Archive for the ‘Posts’ Category
That Space Between
Posted on: June 9, 2016
- In: Posts
- Leave a Comment
What goes through your head during that space between words when you are stuttering? You know what I mean, that often long pause that creates space between two words while you are having a block.
Is it something that you think about? I have. Not often because my blocks aren’t too long, but every once in a while I get one that seems long and definitely creates that space.
I often feel anxious, as it isn’t natural to have long pauses between words. Even when that is done intently by a speaker for emphasis, that space is often not as long as one created by a stutterer.
Sometimes I think to myself, “Oh no, not now.” Or I think, “What are they thinking?” I try to re-frame my thoughts and sometimes think, “Oh good, a moment to catch my breath.” Especially when I am presenting, I can use that space to compose myself and prepare for the fluent word that inevitably comes after the space.
Fluent people probably never give this a thought.
Remember To Breathe
Posted on: June 4, 2016
It always surprises me to hear one person who stutters advise another person who stutters to remember to breathe when facing a stressful speaking situation. It’s not something like remembering to turn off the coffee pot before leaving the house. For that, you have to consciously focus on the act of walking over to the coffee pot and powering it off.
Breathing isn’t like that. There’s isn’t an “on-off” switch that we need to remember to push. It’s not mechanical. Breathing comes automatically. We do not think about doing it. We just do it. Like the Nike slogan. The human body comes equipped with the innate ability to do that which keeps us alive. Unless of course we are injured or gravely ill and mechanical breathing is indeed needed for breathing.
So why then do we often hear people reminding us to breathe? I often get annoyed when people who don’t stutter offer me that advice. Like I have a choice. Like there is a button to push. As if “just breathing” was enough to stop stuttering.
It’s not that easy. Stuttering is a neurologically influenced disorder which interrupts the normal flow of speech. Breathing, which we already do without thinking about it, does not improve our stuttering.
I see and hear this a lot in the stuttering community. Someone will post on a forum that they are nervous about an upcoming job interview and ask for advice. Inevitably, someone will write, “remember to breathe.” That thought doesn’t enter my mind when I am faced with a challenging speaking situation. I am usually thinking about a strategy I can use to lessen repetitions or to get out of a block. Breathing isn’t a trick to pull out of the speech tool bag.
Why do you suppose people who stutter offer this advice to other people who stutter? Is it because they can’t think of anything else?
Amazing Communication Skills
Posted on: May 16, 2016
For years, I believed that stuttering could not be used in the same sentence as effective communicator. The two did not equate. Stuttering to communication was like a bull in a china closet – not going to work.
But ever since I joined Toastmasters and practiced public speaking and realized that I could communicate effectively, things changed. I began to believe in myself as a communicator and others did too. I’ve been asked to speak to many groups about my stuttering journey, something I never imagined myself doing when I was younger.
Last week, I had the opportunity to speak to a high school science class about the neurobiology of stuttering.The students were a great audience and asked thoughtful questions. They also provided me with great feedback.
These are just a few of the comments students emailed me the day after the presentation:
“Listening to you speak was amazing. You’re so confident and knowledgeable on the topic and it was truly inspirational.”
“Your ability to conquer your fear of stuttering was inspiring. I wish I had your amazing communication skills.”
“I truly admire the courage it took for you to present to us! You are an inspiration and I hope you know what a great communicator you are!”
It was so gratifying to talk to these kids and have them share that they think someone who stutters can still be a great communicator.
We CAN be great communicators. Remember, there is so much more to effective communication than being fluent. Speaking regularly and getting feedback proves that.
Stuttering Awareness Week 2016
Posted on: May 9, 2016
- In: Posts
- Leave a Comment
This week is National Stuttering Awareness Week in the United States. It’s an opportunity for people who stutter to talk about stuttering to those who don’t, to educate and raise awareness.
There are many ways to advertise and promote stuttering awareness. Here are a few.
1. Consider wearing a stuttering awareness tee-shirt, wrist band or lapel pin to work or out in the community. If people ask about it, mention you stutter and take the opportunity to explain what it is and how it feels.
2. In your office, display posters or a coffee mug that says something about stuttering. (These items can be found in the store at the National Stuttering Association.)
3. Consider contacting a radio station and asking if you can make a public service announcement (PSA) about stuttering.
4. Read blog posts or articles or literature about stuttering to educate yourself more about stuttering. Great free resources are available at The Stuttering Foundation.
5. Stutter openly this week. If you are usually covert about stuttering, try to give yourself permission to stutter openly. Be open if people have questions about your speech.
This week I am speaking to a high school senior class that is specific to scientific research and public health. I will be addressing my personal experience with stuttering along with talking about the neural and genetic basis of stuttering. I have asked the class to read an article about stuttering research so we can discuss it during my presentation.
I have also submitted a brief article to my local newspaper about how important listening is when engaging with someone who stutters. I am hoping it will be published this week.
What will you do this week?
The Stuttering ID Card
Posted on: April 11, 2016
Up to this point, I’ve been quiet about the Stuttering ID Card that has been created by the Stuttering Foundation for people who stutter to carry in their wallet. This card was created in response to an incident that occurred at an airport where a person who stutters claims to have been detained because of her stuttering.
When I first heard about it, I did chime in on Twitter to say there is going to be hundreds of people who stutter coming through the airport in July for the annual conference of the National Stuttering Association. But I’ve been quiet since, as there has been no word from the airport about what happened and there is always two sides to a story.
The young woman has garnered a lot of attention in the stuttering community. She has written articles for the Huffington Post and was also featured in The Mighty.
Recently, I saw that the American Speech-Language-Hearing Association wrote about the ID card on their blog, The ASHA Leader.
So, now, two prominent organizations have advocated that people who stutter carry this card when going through customs at airports, to help explain that they stutter.
I wouldn’t feel comfortable carrying this card. I don’t need a piece of paper to state that I stutter. I can tell people that myself, if it becomes necessary. Sometimes, it’s very obvious that I stutter, sometimes not so obvious. There are times when I feel comfortable advertising that I stutter and times where I am not.
I’m curious. How do you feel about this? Would you carry this card with you when traveling?
Looking At Ourselves Stutter
Posted on: April 5, 2016
- In: Posts
- Leave a Comment
A very courageous poster today made a comment in a Facebook stuttering group about how hard it is to watch himself and other people who stutter on video.
He shares very honestly that he can’t stand to see himself stutter and can’t bring himself to watch other people who stutter either. For him, it’s not a way of desensitization, but rather a form of torment.
This made me think about how hard a time I had when I was asked to make a video of myself stuttering when I did speech therapy some years back. I remember quite vividly how much I resisted doing it. I just did not want to see myself stutter. I felt my stuttering was ugly and I was aware of how I tensed up when I blocked and I just did not want a video reminder of that.
My speech therapist at the time really wanted to deconstruct my stuttering with me and felt strongly that viewing my stuttering was the best way to do it. She also wanted to be able to “count” my stutters as part of required data collection for her class. I hated that too, as I felt it made me nothing more than a piece of data to be collected and not really a person who just happens to stutter.
It took me the whole semester to allow her to record me doing a very short monologue where I hardly stuttered at all. Even looking at that with her, with very little stuttering, made me feel self-conscious and embarrassed. I just didn’t like to see myself on video. I didn’t believe it could be helpful.
Fast forward, about 9 years later, and I find I am one of the people posting a video of me talking and stuttering in some of the Facebook groups. Something I never thought I could or would do, now I am doing with ease and posting publicly on the Internet. Wow!
What’s changed? Mostly, my attitude. I have reached a point in my life where I am OK with my stuttering and feel that I can help educate and raise awareness about stuttering. I am OK with looking at myself and hearing myself on video. I think most of this comes with maturity and experience and a good dose of “I don’t give a crap.” 🙂
I am in awe of all the members in the stuttering groups who have taken a risk to post videos of themselves talking about their story with stuttering. Some of them have acknowledged that they are new to the community and have never met another person “in real life” that stutters. Through posting video stories, people are seeing and hearing other people who stutter and I think that it’s great to lessen feelings of isolation, which are common for people who stutter.
I’m glad that the poster had the guts to share how he really feels about seeing stuttering. It certainly gave me pause to reflect on where I’ve been and where I am at now.
I’m curious what you think. Have you ever seen a video of yourself talking and stuttering? How did it make you feel? Would you be willing to post a video of yourself in a stuttering forum on the Internet?
Book Review: First Person Shooter
Posted on: March 29, 2016
- In: Posts
- Leave a Comment
A member of the global stuttering community from Australia reached out to me and asked if I would read his new book. I was delighted, as I always enjoy reading about stuttering.
I recently read “First Person Shooter,” written by Cameron Raynes, a person who stutters. The book is a young adult novel, with some adult themes. The book is narrated by young Jayden, a 15 year old boy who stutters. Jayden is addicted to video games and has a crush on his best friend Shannon.
The story is pretty intense, loaded with characters who all have their own story. Jayden and his father are surviving after losing his mother 12 years earlier. Shannon’s mother is due to be released from prison. Jayden is constantly trying to outrun a couple of school bullies. He has a part-time job at a meat shop and looks in on his neighbor, a disabled veteran. The town is bracing for violence from Pete, who is looking to exact revenge for the murder of his father. And Jayden’s beloved dog is dying.
There is a great deal I could focus on in this gritty coming of age story. For the purposes of this blog, I’ll focus primarily on the stuttering. Stuttering is not always portrayed well in the media and the arts, so I was eager to see how the author incorporated it into the story.
The first thing I’ll say is the stuttering experience is beautifully handled. It is obvious that the writer has first hand experience with stuttering. He nails Jayden’s struggle with having much to say, but feeling unable to express himself the way he wants. Jayden has a love of poetry but can’t make his own words flow.
Jayden shares many real and poignant feelings about his stuttering, which at 15, he realizes will be with him for life. Early on, he reflects that “to speak is to be human,” inferring that perhaps he doesn’t always feel human because of the way he talks. When he speaks, his words are ugly. He escapes these feelings by getting lost in his video games.
Jayden also thinks that deep down, something is wrong, that he is broken inside. That is not unusual for a teen who stutters to feel. I sure felt defective when I was his age and often wondered, “Why me?”
Jayden also describes the dread of sitting in class and having the teacher go around the room and know that he is not going to be able to get out of speaking. He speaks of scanning ahead, which is a trick that many people who stutter use to avoid stuttering. In class, he has also tried being funny, to draw attention away from his stuttering, which doesn’t always work.
Jayden has a circle of friends who accept him. Several of them have also been picked on by the school bullies, so they are a small group with commonalities. Jayden appreciates his friends because he can be himself and not be consumed by the constant worry of how he will sound and how they will react.
Throughout the story, Jayden dreads an oral poetry presentation he must do before the end of the school year. Anyone who stutters can empathize with Jayden’s terror of having to speak and stutter for a prolonged period of time. It can be a harrowing experience for an adult, and this is an adolescent dealing with the cruelty of teens. Jayden gets through the experience and closes the door on another school year.
I highly recommend this book for teens or adults who stutter and anyone for that matter. It is well written, with an honest, believable character who stutters. The author lets us into Jayden’s head and we get how tough stuttering can be. Most fluent people don’t really “get” stuttering. Raynes masterfully weaves Jayden’s stuttering into a story that is dramatic, intense and satisfying. You feel for the kid and applaud his tenacity and courage on many fronts. You’ll have to read it yourself to know what I mean. And I hope you do.
Comedy And Stuttering
Posted on: March 15, 2016
- In: Posts
- 5 Comments
I recently had the opportunity to attend a comedy show, headlined by Drew Lynch, a person who stutters. Drew was featured on last season’s reality TV show, “America’s Got Talent” (AGT.) Drew did stand-up comedy on the TV show and wound up finishing the talent competition in second place.
Drew did not grow up as a stutterer. He claims he began stuttering a few years ago, after being injured in an accident. He was hit in the throat by a softball and began stuttering. He had aspirations to be an actor and decided to try his hand at stand-up comedy when fate intervened and he was injured.
I remember last year when Drew was on AGT. A lot of people in the stuttering community did not find him funny and did not think it was cool to make fun of stuttering. Audiences laughed at his stuttering jokes and the way he made fun of himself. He almost always laughed himself after telling a joke.
I found him to be funny and his humor appropriate, but was only seeing him in 3 minute segments.
When I heard he was coming to my hometown to headline a comedy show, I was very interested in seeing him perform. I wondered how he would handle performing for a longer stretch. And I wondered how my hometown audience would react to a comedian that stutters.
My sister had asked me to go with her to the show, which was a surprise, as I didn’t think she would be interested in seeing someone who stutters. She and I don’t talk about stuttering. It’s always been a taboo topic in my family and continues to be so, even though I am very open and public about my stuttering.
So we went to the show and had a great time. There were two opening acts, one which was very funny and the other was just OK. Neither of them stuttered! 🙂
When Drew came out to perform, he immediately started with a joke about stuttering. He laughed and the audience laughed. Drew went on to perform for almost an hour, which I marveled at, given that it’s a long time and a lot of material to remember for the performance.
His material was not all stuttering related. He had funny jokes about every day life which the audience enjoyed. About half of his material was related to stuttering, and making fun of his own stuttering. I think his willingness to poke fun at himself and laugh at his own jokes and funny stories gave the audience permission to laugh. And laugh they did. It appeared everyone in the packed room was having a great time.
I posted something about having attended this comedy show on Facebook. Several people commented that it is not good to laugh at stuttering, because it opens the door for anybody to laugh at stuttering.
I say that most people can appreciate the context and will not laugh at someone stuttering just because they happened to laugh at a stuttering comedian.
After the show, Drew stayed around to meet and greet fans and signed autographs and took pictures. The line was so long, which was a great sign that the audience had enjoyed Drew’s performance. I did not stay to talk to him, although I really wanted to let him know that I stutter too.
Turns out, after my sister drove me back to my car, she went back and stood in the line to get an autograph and a photo. Guess she really enjoyed the performance.
So, what do you think? Is it OK to laugh at someone who stutters when they are telling jokes and making fun of their own stuttering?
Stinking Thinking
Posted on: March 8, 2016
I recently asked a question on one of the Facebook stuttering forums. I was interested in what people think about when stuttering. So I posed the question, “What do you think about during a moment of stuttering?”
I was amazed by the number of responses. This question drew about 40 comments.
And guess what? Most of them were negative. People shared that what they think during a stuttering moment is usually tied to shame.
Here’s a sampling of the responses.
Embarrassment.
“I should have kept quiet.”
“I’m thinking about what the other person is thinking.”
“Panic, panic, panic.”
“My mind goes blank.”
“When will this be over?”
“Scanning my brain for words I can substitute.”
“Please just let this moment end.”
“Why do I bother?”
“Uh oh, too late.”
“Here we go again.”
“How stupid I sound right now.”
“I hope my face isn’t getting red.”
What do you think? What goes through your mind when you are in a stuttering moment? Is there anything we can do to change the way we think so that it’s not negative or shameful?
I am definitely guilty of wondering what the other person is thinking when I’m stuck in a block. I wish I could get myself to think, “it’s OK, I got this.”
Stutterer Wins The Oscar
Posted on: February 29, 2016
- In: Posts
- Leave a Comment
“Stutterer” won the Oscar last night at the Academy Awards for best live action short film. It was up against 4 other short films and clearly moved audiences. The Academy got it right by bestowing the award on “Stutterer.”
Have you seen it yet? It is only 12 minutes long and you can buy it from YouTube and make it part of your personal library.
The stuttering community is abuzz about the film, with people offering mixed feelings about how the character’s stuttering was portrayed. People are also talking about how they feel about another character with “flawed” communication being the one to interact with the stutterer.
The film really helps put into perspective the whole notion of imperfections.
Do check it out when you can.
- In: Posts
- Leave a Comment
Spoiler alert!!!!
I recently went to see the short film “Stutterer,” which was shown as part of five short films nominated for Oscars in the live action category. It is exciting to see another film about stuttering up for an Academy Award. Hopefully it will ignite stuttering awareness.
The short film is only 12 minutes long, but packs a punch. On opening, you see the main character, Greenwood, struggle to speak on the phone. Later in the film, we see Greenwood’s father make the phone call for him.
The film conveys how much of a struggle it is for Greenwood to speak, yet in his head, the words flow eloquently and effortlessly.
He is lonely, because he is terrified of communicating with anyone. He is studying sign language and pretends to be deaf so he can communicate without having to speak verbally.
The crux of the film centers around a relationship he has with a beautiful girl he has met online. He can communicate with ease as he types out witty responses to this girl.
But soon she wants to meet in person. She writes him suggesting a meet up, as she is planning a visit. This brings him to a panic, and he doesn’t respond to her right away.
She assumes his non-response means that he doesn’t want to meet. Finally, after much delay, he gets up the courage and writes to her saying he’d like to meet if she was still interested.
When they meet, he discovers she is deaf and communicates through sign language.
The short film was deeply satisfying and left me wanting more. I wanted to see what became of their meet up and if they started dating. I wanted to see if he got up the courage to seek out speaking situations despite his severe stutter.
I felt the character’s stuttering was very realistic, as was his fear of negative social reactions and judgement.
My concern is the portrayal of sign language as a viable alternative to speaking. I worry that stutterers will see this film and get the idea that using sign language to avoid speaking is OK. That’s not the message we should send to the stuttering community, especially young people who have not yet found their voices.
The film is a romance and really doesn’t aim to raise stuttering awareness. But maybe the title will do the trick and get people talking about stuttering which always provides a good opportunity to educate and raise awareness.
Giving Blood And Stuttering
Posted on: January 26, 2016
- In: Posts
- 2 Comments
Interesting title, huh? What would giving blood have to do with stuttering?
Yesterday, I donated blood at a local blood drive. If you’ve never donated before, you might not be aware of how meticulous blood drive staff are about making absolutely sure they are identifying donated blood correctly. They ask you to state your full name at least 5 different times during the process. Usually, stating my name is not a problem, but yesterday my stuttering showed up big time by the fourth time I had to repeat my name.
When I was asked to state my name, it came out “P-P-P-Pamela.” The staff person snickered and asked if I was OK. To her credit, she did not ask if I had forgotten my name, as clearly I had not, since I had repeated it several times already. But her snicker annoyed me nonetheless. But I didn’t say anything. I gave her the benefit of the doubt that she wasn’t sure what she had just heard.
When I was asked the fifth time to repeat my name, out came “P-P-P-Pamela” again. This time she didn’t snicker but asked me if I was feeling woozy or lightheaded. I told her no, I just stutter. They hadn’t started drawing my blood yet, so I couldn’t have felt woozy or lightheaded yet.
When I told her I just stutter, she just nodded her head and looked slightly embarrassed but didn’t respond.
I was glad I said something to let her know I stutter. Hopefully I educated her a tiny bit and she’ll remember not to snicker or assume something the next time she encounters someone who stutters.
How have you handled similar situations when you’ve had to repeat your name several times? Would you have done something differently?
Make Room For The Stuttering 
What people are saying!