Stonington Lobster Trap Tree

Have you seen the new addition to Stonington borough for the holidays?! The lobster trap tree by the fishing docks is new to our area this month. Constructed of 378 lobster traps standing 24.5 ft tall with 360 buoys and 816 lights decking it. 

The tree in day time.

It took 17 hours for the volunteers to get the tree set up and 4 hours to hang the buoys! This is my favorite part, the buoys were a community involvement project. Each buoy had been hand painted by Connecticut and Rhode Island artists. There’s 44 buoys that were created by children too. The buoys will be auctioned off in February. 

Top image: the top of the doorway. Some of my favorite buoys.

There are already plans to return the tree for the 2022 season. I hope this will be an annual holiday tradition for Stonington! Last year I traveled around New England less, due to the pandemic, this made me realized that there weren’t as many lobster trap trees in Connecticut. I posted on my Instagram asking friends and followers if they were aware of any locally to visit. I was so used to seeing them on my travels in Massachusetts, Rhode Island and Maine during the holidays. 

Oh buoy!

I went to see the lobster trap tree in the first week of December. I was blown away by how beautiful it was, especially the painted buoys. I enjoyed walking around the tree looking at each buoy (remember, there’s 360 of them!!) so it was fun to see the variety of art skills. Most of the buoys represented a local business/organization. There were many buoys dedicated to the fishing village, some buoys were painted of specific fishing boats that you normally see at the docks. Another popular icon that was repeatedly painted was the Stonington Lighthouse. 

The top image is the tree lighted up during sunset. More of my favorite buoys.

There is space on the inside of the lobster trap tree that you can walk in to explore. It is little nerve wrecking, I always fear a cave in but the tree is constructed very securely! The view is amazing on the inside especially at the sunset hour or at night with the lights on. 

Top: Sunset from inside of the tree. Two more favorite buoys. Bottom: the view from the fishing docks.

The lobster trap tree is magical to see. I have gone to visit it several times already. It’s so much fun to watch the lights come on around 4:30 PM. It stays on until 10 PM daily. There is always someone around available to take photos for you, this is a great photo opp location! If you don’t feel comfortable being around many people, it’s almost always empty during the daylight hours during the weekdays. 

The tree at sunset.

Tree at sunset, shortly after lights came on around 4:30 PM.

Where is the tree exactly in Stonington? It’s in the park right next to the fishing docks. You can’t miss it. A bonus for those with kids - there is a playground right by the tree. A short walk from the main street where the shops are. Stonington also created a fun scavenger hunt event with the local businesses when they introduced the lobster trap tree. The scavenger hunt is called “find the buoy”, a postcard with 12 shops to visit and get stamped. You then mail in you postcard to be entered to win some of the prizes. Unfortunately, the last day to enter is December 24th, on Christmas Eve so there isn’t much time to do this! 

We visited the tree often because we love it!

I love how the community rallied together to make this tree happen. A lot of help, monetary donations, time, volunteering, etc. went into this! Thank you to all who were involved to make this wonderful and magical tree! I’ve always loved the holidays in Stonington, it’s always been one of the best shoreline towns to dress up for the holidays. I admire many beautiful homes and local businesses that deck the halls. I attend the holiday stroll and tree lighting ceremony annually. I have fond memories of Christmas in Stonington, and now this new addition will bring more wonderful memories! 

My family photo!

For more information on how to purchase the buoys (auction) and view the buoys (if you are too far to visit!), you can visit the website here. For those who aren’t local, it is worth the drive! Don’t forget that Mystic is neighboring town, so you can easily make a day out of it doing everything holiday-related! Have a Merry Christmas! 

My pup modeling for me in front of the tree.

Pennywise Mystic

As I looked back at my past Christmas memories, I had a realization. For the last 5 years, my Christmas outfits came from Pennywise in Mystic, CT. Pennywise is a high quality consignment store that had been around since 1988. Owned by mother and daughter, they sell women’s clothing, accessories and shoes as well men’s clothing. 

Pennywise shop.

When I moved to Connecticut a decade ago, I discovered their shop that was on Cottrell Street (now Mystic Knotwork). I shopped there several times then they closed that shop and moved everything over to the Greenmanville shop across from Mystic Seaport. I shopped there even more when I hit the Lilly Pulitzer phase for a few years. 

Shopping for Kentucky Derby dress in 2016.

Pennywise sells many great quality and popular brands. They are selective about the brands, as not all will be accepted to be sold in the store. A few of brands I frequent are JCrew, Vineyard Vines, LOFT and Levi’s. Other brands I’ve seen: Madewell, Anthropologie, Banana Republic, Ralph Lauren, Gap and many more. Sometimes the clothing are still brand new with the original tags attached. 

The shop is very well organized. It can be overwhelming but it’s easy enough to navigate through. It’s a two story building with mostly women’s clothing and accessories on the first floor. More women’s clothing and men’s clothing are upstairs. Every time I pop in to shop, I check their color sticker sale of the day. For example: red tags are 25% off - if you find a clothing item with a red sticker tag then it is 25% off. They always have two colors each day that are discounted. 

Loved this red Vineyard Vines sweater!

The prices are reasonable for the designer brands and very affordable for other brands! They really do a great job selecting which clothes they consign - you won’t find any with stains, holes, or weird smell! I’ve always been apprehensive about shopping in thrift stores - secondhand never appealed to me. Pennywise has changed my stance on that but it is the only consignment store I will shop at! 

The customer service is always top notch. As I mentioned, it is owned by mother and daughter team. At least one of them is always there each time I popped in. They have always been helpful in locating items I am looking for or for finding things I would want. One time I passed by the shop and spotted a cute coat on the mannequin outside of the shop. I did a U-turn and popped in to ask what size/price it was. I felt bad about making her do all the work taking it off, I was really hoping it was my size… luckily it was! Even better that it was a great price! Hooray! 

The coat I literally bought off the mannequin! (the brown sweater is also from Pennywise).

A few years after shopping there, I decided to consign my clothes. The system is very effective and easy. I brought in my clothes and they will take 5-10 minutes to sort through and take what will sell in the shop. The clothes will stay on the floor for 6-8 weeks and the unsold will be donated to a charity. A win-win to make a little money and have it donated to appropriate places! The shop keeps 50% of the profits, the consigners will get the other 50%. It’s the best percentage I’ve seen compared to other consignment stores. Also, if you made money - you can request a check on the spot. Otherwise it will stay in the system as store credit which you can use if you buy things. 

Time definitely had flew by, it’s hard to believe that I have been shopping at this shop for 10 years now. Does anyone remember Steve the cat? I miss my buddy! He was the shop cat who lived there and would rub up against my leg while I was shopping or he would be napping on the counter. He lived a long life and passed away a few years ago. It’s not the same to pop in there without Steve’s greeting. 

Be sure to visit this shop, they have a wide variety of brands and prices for everyone! You will guarantee find something to buy! I love that I unexpectedly made it a Christmas tradition to buy my outfit from there each year. It’s something I’ll have to continue! 

Pennywise is located at 22 Greenmanville Ave, across from Mystic Seaport and half mile away from downtown Mystic. If you aren’t local… don’t fret. They started selling online and offer free shipping over $100+. Website can be found here. Happy shopping! 

JCrew button up shirt.

LOFT sweater.

Talbots sweater.

JCrew cashmere brown top.

Interpreters

The topic of interpreters… I’ve put this off for a while, after receiving some questions. So here I am, addressing some questions!

First of all, interpreters can be quite the discussion! We could talk all day long so I’ll keep it short for this blog. I have a strong appreciation for them as they help to facilitate communication between both worlds. Without them, it wouldn’t be possible for me to get the information or get my words across. They work hard interpreting for hours at times, with the constant signing (I can’t even write for hours without my hands cramping!). Interpreters also don’t come without some challenges. As the costs of hiring them can be daunting for some businesses/offices resulting in hiring non certified interpreters.

How do I know if my interpreter is certified? Most of time I can look up the registry database online. When I have medical appointments, I do not know who they call so it was common for me to go to my appointments not knowing if I will have a certified interpreter. I am stuck with whatever interpreter that is there that day. I often ask which agency they worked for to keep in mind if I want to request the same individual again.

Why is a certified interpreter important? It’s highly preferred as they completed a program and passed exams. No difference from you preferring a certified contractor to fix your broken porch over a self-taught contractor. This is an issue because most places will not hire a certified interpreter due to higher costs. If you’re certified, the more pay, right? As a result sometimes we end up with a lower caliber interpreter.

Have you seen two interpreters at the same time at an event, or sometimes there’s only one… and wondered why is that? The more interpreters you have, the better quality of information being interpreted. After 20 minutes, the quality of signing usually decreases. So if there’s a second person, that will allow them the rest they need. It is common for them to switch every 20 minutes to keep more accurate translation. I also like it when the resting interpreter sits, still pays attention to what is being said and adds whatever the interpreter forgot to translate. They definitely help to keep each other in check!

People don’t always realize that even with the interpreters translating for me, it’s not always my voice. Wait… what? Imagine this… you know the telephone/grapevine game? Where you have a group of 6 people… you tell one person at a time a sentence then it jumbles somewhere through the game and the last person says something completely different? Sometimes that’s what happens with interpreting. This leads to another question I’ve got… do I trust them? Sometimes. As much as I appreciate them being that bridge between both worlds, it is hard to put all of me in. I constantly am lip reading them to make sure they are repeating what I say. I have my husband with me most of time, so he’s also listening.

With that, has there been any embarrassing moments? Yes, several. The most recent memory I have is at a doctor’s appointment after having a sore throat for a week. I was sharing my sore throat remedies I had been doing at home. I said that I’m constantly eating cough drops. The interpreter translated “I’m constantly eating ice cream”. The doctor smiled at me and I saw my husband speak up. We laugh about it now, but imagine if he hadn’t been there!

I’ve shared that I’m not thrilled with the skill of interpreters in my area as I live in an area of few deaf people. The majority of interpreters are in metropolis cities an hour away. I’ve had my husband interpreting for me at all of my medical appointments for the last few years now. I know it’s not technically the right thing but I just had enough of the bad experiences. It’s hard because I know my decision of not requesting interpreters is not helping to educate the doctors and medical offices that they are supposed to provide me one. It’s also not fair that my husband is doing it for free too.

I don’t always love having my ‘words’ translated by someone else, but it’s the only way I can be a contributing member of the community. Well, the other option would be everyone knowing sign language… but not realistic! I also don’t like that people aren’t really getting to know me. They’re hearing my words through someone else’s voice. I even got that comment when I started this blog, how some were realizing and learning about MY VOICE. Imagine having your mom, husband/wife, brother or a stranger say everything you want. It doesn’t always match.

I’ve had interpreters since I was in elementary school. I was in a special education classroom with a teacher that signed but I still had an interpreter that came with me to my mainstreamed classes in the afternoons. When I transferred schools, I had one same interpreter with me all day long. She worked so hard to convey information and share my words. There was a misconception that she was my mom! Many classmates thought that. I noticed that it is a common misconception with permanent interpreters. How many of you thought Marlee’s interpreter is her husband or a family member?

When I moved to Rochester (NY) … home of one of the largest deaf communities, there were a boatload of interpreters compared to my rural hometown. Interpreters were not as much of an issue but it doesn’t mean that I still ran across some ‘bad’ ones but it was rare. I miss the quality of interpreters in Rochester all the time! I constantly had different interpreters for every class in college, always had two for each class. I saw the difference in having a team vs being solo. It made me appreciate my high school interpreter even more for her hard work!

The topic of interpreters could be discussed more in depth, both positivity and negatively. Despite the bad/challenges, they are a huge help! I get excited when I see an interpreter on TV for press briefings, at a concert, or anywhere really! I appreciate their effort in helping my community to be inclusive.

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!

Mystic Yachting Center

Calling all brides-to-be and anyone who is planning a party in Mystic!

Mystic Yachting Center.

Mystic Yachting Center.

I received an exclusive invite to a cocktail party at Mystic Yachting Center at Mystic Shipyard last week. It recently had been renovated and updated event spaces. I’ve lived here in Mystic for the last decade and never seen this gorgeous venue in person! I was blown away by the nautical touches of the center. Especially the vaulted shiplap ceiling on the upper level! The entrance foyer was very open and welcoming, the walls were covered with photos of New England scenes. 

It’s the ideal location for a nautical wedding for sure! The tablecloths even had beautiful blue and white waves design on them. There was a beautiful picturesque and panoramic view of the boat marina and Mystic River. 

The venue is small and intimate, which would be perfect for weddings/parties/events up to 160 people. For more information, please contact the venue about the capacity limits. The center consists of lower level which was the event space/cocktail hour space with in-house kitchen. The upper level is the larger room with a dance floor, ideal space for receptions. Both levels had bathrooms and is handicap accessible. Plenty of parking for everyone!

At the cocktail party, we ate some appetizers and New England Paella while enjoying some live music. The event was set up like it would be for an event/wedding. It was gorgeously set up with that nautical charm. You couldn’t beat the waterfront views out of the large glass windows from the upper ballroom! It was a cloudy night so unfortunately we missed out on the sunset, but I know sunsets in that area are amazing! I highly recommend you to contact Mystic Yachting Center for your next party/event/wedding!

Boats and more boats.

Boats and more boats.

The set up for an outdoors wedding (unfortunately it was cloudy that day, but imagine a beautiful sunny day!)

The set up for an outdoors wedding (unfortunately it was cloudy that day, but imagine a beautiful sunny day!)

The main entrance.

The main entrance.

Cookies!

Cookies!

The cocktail hour space.

The cocktail hour space.

Beautiful nautical photography through out the venue.

Beautiful nautical photography through out the venue.

Great views of the shipyard.

Great views of the shipyard.

Some tables on the balcony.

Some tables on the balcony.

Enjoying some food and drinks!

Enjoying some food and drinks!

Pudding for dessert!

Pudding for dessert!

How cute is this centerpiece set up? Loved the Mystic Knotwork knots!

How cute is this centerpiece set up? Loved the Mystic Knotwork knots!

Gorgeous window looking out front of MYC.

Gorgeous window looking out front of MYC.

Upper level - food table.

Upper level - food table.

More food!

More food!

The space where music is being played with some tables around.

The space where music is being played with some tables around.

The stairway was gorgeous!

The stairway was gorgeous!

Again, another shot of the main entrance lobby. The stairs goes upstairs to the ballroom space.

Again, another shot of the main entrance lobby. The stairs goes upstairs to the ballroom space.

Some of nautical interior decor.

Some of nautical interior decor.

MYC at night.

MYC at night.

Deaf role models

Who was your role model? Were they deaf too?

Growing up in a rural area of Upstate New York didn’t give me the opportunity to meet Deaf adults to look up to. So who did I look up to? I knew of Marlee Matlin, the famous deaf actress and Heather Whitestone, first deaf Miss America. So that’s who I looked up to as a child. Both are two Deaf women on polar opposite of the spectrum. 

Marlee Matlin is a well known Deaf actress and activist today. Her performance in the movie ‘Children of a Lesser God’ in 1986 earned her an Academy Award and Golden Globe award. She had acted in several movies and TV shows since then, which included ‘Switched at Birth’ and the recent released ‘CODA’ movie. Matlin released a book ‘Deaf Child Crossing’ during my pre-teen years, early 2000s. I was in awe of her ability as a Deaf person being in Hollywood. I wished that there were MORE famous Deaf people.

Credit: Marlee Matlin’s instagram.

Credit: Marlee Matlin’s instagram.

Heather Whitestone was the first Deaf woman to win Miss America in 1995. I was too young to understand at the time about Miss America and beauty pageants. I had learned about her afterwards. During my pre-teen years, she was doing a lot of work with Starkey Hearing Aid Foundation as their spokesperson. I wrote to her (the snail mail way!) about my deafness and how impressed I was with her accomplishments with Miss America.

Credit: Heather Whitestone McCallum’s instagram.

Credit: Heather Whitestone McCallum’s instagram.

Marlee and Heather lost their hearing at 18 months due to illness. They identified themselves as Deaf but were on the opposite side of the spectrum. What does that mean exactly? In the present day, Marlee Matlin is a strong advocate of using American Sign Language (ASL). Although I do need to point out that she has the ability to speak and previously (maybe still currently?) wore hearing aids during my childhood years. Heather Silverstone grew up orally/verbal. She didn’t use sign language until her senior year in high school. Heather was more mainstreamed in the hearing world, even getting her cochlear implants in her adulthood. 

During my childhood, we didn’t have Internet where I could’ve had an easy access to many other Deaf role models that were out there. My mom clipped newspaper articles during my childhood to show me anything about Deaf people. I started seeing more and more of Deaf examples in my late teens years/college years. The media started having more exposure of the Deaf community. The TV show ‘Switched at Birth’ really opened many eyes about the Deaf culture. 

In my small town in Upstate New York, there were a few Deaf adults but I didn’t have many interactions with them. I did attend some meetings when I was in my high school years. I didn’t find a connection with them back then. There weren’t many others that I could relate to, so it was difficult to find role models, famous or regular folks, to really look up to. I might’ve had Marlee and Heather to look up to, but I didn’t want the same exact goals as them. I did learn that their Deafness didn’t stop them from achieving their goals so that is what was inspiring to me as a kid. 

While I was at college in Rochester, Marlee Matlin released a book ‘I’ll Scream Later’ in 2009. As part of the book release, she toured several cities which included a stop in Rochester. It was surreal to meet her at my college in person after idolizing her my entire childhood. I was so starstruck that when it was my turn for her to sign my book, I froze. I didn’t know what to say! I didn’t say a word! She smiled warmly and thanked me for coming. Oh, how I wish I could go back now and say everything. How she inspired me to achieve the impossible. Don’t let my deafness stop me from my passions. How she gave me that hope that Deaf can do it. Maybe someday again I will get that chance!

When I met Marlee Matlin at RIT, 2008.

When I met Marlee Matlin at RIT, 2008.

Now, it’s different with social media and technology gaining more accessibility to Deaf kids today. They know about Deaf role models out there who are singers, artists, business owners, performers, etc. The kids have their pick now on who to look up to. I’m glad that there are more successful Deaf people out there to be that role model for a Deaf kid to look up to!

CODA movie - Dad's verison

****SPOILER ALERT: If you intend on watching this movie you may want to wait to read this!****

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I remember shedding tears watching the end of Brian’s Song, Terms of Endearment and even Bambi.  I experienced strong emotions throughout CODA! I don’t usually stay for the credits but needed to! This was quite different for me! I realize this movie touched others as well!

As Kelly explained this movie is about a hearing girl with deaf parents and brother. She is challenged to balance her life deciding what she wants and assisting her family. There were so many scenes that I could also relate to as a parent of a deaf daughter.

In the beginning of the movie the parents showed up at the school playing music very loud. This way they can feel the vibrations. This obviously caught the attention of the hearing kids who laughed and ridiculed them. The daughter defended them with no success. Deafness is not visible! We can relate…. as a teenager Kelly was returning a grocery cart to the corral for her mother. A man yelled to Kelly from behind that he would use the cart. Kelly not hearing did not react and put it away. He then threw up his arms in haste & with a very angry face mumbled something. Diane seeing this, informed him that she is deaf! Not so calmly!

At one point the daughter in the movie expressed herself as “I am exhausted”! This was used in context of being torn between helping her family and developing her life. Her family’s demands were so great (doctor appt, court and negotiating for their business) she had missed  her commitments. Kelly has expressed frustration with her family members who sign in group situations. Especially around the holidays! She misses so many conversations and it is difficult for the interpreter to determine what conversation to interpret.

Kelly mentioned in her review that during the school recital the director turned off the sound. The film scanned back and forth with all the happenings but the silence was overwhelming! The deaf parents’ heads were moving back and forth to try to understand what was going on around them! This put all viewers in the place of the deaf characters. Wow! This was a great approach to give you the feeling of their daily life.

The family returned home after the recital. The father and daughter were outside. He was asking questions about the song she performed. He asked her to sing it to him. She obliged and he put his hand on her throat! She seemed surprised but realized he wanted to feel her voice! Kelly started at a school when she was a year old. They worked with Diane and Kelly on her speech. Mirroring mouth movement for repetitive sounds. I remember putting Kelly’s tiny hand on my throat and repeating sounds. I remember her face. Kelly always showed amazing facial expressions as a toddler!

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Toward the end of the movie the daughter was auditioning for admission to a prestigious music school. Her family was not allowed in her performance but found their way to the balcony. They entered quietly not to tip off they were there. She started her performance of “Both Sides Now” by Joni Michell  and she saw them. She started to sign the song about 1/3 of the way directly to her family! This confused the staff evaluating her until they realized her family was there.  The irony of the song was well represented to the struggles she had. She fell back into her role as interpreter where she should be individually focused. You could see the love she had for her family!

“Rows and flows of angel hair

And ice cream castles in the air

And feather canyons everywhere

Looked at clouds that way

But now they only block the sun

They rain and they snow on everyone

So many things I would have done

But clouds got in my way”

Looking at things from Both Sides Now is a constant effort! Understanding one’s perception may not be what you actually see. This movie really made me think! I hope more opportunities come for these people to express their views of the world!

Please watch this movie! I am sorry to give details before seeing it but I wanted to reference these moment to my personal experience. 

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CODA movie

In mid-August, there was a new movie making a splash. Apple+ released ‘CODA’ starring Marlee Matlin.  The term CODA stands for Child of Deaf Adult[s] so it was a movie portraying a life of a CODA. The movie was selected to be shown in limited theaters. I was thrilled that Mystic Luxury Cinemas was one of the theaters to feature the movie. I haven’t gone to the movie theaters in 6 years! While in Rochester, the movie theaters had a limited schedule of when movies would play with open captions (subtitles that appears on the screen). In 2013, the movie theaters moved to offering closed-captioning glasses. It is an accessibility tool, 3-D glasses that have captioning. It appears when you wear the glasses while watching the movie. 

It should’ve been a win, right? Except the captioning glasses are a nuisance. The 3-D glasses have two large boxes on the side which are bulky and heavy! Each time I went to the movies, I found myself leaving with a headache and sore neck. The glasses were so heavy that it always left an imprint on my nose bridge and on the sides of my face. While wearing the glasses, I had to stay still and laser focus on the movie screen to see the captions. If I looked over to a person’s face, the captions would be on their face. Sometimes the color of the movie screen washed out the captions (they’re yellow) so I would have to tilt my head down to the dark area under the screen. It was difficult to go back and forth from reading the captions under the screen to looking at the screen. Going to the movies wasn’t relaxing any more.  

Posing with the movie poster while signing “I Love You”

Posing with the movie poster while signing “I Love You”

‘CODA’ made a move to have burnt in captions on all movies. No matter what, no matter where, everyone could go to the movie theaters and be included with everyone. I was thrilled that I finally had the chance to go to the movies and be comfortable! Especially Mystic Luxury Cinemas, a theater I’ve never been to, had luxury reclining chairs. It was so comfy! I enjoyed it so much that I went back a second time myself one rainy day. 

Before the release of ‘CODA’, I had some hesitance about how good the movie would be. How many Deaf movies do you know out there? Really only one well known movie… ‘Children of a Lesser God’ filmed in 1986, because Marlee Matlin won an Academy Award for her role. Since then, not many movies were made focusing on Deaf characters. Instead, many of them were in the background or played a role with less talking. I was nervous about this movie, if it would have actual representation of the Deaf community. Hollywood also was known to not cast Deaf actors for Deaf roles, which is still being fought for to this day. I had learned that when the director of ‘CODA’ shared the idea of the movie, she was turned down at first because she wanted Deaf actors. She fought to cast Deaf people and ended up getting her way! The Deaf actors casted in ‘CODA' were Marlee Matlin (Deaf mom/Jackie), Troy Kotsur (Deaf dad/Frank), and Daniel Durant (Deaf brother/Leo).

Now, my movie review for ‘CODA’ gets 5 out of 5 stars! It was amazing. I just loved it. I mean, you can’t beat the New England setting which was filmed in Gloucester, Massachusetts. And the fact that the movie focused on a Deaf family. The main character was a CODA girl attending high school, pursuing her music goals while working in the fishing business with her Deaf family. I thought it was a good representation of the Deaf community. Just a reminder, there are so many sub-categories within the Deaf community so obviously the movie couldn’t fit in each and every one of them. The movie showed the reality of the Deaf family’s life, even beyond the deafness. It normalized the Deaf family as a small business owner and in other activities such as going to the bar and drinking, Tinder scrolling, sibling banters, sexual activities and more. It focused on the relationship of the CODA with her Deaf family and the hearing world. 

I loved how there were a few scenes throughout the movie that I could relate to; the interpreter issues for one. CODA’s are often interpreting for their parents because many hearing people see them as available and free. The hearing people take advantage of that, so it has caused many CODA’s to have to grow up faster because they shouldered that responsibility of providing accessibility for their parents. Ruby, the main character, was interpreting at meetings, negotiating fish prices, in court and doctor appointments for her parents. The movie didn’t speak about the accessibility issues with finding an interpreter, but it portrayed the Deaf parents as people relying on a family member. I knew that I relied on my hearing family (and even friends!) while growing up. I’ve always felt like a burden to others. The issue is that I wasn’t given that chance to be independent and speak for myself just like the Deaf parents/brother weren’t in the movie.  

Jackie, the Deaf mom expressed her thoughts with Ruby towards the end of the movie about her reaction to Ruby being hearing. I am not a mother yet, but hopefully someday. I have fears of being a parent of a CODA. Even through my husband is hearing, the child still would be labeled as a CODA because of me (Deaf mom). I know how to do things as a Deaf person, so how do I do some things with a hearing kid? Jackie described the fear as feeling a disconnection. Would my child prefer to use sign language to speak with me? Would my child find me annoying later on in life because of my deafness? I grew up feeling like a burden on my family and worried that my brother resented me. I don’t want that with my kids.  

Another thing that struck a chord with me throughout the movie was Leo constantly trying to prove himself. I didn’t realize how much I grew up focusing on proving everyone wrong. There were so many stereotypes of Deaf people that I didn’t want to be victim of. I worked so hard in school to get far in life. Watching Leo wanting that independence and everyone else to respect him just hit me in the feels. I wanted that respect from everyone too. I want them to think I have the ability to do anything! While growing up, everyone focused on my brother or friends around me, instead of looking at me as an individual. If someone wanted to say something to me, they would look to them to interpret for me instead of writing it down. In restaurants, it was them that servers would look to. I felt like I always had to prove myself, even to this day, I find myself still doing that. 

I enjoyed how the movie tried to show some aspects of being Deaf. The one scene that also struck a chord with me, was the concert. The Deaf family went to the concert for Ruby to support her. Ruby and her classmates sang the first song while the Deaf family had no idea of what was being sung, if it was enjoyable, etc. It showed them having small talks about their surroundings or thinking about dinner plans. It made me laugh because I do that! I always find myself people-watching at events without accessibility. The second song that Ruby sang, the movie cut off the sound and made all viewers live through a few moments of a Deaf person’s life. I hope that really makes the viewers think about that! It was a powerful moment. 

Do I have criticism for the movie? Of course, no movie is perfect. Instead, I want to focus that there was even a movie made about the Deaf community and put the spotlight on CODA. We all in the Deaf community so much deserve that. I hope that many people watch it (it’s still playing in selected theaters, but available to everyone on Apple+ TV). I went to see the movie twice at the theater, and both times it made me feel so good to see other people there. I was in disbelief that the theater was more than half full. I was expecting sparse audiences. The people also varied from elderly, families, couples and even some came alone. It made me feel so good. These people were willing to watch a movie about my world!

My family fingerspelling ‘C-O-D-A’ in the movie theater.

My family fingerspelling ‘C-O-D-A’ in the movie theater.

Lavender Pond Farm

In 2016, I had read about a lavender farm in Killingworth, Connecticut. I went with my husband to explore the beautiful grounds of Lavender Pond Farm. They are opened to the public starting in June, when the bloom season starts. The best bloom window occurs mid-June to mid-July. The farm has 10,000+ lavender plants on their 25 acres of land. There is plenty to do at Lavender Pond Farm!

The entrance sign to Lavender Pond Farm.

The entrance sign to Lavender Pond Farm.

The grounds of LPF.

The grounds of LPF.

Lavender everywhere!

Lavender everywhere!

Only if this photo included the smell of lavender.

Only if this photo included the smell of lavender.

I am able to bring my pup with me as they are dog friendly (leashed and well behaved, of course!). There is a farm dog on the property going by the name of Flora, an adorable lavendoodle. Flora approached my pup to welcome her to the farm the first time we visited in 2016. This year, I decided to have a mother-doghter day, so we returned to the farm last week. Flora unfortunately wasn’t around to greet us this year, which we were bummed about!

The mother and doghter day with my pup!

The mother and doghter day with my pup!

My pretty pup!

My pretty pup!

As soon we get there, we immediately explored the fields. I highly suggest you to take a minute and INHALE the beautiful smell of lavender! It helps you to feel calm. There are a lot of bees as they are attracted to lavender. This made me nervous to sit next to the plants for photos but as long you don’t bother them, they will leave you alone.

Gorgeous gardens through out the farm.

Gorgeous gardens through out the farm.

The bee hives.

The bee hives.

If you want to do more than walking the fields, you can take a tour of the farm on their train, LPF Express. You can’t miss the purple train. The tour goes in depth about the beginnings of LPF and educating about lavender. The tour is 20 minutes long and cost $6 per people. Be sure to check their website for the train schedule. There is also a pond out back of the farm, behind the big barn. There is a gorgeous covered bridge! I’m a fan of any covered bridges, so I was excited to see it.

LPF Express train.

LPF Express train.

LPF Express on one of their tours.

LPF Express on one of their tours.

The pond and covered bridge.

The pond and covered bridge.

In the fields, they also went all out with making visitors feel welcome. There is a large chessboard and corn hole that anyone can play. There are plenty of sitting areas through out the property. Some small tables with chairs too, which would be perfect for couples. I saw on their Facebook page that they offer yoga on Saturdays. Be sure to follow them on social media for updates regarding events like that, bloom reports, newest products in their shoppe and more.

The giant chessboard that visitors can play.

The giant chessboard that visitors can play.

Another peaceful garden in the fields.

Another peaceful garden in the fields.

So many lavender plants!

So many lavender plants!

There is a farm shoppe with lavender gifts to take home to remember your visit. I purchased a few lavender candles the first time in 2016, this year I tried the lavender lemonade. The lemonade was delicious! They offer lavender scented soaps, lotions, pillows, candles and more. Flora, the farm dog even has her own line of pet products including shampoo and beds!

The farm shoppe in the distance.

The farm shoppe in the distance.

Close up of the farm shoppe.

Close up of the farm shoppe.

Flora’s Corner - the dog line in the shoppe.

Flora’s Corner - the dog line in the shoppe.

The delicious lavender lemonade available for purchase in the farm shoppe.

The delicious lavender lemonade available for purchase in the farm shoppe.

Lavender Pond Farm is opened from June-December daily 10am-4pm. The bloom season is June-August. Parking is free and available behind the big barn. No admission fees. It’s worthwhile to take the drive through rustic countryside of Killingworth and see the beautiful purple glory!

This was a first for me to see white lavender plants!

This was a first for me to see white lavender plants!

While you can’t pick lavender, you can purchase them at the farm shoppe.

While you can’t pick lavender, you can purchase them at the farm shoppe.

My years as a Deaf first responder

Happy EMS (Emergency Medical Services) Week!

It is a week that occurs annually in mid May. Honoring EMS for all that they do. It is a bittersweet time for me, as I reflect on my experiences with the volunteer ambulance organization. I have learned a lot from these years.

Some background first, while I was in Rochester, NY I was on the track of joining the fire department after meeting a deaf firefighter. I knew I always had a passion for the emergency field. I went on a few ride alongs with the fire department, which I learned a lot especially about the tools that the deaf firefighter used. Unfortunately I didn’t live in the town of that fire department so I had to go to the neighboring fire department. I met another deaf firefighter there which again, I went on a couple ride alongs. I was about to join officially when a new bylaw was passed that any member of the fire department would have to pass a hearing test with the radio communications. At the same time, my passion for the criminal justice system was increasing as I was majoring in the classes. I spent a lot time with lawyers at the court houses so I decided to pursue this path. 

When I moved to Connecticut, it was impossible for me to stay in the criminal justice field. This is when I decided to re-visit the fire department idea. I met a female volunteer who gave me a tour and explained how the fire department also housed the ambulance organization. She was a dual member of both, so she was helpful in sharing all the information. I decided to try the ambulance organization. I officially joined, after being voted in. I remember I was nervous about other members having some hesitancy about having a deaf responder. At the time, I felt welcomed. 

My pup visited me one night while I was on duty.

My pup visited me one night while I was on duty.

I requested to be a driver, which I was told that I had to be certified in CPR and EMR (emergency medical responder) first. I also thought it would be worthwhile to see all aspects on the ride alongs first to solidify that I wanted to be a driver. In the beginning, it was challenging to find a crew for me to ride with. 

Once a crew was found for me to ride with, I followed someone who was a dual driver/EMT. I acted as an assistant, carrying equipments and doing whatever they asked me. I spent most of time observing and learning. After a couple years of doing the ride alongs, I felt ready to start the process of being a driver but I was still not EMR certified. 

I asked a few times about the training/classes but I wasn’t told when they would be offered. I continued to ride on the ride alongs, but I started to stay with the driver only. I would ride up front with the driver. When the EMTs brought patients into the hospital, I would restock/clean the rig with the driver. I was quickly getting burnt out with doing scut work when I wanted to advance in my driver training. 

On some of the medical calls, it was ALS (advanced life support) so a paramedic traveling in a medical truck (employed by the hospital) would meet us at the scene. The paramedic would ride in the back of the rig. Sometimes a firefighter will drive the truck to the firehouse, the ambulance will bring the paramedic back to the truck after the transport. If there happened to be an extra crew member on the ambulance, they could drive the truck following the ambulance to the hospital. One call, the paramedic asked me to drive. It was a big moment for me! I felt responsible, trustworthy, and really good! 

Ambulance rig and medical truck (the one that I drove several times) parked at the hospital.

Ambulance rig and medical truck (the one that I drove several times) parked at the hospital.

The same paramedic quickly took me under his wings on the calls. I started riding in the back to the rig if he was there. He showed me how to start up the heart monitor machine, get the supplies together and ready for him to use, etc. I felt motivated again! We had a long conversation off duty one day about my goals, as well my frustration about being certified. He stepped up, continued to show me how to do things to my abilities and allowed me to try more things. One of most rewarding experiences the paramedic allowed me to try was administrating narcan. It was a couple weeks after getting trained in narcan, that we had a drug overdose call. The paramedic was already on scene and gave the patient the first round of narcan. I had just told the paramedic the previous week that I got the training and he remembered. He told me to ‘come over here and do it’. I was terrified! It was amazing feeling that I actually did something physically life saving. 

I met another paramedic from the same hospital through a mass causality training exercise. The exercise had multiple departments participation. I wasn’t able to do a lot with the lack of certifications. I followed around a few people, feeling helpless and frustrated. I knew that I had the abilities to do some tasks. The paramedic never met me before this day, so when I was placed in the back of the rig with her, she didn’t realize that I was deaf. It didn’t stop her from telling me to get the patients’ information (there was 4 ‘fake’ patients with us). I froze because I’ve never did that basic step! This was 3 years in of being a volunteer with the ambulance organization. I was embarrassed but it turned into a training session for me to learn how to do this step. The ‘fake patients’ were very willing to help out, writing via paper and pen (of course I know this would be unrealistic in real emergent situations) but the point was these 5 people took the time to focus on me to learn something that day. I felt very accomplished.

A selfie after completing a call.

A selfie after completing a call.

This is when I felt like I wasn’t being advocated well enough to try more tasks on the ride alongs enough that both paramedics saw that. I realized how much I was being held back from furthering. On the other hand, I was voted the scheduling officer within first year of being a volunteer. I was responsible for assembling shifts, finding coverages, maintaining updated rosters and assemble coverage for special events. The members were very accommodating with me in my position as the scheduling officer by texting or emailing me. As the time went on, it was getting difficult to do one task which was assigning new incoming members to their mentors. I watched them move up the ranks much faster than me. I felt like other mentors devoted their time to educate them. It wasn’t fair to me. I felt stuck and that I wasn’t going anywhere. I felt that they only saw my skills limited to administrative duties. I really wanted to further my training to get certified and actual help people out in the field. 

After being a volunteer for 3 years, the local newspaper contacted the director of the ambulance organization wanting to do an article on me. I was thrilled that they thought I was newsworthy and saw this as a great opportunity to show everyone that DEAF CAN! I also felt conflicted, because I couldn’t brag about all the tasks that I knew I was capable of that I wasn’t doing. When the article was published, I received so many praise from family, friends, coworkers and the community. I was proud but also frustrated. 

The professional photo from the article.

The professional photo from the article.

The article gained so much attention from outside of the region, including other deaf responders. I got in touch with a few from New York, New Jersey, Illinois, Ohio, Maine, Massachusetts and more. Two deaf firefighters from Connecticut had contacted me too, after talking to them about our limitations, I realized that I was really limited! 

It motivated me to start asking questions about why I wasn’t close to my goal of being a driver. I was finally given a reason… ‘insurance liability’. I got in touch with a disability lawyer who had a deaf husband working as an EMT in Washington D.C. so she was very aware about disability laws. She was very helpful in guiding me with what next steps to take. I contacted the insurance agency that the town had a contract with, which he refused to share the information but forwarded my inquiry to the town mayor. 

The town mayor invited me in for a meeting. When I joined the ambulance, it was a different mayor at the time but the assistant was same person who had been there for the original meeting (that I wasn’t aware of) to determine whether I would be allowed to drive. The mayor explained that he was summarized about this by his assistant and stated that ‘insurance liability’ never was an issue. AND that I was allowed to drive as long there was reasonable accommodation. I was baffled. Wait, what?! My mouth literally dropped to the floor. I came to the meeting with my sleeves rolled up prepared for a fight only to feel that I wasted my time. I left the meeting in disbelief, beyond frustrated, embarrassed and defeated.

I had to really analyze if this was something worthwhile to fight for. Did I have passion for this? I went to the monthly executive board meeting (as the scheduling officer), the training officer who had been at the meeting with the mayor had already taken the steps to research tools for the reasonable accommodations. I had felt sad for that week so when I saw what he had done, I felt supported. He saw my abilities and wanted to help. This is exactly what I had needed.

I finished cleaning the rig and was waiting for my crew.

I finished cleaning the rig and was waiting for my crew.

I went on a few more ride alongs and resigned from the scheduling officer position. I started to find out more and more. When I first joined, there had been an executive board meeting to decide about my request to be a driver. Why wasn’t I present to advocate myself? How would anyone know what resources were available? I’ve lived my entire life deaf, so I knew better than anyone. I also got the impression that the organization might’ve been concerned about the financial aspect of supporting me. Eventually, I took a leave of absence to see if my heart was still in it. After 3 months, I officially resigned. 

It is very likely that I was the first deaf person for the majority to meet. I hope they learned that I was capable of doing anything. I hope in the future, they can be open minded, allow others to grow and support them in their goals. If you are in a position to support someone like me to accomplish their goals, be that person! You want to be remembered as someone who helped, not someone who didn’t help. Nothing more rewarding than that.

Resigning was the most difficult decision because I felt that I failed. I was so hurt. I felt betrayed. The 4 years would’ve been so different if I knew right at the beginning about the reasonable accommodation. I had invested a lot of my time to respond to those calls and attend all the meetings to not get the results I had aimed for. This is not the story I had hope to write about. I wish this was a successful deaf role model story for others to be inspired by, but I know in my heart that I tried. I try to not look at this experiences as a waste of time, because I did gain a lot from the experiences. I met many people in the field who taught me things, learned about myself and met some life long friends. 

I attended the CT EMS Expo annually, one year I met the crew of Nightwatch TV show (based in New Orleans, LA).

I attended the CT EMS Expo annually, one year I met the crew of Nightwatch TV show (based in New Orleans, LA).

Holiday Lights at Olde Mistick Village

‘Tis the season!

December is one of my favorite months when all towns gets into the holidays festive mood! I love walking around to see garlands, wreaths, trees, ornaments and all the decor. It is different this year without our usual events. The season typically kicks off with the annual holiday boat lights parade that happens the weekend following Thanksgiving. This year it was the lights show at Olde Mistick Village!

Olde Mistick Village (as previously blogged about here) is having their holiday lights spectacular show. The lights have already been lit since the week of Thanksgiving and will remain on until January. According to their website, it is the largest lights display in southern the New England region with over half a million lights! It is decorated throughout the village, which is very walk-able and perfect for social distancing activities. Come see the Christmas wonderland!

Shops are also open later for holiday shopping if you haven’t finished your shopping! Please consider shopping small to help businesses to keep thriving in our community through this difficult time. I’ve listed my recommendations in the previous blog (linked in last paragraph). The shops are opened until 8pm, with exception of the weekends (9pm Friday & Saturday and 6pm on Sunday).

To add to the festivities at Olde Mistick Village, Jealous Monk brought out some igloos in their beer gardens! It can fit 4-8 people. Reservations are strongly encouraged as they only have a few time slots per day (to allow cleaning in between uses). Email: Brittany@jealous-monk.com

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Sailing Tall Tales

My parents recently visited me for the week from Upstate New York. One of my dad’s favorite activities is being out on the water, so he arranged us to go on a sailing adventure. I get super nervous when it comes to being on a form of transportation (ferry, boats, trains, etc) with many strangers and when I’m not operating it. Luckily, the sailing adventure my dad arranged for us was on a private sailing vessel and the best part? My family and I were the only passengers on the sailboat!

We headed to New London, CT to the boat marina located right next to Captain Scott’s Lobster Dock. The private vessel named Tall Tales was docked in the marina, which is where we met Captain Stu Reininger. Captain Stu is an interesting person with many stories from his life experiences! Throughout the cruise, he shared tidbits of his professional sailing career and educated us on how to sail. His passion for sailing has been documented in several books that he wrote (see more details on his website). I plan to get my hands on a copy of ‘A Reef in Time’ to read about his adventures.

Tall Tales took us down the Thames River which neighbors the City of New London and Groton. It was a beautiful day for a cruise so we enjoyed the picturesque views. We passed by General Dynamics Electric Boat, UConn Avery Point, Fort Griswold, Fort Trumbull, Ocean Beach and USCG base. At one point, we were able to see four lighthouses at same time (Ledge Light, Avery Point, New London and Race Rock). That was an amazing sight to see!

We were able to move around on the sailboat. I started out by standing on the stern (back) then sat up front on the bow. Sitting on the bow was relaxing as I sat there inhaling the smell of fresh ocean water and summer air. The water wasn’t rough that day so it was a smooth sail!

Book your cruise with Tall Tales via their website here. There’s a minimum of two passengers up to a maximum of 6. Captain Stu can take you for a lunch cruise which is one hour long with lunch from Captain Scott’s. Contact Captain Stu for further questions or inquires!

Headed towards Thames River.

Headed towards Thames River.

Captain Stu setting up the sails.

Captain Stu setting up the sails.

Red buoy with General Dynamics in the background.

Red buoy with General Dynamics in the background.

New London Lighthouse.

New London Lighthouse.

I spy the Ledge Light up ahead!

I spy the Ledge Light up ahead!

Self portrait.

Self portrait.

Another sailboat on Thames River.

Another sailboat on Thames River.

The sail.

The sail.

Ropes, ropes and more ropes!

Ropes, ropes and more ropes!

Closer to the Ledge Light.

Closer to the Ledge Light.

A relaxing moment on the water.

A relaxing moment on the water.

Posing on the sailboat with City of New London in the background.

Posing on the sailboat with City of New London in the background.

US Coast Guard Eagle ship and City of New London.

US Coast Guard Eagle ship and City of New London.

The City of New London is a pretty sight from the water (I see the fire boat FireFighter too!).

The City of New London is a pretty sight from the water (I see the fire boat FireFighter too!).

Summary: Deaf and Employment

Over the last month and a half, I published a 6 part series focusing on my experience with employment. Many had asked me to share these experiences, such as what it is like to go on interviews or what it is like to work in a hearing dominated environment. I was asked to share this a few years ago. Why did it take so long for me to share? I had a lot of hesitancy to publish any of those posts. I felt like each post was so negative. I’m not typically the kind of person to be excessive and pessimistic.

So why did I decide to do it? I felt that it was important to share these experiences from the perspective of a Deaf person. It is such a challenging task for any Deaf person to seek or obtain employment. My experiences are my own, but it is similar to so many other Deaf people’s experiences. We are often faced with rejection and discrimination. Deaf people are hesitant to share with the employer about the deafness prior to interviews because of the fears they have. I shared this hesitance in Part 2 of the series. My Deaf friends have shared that their interviews sometimes were suddenly cancelled when an interpreter was requested. They were told that the job had been filled. The attitude of the employer often drives away the Deaf candidates. When the companies are wary of hiring a Deaf candidate, it’s because they assume that the Deaf candidate will be a burden with their accommodations and the costs of it. Even if the Deaf candidate got hired, some still face hostility from coworkers.

One main issue that I faced from a few of my jobs was that I couldn’t climb up the ladder as a Deaf person. I felt stuck. I’m a dedicated worker who has the loyalty to stay as long as possible. It was difficult for me to leave each job because I felt like I failed. I know what I am capable of doing and that I deserve to considered for internal growth. When I don’t have the ability to grow in a role, it affects my self esteem.

Seeking employment affects my self esteem! Working in my employment affects my self esteem! Why am I never good enough? This is what I often feel. I attended a prestigious college and received a bachelor’s degree. How do you think it makes me feel when Kohl’s thought I was only capable of unloading the truck for 4 hours a week? Do you know how much work I put into RIT earning the bachelor’s degree? It bothered me so much upon my graduation from RIT, to see my fellow classmates succeeding in the criminal justice field. I invested so much of my time at RIT in the classes, being the Vice President of my criminal justice club, attending informal meetings and much more. My bachelor’s degree in criminal justice DIDN’T MATTER. It was hard for me to be working in jobs where a college degree wasn’t even required. I felt like I put in all of that effort at RIT, only to have this as my reward? Why can’t anyone see what I’m capable of?

My deafness has nothing to do with the job, it’s just a part of me. It’s part of me just like a pair of glasses or hearing aids is to you. I’m always working extra to prove myself to everyone, trying to educate, and helping to ease the fears with communication barriers. This puts more pressure on me to accomplish the best. I know what I am capable of. When I am given a task, I am very dedicated to get it completed. I am very loyal. I accept feedback and work even harder. I hope that someday someone sees my full potential!

My goal from sharing the 6 parts series is to EDUCATE. I hope that if you are someone in that kind of position with the authority to hire, to meet everyone with an open mind. Do not assume what they are capable of. Let them tell you about themselves and their abilities. I believe that everyone at some point has been judged by others, right? It sure isn’t a great feeling so don’t do that to us! Also it will be worthwhile to be that person to help a Deaf person grow by offering opportunities or creating a chapter for them in their lives. Don’t you want to be remembered as that person who helped?

Part 1: The employment challenges of the Deaf.

Part 2: The search in CT.

Part 3: American School for the Deaf.

Part 4: TSA.

Part 5: The continued search.

Part 6: My journey as a Deaf Paraprofessional.

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

Part 6: My Journey as a Deaf Paraprofessional

Yesterday marked the end of Deaf History month, so to wrap up the series about challenges I faced with employment, I will talk about the recent and last job I had. Over the last 4 years, I worked as a special education paraprofessional at an elementary school. I interviewed for a position at the high school level and had accepted the offer, until the Special Education director convinced me to interview for the elementary school position. He thought that the student was in need of someone like me more than the high school student. I went to the interview at the elementary school and requested an interpreter. I showed up to only the principal and the special education teacher. The special education teacher did all of the work by asking questions (writing with me), telling me what the job would consist of, the requirements, and answering my questions. She took me to the classroom to meet the student. Looking back at this experience, I honestly believe if the principal was solo at this interview, I wouldn’t have been hired.

I worked under the special education teacher, so we had a good system going where we would write back and forth. We communicated about the tasks, the student’s needs, etc. It was never a challenge to communicate with her. My student that I worked with 1:1 with had Down Syndrome. He was non verbal, so I had to teach him some sign language. We worked in his regular mainstreamed classroom, so I also had to work with the classroom teacher. The school was hearing-dominated so I was the only deaf employee. I had to write on paper to communicate with any of my coworkers. The teachers and other paraprofessionals were flexible with that, and very willing to communicate with me.

The school was a small community with 300+ students and 100+ staff. It didn’t take long for everyone to realize my deafness and pick up on how to work with me. It was the largest workplace that I’ve had to work for with no awareness of deaf culture. I thought it’d be more difficult but it wasn’t. Within 2 years of being there, the students were also accepting me. They were learning sign language, asking me questions about my deafness, etc. I was happy to educate them. I felt like with me being there, I was also teaching those students to be inclusive.

The students were very adaptive to me, picking up from the beginning on how to communicate with me. I actually found that most students were able to understand me more than the adults. I’m not sure why, but it was an interesting observation! The students were able to communicate with me by gesturing or writing. There were times when I didn’t understand and I felt very helpless! The worst was when I had students coming up to me crying (which 80% of the time, it was just over innocent arguments). I would do my best to consult them but had to get another staff member to help sometimes. It wasn’t a great feeling, especially with me having a lot of pride. Asking for help isn’t something I really enjoy doing.

Luckily, I worked with a great community of teachers and paraprofessionals at the school. The paraprofessionals were understanding and always jumped in when I asked for help. I recall one year when we were all in the regular classroom, the principal had come on the loudspeaker and announced something. I saw the students’ expressions turn to panic. I started stressing. After the principal finished, the teacher took the time to explain to the students in better terms to calm them, then I saw her saying “Hold on, I need to tell Miss Kelly”. She wrote down and explained there was an incident that had happened on the school grounds but was handled by the local police agency. I was very appreciative of that! The incident was already over, so the teacher didn’t have to take the time to do that for me, but she did. Imagine if she didn’t, I would be wondering why the students were panicked. There were other situations similar to that, when there was information shared over the loudspeakers, and some staff did their best to let me know.

A challenge of working in the school was the new changes every year, moving onto the next grade level to a new teacher, new kids. The second year, I was lucky to be with the same teacher from the previous year. She helped to ease the new students by explaining my deafness and did demonstrations. She stood behind me (while I was pretending to be clueless), calling “Miss Kelly!” to explain that was the incorrect way to ask me for help. She demonstrated the correct way, which was to tap on my shoulder then ask for help. I never asked her to do that, but I was taken aback. I was impressed and so grateful for her to set the base for me. It truly helped the students understand right away, with the information stuck in their heads throughout several grade levels. I was super nervous to work with any new teachers, but so far I was lucky with all of them!

Each of the relationships I had with all teachers were so different every year. I worked with a total of 4 (classroom) teachers. The first year was awkward with me establishing a routine so it took a while before I started to really know the teacher personally. We were able to communicate via paper and pen. This was the same with the second teacher that I worked with. It also helped to have social media (Facebook) to be in the know of what was going on with our lives. That gave me some info on what to talk about in person at work. The third teacher I worked with was different from the first two. We exchanged phone numbers, so we texted. I noticed with this, I was able to express more. Writing via paper and pen can be painful if you want to have the level of what would be said in a verbal dialogue! For the first time, I felt like I had someone to really talk with and we talked about our common likes and our lives. It was weird to have someone to know so much about me, because I was able to share more through texting. He knew more things about me than anyone else in the school so I truly felt like I had a friend. It was difficult when I wanted to interact with other paraprofessionals, because they would be in groups and talking. I would be singled out. The paraprofessionals also chatted with teachers in the classrooms whenever there was down time. This bothered me a lot. I wanted to be included. I ate lunch alone. How can I lipread people with food in their mouths? I was lonely, but at the same time I wasn’t because I knew they liked me from their actions. Again, social media helps so much to keep me connected with them. This is why I felt like I had a ‘family’ in the school, I know that they are there for me despite the communication barriers.

The school started to take an interest in sign language. Many students would approach my student or me to ask for new signs. We were invited to come to first grade to teach some signs. The last school assembly last year surprised me with the Kindergarten class singing a song all in sign language! It was such a heartwarming moment to see that, to feel inclusive AND because my student enjoyed it so much he signed along with them while sitting in the audience. I had a student in the regular classroom that attended sign language classes at the local library too. She’d come back every day proudly showing off what she had learned. She learned so quickly that we were able to hold conversations! It was huge to me. Coming from the first year when the students would share their weekend news, I would have no idea what most of them said. I was always disappointed that I didn’t know what was happening in their daily lives and couldn’t use information to help build bonds with them. Do they like swimming? Do they like to play sports? Did she have a little brother like I do? There were many students that I didn’t know very much about so I had to learn a lot on my own from observations. To be able to hold a conversation with the student entirely on our own with no outside help was an accomplishment. I felt proud!

The students might not have been able to communicate with me much through sign language at first, but they did learn a lot about me. I established bonds in another way; instead I would show pictures of my Dalmatian. A girl drew a picture of gymnastics, so I wrote a note saying that I did gymnastics when I was younger. I relied on their drawings, their actions, their clothing, etc to build the bonds. We didn’t have the language but we were able to relate in a unique way. For my birthday and Valentine’s Day, the students drew cards decked out with sign language or Dalmatians. I loved that they knew me despite the lack of language between us.

I did have a huge ongoing issue with requesting interpreters for the team and paraprofessional meetings. The school never got me an interpreter until my 4th year of working at the school. I attended the paraprofessional meetings which were monthly. I would sit there clueless of what was being said. One meeting, the principal asked me a question directly and I didn’t understand. Few staff members around me scrambled to get paper and wrote down the question. By the time I could answer, the discussion had already moved on. It didn’t matter for me to answer. The part that bothered me was that I felt like an idiot, thinking the others probably looked at me with sympathy. Did they feel bad for me? They should not. They should’ve been bothered by the principal for not being accommodating to me. I missed training (which was an opportunity for growth as well as an opportunity for extra income) because they couldn’t request an interpreter for me. It frustrated me so much.

I emailed the principal in the beginning of my 2nd year of working there, explaining to her the difficulty of lipreading multiple people at once in a room; how I needed an interpreter for all of those times. I referred her to call the local agency that provides interpreters. She had a sit down discussion with me, proudly sharing that she called them. It was mentioned that the cost was shocking, but went on to say if I request a job coach it would help. I was speechless. Did she understand what a job coach was? This is after working at the school for a full year. I know what I do in my job. I received a positive evaluation at the end of the previous year (and even verbal praise from other staff and the parents). I realized this was a strategy to get the cost of interpreters down. The school did not want to pay for my accommodations.

The unwillingness to accommodate me made me feel that the principal didn’t value me as a team player. It was particularly hard when I wanted to contribute in the team meeting for my student. I knew my student better than anyone because I was the one with him constantly. Luckily his parents were aware and established great communication with me. I had a great relationship with the special education teacher too, so I was able to share a lot of information with her which she would discuss in the meetings. I couldn’t imagine what I’d do if I didn’t have her to help me out. She always tried her best, even went beyond her duties to accommodate me when it wasn’t her job.

I decided to look at the positivity which was my amazing student, the wonderful special education teacher, as well the classroom teachers, the students who were so accepting of me and the paraprofessionals. I truly had a little school ‘family’. That’s how I got through the first three years. No matter what, it still took a toll on me with the lack of accommodations. In the final year of working at the school, there were also a lot of changes that came along with the merge of another elementary school to my school. The small school was no longer the community I once knew. I didn’t have any teachers or staff that I once worked with before. I had to start completely over.

It was even more difficult to establish my role with a new community who wasn’t familiar with me. I felt like the larger mass of people somehow made it hard. I was working in the new special education classroom with 5-6 other paraprofessionals. They were having meetings in front of me. I didn’t realize they were having the meetings! I was shown the new plans or directions after hand. No input from me at all. It was extremely difficult to communicate to anyone about my student’s progress. I felt awful as I felt responsible for my student’s regression. I also struggled with the lack of interactions with staff. It made all the frustrations I had in the first few years seem so little. I got lost with the merge. It affected me so much, even outside of school. I was unhappy and I felt sad. It was with extreme difficulty that I had to leave the school. I pictured a different ending. I missed my student and the school ‘family’ terribly.

Part 5: The continued search

The search for a job after American School for the Deaf took a long time again. I faced many rejections as I mentioned in Part 2 here. This time, I contacted the vocational rehabilitation counselor to help me with the search. She assigned me a headhunter, which is an individual who helps me find opportunities. I spent a lot of time with the head hunter applying to jobs, fixing up my resume and following up with the businesses. I saw a huge difference in the search process with a headhunter. Instead of having those companies contact me for an interview, they had her phone number. She would talk with them, reassure them with their concerns of hiring a deaf person. I received more interviews during this cycle than the first time when I was alone.

I had mixed feelings about working with a headhunter. I was appreciative with what she did for me. She came along with me on interviews to help with communication since she was skilled in American Sign Language. However, the headhunter’s goal is to encourage businesses to hire people with disabilities. As part of that outreach service, she offered them an incentive, job training, etc. If I was hired, she would become my job coach. She would stay with me at the job, train me in whatever I needed and check in with me. It was part of her job, so I didn’t like how that took away my independence. It felt like I was bringing my mother to the interviews at times, the people were always focused on her. They talked to her more than me. She negotiated with them. When I answered questions, she added in her own words to help me ‘sell myself’. I was being overshadowed. Working with a headhunter showed my deafness more whereas before I was trying to hide it until the interview. I wanted them to see my abilities not my deafness.

I applied for a security guard position at a defense contractor in Southeastern Connecticut. I was told that they had several deaf employees in a variety of positions. I never personally met them. I was invited in for an interview so I went with the headhunter. I met with the security director and a security guard. Throughout the interview, I thought it was one of the best interviews. The men were respectful and looked at me, instead of relying on the headhunter. The radio issues were brought up, but the director immediately stated “we aren’t going to say no to you over that”. I was taken aback by the comment because I was used to rejection.

At the end of the interview, the other security guard who was at the interview, came up to me. He signed to me. I was shocked. Turns out that he had been a graduate of Rhode Island School for the Deaf. He was hard of hearing but knew some signs. This got my hopes up even more, to think they were flexible with someone like him already, so they were familiar to work with folks like us! I felt like there was hope for me. I contacted them several times only to have no callbacks since the interview.

I found employment through my head hunter. She had gotten word about an agency needing someone who was fluent in American Sign Language. The agency focused on providing services to adults with developmental disabilities. The job position was a provider who would work with those individuals in their daily routines whether it is with their jobs, teach them life skills, etc. I went for an interview at the headquarters in Middletown, CT by myself since the lady I had been in contact with knew sign language. She was a child of deaf adult (CODA), growing up in a deaf family! The interview went well. I was invited for a second interview at the location where I would be working out of (New London, CT). I asked for an interpreter. I was told that they had someone who would be able to help out with that.

I showed up to the interview where I met with the manager and the “interpreter”. The manager had a non verbal client who used sign language to help convey her information. It was awkward at first, because I didn’t realize she was non verbal. When I realized, I wrote down my answers to the manager. The interview went well, I felt like the manager was patient with me. Even though the interpreter was not a professional, I saw the open mindedness. She was flexible with me. It helped that the agency had people with disabilities so it wasn’t a frustrating experience to get hired.

The manager I worked for was one of the best that I had worked for. She didn’t hesitate to communicate through writing or email. Other coworkers were flexible with me too, some of them knew sign language. I was able to communicate with some of them. They didn’t look at me differently for my deafness. However, when we went out in public, I was often mistaken to be a client! It wasn’t the greatest feeling because people thought I was incapable to be an employee.

The job required transporting clients, so I had to get a special driver’s license. I went through the testing, got fingerprinted and photographed, and had my background check completed. In the end, I wasn’t allowed to have the driver license because of my deafness. The agency had a pay increase when you got the driver license too. I was furious! Luckily, my supervisor and her boss were understanding of the situation and didn’t hold it against me. I was able to get the pay increase for the effort.

My only regret from this job is that I didn’t push them hard enough to hire an interpreter for the team meetings. A coworker, who had a deaf family member, interpreted at all of the meetings. It was challenging because she had to convey information to me, as well as be able to input her comments and interpret my comments. I could see that it overwhelmed her to be in multiple roles. I felt like I was a burden on my coworker and I hated that feeling. Over time, I contributed less and less to the discussions.

After a year of working for the agency, I needed a change of scenery. I felt like I couldn’t grow. There weren't any further job opportunities for me. I knew I had more to offer!

Stay tuned for the last part of this series!

Part 4: TSA

Upon my resignation from American School for the Deaf (read Part three here), I was still reeling from the loss of the new plans I had made to be a teacher. I decided to go back to searching for a job in the criminal justice field as I originally planned.

This is when I signed up for a 4 year long commitment with the Transportation Security Administration (TSA). It should be listed on my resume because you totally can see the dedication right there. All joking aside, it was my biggest fight in trying to get the job.

I applied for the TSO (transportation security officer) job to screen the travelers and check luggage at the airports. I had to pass a pre-exam consisting of questions and images of x-ray images to identify items. The exam was good for up to 3 years. During that window, whenever a job opportunity was posted, I could apply and be called in for an airport assessment. I drove an hour north to East Smithfield which is outside of Providence, Rhode Island to take the test. The test didn’t require extra accommodations since it was all on the computer. The folks who administered the test told me I passed with “flying colors”. I also received an email the next day to confirm that I had passed. I applied to several listings at airports in Providence, RI; Hartford, CT; New Haven, CT; and Boston, MA. The 3 year window went by with no callbacks. When the window expired, I took the test again. I drove back to East Smithfield, RI. For the second time, I passed.

During the original 3 year window, I received a call back while I was employed at American School for the Deaf. I called them back through the relay service and wasn't able to get a live person on the phone so I left 3 voicemails in a week’s time. A month later (See? I never gave up!), they claimed that they never received any of those voicemails I had left and that the position had been filled.

Shortly after taking the test for the second time, T.F. Green airport (Providence, RI) invited me in for an assessment. The airport assessment was an interview, color vision test and complete paperwork. I was thrilled to finally get this far. My hopes got really high. I knew what I was capable of. I was proud of my heightened vision skills (deaf people are known to be very alert and very observant).

The woman who called me to schedule the assessment recognized that I was deaf on the phone because of the relay. I use a relay service which is when I call the agency, give them the caller’s phone number that I want to call, then have that interpreter as the ‘middleman’ of the conversation. The TSA woman told me I had to request the accommodations (interpreter for the interview) by putting in a formal request with TSA headquarters. I went ahead and confirmed that I will be at the assessment so I had a week to submit the request and have it approved in order to participate in the assessment. The week was stressful, consisting of calling headquarters DAILY to get the paperwork through.

The day before the assessment, headquarters sent me a letter that was sent to me via FedEx overnight stating that the accommodations request was REJECTED. The director of accessibility services at headquarters said I couldn’t have an interpreter at the assessment. It shattered all my confidence!

The letter stated that one requirement of the TSO job was that I had to pass a hearing test. I knew it was a possibility down the road after the interview. How did they know the level of my hearing loss at this point? I didn’t even get a chance to try the test.

I contacted lawyers from the State’s Office of Protection and Advocacy for Persons with Disabilities. I asked for help to see if TSA actually had the grounds to deny me my right to the interpreter. The lawyers got right onto it, investigated this. After a few days, they told me TSA did have the authority because they were a federal based agency. The letter from TSA stated that I could still participate in the assessment without an interpreter.

So therefore I decided to try. I thought it’d be ok to try to communicate verbally as much as possible and resort to writing if I needed to. I scheduled the day for the assessment with T.F. Green airport. I got another email from the director of accessibility services at TSA to confirm (more like reminding me) what the letter said about no interpreter then it went on to say that I could NOT bring any other form of alternative method of communication. Far enough to say that I would NOT be able to bring paper and pen! The assessment would be a group style interview with 3 supervisors/employees with 3 other candidates for the position. I knew it would be too difficult; I don’t always have clear pronunciation and I can’t lipread in a group setting. When I read that email from the director, my heart broke.

I broke!

I felt it was IMPOSSIBLE!

TSA was doing everything in their power to eliminate any opportunity to present my abilities!

I was SO disappointed in how little Americans with Disabilities Act (ADA) could help me in this situation. I didn’t realize federal agencies were exempt from the law and can discriminate against me. I truly believed that I could get this job. I saw Deaf agents at other airports (Pittsburgh, Rochester, etc). If they were able to do that, I CAN TOO! As I mentioned earlier in the post, deaf people have stronger vision than an average person. With the hearing loss, our other senses are heightened. That heightened vision skill would’ve been very beneficial as a TSO since the primary job task is inspecting. Why do we need hearing for that task? I hope to see TSA open opportunities to the deaf community… someday!

Part 3: American School for the Deaf

Part Three of the challenges of employment for the Deaf series. Read Part One here and Part Two here.

One summer I applied to a residential counselor position at American School for the Deaf (ASD) in West Hartford, CT. ASD is an institute for deaf students from K-12. Some students commuted daily to the school on the school buses. Some students stayed at ASD in the residential dorms since they lived in NYC, New Jersey, all over Connecticut, or Massachusetts. The job I applied for was to supervise these kids who stayed in the residence halls.

It was definitely the easiest interview I had. I didn’t need to worry about asking for an interpreter. I felt like because of the deaf culture, with me being deaf, it was an automatic hire. They’re always looking for deaf role models for the deaf students. I did get the job and worked through the summer while the students attended summer programs. It was the only job I had in my life where I felt no frustration with communication.

Throughout the employment at the school, everyone I spoke with knew sign language. Not all of my coworkers were deaf but there were also many hearing who knew ASL. The students all were deaf. It was such a relief for me when I got the job, in a deaf world among people who spoke my language. I enjoyed it a lot in the beginning. It was so easy to communicate with anyone.

Although the communication was easy, there were still challenges. I noticed it was hard for me to be accepted. Yes, despite being around my OWN kind of people, I wasn’t accepted. The deaf community is very protective of preserving their culture. I came across as a deaf person who was “not deaf enough” with my mainstreamed background. It was a challenge for me to make friends among the coworkers. I felt really lonely. I noticed that I was close with the hearing coworkers, whom I loved but I craved to have more deaf friends in my life. I missed the deaf friends, the deaf community in Rochester, NY and having friends who understood me.

Despite the challenges of being accepted by some deaf coworkers, I loved being immersed in the deaf world where everyone signed. I ignored that I felt lonely among my own peers, but at least I had people to sign with. The students looked up to me. I was so motivated to stay there as long as I could. I finally felt like I was at a job that I would be at for years. I didn’t see myself in the residential counselor position in the long term so I started looking into getting a master's degree in education. That Fall, I applied to Gallaudet University, hoping to pursue the goals of being a teacher at ASD. The master’s degree program allowed me to stay with my employment at ASD, while taking the courses online. I would only have to go down to Washington D.C. for 6 weeks for one summer. The term didn’t start until the following Fall so I still had another year before I could start on the master’s degree.

At the same time, during that Fall, it quickly got difficult to work at ASD. There was a lot of workplace politics starting to affect many people. It created a toxic environment. It was difficult to maintain a positive attitude, but the students motivated me to keep going. I worked there as long as I could. Unfortunately, it got to be too much so I had to resign in the winter. I was really disappointed that they couldn’t recognize the importance of having deaf role models for the deaf students. A month later, I received the acceptance letter from Gallaudet University. I put that plan aside since ASD was the only local deaf institute where I could work at. There were deaf institutes in Massachusetts and Rhode Island but it would be a super long commute. I didn’t have the flexibility to move.

I missed the deaf students terribly when I left. Despite not being accepted by some coworkers, it still was a slice of heaven to be in my world for a while. It was difficult to accept the loss after leaving the deaf community in Rochester, NY. I felt that all over again. It took a long time for me to recover and get back to the reality of working again in the hearing dominant world.

Stay tuned for Part 4.

Part 2: The search in CT

Part Two of the challenges of employment for the Deaf series. Read Part One here.

When I moved to Connecticut, I reminisced about the days of the Probation department. Naturally, that was the first place I went to seek a job. I interviewed for the probation officer position in my county. It turned out to be one of the worst interviews I’ve been to.

Before I dive in about what happened with the interview, let me explain some things. I’ve gone to numerous job interviews. Beforehand, I usually try to ask for an interpreter or give a heads up about my deafness. Most often, they are not aware of the ADA law that they need to provide accommodations so I would find myself easing their worries that we can communicate via paper-and-pen method. It’s a difficult position for me to be in. When I should’ve been educating them about the ADA law accommodations, but instead I am trying to get on their good side and be likable for them to want to hire me. I worried that if I came across as demanding and made them uncomfortable, they wouldn’t consider hiring me.

With every job application I have submitted, the furthest I’ve got was them calling me to schedule an interview and this is when they find out about my deafness. I would normally not receive another call back from them. It became a common occurrence so I stopped telling them beforehand that I was deaf. I wanted to show them that I have the ability to do the job! I started showing up to interviews with paper-and-pen in hand and ready. I received a variety of reactions; most would be surprised. Some were willing to go along with the communication method I showed them.

Some were not willing to accommodate which is what happened at the probation job interview. I showed up, dressed professionally, proud of my strong criminal justice background and excited to ace this interview. I left the interview wishing that I wasn’t born deaf and felt very down for the rest of the day. The interviewer was a woman, who acted unhappy about the communication barriers. She had a list of questions she wanted to verbally ask me, but I had to write down every response. Throughout the interview, I also struggled with understanding her so I asked her to write it down and she refused to. At the end of the interview, she explained the high fast paced environment in the courts. I was very familiar with it from my previous experiences. I spent a good half hour selling myself with that amazing background and the ability I had for the job only to have her belittle me. She was clear about how it wouldn’t work with my deafness. It was a straight rejection right there at the interview. She only saw my deafness, not my abilities. It was impossible to change her mind because she never gave me a chance.

Unfortunately it was a common result of the many interviews I went to where the people rejected me right there. It was difficult for me to keep applying when I kept running into these roadblocks. Eventually, I started applying to jobs with less demanding qualifications. I applied to stores, restaurants, hotels, etc.

Kohl’s invited me for a group interview with 3 other young ladies for a sales associate position. It was an hour long interview specifically explaining the position. Kohl’s offered me a job afterwards. I was excited thinking it was at least something to get me out of my apartment and earn some income. Later that week, we were discussing the schedule and training. I found out that they planned on having me unload the trucks for 4 hours per week. I was in disbelief. This is all they see me capable of doing? I was so insulted that I told them I didn’t want the job.

I went on websites where parents posted listings for babysitters or nannies. I decided to try my luck there with my previous background of babysitting for my neighbors’ kids and cousins. I was faced with many similar responses from parents saying they didn’t think it’d work because of the communication barriers. One parent even asked if I was a parent, and stated that I shouldn’t even have a kid because “how can I hear them crying!” Communication barriers were the most often used excuses from anyone for why I wasn’t being hired.

I interviewed for a real estate assistant position. The real estate agent was a super friendly Italian guy, who was willing to talk with me via paper-and-pen. I had hopes with him based on his positive attitude. During the interview, he was super skeptical of the communication barriers that I would have with his clients. I never heard from him again.

Through these challenging times of waiting on getting a job, I did find a way to make some income. I started cleaning out my closet, selling it online.

Stay tuned for the next experience which is when I finally got a job in a deaf environment.