About the Author:
Hi! My name is Kory Tran and I’m a person who stutters in the Bay Area. Well, I suppose I’m a person who stutters outside the Bay Area as well. I am an aspiring UX designer/writer with a background in journalism. My work has appeared in the Mercury News as well as the American Drivel Review journal of literary humor. I am currently active in the National Stuttering Association as the co-chapter leader of the South Bay/Silicon Valley chapter. |
There is a TV show I like called “The Blacklist.” One day I watched an episode where the main character is abducted by a group of road bandits, one of whom, T-Bone, has a noticeable stutter. I waited for T-Bone’s stutter to factor into the storyline. I figured, there has to be a specific reason this character stutters, right? The plot will hinge on his stutter somehow. Or the other characters will make fun of his stutter to emphasize the depth of their villainy. But by the end of the episode, I was surprised—the apparent stutter was never mentioned. To me, this was groundbreaking. But also, I wondered why something so simple was groundbreaking.
For a significant part of my life, I worried that having a stutter would define me. “Oh that’s Kory,” I imagined they’d say, “That’s the guy who stutters.” I was worried I wouldn’t have personality traits independent of my stutter.
A stutter was something I felt I had to minimize, or be in denial about. “Oh I didn’t stutter. I just didn’t know the right words to say.” “Oh I didn’t stutter, I just wasn’t sure how to pronounce this.” Having a stutter just seemed so negative. I wanted to sweep it under the rug, throw some furniture on the rug, and then stand in front of the furniture saying, “Hey hey! There’s nothing to see here!”
By my junior year of college, I thought I had kind of hidden my stutter. I thought, if I were a Google search, the word “stutter” would be buried on the third page of my search results.
Then one day a classmate said to me, “I think it’s so cool and brave that you’re majoring in journalism even though you stutter. Honestly, if I had a stutter, I wouldn’t know how I’d deal.” At that moment, the carefully crafted image of myself as a person who didn’t let my stutter bother me came crashing down. My classmate might have intended the comment as a compliment or an offhand remark, and yet I felt the sting…that no matter what I did in life, I would always carry the stigma of a person who stutters.
When it came to journalism, I became hyper-aware of my stutter and I dreaded the reporting work—making cold calls, approaching people I didn’t know, winning sources’ trust enough to garner information from them. Once, as a student correspondent for a major newspaper, I interviewed a veteran reporter and blocked many times. Afterward, the veteran reporter offered me tips on how to relax and sound more confident, she said, “so that people will take you seriously as a reporter.” She was aiming to be kind, but afterward I wondered if people would ever take me seriously as a reporter. When I was transcribing my recorded interviews, my stutter was all I could hear.
Now, this is the point in the essay where you’re probably thinking, “Wait, where is the inspirational part? I came here for an uplifting read and it just seems to get worse and worse. What wonderful event happened that turned everything around for you?!”
Well…a fairy godmother didn’t appear out of the blue and say, “Bibbidi bobbidi boo. Congratulations, your stutter no longer bothers you.”
But when things get really low, when you feel like you’ve hit the bottom, there’s nowhere to go but up. I threw out the furniture, lifted up the rug and admitted to myself that my stutter was still there. Once I accepted that this stutter was here to stay and that it was OK, it seemed much less imposing.
I joined the National Stuttering Association, where I met people who asked me to stop apologizing every time I had a block. I joined Toastmasters where I discovered, surprisingly, that a lot of people wanted to hear what I had to say, even if it took me a bit longer to say it.
In the past, I would often avoid telling jokes in case I’d have a block on the punchline. I would also avoid arguments in case my stutter appeared to undermine my credibility. But those avoidances prevented people from getting to know me. Now, if people dislike me, I hope it’s just because I’m a terrible person.
Are things much easier now? Not always. As I am pursuing my new career in UX (User Experience), sometimes those old concerns still creep in, like: If I stutter during an interview or a presentation, would that make me seem unsure of what I’m saying? Would they be more inclined to hire someone who could speak with more ease? People in the industry are so confident, how do I make myself heard?
But to make a long story shorter, and also because this essay does have a word count limit, I learned that having a stutter didn’t prevent me from having other qualities. Instead of having a stutter or being funny, I could stutter and be funny, weird, imaginative, and many other adjectives.
Having representation in the media helps. “The King’s Speech” is the example a lot of people cite when they talk about stuttering. But I’m more eager for examples like “The Blacklist” where if a character has a stutter, it wouldn’t necessarily be a plot point. The more that a stutter is normalized and not portrayed as harrowing or quirky, the easier it gets for people like me to show our other qualities, our other personality traits.
In addition to being a person who stutters, I’m also a person who dances awkwardly, a person who dislikes running, a person who can be shy and outgoing on the same day. And a person who watches “The Blacklist.”
Kory thank you for writing this wonderful piece. The part that really resonated with me is when you were watching “Blacklist” waiting for them to make the show around the person’s stutter. It is amazing how our mind obsesses over it that when we see it or hear it, we think EVERYONE MUST want to only focus on that but it is just not a true narrative.
However, can totally relate when those various individuals pointed it out as well as I think that is so true to the overall reality of mankind. People are different and some are more accepting than others just like some have more sensitivity than others.
Fully agree that representation is everything as it is hard to make progress in awareness and normalization if we never see our kind in the media. I am deep in the improv world and trying to help bring improv to more disability groups so we can help bring more disability groups up on stage.
The question I have for you now is how do you feel about your stutter? Still insecure and resent it or do you feel proud now to have a stutter? I am very curious about ones attitudes toward their stutter as I know we all have a different view of it.
I have always wanted to explore improv and take classes, but never had the time! It’s nice to hear you’re deep in that world and taking it on.
To answer your question, I don’t feel “proud” to have a stutter. On most days, I feel like it’s just a part of me, like someone who is left-handed might have to do things slightly different from a right-hander. On some days, I feel a bit more frustrated, like if I’m in a situation where I have to compete with a fluent person to get heard, but I’m usually more frustrated at the situation than at my own stutter.
I like your sense of humor, I was chuckling from reading your bio alone. Thanks for stuttering outside of the Bay Area, and for writing this 🙂
Thank you! I knew you’d appreciate the humor. One of my earlier drafts had more jokes, but I didn’t want to detract from the message.
Kory, Thank you so much for sharing. I agree with you completely, we need to normalized depictions of stuttering through the media. I am happy that you acknowledges you are not just a PWS. I know it’s very difficult to introspectively define ourselves by the characteristics we love rather than the features we struggle with.
Thank you! We are all such complex beings and should celebrate so many aspects of ourselves.
Beautifully written, Kory! I love your attitude towards stuttering
Thanks, Adriana! It took me a long time to get there.
Thank you so much for Sharing, Kory!! I am so happy that you have been able to feel comfortable in your own skin and that you have learned that your stutter does not define you. You are brilliant and will continue to do wonderful things. I love that you mentioned how individuals make statements such as about how it was “brave” to major in journalism with a stutter. Many individuals feel that they are making compliments but it may not feel like a compliment to a PWS. I love that you mentioned this, as individuals who do not stutter can be more cognizant and aware when they are making comments.
Thank you! Yes, sometimes compliments can feel patronizing or backhanded if they’re reinforcing the person as an “other.” Thank you for your kind comments.
Kory, thank you for sharing your story! I really enjoyed reading about your experience and how it has shaped who you are today. My question for you is how can we continue to normalize stuttering? You mentioned the lack of a storyline for the individual who stuttered in “The Blacklist” as groundbreaking and how an individual who stutters doesn’t just stutter but can dislike running or be shy, so what can be the next big step in normalizing stuttering in our world?
I think the next step is just having more representation without having to always making it into an inspirational moment. For example, America’s Got Talent recently published a video entitled “Singer with speech impediment moves judges to tears.” I thought it would’ve been better if they titled it “Singer moves judges to tears” or used some other qualifier/adjective to describe her. Then people would still notice her stutter but would consider it “normal” because not a lot of attention was called to it.
Hi Kory, What a GREAT article. Thank you for sharing. Have you thought of being an actor? I recently saw a comedian who stutters and he does an amazing job. You can Be Anything!
Warmly, Nikki Rader
Thank you for your kind comments, Nikki!
I actually studied acting for two years in college before deciding it wasn’t for me.
This is an awesome paper, Kory! Thanks for submitting it and sharing your perspective. I am so glad to be your friend and that you chose to participate in this conference this year! 🙂
Best,
Tiffani
Thanks, Tiffani. I am so glad to call you a friend as well!
Kory, thank you for sharing your story.
I think it is amazing that you are a co-chapter leader of the National Stuttering Association. my question to you is what situations do you feel frustrate you the most?
Thanks, Haley.
To answer your question, the situations that still frustrate me the most are job interviews and other occasions where you have to confidently make your case, especially in a limited amount of time. Unfortunately some people still equate stuttering with nervousness and not being prepared.
Hi Kory! I loved your story and I’m glad you accepted your stutter as something that is part of you 🙂 How did you feel seeing the King’s Speech for the first time? I’m sure it was exciting to see representation for the first time!
-Justin
Thanks, Justin!
When I watched “The King’s Speech,” I really related to the fact that he tried everything and was still frustrated. And I was pleasantly surprised to see that it ended with him still stuttering and being OK, instead of it being magically cured and overcome like one would expect in a movie.
Hi Kory,
Thank you so much for sharing your story! I really appreciate your point that there is no magical fairy godmother who made everything all better with your stutter magically disappearing. You had to learn to accept it, and I feel people often hope that everything will magically get better in numerous aspects of your life. However, you worked hard to improve your mental health, for yourself. I am so impressed with you and your article! Thanks for sharing.
Thanks, Emily! Yes, sometimes we just kind of have to be our own fairy godmother. It’s not easy, but just taking a small step in the right direction goes a long way.
Hi Kory! I really loved reading your story! I am also from the Bay Area so when I read that you were from there I instantly knew I would enjoy your story. I then read that you loved Blacklist and so do I!! I found it very inspiring that you accepted your stutter and tried your best to embrace it! I am curious as to know who is your favorite character in Blacklist?
-Ariana P.
Thank you, Ariana!
My favorite character was Samar, but unfortunately she left the show. I do like Dembe as well. How about you?
I also loved Dembe!!! He is my favorite for sure
I loved your story and the perspective you shared.
I recently went to a family dinner with my in-laws and my brother-in-law shared a story about one of his friends and coworkers. He prefaced this story about how his friend had a stutter, which was entirely unrelated to the story, which was about how his friend had gotten into a bar fight one time in Iceland.
We ended up having a discussion about why he felt the need to include this unnecessary detail and he did not understand why it was a big deal. It wasn’t until his wife chimed in and said that she would be irritated if he started all his stories about her by noting her hearing loss/speech sound disorder that it clicked, and he backtracked.
Like the people you mentioned, most people think they’re being nice or helpful, or at the very least that their comments are harmless. But as you noted, even things that should be simple are still groundbreaking. It’s great that you found a positive representation in the media, though, and I hope we get more accurate portrayals of stutters as traits instead of defining features in the future.
Thank you for sharing that story. When someone’s stutter is pointed out in a situation where the fact is irrelevant, it can really make us feel like an “other.” I’m glad to hear your family had that discussion with your brother-in-law.
Hi Kory,
I did a research paper last year about the stigma around stuttering. Media has so man negative portrayals and it honestly may affect people’s point of view toward stuttering. I’m really glad that the Blacklist had that representation without negative connotations surrounding the character. I have never seen The King’s Speech, but it’s on my watch list. I’m excited to see that representation too. Thank you so much for sharing your story!
Madi
Thanks, Madi! I am glad the representation is improving, even if gradually.
Hey Kory!
Thank you for sharing your journey with stuttering! You made it very easy to understand your experience with your relatable examples and by adding in some good humor as well! I am glad you have found good representation in the media with people who stutter. I think that type of representation is hard to come by, so I am encouraged by what you have experienced on “The Blacklist.” My current job in research during my undergraduate years has focused on how children can have language disorders within a dialect, not one over the other in a disorder versus a dialect format. I think this concept transfers well to many other areas of life, not just language disorders, because in the end individuals are not just one defining characteristic in a limited box of opportunities. That being said, my favorite part of your post had to be your mention that you stutter AND you are funny. You definitely can be do both, along with many other things!
Thanks again for sharing!
Tatum Carver-Dews
Thanks, Tatum! Yes, I’ve also been told by many people who stutter that they stutter differently when speaking in a different dialect/language. It’s always so interesting to hear how vastly different everyone’s experiences with their speech disorders can be.
Hi Kory! Thank you for sharing and being open to all of us about your journey. I love that you believe that your stutter isn’t who are you, because that is SO true! I’m a graduate student in speech language pathology, and I’m learning so much about how acceptance and confidence is very important for PWS. Thank you again for sharing this story with us!
-Kelby
Thanks, Kelby! I really appreciated your comment. It took a long time for me to reach acceptance and it’s still a journey.
Hi Kory! Thank you for sharing your story. I am in a fluency class and trying to learn more about people who stutter. I admire your bravery and humor when conquering life. I now understand how simply putting a PWS in a movie does not necessarily create inclusion. More portrayals of PWS should be represented subtly rather than be the main focus. I am going to school to become an SLP assistant and wondering how we, as professionals, can help others feel confident in their speech. I would love to hear your advice. Thank you!
– Sarah
Hi Sarah, sorry I didn’t see your comment earlier! To answer your question, I think the best way to help others feel confident in their speech is just to be a good listener, but not in a patronizing way. I think all of us, whether as people who stutter or not, just want to feel included and like our voice has meaning. Thank you for your question!
Hi Kory,
Thank you for posting this. I’m in school to become an SLP. Do you have any advice/thoughts on how interactions with an SLP could help someone embrace who they are?
Hi Laura,
My advice would be to treat each person as unique. When I was a kid in school and had to meet with a speech therapist, I always appreciated the more personal interactions as compared to the ones where I was grouped with other kids (who didn’t have a stutter) in a “one size fits all” session.
Hi Kory,
I wanted to thank you for sharing you’re story/journey with all of us it was I really appreciate it. I am currently in my undergraduate program to become an SLP. I finding truly inspiring that you have come so far in your journey with stuttering. I have a nephew who stutters and he is one of the many reasons I have decided to purse this career path. I am currently in a fluency class this semesters and it has provided a lot insight and understanding to people who stutter. I often times think about what it is my nephew is going through and what he is feeling, he doesn’t share his feelings too much with me or my other family members, even though we support him support I still feel like there is more I can do. This is why Ive enjoyed reading your story it was uplifting and funny! It also gives me hope. There is one thing that I would like to ask…do you have any advice on how I can help my nephew or others feel more confident with their speech?
-Isabel
Hi Isabel,
First off, I want to thank you for being so thoughtful! My advice to help your nephew feel more confident with his speech is to be a more focused listener, make eye contact and give him the space to make him feel like his speech is valued. Growing up, I was often interrupted when I stuttered, so I came to feel like my speech was worthless. But when I joined Toastmasters and people were actually quiet and paying attention to me, I thought, oh wow I actually have something worthwhile to say.
Hi Kory,
I really loved your essay. I too am a person who stutters and it truly was liberating to me when I finally realized (after many years) that I am more than my stutter. I had let that consume me for so long, to the extent of hijacking my personality and hiding other more important parts of me.
Thank you for being so honest.
Pam
Thank you, Pam! I try to be as candid as I can and usually the response is positive. I think you’re very similar as well.
Hey Kory!
Thank you so much for sharing your story and your journey with stuttering! One thing in particular that stood out to me was when you saw the episode of the “The Blacklist”, you were surprised. I love your comment about how something so simple should not be surprising because that is true! I think there should be more instances like this in our media representing people who stutter!
-Madison
Thank you, Madison! I think growing up, we get so focused on how we’re different, leading to people unnecessarily feeling like outsiders. The more that stuttering is represented in the media, the more that people will eventually say “no biggie” and come together more easily.
Hi Kory!
First of all, I just want to say thank you so much for sharing your story. As someone who does not have a stutter, I want to hear more stories like yours to help myself learn more about the world of people with speech impediments. I’m currently studying to become a speech language pathologist, so stories like yours inspire me to continue studying in this field. So, thank you!! I feel like stuttering isn’t portrayed positively or normally in the media as much as it should be. I love how you mentioned that one of the characters in “The Blacklist”, is portrayed as a completely normal person, and not just someone with a stutter that hinders them. It’s so important that this happens more often to help spread more awareness on stuttering! Other than some shows, stuttering isn’t something that is spoken about often to the normal, everyday person. Before I began studying to become an SLP, I never was exposed to the world of people with speech impediments. That really should change, and your essay brings a lot of light to that issue. Also, it makes me sad that stuttering can impact someones credibility. If people became more aware and were more understanding, maybe that would change. But like I mentioned before, people like you are already helping inspire that change:)
Something that you mention is that stuttering doesn’t go away, it’s something that someone has to accept and be okay with that. Was there a person or a group of people that helped you accept your stutter, or did you learn to do that on your own?
Hi there! Thank you for your comments and questions! Before I joined the NSA in my 20s, I can’t recall really interacting with another person who stutters and having a conversation about it. In fact, I think I’m the only person in my family tree who stutters, so growing up my family didn’t really know how to deal. They just felt that it was something that had to be cured, stamped out. So when I joined the NSA and got to meet people who were in their 60s, 70s, etc., who were still stuttering after a lifetime of speech therapy, it made me realize that stuttering may not go away, but it didn’t prevent people from leading happy lives.
Hi Kory! I really enjoyed reading your article and seeing how your perspective on stuttering has changed. You mentioned two examples, on of your classmates and the other a reporter, where what they said came across differently than they may have intended. I was wondering what is something you would say to someone without a stutter to prevent instances like this from occurring?
Hi Beccah,
It’s difficult because I don’t want to seem preachy and defensive, so I would just be honest and say I have a stutter and sometimes it makes things difficult for me. I don’t think it would prevent instances like those from happening, but I guess the main point is to get the conversation going.
Hey Kory!
Thank you for sharing, this provided me with a great perspective for how small changes in the way stuttering is portrayed can be essential in normalizing stuttering. I love how you talk about being someone who is funny, weird, imaginative AND a person who stutters rather than being funny OR a person who stutters. So much of how our perspective on things form is from the wording used to describe it. Changing the wording is a huge step towards normalizing stuttering.
What are some other tangible ways people who do not stutter can contribute to normalizing stuttering? What about ways people who do stutter can continue to normalize stuttering?
Thanks for your comment! To answer your question, I think a great way for a fluent person to help normalize stuttering is to be a good listener and avoid interrupting. It doesn’t have to be a grand gesture, just showing that you’re present without being patronizing is simple yet so effective. For people who stutter, I would suggest to just get the fact out in the open more, and then shrug at the fact like it shouldn’t be a big deal. But of course, everyone’s journey is different and I’m just showing what has worked for me.
Hey Kory!
Thank you for sharing your story with us! I love how open you are about the struggles you have had coming to terms with your stutter. I am a graduate student in speech-language pathology, and it is so helpful learning about the experiences of people who stutter and the struggles they face in their day to day lives. I know that learning from you and others who stutter will help me to become an empathetic SLP that can help those who stutter to become confident in sharing their voices with others!
Have you had any experiences in speech therapy (good or bad) and how have they helped you?
Hi and thank you!
To answer your question, I attended speech therapy at school from the time I was in first grade through maybe fifth grade. But as a kid, I moved around and changed schools so often and many different SLPs that now it’s kind of all a blur. The experiences that I found most helpful were the one-on-one sessions where I was really listened to, as opposed to the group sessions where I participated in activities with kids who didn’t stutter. I also remembered being told by SLPs to “slow down” or think more about what I wanted to say before saying it, and those experiences were not helpful as I felt like they didn’t “get” me.
Hi Kory,
My name is Aminah and I am an undergraduate student in communication sciences and disorders. I thought your story was inspiring. Seeing someone on tv that deals with something that you deal with daily can be inspiring. My question is has there been any instances that tv has negatively impacted your confidence towards stuttering?
Hi Aminah, thanks for your comment.
Off the top of my head, I can’t think of definitive negative portrayals, but I feel like people who stutter are always portrayed as nervous or timid, and often the side character. I can’t remember any instance of a character who stuttered being seen as really confident or popular or even really charismatic, and I think a portrayal of that would go a long way toward normalizing stuttering.
Hey Kory! This was such an inspirational story and I could not be more proud of you for accepting your stutter and not letting it define you. I can tell that you love to make others laugh! So NEVER stop being YOU. Thank you for sharing this amazing story! -Kenslee Maines
Aww, thanks, Kenslee! Your comment made me smile.
Hi Kory! I really enjoyed your article and found it very inspiring. Thank you for sharing and being so honset and open and funny at that! I am currently in school aspiring to be a Speech Language Pathologist and hoping to be able to help others in the future. The question I have for you is what are some ways or strategies you used to help you minimize your stuttering? Also, have you become more fluent as you got older?
Thanks for your comments, Susie!
To answer your question, when I was younger I would substitute certain words for ones I knew I wouldn’t stutter on, or just generally wouldn’t speak as much. I find that I sound slightly more fluent as I got older, but more significantly I sound less nervous and more sure of myself.
Hi Kory, thank you for sharing your inspirational story. It’s funny how something so small, such as a comment or remark, makes the biggest impact in our lives, whether it be positive or negative. I believe that these moments happen in our lives to confront our challenges. I’m very glad you were able to remove the “rug and furniture” and see yourself beyond the stuttering, embrace it, and share with the world all your talents. – Maria Balkji
Thank you. Yeah, it’s amazing how a small comment or remark, one we may think is so trivial, can mean so much to others. I’m glad for all these experiences. Take care, Maria.
Hi Kory, thank you for sharing your inspirational journey with us! My question for you is, what made you want to become a reporter? Now that you are older and learned to be confident and prod of who you are…have you become more fluent?
Thank you, Zoe!
To answer your question, I’ve always liked to write, and during high school I joined the school newspaper because it afforded me a great opportunity to write. In college I studied both creative writing and journalism, and being a reporter seemed like the more steady route.
I don’t know if I got noticeably more fluent, but I find I’ve gotten better at communicating.
Hi Kory! I really enjoyed reading your article! I thought that the point you made about how something so simple, such as a TV show having a character who stutters and not have it factor into the plot in any way, can be so groundbreaking was very interesting because it is so true! It shouldn’t have been such a surprise that the character’s stutter didn’t have a point in the plot. I completely agree that having a stutter without using it to portray a character in a certain way needs to become more normalized in the media. I also loved how you talk about how a stutter does not define a person and a person isn’t limited to just that one trait, and how you can have many different qualities and traits! Thank you for sharing!
Aww thanks for the kind words, Kate! I hope to see more media portrayals of a person who stutters just existing and being themselves in the world without the point being hammered down that they stutter.
Hi Kory!
First of all, thank you so much for sharing such a personal and raw story. I really enjoy how real and transparent you are in explaining your thought process, experiences, and feelings toward what it means to stutter. I agree with your thoughts regarding representation in the media, for mass media and pop culture truly shape our lives in many aspects.
I was curious as to what you would do in order to create better representation in the media for PWS?
Thank you for your comments! To answer your question, I’m not sure what I would do to create better representation as we are a very small percentage of the population. But I would encourage people who stutter to let themselves step into the spotlight and not be afraid to own their stutter.
Hi Kory!
Thank you so much for sharing your story, I really enjoyed reading it! I loved the part where you talked about how you are not only a person who stutters, but you are also all of these other things like a journalist, a person with a great sense of humor, and a fan of “The Blacklist,” of course; having a stutter isn’t the only thing that should define a person, and I love how you worded that in this piece. I appreciate how raw and open you are about sharing your struggles; as an undergraduate student studying communication sciences and disorders, I thought your story was incredibly eye-opening and helped me to know more about the daily lives of people who stutter.
Thank you! I’m glad my essay was helpful and eye-opening. I really appreciate you taking the time to leave this comment.
Hi Kory!
This was such a great read for me to read, and I truly enjoyed it. Not letting your stutter define you is something I feel is really empowering to acknowledge and live by. One of my best friends from when I was younger stuttered, and I remember getting very protective over her because I did not want others to be rude to her because of her stutter. However, as I grew up I realized I spent so much time trying to “protect” her, that I made a lot of our conversations centered around that, and it really was probably draining for her to be around. Through grad school and just life in general, I have learned the importance of not letting the stutter identify the person. This helps me even more to understand this. Thank you so much!
Thanks, Meg! And thanks for sharing the story about your friend. It was kind of you to be protective of her and I’m sure she appreciated it at times, but yes there’s a point where it might become patronizing. Thank you for being a thoughtful ally though!
Hi Kory,
I really enjoyed reading your story.Thank you giving some insight into how stuttering can start defining you. It makes total since how watching the Blacklist episode where they don’t make a big deal of the actor that’s stuttering is just refreshing to see.I love how you don’t let stuttering define you because you’re so much more than that.What has been helpful to you in embracing your true self?
Best,
Cynthia
Thank you, Cynthia. I have to admit, what’s been helpful in embracing myself has a lot to do with getting older and having less patience contorting myself to hide my stutter. It also has helped being more open and being met with thoughtful responses instead of the immature bullying one might experience as a child.
Hi Kory! Thank you so much for sharing your story. I am currently in my first year of grad school, and I work with a couple of patients who stutter. So hearing stories like yours is so helpful in gaining understanding. I also think that it is groundbreaking that “The Blacklist” included someone who stutters and never addressed their stutter. However, it shouldn’t be that groundbreaking. There should be more representation of people who stutter in the media, and it should be more normalized like it is in “The Blacklist.” I know for me, before I began college I did not know much about stuttering and to be honest, I did not think about the experiences of people who stutter. Your experience with the veteran reporter makes me upset. I just can’t understand how your stutter could make someone not take you seriously? However, I think it is really awesome that despite these comments you have a positive acceptance of your stutter and that you have learned that your stutter does not prevent you from having other qualities!
Thank you for your comments! I myself didn’t really interact with anyone else who stuttered until I graduated college. I didn’t have any people who stutter in my family tree. So it took joining the National Stuttering Association to meet others who stuttered and realize I didn’t need to be ashamed of my stutter. I’m hoping more kids will see this representation growing up and know that they are “normal” and loved.
Thank you for sharing your story! I will be graduating this december, I will be receiving my bachelors. I am actually taking a class right now called Introduction to fluency disorder and i have read a lot about stuttering and been learning about it. There for my question to you is, how do you stay so positive? What are some tips you would give someone else who has a stutter?
Thank you, Kathy. To answer your question, I don’t stay positive all the time. In fact, there are times where I still feel really down about it. My advice to someone who stutters is to seek out more people who stutter, whether it’s through an NSA chapter or a conference, because the more people you meet who are in the same boat, the less you feel alone, and the more encouraged you feel to accomplish things.
Hi Kory!
I loved reading your story. I’m finishing up my last year of undergrad and hope to get into grad school after this! I think the king’s speech is a perfect example of someone with a stutter and outlook on life. My question for you is: how long did it take for you to be comfortable talking and communicating with others while also having a stutter? 🙂
Hi Caroline, my story might be a bit atypical, as despite my stutter I was a pretty outgoing kid and it wasn’t until I got a bit older that my stuttering really bothered me and made me shy. So it took a long time, years, but I was able to remind myself that I could be that outgoing kid again. It also helped that I joined a bunch of clubs and activities that forced me to speak more, and the more you do something, the more you get comfortable with it.
Hi Kory! Thank you for sharing your story! I really enjoyed learning about your personal journey and how you learned that you could have other qualities! Is there was one thing you wanted the public to know about stuttering, what would it be?
Hi! If there was one thing I wanted the public to know, it would be that people’s stuttering can vary greatly from day to day, as I often get asked why my stutter is more noticeable on some days compared to others.
Hi Kory!
Thank you for sharing your story. I enjoyed your sense of humor; it’s similar to my own. After reading your article, I’ve taken the time to reflect on how much stuttering is underrepresented in the media. I’ve never actually watched The Blacklist, but I want to check it out. I have a question for you, how do you feel you’ve changed as a person since you’ve gone through these experiences? Whether it’s because of The Blacklist, journalism, or other things you enjoy. Again, thank you for sharing!
Thanks for the comments, Springrose. It’s hard to say how I’ve changed as a person. Sometimes I wonder how my life would be if I had grown up without a stutter, if I had been able to just easily say everything I ever wanted to say. But I believe my experiences with my stutter has also made me a much more empathetic and patient person than I would’ve been if I had grown up fluent with no challenges.
Hi Kory! My name is Muna and I am an undergraduate student in communication sciences and disorders. I recently watched “The King’s Speech” for class assignment. As I was reading your article I wondered if you ever watched it and if you did what did you think about it?
Also want to say thank you for this inspiring story and for giving a voice to so many wonderful people!
Hi Muna, thanks for your comment! I did watch “The King’s Speech” and I thought it was great that at the end, his speech didn’t get magically cured and he didn’t lose his stutter. That was the major positive aspect for me, that it showed that he carried on and gave a big speech despite his stutter still being there.
Hello Kory!
Thank you for sharing your experience with stuttering and also your struggles. I totally agree with you some people might not think that their comments are offensive or they they its a compliments. What do you think really helped you change your point of view of people commenting like that?
thank you !!
Michelle Enriquez
Thank you, Michelle! It’s difficult because sometimes you can’t tell the intention people have behind their words. These days I like to think that if people are making a comment that seems offensive, it comes more from a place of ignorance rather than mean-spiritedness.
Hi Korey!
I really appreciated hearing your story and perspective about your stutter. I think it’s important that other PWS know your story because they would find it inspiring. I thought it was funny when you said, “so when does the inspiring part come”. I think telling others that your stutter doesn’t completely go away is inspiring in itself! It’s real and I think people appreciate that you are being true to yourself. I did end up watching King’s Speech in my class for fluency disorders and I think it’s important to bring light to PWS in the media. People want to know your story so thank you for sharing!
Thank you for your comments! I’m glad you enjoyed reading my essay and found it inspiring. That made my day. 🙂
Hi Kory,
Thank you for sharing! I’m curious, what was the first movie/show you watched that showed a PWS? How did you feel about this representation?
Hi Nandini,
I can’t remember the first time I saw a portrayal of someone who stuttered, but “Pan’s Labyrinth” was one of the ones that stood out, unfortunately because it’s a sad portrayal.
Hi Kory! My name is Genesis Melgar. I Enjoyed reading your story so much and felt so connected to it as well. I find it so inspirational that you grew to not let your stutter define who you are, you made peace with it, and you’ve learned how to live with it- without overshadowing all of your skills, and characteristics that make you who you are.
I’m majoring in speech pathology, and I want to share with you that I am not the best public speaker or speaker in general. I stutter, I mumble, and I speak extremely fast. I would be lying if I said this hasn’t impacted my life or made me feel like I should choose another career where I’m not teaching people how to speak fluently when I seem to have trouble myself. However, after reading so many articles and talking to a few professionals on here, I noticed there are many speech therapists that stutter and speak in a fast manner as well. It isn’t something to be ashamed of, and I’m glad that we’re working to get rid of the social stigma that comes with stuttering. Be well Kory, sending you my kindest regards. I look forward to seeing you on television and witnessing all of your achievements that I know are so near!
Oh wow, Genesis, thank you for your wonderful, kind comments!
I am friends with a couple of SLPs who stutter, and what I’ve learned is there is not one “perfect” or “right” way to speak, we all have our little differences that set us apart. We really just want to improve the effectiveness of our communication.
I wish you the best in pursuing your career of speech pathology, you already like a very thoughtful, empathetic person.
Hi Kory! Thank you so much for sharing your story! I am happy to hear that you are comfortable and confident. I am enrolled in a fluency class and the ISAD conference has allowed me to gain better insight coming directly from PWS. Portrayal and normalization of stuttering is something that the media should work towards, as representation is something that we all look for.
Thanks for reading my essay, cdm! I hope your class goes well and you have a great experience.
Hi Kory,
Thank you so much for sharing your story. You are truly very inspiring and admirable. It seems that you persevered through much diversity and learned to cope with your feelings well. Ive been learning throughout this conference that it is difficult for PWS to not define themselves as that. It seems like you are such a strong character and embrace your differences (like any other person should). I liked reading when you said “The more that a stutter is normalized and not portrayed as harrowing or quirky, the easier it gets for people like me to show our other qualities, our other personality traits.”
As a PWS, how do you see people in this world helping reach that goal of normalizing a stutter? What type of people have you came across to help you show your other qualities and personality traits?
Hi Lali, thank you for your comments! You have very good questions. I think the easiest way to normalize stuttering is just to expose people to more people who stutter. I grew up not knowing anybody who stuttered, not even in my family tree. It wasn’t until I finished college and started attending National Stuttering Association meetings that I really got to know other people who stutter, and it was eye-opening. I met people who were leading full, accomplished lives and having successful careers and it made me feel for the first time that I didn’t have to let my stutter hold me back. Meeting the various PWS in the NSA also helped me see that we are not a monolith, that we all have very different personalities despite this one common thing of us having a stutter. So that made me realize I was free to explore my other qualities and traits.
Back to the normalization topic, I also know people who were/are not “out” with their stutter, maybe because they grew up in an environment where they didn’t feel safe admitting that they stutter. So I hope that the more stuttering is seen and normalized, more people will feel OK to say “I stutter too.” And then that would help even more PWS open up.
Hello, I deeply enjoyed reading about you overcoming your stuttering insecurity. What do you think is the most important piece of advice you could give a young adult who is struggling with confidence as a result of their stutter? Thank you in advance, your advice will be deeply beneficial.
Hi Desiree, what I would say to a young person who stutters is that they are worth listening to, even if it takes extra time. And I would suggest to do things that are outside of their comfort zones, like public speaking. One of the advantages of youth is that they have lots of time to try different things without limiting themselves or putting themselves into a certain box. And once they find what makes them special or unique, they’ll gain confidence.
Hi Kory,
I really enjoyed reading about your experience! I agree that we need more PWS represented in movies and media, and without the stuttering being a plot point or representative of negative character traits. This will help PWS have characters they identify with, as well as normalize stuttering in society at large. Many PWS have never met another PWS, and many people do not know a PWS, so the only times they may have seen someone or someone else stuttering would be in a movie, which is not often a positive representation. Another point to be considered is that most characters in movies who stutter are not played by a PWS. I think this is another area that could be advocated for, is having these parts played by a PWS. Do you have any thoughts on this or how to best advocate for this?
Thank you,
Isabella
Excellent point, Isabella. I think many of the actors who say they stutter are the ones who only stutter as a child, so I would love to see representation by actors who still stutter as adults. After that episode of “The Blacklist” aired, I tried finding out if the actor stuttered in real life as well, but I had no luck. I think a good way to advocate for this is to just be more visible. We are a very small percentage of the population—I believe it’s 1 percent—but the more we show up, the more a stutter may just be something we all consider “no big deal” in the future.
Hi Kory! Thank you for sharing.
I really enjoyed reading story, and I am so glad you did not let stuttering define who you are.
I do believe that having a representation in the media, will help. Do you recommed anything other than “The King’s Speech” or “The Blacklist”. I would love to see more movies/tv shows that represent people who stutter.
Btw I am also a person who can be shy and outgoing on the same day too!
Very good question, Itzel, that really got me thinking. I tried googling more examples of portrayals of people who stutter and nearly all portrayals I found were negative, or so slight that you could blink and miss it. I wish I could find better examples.