose.com/

Deaf Identity - https://www.deafidentity.com/aboutus

dirty beard press - https://www.dirtybeardpress.com/

Sisters in Style Online - https://sistersinstyleonline.com

ART

58 Creativity - https://58creativity.com/

Jena Floyd Art - https://www.etsy.com/shop/jenafloyd

Love Letters by Emily - https://www.lovelettersbyemily.com/

J9 Art Shop - https://www.etsy.com/shop/J9ArtShop

Viva Jess - https://www.etsy.com/shop/VivaJess

Kellie Martin Art - https://www.etsy.com/shop/KellieMartinArt?ref=seller-platform-mcnav

CRAFT

Raine Collective - https://shopraineco.com/

Strings and Things Handmade Macrame - https://www.instagram.com/stringsandthings_gi/?hl=en

Kissfist Stitch - https://www.instagram.com/kissfiststitch/?hl=en

Garden Stick Designs - https://www.etsy.com/shop/gardenstickdesigns

WELLNESS/CANDLES

Blue Organic Kitchen - https://blueorganickitchen.com/

Purple Rose Wellness - https://purplerosewellness.com/

Hotsy Totsy Haus - https://www.hotsytotsyhaus.com/

Kova Kandle - https://www.etsy.com/shop/KovaKandles

JEWERLY

Eden and Clay - https://www.edenandclay.com/

FOOD/BAKING

Bake It with Sass - http://bakeitwithsass.com/

There are so many other Deaf owned businesses that I couldn’t cover in this post! I’m excited that there are so many deaf talent. If you’re looking for something in particular, please don’t hesitant to contact me and I can try to help you find a deaf owned business specializing in that. 

Happy shopping! 

Deaf books

For Deaf Awareness Month, I complied a list of d/Deaf books that I recommend:

True Biz by Sara Novic [adult fiction]

This will always be one of my favorite Deaf books! It is a fiction read, following three characters at a deaf school. I found this to be a very informative read. It covered a variety of important topics within the deaf community such as the risks of deaf schools closing, the controversy of cochlear implants and language depravation. The book also shows the spectrum of deaf lives. Each character is deaf but are so different based on their communication methods. The book reads like a love letter to deaf community!

El Deafo by Cece Bell [middle grade/graphic novel]

An adorable graphic novel about deafness. It follows a girl who transferred to a new school. She showed and taught people about her deafness. The artwork in this graphic novel was very clear and showed how to interact with deaf kids. I laughed and cried. I could relate so well because I changed schools in 5th grade. I strongly recommend this book to young adults/kids but even adults would enjoy this too!

Haben, The DeafBlind Woman Who Conquered Harvard Law by Haben Girma [memoir]

A memoir by the first DeafBlind person to graduate from Harvard Law. It shared her experiences from her childhood up to her college years. I found her to be a very strong and influential person. This book shows how to be a strong advocate. It was written beautifully, especially when the author shows her humor. I have been following her on social media where she continues to teach, so I’m still learning! It’s important that we recognize the spectrum of the deaf community which includes the deaf blind community. Haben’s story is an aspiring example.

You Don’t Know Everything, Jilly P! By Alex Gino [middle grade/fiction]

A fiction YA read about Jilly who has a new deaf baby sister. Her family maneuvers through deafness, finding the best resources for the baby sister. Jilly also has a new deaf friend who teaches her how to be an ally. I appreciated that the author explained, in the author’s note, how they were not deaf so that’s why Jilly was a hearing character. The author did not want to be inauthentic so they wrote the perspective of a hearing person learning about deafness.

Silent Alarm, On the Edge with a Deaf EMT by Steven L. Schrader [memoir]

I was excited to find this book when I joined the ambulance organization as a first responder a long time ago. It was really interesting to read about the author’s experiences and how it differs from mine, he was in a large/busy city while I was in a small town. There were still so many stories and experiences that I could relate to, as well the challenges and discrimination. This book was very encouraging to chase your dream. Well written book!

The Invention of Miracles, Language, Power and Alexander Graham Bell’s Quest to end Deafness by Katie Booth [non fiction/history]

One of most powerful books about deaf history. Alexander Graham Bell is known to many as the telephone inventor but he was controversial figure in the deaf community. He wanted to eliminate sign language and deafness. Bell was a huge supporter of the oral method education for deaf students. I read this well researched book and learned a lot! It’s also frustrating to see how much AGB shaped my life. I had plenty more to say about this book so here is a dedicated blog.

T4 by Anne Clare LeZotte [young adult/historical fiction/poetry]

Nazi Germany adopted the sterilization law program from the United States. The program was renamed T4. The Jewish people weren’t the only ones targeted, also disabled, mentally challenged, deaf, gay, people of color and many more. This book is a historical fiction, written in poetry style. It is a fast read with only 108 pages but powerful enough! There aren’t many stories about T4 or deaf experiences in Holocaust.

The William Hoy Story by Nancy Churnin [children/picture book/biography]

An adorable picture book about the deaf baseball player, William Hoy. Did you know baseball signs were created because of him?? The universal signs you see for Ball, Strike, Out, etc. It wasn’t common to use sign language back in the 1880s. While playing baseball, Hoy asked umpires to help him understand the games, they came up with hand gesture/signals and that’s how it came to fruition. I enjoyed this picture book about Hoy’s life and the history of baseball signs.

I’ll Scream Later by Marlee Matlin [memoir]

A memoir about her experiences in Hollywood, also some from her personal upbringing. She was one of my idols growing up because there were so few successful deaf people visibly out there. She is very honest and blunt, she shares and doesn’t hold anything back in this memoir. It was very interesting to read! I laughed at some parts because Marlee focused on 1980’s-2000s era, which included the technology we used back then. In the book, Marlee mentioned the closed captioning box… I remember toting that box to sleepovers. I met Marlee in Rochester, NY during her book tour in 2009. I was so excited and so shy, I froze and couldn’t say anything to her!

Hands of My Father, A Hearing Boy, His Deaf Parents, and the Language of Love by Myron Uhlberg [memoir]

A memoir by a CODA (Child of Deaf Adult/s). Beautifully written. He lived in Brooklyn, NY during the Great Depression with his deaf parents. This was my first CODA book. He shared a lot, especially the resentment/burden that he felt with having to interpret for his parents. Yet, he had a very close relationship with his dad. I was mesmerized by the way he wrote about his dad’s signing/hand movements. Even through this book was from my deaf culture but it felt foreign to me! Worthwhile to read because CODAs are part of the deaf spectrum.

Song for a Whale by Lynne Kelly [young adult/fiction]

The book focuses on the isolation of a deaf girl in the hearing world. Iris is a 12 years old who is mainstreamed in a hearing school. She is often lonely and her classmates saw her as stupid. Iris learned about a hybrid whale that has its own song, that other whales doesn’t recognize. As a result, the hybrid whale is isolated and lonely. Iris was able to relate with the whale so she seeks out a solution to this problem. This book struck a chord because I understood the isolation. Heartwarming and adorable book!

Train Go Sorry, Inside a Deaf World by Leah Hager Cohen [nonfiction]

Even through the book was published in 1995, it still is worthwhile to read! It focuses on many stories of students, staff and alumni from a deaf school in NYC. It was a very engaging book, including debates within the deaf world - oral vs ASL, cochlear implants, etc. The book also included the history of the deaf school. The author herself was not deaf, but was the daughter of the principal of the deaf school (back in 1995) and her grandfather had been one of the original deaf students at the school.

Show Me a Sign by Ann Clare LeZotte [middle grade/historical fiction]

A historical fiction about Martha’s Vineyard Sign Language. The author is deaf and did a great job of researching for this book. The book follows an 11 years old girl who lives on Martha’s Vineyard with her family. Despite it being sad in some parts, it is very fascinating to read about the history of Martha’s Vineyard and the deaf community!

Everyone Here Spoke Sign Language, Hereditary Deafness on Martha’s Vineyard by Nora Ellen Groce [non fiction/history]

A history/non fiction book about Martha’s Vineyard and its deaf community. The deaf community existed on the island from 17th century until around 20th century. There had been a large deaf population, so Martha’s Vineyard Sign Language was invented. The hearing islanders learned it too. Imagine an entire community that could communicate with each other! I wish this still existed today. It was a well researched book but I was disappointed that no deaf people were interviewed. Still very interesting to read about this deaf history!

Silent Night by Sue Thomas [memoir]

Sue Thomas had been one of my biggest role models growing up. There was a TV show called ‘Sue Thomas FB Eye’ that focused on her experience working for the FBI. I had a strong interest in criminal justice and ended up majoring in it at college. This book focuses more on her personal life, it was really interesting to read about one of my role models! It was heartbreaking because she had a tough life, but I appreciated her honesty. The book was still very enjoyable to read.

Deaf President Now! The 1988 Revolution at Gallaudet University by John B. Christiansen and Sharon M. Barnartt [nonfiction/history]

In 1988 at Gallaudet University, a college for the deaf located in Washington DC, had a week long protest. The deaf students got frustrated when a hearing president was appointed, when they had request for a deaf president. This became one of the most important deaf historical event. The week long protest did conclude in Gallaudet seeing their first deaf president, I. King Jordan. It is a very inspiring read. DEAF CAN!

Deaf Utopia: A Memoir - And a Love Letter to a Way of Life by Nyle DiMarco [memoir]

Nyle DiMarco, known from his time on American’s Next Top Model and Dancing with the Stars. He won both! This is a personal memoir written about his childhood, upbringing, his deaf family, and more. It definitely read like a love letter to ASL and deaf pride/culture. I’m 3 months older than Nyle, but our lives were so different. This is a good example that not all deaf lives are same. There were some parts where I could relate to similar life experiences. I enjoyed this memoir!

Deaf Child Crossing by Marlee Matlin [fiction/middle grade]

This book was released while I was in elementary school. It was my first book with a Deaf character, so this became really special for me! It focuses on a Deaf girl who makes a new friend in her neighborhood. The new hearing friend learns sign language to communicate with her. This also struck a chord with me, reminding me of my childhood friend that I grew up with, who also learned ASL to communicate with me. A beautiful book about friendship.

Give Me A Sign by Anna Sorino [YA fiction]

I loved this book that came out in 2023. The book covered a wide spectrum of Deaf identities. The story takes place at a deaf camp following Lilah, who struggles with being “not deaf enough”. Something I am very familiar with! I wish I had this book when I was a teen! The author did an amazing job of educating about communication (ASL vs voice), the cochlear implants controversy, ableism, and many more.

On The Bright Side by Anna Sorino [YA fiction]

Another amazing book from Anna Sorino — I related a lot to the main character, Ellie who had to go to a new school and be mainstreamed. She meets a new friend, Jackson who has his own disability. The friendship between them is powerful as they maneuver through their journeys of being disabled. I love having more books with deaf/hoh rep!

Signs of Survival by Renee Hartman with Joshua M. Greene [YA memoir]

Renee is a Holocaust survivor, with her deaf sister. The book focused on their experiences as Jews living during the war and the camp. It is a raw and powerful read. The book is a transcribed compilation of video interviews that Renee did for Yale’s Holocaust testimonies archive. There aren’t many stories including deaf people during the Holocaust so this is important book to read.

The Deaf Girl by Abigail Heringer [memoir]

I enjoyed this memoir as I was a fan of Abigail during her time on The Bachelor. This is the first memoir I’ve read about a deaf person with cochlear implants. It is very interesting to learn about her experiences and there were quite a few experiences that we had in common. There’s such a wide spectrum of deaf identities so I highly recommend to have this book on your to be read list!

There are just some recommendations of what I’ve read… there are so many more d/Deaf books out there that I have yet to read! I encourage you to read these books to learn about the deaf culture and expand your knowledge about our deaf world!

How can you be accessible for the Deaf?

Recently I had a conversation with some of my family telling them how I love my dentist because of how accessible they are. I thought that I’d share this with you, especially if you are a business owner. How can you be accessible for the Deaf community?

It is in the Americans Disabilities Act (ADA) that all medical offices and businesses must provide an interpreter if a Deaf person requests one. Not all Deaf people will request an interpreter, so I thought I’d share how you still can provide accessibility without an interpreter.

I do not request an interpreter for the dentist because there’s so little conversation that takes place. So I feel comfortable to go sans interpreter. Every time I walk to the chair, I’m always impressed with how the hygienist has everything ready for me. There is a TV monitor near the chair that is typically used for viewing charts, x-ray scans, etc. She would have a Word document open with a message for me, greeting me and informing me about what’s on the schedule (we need to do x-ray pictures today, etc). She also has a notepad with pen ready on the chair. The hygienist would take the time to ask me questions and make sure I’m ready before she starts the cleaning. When the dentist comes to checkin, sometimes I can lip read her but the hygienist still types what is said. This is how you provide accessibility, offering ALL options. I have the option of lipreading or to look at the computer. It is so helpful because I do understand my dentist pretty well but I STILL miss some words here and there.

This was super helpful when my dentist was absent on one of my visits, I had a different dentist that day. It’s harder for me to lip read someone I not familiar with, that day I relied on the computer for all my information. Imagine if the hygienist didn’t do that? I would’ve left that day not knowing half of what was said.

As I mentioned, the hygienist places a notepad with pen on the chair. These days with technology it is easier for Deaf people to type notes on the phone if needed. The thoughtfulness of providing paper and pen even through I didn’t need them, still gives me the sense that the hygienist is trying. That act alone makes me much more comfortable, calms my nerves and I do not feel that communication with be stressful. She’s not leaving it all on me to ‘work’ for the communication, but making that line open for both of us. I appreciate her so much, she does this EVERY visit and never misses.

It still is so important to provide paper and pen especially if we don’t have access to our phones or something. For example in hospitals: if we are doing medical procedures, or are some place where phones are prohibited, and there’s no interpreter - you need to remember to give the Deaf people something to communicate their needs. It’s important to not only focus on HOW you can communicate, but also remember to give THEM that accessibility.

When people ask me if I can lip read, I know many aren’t aware that question can be ableist. It’s implying that the Deaf person should do all the work of lip reading, communicating, and understanding. Make the communication easier for the hearing people because that’s what they know. Think about if it was reverse, if we (Deaf people) ask EVERY hearing person we meet, “Do you know how to sign?”. I would think many of you may feel some kind of guilt (for not knowing sign) or feel pressured to communicate because of the implication behind the question.

The dentist office is the best accessibility out of all medical offices/appointments I’ve had in my lifetime. My doctor’s office is getting there too. Growing up, I’ve always relied on my parents to do all of the communication with my doctors but this is naturally for children. Once I moved to Connecticut I had to find a new doctor as an adult. My first Doctors was not a good experience, there was a lack of communication, accessibility issues and the office had difficulties providing me a certified interpreter.  After a while of this, I switched to a new doctor. I was so traumatized by the interpreter issues from the prior office that I didn’t request one with my current doctor. My husband does it all. However, I did noticed a growth of awareness over time with the doctor office. They email me instead of calling my husband, I can email my doctor with questions or place pharmacy orders. That gives me a huge sense of independence. The front office staff also seems to be learning some ASL.

I like to be looked at as an individual when I visit a business instead of relying on others for communication.  They should not rely on my husband to interpret for us. It gives me more confident when they give me that accessibility because that is a sense of independence for Deaf people. So how can you be better if you have a Deaf customer without an interpreter? Always have all options ready.

Aside from medical offices or professional businesses, I do favor stores and places where there’s someone who is helpful in communicating. When I have a great experience (even if it was only once), I’ll be a loyal customer. I have to admit that I even pay attention to the schedules so I know when a specific person would likely be working.

If you don’t have the ability to provide pen and paper, or there are no phones near by … gesturing still goes a long way. Patience too, I always get tense when I stand in a line, with more people behind me.  I have no idea how patient the employee would be with me. I’ll share one ‘wrong’ example. I went to a local donut shop to get donuts and coffee to surprise my husband. I’m not familiar with coffee orders because I’m not a coffee drinker. I don’t know all the jargon. I asked for ‘white chocolate mocha coffee.’ The barista stood there and stared frozen at my phone screen.  I could sense that the wheels were turning in her mind, I knew she had a question. She didn’t ask. I pointed at the menu behind her, implying she could point to what she was trying to ask me. She didn’t do that, but instead walked to another employee and talked a little. That was it. I assumed she got the order. I ended up going home with an iced coffee with mocha syrup. I had asked for a HOT coffee and the coffee that was already white chocolate mocha flavored without additional flavors.

I was frustrated that she didn’t have the patience to gesture or try to ask her question. She didn’t even try to talk to me. That’s a huge wrong example how to treat your Deaf customers. I understand that the girl might’ve been nervous and never met a Deaf person so she froze. We are so used to that, we have the patience to wait and be sure that we are understood. We WANT to be understood. Do not assume. Just TRY.

I have so many more right and wrong stories but it’d make this blog post too long. I’m very willing to have further conversation with anyone who wants more tips or advices on how to provide accessibility. If your situation is more specific, please don’t hesitant to reach out to me for more help or ideas. It will make every Deaf person’s day if someone puts in the effort to provide accessibility for all of us at your business. Truthfully, that also will get you MORE customers because we will be raving about you.

Cochlear implants

Cochlear implants. A taboo word in the deaf world.

For those who aren’t familiar with what cochlear implants are - it’s an electronic device installed under the skin behind the ears. It consists of many parts to help transmit sounds to the outer device (it looks similar to hearing aids). This process requires surgery which is usually done in the same day or overnight. It is a common misconception that cochlear implants would cure deafness. It does not. The cochlear implants are another aid for deaf people to be able to hear some sounds and speech. After surgery, they have to go through intensive therapy on speech and learn the sounds.

So many people describe cochlear implants as a “medical miracle” but yet dumbfounded when they come across deaf people who turned it down. It is a controversial topic in the deaf community. There are some deaf people who are against it because they feel that it oppresses them so they actually frown upon the deaf people who do get cochlear implants. Most often the deaf people with cochlear implants feel rejected from the deaf community.

I learned about this controversy when I attended college. I went to Rochester Institute of Technology (RIT) which had many colleges including National Technical Institute for the Deaf (NTID). This is the reason for the large deaf community in Rochester, New York. I observed many sub groups within the deaf community at RIT. There was the “deaf pride” group who were raised by deaf parents, attended deaf institutes, fully emerged into the deaf culture. There were the “mainstreamed” folks who were raised in a hearing world but immersed some deaf culture in their lives such as using sign language. There was the “oral” group which often applied to those with cochlear implants; they often didn’t use sign language but relied on lipreading and talking. It was interesting to learn about from all kinds of D/deaf lives.

Those who are against cochlear implants don’t see their deafness as something that needs to be fixed. They use examples of successful deaf people out there in the world - famous actors/actresses, artists, athletes, and even musicians proving that there are many who are satisfied with being deaf. It’s often explained that deaf people can do everything but hear. Another reason why the fear of cochlear implants is impacting the deaf culture is the belief that if technology continues to be used to help deaf people then sign language/deaf culture would decline.

Most deaf children are born to hearing parents. It is common for doctors to push cochlear implants. With the hearing parents’ initial shock once finding out their child is diagnosed with deafness, it can provide a false sense of hope that they will be cured with cochlear implants.

During college I met so many deaf people who received cochlear implants at a young age and were no longer using it. When I asked them for their reasons, the common replies were (1) that they weren’t happy with their parents’ decision (2) it causes a lot of headaches or (3) did not see a benefit in using them/were not a successful tool for them. Those that I did know that actively used cochlear implants were the ones who decided later on in their teens/young adult years. Again, that does not apply to everyone but it was an observation I had from my college years.

So what is my opinion on cochlear implants?

My parents heard about them when I was 8 years old. They met with someone to discuss the whole process of getting cochlear implants for me. At the time, it was determined that I was not a viable candidate for cochlear implants because the company who manufactured them was very new. The technology at the time also was not advanced for my level of hearing loss (profound loss). The company was specifically targeting senior citizens who lost their hearing or late deafened people.

The technology advanced over years so cochlear implants were a possibility for me again. I was asked in my high school years if I would consider getting them. I let the fear of being in surgery prevent me from making a decision.

When I went to college, I had many friends who had cochlear implants so I was able to learn more about them. As I mentioned before, some friends described they received more headaches which I did not want. The implants also would take away any residual hearing, which I have a tiny bit of, that I wanted to hang onto! Another turn off for me was having to get the cochlear implants updated every few years so that meant going in for a few surgeries throughout my life. I still have a fear of being in any kind of surgery so that wasn’t appealing to me!

I am not against cochlear implants. I support people who want them. I have seen where it is successful for some people while it wasn’t for some other people. The key in my final decision was that I am comfortable with being deaf. I like my silence. I don’t like major changes. I couldn’t imagine going from my silent world to a world with sounds. I’ve had so many people who couldn’t understand how I would pass up on them when they could be a huge asset. The results of cochlear implants aren’t same for everyone so there is no way of knowing how successful it would be for me. It wasn’t enough of a risk for me to take because it took a long time for me to love myself as a deaf individual.

All opinion in this blog are my own. It does not reflect the opinions of other deaf members.

Deaf Movies/TV series

It’s binge watching season! With the colder weather here, we’re starting to stay indoors more. Ever since the blog I wrote about the movie ‘CODA’ last summer, many have asked if there were more Deaf movies/TV shows. I’m finally here to give you the scoop!


Deaf movies to watch:

Children of a Lesser God (1986)

This is probably the most well known deaf movie. Marlee Matlin, a deaf actress, won the Academy Award for her role. It is about a new speech teacher who fell in love with a deaf janitor while working at a deaf institute. He pursues her to use her voice/learn speech as she wasn’t verbal. This is a good movie, but really focuses on speech/oral aspect of deafness. It’s also ‘based’ in New England (but actually was filmed in Canada)!

Sound of Metal (2019)

A powerful movie! It follows the journey of a rock band drummer who lost his hearing. It showed how he was in a hurry to find a quick ‘fix’ or cure. While he was re-adjusting to his life without hearing, he was immersed in a small deaf community in which he learned about the deaf culture. I thought this movie was perfect for people who are stuck in both worlds! I also loved how the deafness was portrayed as a culture, not a physical disability in the movie.

Audible (2021) Netflix

This short 40 minutes documentary focuses on a deaf football player at Maryland School for the Deaf. It shows clips of his life as an athlete, a friend who lost someone to suicide and being a teenager. It also interviewed some other deaf people. The documentary captured a lot of moments showing what it feel like to be immersed in the deaf world. 

…and Your Name is Jonah (1979)

The deaf boy had been misdiagnosed so he was institutionalized with intellectually disabled. It shows the journey of the deaf boy adjusting to living with his family. This movie is a great example of language deprivation.

The Hammer (2010)

A biography/drama/sports movie about Matt Hamill, the first deaf wrestler to win a NCAA. It followed his youth years in Ohio, discovering wrestling then his success during college. I was particularly excited when this was released back in 2011 because he is a RIT (Rochester Institute of Technology) alumni. Go Tigers! I really enjoyed this movie, which had many deaf actors/actresses! The movie also was filmed through out Rochester, NY. It is one of my favorite deaf movies.

A Quiet Place (2018)

A horror/sci-fic movie about a family living in silence to hide from monsters with ultra-sensitive hearing. One of the family member is a deaf girl so the entire family uses sign language to communicate. Horror/Sci-Fic is NOT my genre at all, but I had to watch this movie. I felt like it was more suspenseful thriller but enjoyed it a lot! The girl is played by a deaf actress, Millicent Simmonds. Also, A Quiet Place II was released this year, but I haven’t seen it yet!  

Sound and Fury (2000)

A wonderful documentary showing the controversial of cochlear implants. It shows the conflict of deaf identity and struggling to belong. Definitely worthwhile to watch!

Sweet Nothing in my Ear (2008)

Another movie about cochlear implants. It is a family drama about a hearing man and his deaf wife (played by Marlee Matlin) who are conflicted on whether their deaf son should get the cochlear implants. This showed all sides/opinions. 

Born to be Wild (1995)

This may not be classified as a ‘deaf movie’ but sign language is included. It’s a kid-friendly movie of a gorilla learning sign language to communicate. The gorilla develops a relationship with a rebel teenager and they communicate using ASL. It is a cute and heartwarming movie!

Listen to Your Heart (2010)

One of my favorites! Ironically it is music-based movie which I try to avoid. A singer fell in love with a deaf girl, but the love inspires him to write music. It is a romantic drama movie, but it shows that nothing is impossible! 


If you want to binge on TV series. There are some recommendations: 

Deaf U (2020) Netflix

A reality series following several deaf students at Gallaudet University in Washington DC. I felt like I was watching ‘Real World’ on MTV but with deaf college students! I do have to warn, this series is unfiltered. 

Switched at Birth (2011-2017)

A drama series starting out with a hearing girl who found out that she was accidentally switched when she was a baby. She meets the other baby that she was switched with, which was a deaf girl. They both immersed into each other’s lives. A lot of deaf culture and aspects are portrayed in the show. A fun and worthwhile series to binge!  

Deaf Out Loud (2018)

Only 1 season, this documentary follows around three deaf families. I am so, so, so sad that more seasons were not signed for this show. I loved it! It showed a variety of deaf identities, how all deaf people aren’t the same and different opinions. If you want a glimpse of true deaf world, this is the show to watch. Also, one of the deaf families is based in Connecticut! 

Sue Thomas FB Eye (2002-2005)

A police-drama TV series following a deaf FBI agent who works in fingerprinting. Another agent noticed her lip reading skills promoting her to an elite surveillance team. This is inspired by Sue Thomas, a deaf woman who works for FBI so this show is loosely based on her life. 


There are many more that I haven’t seen yet. I have a long list of movies to watch! Hope you enjoy some of those and let me know what you think! 

Alexander Graham Bell and the Deaf community

Book Review of The Invention of Miracles: Language, power and Alexander Graham Bell’s Quest to end Deafness by Katie Booth. I mentioned in the last blog how this book had made a great impact on me enough that it earned its own post! Here are my thoughts:

Whoa! This book was such a powerful read about a controversial person in the deaf community, Alexander Graham Bell. I didn’t know about the release of this book back in April 2021, but had spotted it in the bookstore. Only because the cover had “The Quest to end Deafness” on it grabbing my interest. I knew of Bell, learned that his name was an adversary in the deaf community while I was at college. Many of you only know him as the inventor of telephone but he also had worked as a teacher for the deaf.

I picked up the book and read the prologue. Right away, I was drawn into it with the author growing up with deaf grandparents whose lives had been impacted by Bell’s oralism. The local library finally had this book available so I read it and boy, was I glued to EVERY page! I had figured that I’d be skimming through some parts since it had explained Bell’s invention of the telephone. I’m not the one for science, but the author did an amazing job of explaining.

The book was very complicated. Like I mentioned, I only knew that Bell wasn’t liked in the deaf community but never really knew the depth of where it stemmed from. I knew he pushed for oralism. The book is 400+ pages long, divided into 3 parts. The first two was about Bell’s romance with his (deaf!) wife, his invention and brief stories about his work with the deaf. The last part focused greatly on the deaf.

At first, I respected his hard work for inventing the telephone. He was a smart man. Later on, when I read about his time with educating the deaf on how to speak… my mind frame of Bell shifted quickly. He advocated greatly for the oralism method, wanting sign language and deafness to be eliminated. It was his goal to teach the deaf people to forget that they are deaf.

There were several excerpts from the book that parallel so much to today’s world. I didn’t realize that even in the 1880’s that deaf people were being asked “did you ever try to learn to hear by the motions of the lips?” Which is equivalent to “can you lipread?”. I’m still asked that TODAY in 2021! The implication of Bell’s oralism probably gave hearing people that exception that deaf people are able to lipread.

As I was reading this book, there were several descriptions of speech lessons…bringing up memories of my own speech lessons during my childhood. I have NEVER enjoyed speech. I disliked it so much. Just like the students in the book struggling to make specific sounds, I had some difficulty with specific letters such as “k”, “c”, “p”, etc. I remember being frustrated but had to internalize that anger until I was home. I didn’t like how speech lessons also took my time away from the classroom. I felt like I was missing out on what was going on with my classmates. This was an argument used by the pro-ASL advocates against Bell’s oralism, that teaching the deaf oralism took their time away from their general studies.

I was interested to see so many similarities or connection with Mystic Oral School (MOS). If you recall, I wrote a blog about the school here. It was Bell’s oralism method that was taught at MOS. During Bell’s era, they struggled with many oral deaf students signing in secret which were many stories I heard from MOS alumni. How they would secretly sign with their friends in the dorms or at home. It seemed to be a reoccurrence for sign language to be snuck in among the oral deaf students. The book mentioned Bell advocating against ‘signing schools’ to receive public funds. I remember reading court papers from when Bell came to Hartford, CT to support MOS getting funds they needed.

Bell is a very complicated person. He was smart but unwilling to listen to the deaf voices. He knew that he wasn’t liked by many. It continued to be his goal to eliminate deafness/sign language. It was implied that Bell had a little soft side towards his deaf students, as it mentioned in the book that he helped them in finding jobs, paid for their education and bought them clothes. Yet, he still believed that ASL shouldn’t be taught. I also mentioned earlier that Bell even had a deaf wife. He also had a deaf mother, who he used sign language with at home during his childhood. His wife had been one of his former students who he taught oralism to, so his wife knew how to lip read him/spoke well. She became the example of his oralism success. Bell’s wife also had a strong dislike towards teachers of the deaf because they often looked at their students as ‘cases’ which is exactly what Bell did, especially with Helen Keller!

One part of the book that made me angry was Bell’s involvement with eugenics committee on passing sterilization laws. Indiana had been the first state to pass the law in 1907. This law inspired Nazi Germany to adopt and establish their version, resulting in 40% of German deaf being sterilized. I had no idea the connection. Many don’t realize that Holocaust targeted deaf (and disabled) among the Jews. The sterilization program they adopted from the United States eventually turned into ‘T4 program’ which was a euthanasia program. This had upset me so much that I had to put the book down briefly because I was recalling a video I watched last year of a German deaf woman who had been sterilized. She shared her sadness of never being able to conceive.

This book was excellent written, very well researched and put together perfectly. The author had really dug in the archives. It was a book full of history but so powerful that it will spark dialogues about one’s personal experience as a deaf person in today’s world. It brought out so many emotions for me. I thought about my childhood that had been shaped by Bell’s oralism. I learned how to speak/lipread first until learning sign language 3 years later when I moved to a new school that combined use of speech/ASL. I felt like I spent the majority of my childhood being embarrassed of my own deafness. There were a few incidents when I’d tell my family to stop signing in public when people were staring. I always apologized for being deaf when hearing people tried to talk to me unaware of my deafness.

How people perceived the deaf people was definitely influenced by Bell. Oralism still exists today, not as popular as it was during Bell’s era. We still face discrimination especially with jobs and accessibility challenges. Many hearing parents still aren’t receiving the resources when they give birth to a deaf child resulting in language depravation. The majority of doctors today are in favor of cochlear implants. The issue is that it’s implied that it’s a cure, instead of an assistance tool.

I thought so much after reading this book. How my life would have been different if Bell had listened to the needs of the deaf people. If he had worked with them, how much more successful would we have been today? Would we still be facing discrimination? People’s opinions of us might’ve been different? After all, Bell was a smart man and could’ve achieved a lot if he had collaborated with the deaf community. In the end, he only ended up causing great harm on the deaf community. I’m so grateful that the deaf people during Bell’s era had persevered and allowed us the freedom to use sign language today!

Don’t wait on picking up this book like I did, it’s so worth the read!

Can Deaf people drive?

“Do you drive?”

“Can Deaf people drive?”

“We can drive, but Deaf people can’t.”

Those are the questions or statements I’ve heard since childhood. I recall being in ASL class in middle school. The teacher asked the class to name one thing that they can do that deaf people can’t do. A girl said “we can drive”. I reacted to that with surprise that some people thought that way.

“What about the emergency vehicles/sirens?”

“How can you hear the car horns?”

Usually the follow up questions would be about sounds that most hearing people hear while driving. Yes, I can’t hear them, but I can see the emergency vehicles. I can’t hear car horns. I do have the added expectations to look around more.

It helps that Deaf people are known to have expansive peripheral vision. At the driver’s license testing, the evaluator even made a comment that he especially likes the Deaf drivers because they pay attention more.

There is no proof that Deaf people cause more accidents due to their hearing, or hearing loss making them less safe drivers. We are allowed to receive a regular driver’s license but any type of other licenses may be more challenging. It was only recent that Deaf drivers can be truck drivers (2013).

It was frustrating at one of my old jobs when I was a direct support professional. I was responsible to help my client learn how to be a member of the community i.e. having a job, participate in events, etc. All direct support professionals at the agency were required to get a special driver’s license to be able to transport clients. I went through the whole process of being fingerprinted, blood tested and paid fees to find out that I couldn’t get it because of restrictions about my hearing loss. Oh! I forgot to mention that getting that license also meant a pay bump. Luckily, the agency was understanding that I tried and they honored the pay bump for me anyways. It still wasn’t fun for the entire employment to feel like I couldn’t be relied on for driving. We had a team 2:1 so the other did all of the driving. I felt a lot of guilt for not being more helpful.

Emergency vehicles nowadays don’t seem to use sirens anymore. I can spot the flashing lights coming from behind me or ahead of me a mile away! There was only one moment that worked against my Deafness when I drove to my job in downtown Rochester, NY. I came to an intersection that was blocked by tall buildings and once the light turned green, I started going when a police cruiser was speeding towards me. I slammed on the brakes hard, and let the cruiser continue even though he had to slow a bit.

Being a Deaf driver can still be a challenge, but thankfully my expansive peripheral vision helps tremendously. I know that I always have to be alert. I still work hard to this day to not have any distractions. I often do double-checking at intersections/stop signs. To this day, I’ve never received a ticket (*knock on wood*). It’s a common misconception that people think Deaf people can’t drive legally but they can!

Can you lipread?

The very first question that I get asked every time once someone finds out about my deafness is “can you lipread?” (and yes, they’re verbally asking me this). It’s a misconception that every deaf person knows how to lipread. It’s a skill that is learned. As mentioned in my background blog, I grew up in a mainstreamed setting so I learned how to lipread at a young age.

Lipreading is a difficult skill to learn. It varies on the level of hearing loss and preferred communication method - some deaf people may be experts but some may be lousy. Hearing people often think this is the best method of communication but it is not. I grew up in a mainstreamed setting so I use simultaneous communication - speech and American Sign Language (ASL) as my main method of communication with my family and friends. Signing is the easiest method of communication but I also use speech to help them understand me more since they don’t know EVERY word in sign language. I understand everything when they use ASL with me.

I lipread a little when I’m interacting with strangers in public like at the stores, appointments, etc. If I am aware of what the conversation will be about, I have the ability to lipread most of what is being said. For example, if I go into a coffee shop - I know they will be asking me what size cup, what kind of milk, do I want this added in the drink, etc. It throws me off if they started a conversation that is not topic-related. Often, I would panic and wonder “what are they saying?”. It will take me a few minutes to try and figure out what is being said.

Many people have asked me if it makes a difference if I’m in a one-on-one dialogue vs a group setting discussion. Either way, I am only able to catch a few words from the entire conversation. The benefit of having 1:1 conversation is that I am able to focus on one person and I can ask them to repeat if necessary. Forget it with a group setting! I never catch anything from multiple people talking and they don’t always directly look at me (which helps me to lipread). It is extremely difficult and most of the time I leave those groups wondering what the discussion was about.

One issue that I have faced while trying to lipread a stranger in a public setting is that they get annoyed with me when I ask them to repeat or gesture. They either give up or cut the conversation short. So many people do not realize that lipreading is a substantial task for deaf people. It really requires us to put in a LOT of effort. In the end, I always feel guilty for any miscommunication that happens which isn’t always my fault. I try to ask people to write since that is better than lipreading.

You wouldn’t believe the misunderstandings that can happen from attempting to lipread! When I’m in a dialogue with a stranger, I am likely to catch a few words so I play the whole “fill in the blank” game. There have been some assumptions where I was entirely wrong and made the situations very awkward!

How long does it take me to lipread a new person that may come in my life? I am employed at a public school and I am the only deaf person there. How do I communicate with my hearing co-workers? I do have to lipread most of them. It is always challenging in the beginning of every year when I work with new co-workers. It does help when I see them daily and practice lipreading them. For example, if my co-worker verbally reads a book that I am familiar with, I am able to practice lipreading. It takes me about a month and a half to be able to lipread the majority of what they are saying but I do still occasionally miss some words.

Many people also don’t realize there are things that can prevent me from lipreading! One time at work, we lost power so we were in complete darkness. A co-worker started talking to me but I couldn’t see their lips in the dark! There have been some men that I wasn’t able to lipread because of their mustaches or beards. I can’t read lips when they’re covered with facial hair. It can be very distracting to lipread when someone has objects in their teeth/mouth or any kind of deformity around their mouth.

Accents also prevent me to lipread since people pronounce their words differently. I’ve traveled to Ireland twice where I’ve met many friends. They all spoke English but pronounced their words differently so I wasn’t able to lipread. I have came across New Englanders with strong Boston accents, which again I can’t lipread. I wasn’t raised in Boston so I never learned their pronunciations.

In the end it’s best that you do not assume that all deaf people can lipread. Don’t be afraid to ask them what their preference method of communication is. Most of the time it will be writing on paper or gesturing. Of course it’s most helpful if you know sign language!

All opinions in this blog are my own.