Category: Hearing Loss
Unlocking Clearer Sound: A Closer Look at Ceretone Hearing Aids
my auditory journey. Their commitment to innovation and reliability truly sets them apart.
Comfort and Fit
As someone with smaller ear canals, finding a comfortable fit was always a challenge. Ceretone OTC options provided a perfect solution, fitting snugly without discomfort.Mission and Dedication
What struck me most about Ceretone is their mission to empower communities affected by hearing loss. It’s not just about selling devices—it’s about enhancing lives through technology. Their products meet rigorous FDA standards for quality and reliability.Technological Excellence
Ceretone is dedicated to empowering communities affected by hearing loss. Their mission goes beyond selling devices; it’s about enhancing lives through advanced technology. Each product meets rigorous FDA standards for quality and reliability.- Digital Signal Processing: Enjoy clear, natural sound in any
- Adaptive Clarity: Conversations are clear, whether in a bustling café or a quiet park.
Ergonomic Design
Comfort is another area where Ceretone excels. The ergonomic design ensures that wearing them feels natural, almost like they’re not even there. Customization options allow me to tailor settings to my specific hearing profile, enhancing overall satisfaction and comfort.
Enhanced Quality of Life
Choosing Ceretone has improved my quality of life. I feel more confident and connected in social situations, thanks to the improved speech comprehension and sound quality. The extended battery life minimizes disruptions, allowing me to go about my day without worrying about power.Customer Testimonials and Support
Reading testimonials from others who have experienced similar benefits reaffirms my choice. Their stories echo my own sentiments—Ceretone has truly made a difference in our lives. The support and warranty they offer further solidify my trust in their products, knowing I have comprehensive coverage and expert guidance whenever needed.Take the Next Step
If you’re considering enhancing your auditory clarity and comfort, explore Ceretone today. Visit their website to see their range of products and find a solution that seamlessly fits your lifestyle. Experience clearer sound with Ceretone and enrich every moment to its fullest potential.
What Is Tinnitus And What Can You Do About It?
Imagine you are sleeping soundly in your bed. You are relaxed and dreaming, when suddenly you hear a scratching against your window that causes you to awaken suddenly. Your brain perks up and your heart rate increases. “Fight or flight” kicks in. Your eyes scan the room for an intruder or other danger. You notice that while you were sleeping, a thunderstorm was brewing outside. The wind and rain caused tree branches and leaves to strike your window, resulting in the strange sounds that caused you to wake. As you return to sleep, the sound of the storm outside persists, but your brain knows there is no threat, therefore, you can return to rest. This example is one I used regularly while working as a clinical audiologist to explain the brain and its reaction to the phantom sound of tinnitus.
Tinnitus is defined as a sound heard by an individual when there is no external source creating the sound (that is, the sound cannot be heard by anybody else). Tinnitus is commonly described as ringing, hissing, roaring, or buzzing. The National Institute on Deafness and Other Communication Disorders (NIDCD) estimates that over 10% of the U.S population has experienced tinnitus (What is Tinnitus? | American Tinnitus Association (ata.org). It is also the most common service-connected disability among those who served in the military.
Although many individuals have experienced tinnitus at some point in life, NIDCD estimates that approximately 2 million Americans suffer from debilitating tinnitus—meaning that the ringing in their ears significantly impacts their daily life.
Below are answers to three key questions about tinnitus. Whether you suffer from tinnitus yourself or have a friend or family member who experiences tinnitus, this information can help you gain a better understanding of this mysterious phantom sound.
- Is there a cure for tinnitus?
To date, there are no FDA-approved medications specifically proven to cure tinnitus. However, there are some treatment measures that can help people reduce their perception of this sound and annoyance from tinnitus. Common treatment plans include Tinnitus Retraining Therapy (TRT), Cognitive Behavioral Therapy (CBT), and/or hearing aids with the option for combination sound therapy features that reduce the perception of tinnitus (e.g, by providing a more soothing sound that balances or “drowns out” the unpleasant tinnitus noise). For tinnitus sufferers looking on the Internet for help, be wary of any product or pill that makes claims to cure tinnitus—as there is no evidence to support such claims.*(Note: for more information on TRT and CBT: Tinnitus – Diagnosis and treatment – Mayo Clinic
- What research is being done to treat tinnitus?
Tinnitus, including its origins and treatment options, has been studied since the 16th century. Recently, there have been devices approved by the FDA to help manage tinnitus using external stimulation. Many of the newer tinnitus treatments focus on some form of sound therapy delivered to the auditory system, either sound generators or tinnitus sound therapy in combination with hearing aid amplification. Even though there are now some tinnitus treatment devices available with data to support reduction of tinnitus perception, there is not one “gold standard” treatment that works for everyone. Currently, these devices have FDA approval for tinnitus treatment and are available in the United States:
*(Note: this author does not promote or endorse any specific product of manufacturer for tinnitus management. The recommendation is to consult with an audiologist who specializes in tinnitus to discuss options that work best for each individual’s tinnitus management needs).
People who suffer from tinnitus are such a diverse group that it is difficult for researchers to control other variables and focus solely on tinnitus. Tinnitus perception is subjective to the listener; audiologists can measure tinnitus with loudness and pitch matching evaluations, but these tests rely on the listener to determine the tinnitus pitch and volume. Additional variables to control are degree of hearing loss, medications, pre-existing conditions, and general overall health. All these variables lead to challenges in finding a uniform group of tinnitus sufferers to examine, but these challenges do not keep researchers from trying to find solutions. On the American Tinnitus Association website, you can find a link to clinical trials for tinnitus and explore what research is currently being performed: Clinical Trials | American Tinnitus Association (ata.org)
- What type of professional do I see for my tinnitus?
An audiologist will be the professional to seek evaluation and care for tinnitus. The audiologist’s first step will be to examine your ears to check for earwax build up. They will then conduct a comprehensive hearing evaluation, which will help them determine how well your outer, middle, and inner ear are working. It is also important to have a medical evaluation if you have tinnitus, especially if the tinnitus is new or if it is in one ear and not the other. The physician to see for medical evaluation of tinnitus is an otolaryngologist, also known as an ENT (ear, nose, and throat doctor). The ENT will determine if further testing to evaluate the tinnitus is needed (i.e., MRI, Doppler test, CT scans, etc). If you are going to seek treatment with hearing aids or tinnitus devices, the audiologist is best equipped to determine what will best suit your individual needs. Some tinnitus patients find it beneficial to seek care from a psychologist to see if CBT is an option for their treatment (Behavioral Therapies | American Tinnitus Association (ata.org)). Lastly, consulting with your primary care physician to review the medications you are taking is an important step in tinnitus management.
If you or a loved one suffers from bothersome tinnitus, consult with an audiologist to discuss options for treatment (refer to the American Speech-Language-Hearing Association’s professional search tool to find professionals in your area: Find Certified Audiologists and Speech-Language Pathologists (SLPs) (asha.org). Lastly, bookmark the American Tinnitus Association (ata.org) homepage to check in for news and updates.
Bria Collins, AuD, CCC-A, is a certified audiologist and currently serves as Associate Director, Audiology Practices, for the American Speech-Language-Hearing Association
Dating Tips
If you have ever been romantically interested in a deaf person, this article is for you! At DeafandHOH, we want to help you have fun and have the date go as smoothly as possible. It’s ok to be nervous; keep an open mind and have fun! We have developed several tips just for you.
If you are not deaf, or hard-of-hearing, then you may have many questions about deafness. However, the most important questions you can ask are about their communication preferences. Deaf people are diverse and have a variety of communication styles. Below we will begin with the basics to help you out.
The Basics: Find out your date’s preferred communication method.
- Some deaf people can speak and lip-read. However, it’s important to note that not all deaf people prefer to speak or lip-read. If they choose to speak and lip-read, we highly recommend going somewhere that is not noisy. Unless the person says it’s ok with them, avoid places like bars, or anything with large crowds and/or loud music playing in the background.
- Remember to keep in mind that not all deaf people wear hearing devices, and these subjects can be sensitive.
- Make sure the place you are making a reservation at is well-lit enough for the person to read your lips, see your face, or even see you signing clearly.
- Get the items on the table out of the way. If you plan to sign with a deaf person, it is important to be sure the person can see you clearly. Getting the items out of the way shows that you are centered and they have your full attention.
- Allow the deaf person to order their food or whatever they please. Do not infantilize them. It is very likely they have been infantilized by other hearing people in the past or they have faced marginalization in their lives. If they’re giving you the chance on a date, they most likely trust that you will treat them as equals.
Date Ideas and Planning Tips
You’re not just picking a location; you’re picking an experience! Be thoughtful and impress your date by researching and requesting accommodations ahead of time. If you aren’t sure where to go out, check this link out: www.deaffriendly.com. They have helpful reviews that rate a business on its deaf friendliness! Keep reading for tips on movie dates, lives shows, and at-home dates.
- Movie Theatres: Before going out, check to see if there’s open or closed captioning. While you can check local AMC theaters, don’t forget about drive-in movie theaters! Check our previous article about the local AMC theaters; [insert link]
- Live Shows (Ballet, Theatre, or Dinner Shows, etc.): You can request an interpreter to interpret the shows. If they say they cannot hire an interpreter, there is an ADA document that you can show them. Go to https://www.nad.org/resources/advocacy-letters/ and download it before attending places or making reservations. They will most likely comply with the request.
- Musical Concerts: If you are interested in having an ASL interpreter, you can go to www.deafinitelydope.com and request a musical interpreter to be at the concert. You can also call the venue and request an interpreter to be there. If they refuse to provide accommodation, you can also show them the advocacy letter mentioned above.
- Dinner at Home: To create a dating-like setting, you can cook with ASL pasta and practice signing skills with the deaf person you are interested in. Check this small deaf-owned business out: pghiatus.myshopify.com. They created ASL pasta to help enrich families by practicing signing with their deaf children.
- TV at Home: You can watch a movie off Amazon Prime, Netflix, or Hulu with your favorite snacks. Be sure to set closed-captioning on.
- Gifts: Lastly, don’t forget to get your sweetheart a card in ASL! It will make their day! Check out an incredible deaf-owned digital art shop here: www.58creativity.com.
PRO Tips: Want to take the next step? Learn ASL for your signing sweetheart!
- When you are talking with a deaf person, keep in mind that you already have gestures within you that you use in daily life that you may not have noticed before. Using these gestures will come in handy. For example, some of the gestures may be holding your hand out and saying “what?” The gesture of tapping your belly indicates that you are hungry. The gesture of drinking indicates that you are thirsty and want a drink. Don’t be shy/afraid to try ASL! Using gestures allows you to be creative, and you may be surprised to find yourself being naturally expressive. If you are interested in learning specific signs or phrases, check this website out; www.signingsavvy.com
FAQs
Is it hard to date a deaf person?
Some people assume that dating a deaf person is difficult because they often assume they are not able to enjoy music or go to the movie theater. However, there are a lot of deaf people who enjoy music and can feel the music through the beats. Fun fact: You can hold a balloon by the speaker and feel the bass through it. This was commonly used in the past at parties. When it comes to communicating with another person, there are barriers but there are also solutions. The solutions include learning how to sign, requesting interpreters, and using writing. Don’t worry much about it and go with the flow!
Is it hard to learn sign language?
Some people think it is hard to learn sign language. It isn’t hard if you put the effort into it and use it daily. It is only hard if you don’t use it. It all depends on you and your interest. It can take a person 6 months to learn or it can also take up to a year to become fluent in sign language. It all depends on who you hang with and how much you work on it. If you hang out with deaf people every day or your deaf partner, then you will absolutely pick up on a lot and become fluent within months.
Isn’t lip-reading enough?
Try putting yourself in the shoes of a deaf person who speaks and lip-reads. Lip-reading is a full-time job, and it is estimated that only 30% is accurate on the lips. Speaking is also hard because many sounds look similar or sound the same. For instance, try saying “I love you.” It also looks like you are saying “olive juice” and “elephant shoe.”

Ilya Kaminsky
Ilya Kaminsky is a well-known deaf poet who was born in Odessa. He was born hearing and eventually lost his hearing at four years old from mumps. His father’s death resulted in him expressing through in poetry. Interestingly, Ilya expressed that the sole reason for his love for poetry was that no one in his family knew English, and he felt it was a sense of freedom (Kaminsky, 2013). Ilya became a resident in New York during the year 1993.
In his book, Deaf Republic, the book reveals a tragedy during a protest which resulted in a soldier killing a young boy who happened to be deaf. It also affected the entire town and caused them all to become deaf. It becomes a drama series and will lead the readers to realize that disability has power. The whole anthology of poems is a story including a married couple who are expecting a baby and teaching signs daily, luring soldiers one by one to their deaths behind the scenes (Kaminsky, 2013). The book is unique because it includes sign language images throughout the pages. Two quotes that felt powerful from Kaminsky were, “Silence is the invention of the hearing, and the deaf do not believe in silence.” He also expressed what silence is like for deaf people throughout the book, which is vital for the readers to understand.
Here is one of the poems that I really think portrays a deaf person’s picture of witnessing a tragedy in its true sense. Reading these poems helps the reader imagine what it is like for those who experienced suffering through war and tragedy, like current events in Haiti, Ukraine, Palestine, and other countries that are not getting enough attention or support.
“That Map of Bone and Opened Valves“
I watched the Sergeant aim, the deaf boy takes iron and fire in his mouth- his face on the asphalt, that map of bone and opened valves. It is in the air. Something in the air wants us too much. The earth is still. The tower guards eat cucumber sandwiches. This first day soldiers examine the ears of bartenders, accountants, soldiers, the wicked things silence does to soldiers. They tear Gora’s wife from her bed like a door off a bus. Observe this moment – how it convulses – The body of the boy lies on the asphalt like a paperclip. The body of the boy lies on the asphalt like the body of a boy. I touch the walls, feel the pulse of the house, and I stare up wordless and do not know why I am alive. We tiptoe the city, Sonya and I, between theaters and gardens and wrought-iron gates – Be courageous, we say, but no one is courageous, as a sound we do not hear lifts the birds off the water.
-Ilya Kaminsky
Ilya Kaminsky’s Achievements
Bachelor’s Degree in political science
Georgetown University
JD Degree
University of California’s Hastings College of the Law.
Co-founded Poets for Peace
Author of “Dancing in Odessa,” which resulted in winning several awards
Author of “Deaf Republic,” winning National Book Critics Circle Award.
If you are interested in learning more about Ilya Kaminsky’s background and poetry, check out the link below.
https://www.poetryfoundation.org/poets/ilya-kaminsky
If you are interested in purchasing the Deaf Republic poetry book, you can order it through Amazon. Click on the link below or contact DeafandHOH to request borrowing the book.
References:
Kaminsky, Ilya. (2013). Deaf Republic. Minneapolis, MN. Graywolf Press.

The world’s largest movie theater provides open captions NOW!
AMC theaters is the largest movie theater chain to provide open captions at 240 different locations in the United States (Treisman, 2021). AMC plans to continue moviegoer accessibility of closed caption screenings and electronic listening devices in many of its theaters (Treisman, 2021). Additionally, the movie theater chain will provide weekly showtimes for new releases to viewers who want to watch movies with open captioning (Treisman, 2021).
If you are interested in watching open captioned movies at your local AMC theater, you can download an app on the smartphone or check the website. If you are unsure whether your local area has an AMC theater, don’t fret! Click on the link at the bottom of this page to get help locating the closest movie theater in your state of residence. This comes with perfect timing for many deaf and hard of hearing Marvel Universe fans that want to watch the early November release, “Eternals” in theatres. The new Marvel movie includes deaf actress Lauren Ridloff, making her Marvel’s first deaf superhero (Treisman, 2021).

FLASHBACK TO THE PAST – 1990’s.
Many DHH are still looking forward to the day where they don’t have to advocate for themselves to watch unlimited videos with closed captions. And thanks to AMC, we may be halfway there! AMC theaters is the largest movie theater chain to provide open captions at 240 different locations in the United States (Treisman, 2021). Did you know “The Caption Center” was the United States’ first captioning agency (Allen, 2015)? Closed captioning became widespread with the rebroadcasts of Julia Child’s television show “The French Chef.” Julia Child was the first to rebroadcast a show with closed-captioning in an attempt to be more inclusive of deaf and hard of hearing viewers watching from home (Allen, 2015). The Federal Communications Commission was established in 1972 and is a non-profit national captioning institute that provides access to closed captioning (Allen, 2015). It wasn’t until 1990 that “The Television Decoder Circuitry Act of 1990″ went into effect, requiring all televisions to have caption decoders (Allen, 2015). However, television programs were still able to exclude captioning from commercials so long as they ran less than five minutes (Allen, 2015). They were also allowed to exclude captioning if the programs ran between the hours of two to four in the morning. Programs having the ability to opt-out of captioning has made it difficult for DHH individuals to enjoy watching television with captions for more than thirty years.
30 YEARS > PANDEMIC
Although closed-captioning has been around since the 1990s, it is not yet a standard for public places such as; movie theaters, bars, restaurants, and open public events. It is slowly becoming widespread and that is wonderful for people with disabilities. Closed captioning provides language acquisition, improves reading skills, and improves receptive skills. With the increase in online consumers over the past thirty years, it can be difficult for DHH consumers to enjoy things like social media to the fullest. Many online videos do not include closed-captioning, including those that come from media outlets. Since the pandemic hit, many people have opted to stay home and use social media as a digital platform to connect and share videos with others. However, a lot of these videos are inaccessible due to the lack of captioning included in them. Thankfully, some digital platforms like Instagram have responded to this influx of online users by providing captioning in the video creation process. Instagram will review the video and add captions as an overlay before users submit the final video for upload. Accessibility continues to evolve, reduce barriers, and provide opportunities for those with disabilities including deaf and hard of hearing consumers. While the pandemic brought about a lot of barriers and obstacles, it also helped digital platforms recognize potential changes they could make to some of their features for captioning, like Instagram.
What is the difference between open captions and closed captions?
Open captioning is always on the screen and the person watching does not have access to turn it off whenever they please. Differently, closed captioning can be turned on and off by the person watching the screen. Open captioning is beneficial for everyone since it is universally designed (UW, 2021). For instance, it’s helpful for noisy environments, people who speak a different language than the original content, and people who struggle with speaking (UW, 2021).
DID YOU KNOW…
People who work as stenocaptioners or captioners make more than $100,000 a year (Allen, 2015)? They are responsible for maintaining high quality captions without making any mistakes.
References:
Rachel Treisman. 2021. The world’s largest movie theater is adding open captions at 240 U.S. locations.
Scott Allen. 2015. A Brief History of Closed Captioning.
University of Washington. 2021. What is the difference between open and closed captioning?
What is Dinner Table Syndrome?
Many deaf and hard of hearing children come from hearing families in which the majority do not know sign language. Consider the experience a deaf individual might have compared to a hearing individual at the dinner table. As a result of this, many DHH people struggle to gain regular access to socialization and communication in their daily lives. Imagine a group of people starting to laugh uncontrollably at the table while a deaf individual questions themselves and asks the nearest person, “What’s so funny?” Often, they will receive a response like, “Oh, it’s nothing” or “I’ll tell you later.” This type of social interaction could lead anyone to experience the depths of isolation and frustration.
According to Sara Novic, “Deaf people have a term for the isolation that grows out of being surrounded by non-signing hearing people: ‘Dinner Table Syndrome’ ” (2016). Many hearing families do not realize they are contributing to language deprivation and inaccessibility to their deaf relatives. Dr. Henner, a deaf assistant professor at the University of North Carolina stated, “People learn language and get information not only from direct teaching but also indirect exposure” (Novic, 2016). Hearing children are exposed to things like background noises that constantly reinforce their language abilities— while deaf children do not always have the same privilege. Since many families do not sign, deaf children are deprived of important information that may be happening around them, such as background conversations. Many DHH children may recluse themselves by going off in their room to read or watch television. It’s become easier for DHH children to excuse themselves and interact virtually rather than experience things like family time and forming deeper connections with others face-to-face.

For many families, the upcoming holidays are perfect for catching up and spending time with one another. But for some DHH individuals, this time spent with family can leave them feeling full of dread and isolation. It’s important to note that communication with deaf relatives is still possible for families that do not know sign language. Perhaps they are just not familiar with some of the basic accommodations that can be made during these gatherings. For instance, using gestures can go a long way. And with a lot of relatives watching television during the holidays, it’s important to be mindful if the big game or holiday parade is on to include deaf guests (NDC, 2019). The most important thing you can do is to turn on the closed captioning on the television before guests arrive (NDC, 2019). If you do not know how to turn closed captioning on, you can ask a deaf guest when they arrive. They will appreciate your consideration and efforts to include them. By simply adding captions, families can “help deaf people follow what is happening on the television, especially in a noisy or busy environment” (NDC, 2019). Another accommodation for families to consider is pitching in funds to hire an interpreter (NDC, 2019). This could be an exciting experience for everyone involved—and who knows, maybe hearing relatives can learn some new signs. And if hiring an interpreter is not possible, there are still other options available such as speech-to-text services (NDC, 2019). Speech to text is an app which is similar to common tech devices like Siri or Alexa. It can translate what is being said to text.
Understanding the importance of language deprivation is critical in helping families recognize the problems faced by their deaf relatives and friends. Families can work toward solving these problems by providing the support and accommodations necessary to include deaf relatives. By familiarizing oneself with the different accommodations available to DHH individuals, it should be much easier for hosts of gatherings to create an enjoyable experience for all.
References:
NDC. (2019). A Holiday for the Whole Family: Tips to Include Deaf Guests.
Sara Novic. (2016). Why ‘Dinner Table Syndrome’ is getting worse for deaf people.
Four Degrees of Hearing Loss, Part 1: Navigating Mild Hearing Loss in a Hearing World

Affects of Mild Hearing Loss
Mild hearing loss affects about 25 million people in the United States (source), and is the least debilitating of the four degrees of hearing loss – the others being moderate, severe, and profound. Hearing loss is usually categorized in terms of decibel receptivity. A person who cannot hear sounds of 25 decibels (as loud as whispering or rustling leaves) to 40 decibels (quiet ambient noise in a library or urban environment) may identify as having mild hearing loss.
Erwan’s Experience with His Hearing Loss
Until his recent (mild hearing loss) diagnosis from an ENT specialist, Erwan, 28, thought that his difficulty in noisy crowds, his loud speaking voice, and his slight reliance on lip-reading were typical experiences. Getting hearing aids made a fast difference in how he adapted to situations where hearing might be an issue. “I must have had this [hearing loss] since I was a kid without realizing it,” Erwan, 28, says. “I’ve always been able to adapt and deal with it.” Receiving his first pair of Phonak hearing aids in March 2021 helped Erwan rediscover small sounds, like the bass in a song or the boiling of a pot of water. For Erwan, getting hearing aids was “one of the best things to happen to me this year!”
Jordan’s Experience with Her Hearing Loss
Meanwhile, Jordan, 30, has been wearing hearing aids for the past four years. As a professional with mild-moderate sensorineural hearing loss, she often needs to make careful decisions on how best to navigate in a certain situation. Is there a place she can stand in a crowded room where the surrounding conversations will be least overwhelming? Will she be able to wear behind-the-ear hearing aids, glasses, and a mask all at the same time, or is it better to pick the invisible-in-canal aids of a slightly lower quality?

Although Jordan greatly benefits from hearing aids, she wants people to know that the common parallel between glasses and hearing aids isn’t completely accurate. A pair of glasses will clarify a blurry object, but hearing aids are meant to amplify, not clarify; a mumble will just become a somewhat louder mumble. In addition, quiet noises brought to focus by hearing aids can quickly become exhausting or overstimulating. “No matter which way I slice it, wear my aids or don’t, I end up cognitively more tired than I used to after social interactions,” Jordan says.
Complications They Both Faced
For both Erwan and Jordan, the COVID-19 pandemic illuminated the difficulty of navigating conversations without the ability to lipread, and neither of them were aware of the extent they relied on it until people’s faces were covered with masks. Still, even before realizing their hearing loss, they have been able to adapt and cope in a hearing world.
Questions
Do you have questions about the benefits of hearing aids, or are you wondering about how to deal with masks in a post-COVID world? Visit our Frequently Asked Questions page for quick answers, or reach out on our community Facebook page for resources and advice.
The Camp
As a child of the 70s, having been born in ’72, growing up was a huge learning experience, not just for myself, but for my family, my friends, my school, my job(s), but especially for myself. Back then, I was unique because I had a disability that not many people knew about, much less understood. I was born with a severe hearing loss due to the results of birth complications. During the ’70s, and perhaps into the ’80s, those with some form of hearing loss or deafness would be sent to a school for the deaf. In Maine, there was only one such school, and it was called Baxter School of the Deaf.
My parents wouldn’t have any of it. They refused to send me somewhere so far away. The only time I’d ever see them was during the weekends, if that. They fought for me to stay home and go to public school in our area, and miracously, with the help of several doctors, speech therapists, etc, they won the right to keep me home and send me to public school.
As I said, it was a learning experience. Not only did I had to adjust to a life with hearing loss, but so do others had to adjust to a child with a hearing loss. Thankfully, my mother made sure that I lived a “normal” life, a life that would be considered the life of a “hearing person”. Among those I still count as friends are kids, and now adults, who had perfect hearing all their lives. If I did not have those guys as friends, I’d have been very, very alone indeed, because of the simple fact that there were no kids my age who had the same disability I did.
One such experience I will relate to you now. A few years after my parents found out of my severe hearing loss, when I was but a wee kid probably still sucking my thumb, my parents decided maybe I would benefit from meeting kids who had the same issues I had. Deafness. Hard of hearing. So my father took a day off from work, and hightailed it up north with myself and my mother in tow to a Camp for the Deaf Children.
Little did I know that I would remember this experience for the rest of my life.
We arrived at the camp, and to all appearances, everything looked normal. People were normal. Kids were normal. The campgrounds were normal. Everything was just fine and dandy. My eyes probably lit up then, seeing all the fun things I could do for three, maybe four months!
We were ushered into a room and spoke with a guidance counselor. And then he showed us around on the camp grounds. As we walked around, we passed building after building where the kids would sleep or stay inside during rainy days. As chance would have it, it had just rained about an hour before our arrival, and the children did not yet leave their bunks.
Have you ever seen an old black and white film where a car would be cruising a dirty old neighberhood, and kids would be standing in their doorways, just staring distrustfully at the car as it drives by? That an ominous silence filled the air, only to be shattered by the voice of the counselor as he introduced us to other counselors, or when he showed us around? It was like a scene straight out of a horror movie, to be honest.
I thought I was home. I thought I was with kids who are…Just. Like. Me. But it was furthest from the truth. You see, I am hard of hearing, not completely deaf. Strike one against me on that one. I did not learn sign language, having been able to communicate just fine with other kids my age. Strike two against me. And finally, I was an outsider, regardless of our mutual disabilities. Strike three.
People with deafness, they are empaths. We can read lips. We can read body language. And kids? Well kids are honest to a fault. And their body language was so plain and open to see. I was not wanted. I was an outsider. And I felt every stare, every distrustful stare that day. I broke down and cried that day, so powerful were the emotions I felt emanating from the children in their houses of wood.
My parents took me out of that camp as fast as their feet could go. They knew what I saw. They felt what I saw. And I never attempted to do that again, never. Ever. Again.
Here’s the thing I learned since. I am thankful for my parents with what they did. They did not shelter me from the world, as cruel as it is. They did not inhibit me by defining me as a child of deafness. They chose to treat me as their son, a child, a child who loves to play ball. Who loves his video games. Who loves to read and write, and play games with his friends. They did not let my disability affect my happiness; they would not allow me to let my disability define who I am. And what I am.
Because of that, I was much better able to deal with the real world as a consequence. Did I have some problems as I became an adult (and afterwards?) Certainly! No matter what, there will always be ignorant, selfish, uneducated people who will judge you no matter what. But I was better able to deal with such things, and still retain a semblance of a “hearing person’s” life.
It’s okay to have friends and acquantainces from all walks of life. It’s okay to accept your deafness as a part of yourself, and it’s okay to mingle and mix with people of different race, color, religion, and last but not least, with people who can or cannot hear.
I don’t let my deafness define me. I define who I am, me alone. And you know what taught me to do that? Walking in a camp of deaf kids changed that.
Morale of the story? Don’t let anyone or anything define who you are. You are who you want to be.
Living In Between
When most people look at me, they probably don’t see my hearing aids. They probably don’t know that I struggle with comprehending a spoken conversation. They most definitely don’t know that I am juggling life between two worlds.
Many of us in the Deaf and Hard of Hearing community wear hearings aids or cochlear implants, however, this doesn’t mean we can understand every spoken word. With my hearing aids, I simply hear more noise. The noise itself is not distinguishable between rushing wind and someone shouting my name from far away.
From the time I was five years old and I received my first hearing aids, I was encouraged to “be hearing.” I went to speech therapy but was never introduced to American Sign Language. I didn’t even know the Deaf community existed, until I was in high school. While my parents weren’t supportive of me attending the American School for the Deaf, I could take ASL classes. It was there that a passion was born. I finally found a place where I wasn’t an outcast. I wasn’t the only one who was different. I could breathe.
I remember when I was in elementary school trying so hard to fit in. I purposely left my hearing aids at home, “forgot” my FM unit in the audiologist office and must have done the Deaf Nod a million times a day. I always felt like the odd ball. The misfit. I was constantly fighting what made me different – unique. I didn’t want to be that way. I wanted to be like everyone else, you know, normal. It didn’t become painfully apparent that I would never be normal until I was in high school.
My high school experience was not a good one. Honestly, I’d rather pretend those four years never happened. Not only were students picking on me for not being able to hear them, teachers did it too. They could be in earshot of someone bullying me and wouldn’t say a word until I retaliated. The one memory that is forever burned is when one of them called me a retard. That word haunted me and still does sometimes. Any time I wanted to try something new, his voice would echo in the back of my mine until I decided not to try. I had started to believe that word was synonymous with my name.
Since no one in my family learned ASL, I was forced into a life of lip reading everyone all the time. Whenever I went home after school, I rarely wanted to have a conversation because my energy was often tapped out. I’d go to my room, crawl into a comfy chair and read a book. In those fictional lands, I didn’t have to work as hard to understand what was going on. If I missed something, all I had to do was turn back a page or two. Whereas in a real-life conversation, I was always lost. If I had to ask, “What did you say?” more than once, I usually just read their facial expressions to figure out how I should react. It got to the point where sometimes, I was 100% guessing during a conversation.
During the pandemic, I have been guessing all the time. My insecurity is now through the roof! I can no longer hide my hearing level as well I used to. I have started to use alternative methods for communication among general public like Sprint IP Relay and typing my food/drink orders in my phone. Lip reading and facial expressions were the skills I could use to understand what I couldn’t hear. Now, I have less to work with when figuring out the correct response to a question or statement. Every Deaf and Hard of Hearing person would probably agree to this, I can’t wait till we no longer have to wear masks in public!
While hearing aids allow me to hear sounds, I can’t otherwise hear, this means many people I encounter think I am hearing. Since they assume that I am hearing due to what I can understand and my speech, I have always been embarrassed whenever I need to ask, “What did you say?” I am positive that they will think less of me, if I told them the truth. In reality, I think of myself as less than. Not good enough. Subpar. Don’t get me wrong, the bullies from high school and others I have run into over the years who have said, “Never mind” or looked down on me, played a part. Those looks, words and vibes chipped away at my self-esteem, as I grew older. I hardly thought of myself as successful or worth anything. This is something I still struggle with.
So, when it came time to move almost halfway across the country to start my own life, that mentality followed me into every kind of relationship. Whether it was trying to find a job, friends, boyfriend, or roommate, I was constantly second guessing myself. When they looked at my hearing aids, they automatically saw what I couldn’t do, instead of what I could do. Eventually, I met individuals who saw my potential, my worth, my essence as something to be cherished instead of frowned upon. In an effort to acknowledge my own self-worth, I have a mantra. I am a Black Deaf Queen who deserves to have space to be me. I will accept nothing less. I can do anything, except hear.
