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This video is making the rounds of the stuttering sites on social media and for good reason. A dad with a stutter is seen reading to his daughter before she falls asleep and it is clearly a challenge for him. But he perseveres and does what he wants to do for his child.

I applaud this dad for doing what thousands of parents do with their children – read to them before bedtime. The fact that he decided to record this for others to see took a lot of guts. I am glad he did, so you can see it here. He allows us to see the very vulnerable side of stuttering.

Earlier this week, I gave 4 presentations to high school students about career planning and options for scheduling for their last two years of school. This is something I do every year as part of my job as Outreach Specialist. Every November and December, I go out to school districts in my area and present about vocational programs that students can choose.

As I’ve been doing this now for many years, you’d think I would be totally used to the challenges of public speaking with a stutter. Right? Wrong! I still feel self conscious when I have lots of stuttering and sometimes my mind wanders with thoughts that the students are thinking there is something wrong with me.

Monday happened to be one of those days where I stuttered a lot and was very aware of it. I did not disclose to the audience ahead of time like I sometimes do, because I didn’t want students focusing on my stuttering. I wanted them paying attention to the information I was sharing.

In between two of the presentations, I overheard two students whispering (loudly enough for me to hear) and laughing about speech impediments. Clearly they had heard me stutter and were talking about it. I felt very uncomfortable but didn’t react or say anything to them. Maybe I should have. Maybe I should have disclosed that I stutter at the beginning of the presentations and just trusted that the students would take it in stride and act respectfully. Maybe I didn’t give them enough credit.

It bothered me that I let stuttering and someone’s reaction to it bother me as much as it did. I did a pretty good job of not letting it show though. I’ve always believed that when you’re speaking in public, you should never let the audience know that you’re uncomfortable or “sweating something.”

Someone told me yesterday that there will always be another day where I’ll have a more positive experience. He’s right. I’ll have plenty more opportunities to present in the coming weeks and choose to disclose my stuttering if I think that will be helpful.

What do you think? How do you handle the challenges that come with public speaking and stuttering?

I am so happy to have a piece published today on The Mighty about stuttering. It’s called 5 Things I Wish My Younger Self Knew About Stuttering. The older I get, the more I appreciate what I’ve learned about stuttering. And I often think how things would have been different if I knew some of these things when I was growing up.

Here is the piece:

When I was growing up as a kid who stuttered, I felt so isolated. I didn’t know anybody else who talked like me, and no one ever talked about my stuttering. My father would yell at me when I stuttered, which made me feel scared and ashamed. When I started school, I remember my kindergarten teacher also reprimanding me for the way I talked, which again made me feel so ashamed.

I got teased a lot for my stuttering. Kids mimicked me and laughed and I began to not want to talk at all, because of the reactions I got and the feelings I had. It was a very lonely experience growing up thinking I was the only person who talked like this. I felt weird and awkward and like somehow stuttering was my fault.

I worried about stuttering all the time and constantly figured out ways to not stutter openly. I developed a huge vocabulary as a kid, and became an expert at substituting words that I knew I would stutter on with words that were safer to say. And I also avoided speaking situations a lot. Sometimes it was just easier not to talk – then it was guaranteed that I wouldn’t stutter.

As I got older, things changed. Dealing with stuttering became a little easier, because I learned to not care so much about what other people thought. And I met other people who stutter, which changed my life dramatically. I realized I wasn’t the only one and there was no need for me to feel so weird and awkward anymore.

These are the things I know now about stuttering that I would have liked to know when I was younger.

1. Stuttering is no one’s fault. It is a speech disorder that interferes with the normal flow of speech production. It is widely thought today that stuttering is neurological and also genetic. No one in my immediate or extended family stutters, but it definitely wasn’t my fault. I didn’t do anything to cause my stutter, and neither did my parents.

2. When you get older, stuttering is easier to deal with. It’s a bigger deal in our heads than it really is to other people. Adults have their own issues – they don’t care that someone else stutters.

3. Stuttering does not mean that we are less intelligent than others or that we have emotional problems. We are not nervous or shy. We just stutter. We’re as smart as anyone else and can do anything that anyone else can.

4. There are lots of people who stutter. In fact, there is a whole community of people who stutter, from all walks of life. People who stutter are very successful and have careers as lawyers, doctors, educators and many more. When I was growing up, I was afraid that I wouldn’t be able to get a good job just because of the way I speak. That’s just not true.

5. Stuttering make us unique. Only 1 percent of the general population stutters, which means I have something that 99 percent of the world doesn’t have. And that’s kind of cool.

On Saturday, I had the pleasure of attending a one-day NSA conference sponsored by the Boston chapters of the NSA. The conference was held at Boston University, where one of the coordinators of the stuttering program arranged for space to be used for the day.

I drove over to Boston from Albany, NY where I live. It was about a 3 hour drive, and most of it, both to and from, it rained. It even snowed a little on the way back, which I was totally not ready for in October.

I had no expectations of the one-day conference, except that I was looking forward to spending the day with other people who stutter. And what better day for this than International Stuttering Awareness Day (ISAD) which is recognized every October 22. I met lots of people from the Boston area as we spent the day together in workshops and at lunch. I really enjoyed hearing so many Boston accents!

The first workshop of the day was on self-advocacy, something that is near and dear to my heart. I believe that everyone who stutters should advocate for themselves because no one else is going to do it for us. Jess facilitated this workshop by sharing some scenarios she created to use as discussion points. Our group only got through 3 of 8 scenarios because we all shared our experiences with advocacy – both what we found easy to do and what may be more difficult.

The next workshop focused on choosing activities that we could participate in that would stretch us out of our comfort zones or be a real peak performance for us. People shared what they were willing to try when they got back home. One guy said that he wants to get up the courage to ask a question at a meeting that usually is comprised of 200 people. He wants to be able to do that with no shame of stuttering openly. Another guy said he wants to check out a Toastmasters meeting. Another guy said he wants to make more phone calls than always relying on the internet or email.

The last workshop that we attended was the screening of the short film “Stutterer.” We watched it as a group – adults, parents and SLP students. I had already seen the film but delighted in seeing it again with people who were seeing it for the first time. We had a great discussion about whether we thought the film portrayed stuttering realistically. We also talked about how it made us feel and what we thought about the ending, which had a surprise twist.

It was a great day of coming together, sharing experiences and supporting each other. We wrapped up with watching a video the kids had made about stuttering and how they want to be treated by others when they are stuttering. The kids were amazing with their open and shame-free stuttering.

The Boston NSA chapter leaders Sarah and Jess did an amazing job putting this conference together. I was very glad I went and got to spend time with other amazing people who stutter on International Stuttering Awareness Day.

On the last night of improv class, one of my classmates came up to me to talk for a minute. She had a sheepish look on her face, as if she was wasn’t sure how I’d react to what she was about to say.

She said, “You know, how, like you stutter” and she had her hand cupped over her mouth as if she didn’t want anyone else to hear it. She went on to say, “I have a friend who stutters too and I really think you two should meet. She’ll be here tonight.” I said, “OK.”

Well, we got busy with the show and performing and all and before we knew it, the night was over and I was saying my goodbyes. My classmate mentioned that I hadn’t met her friend. I told her I had to get going, as I was driving my mom home. She said maybe another time then, as she was sure we’d hit it off.

I laughed to myself. How many times has this happened to you? That someone wants to introduce you to someone just because you both stutter. Like we’d be fast friends because we have stuttering in common.

Note to readers: just because two people stutter doesn’t mean they will be best friends. Just like with anyone else, you may not like each other, one might rub the other the wrong way or maybe one is a jerk, (not me of course!) despite being a person who stutters.

It is true that people who stutter definitely have something in common, but it doesn’t automatically mean they will hit it off and become best friends. I just think it’s funny that people automatically want to introduce me to someone else who stutters because they’re sure we’ll hit it off.

This has happened to me several times. What about you?

Last month, I wrote about how I had joined a beginners improv class. I was nervous and apprehensive at the beginning of the class, for several reasons. I had zero experience with improv and was afraid I’d make a fool of myself. And I worried about how my stuttering would play into it.

Well, last week I completed the class and actually performed with my group in front of a live audience, after just four weeks of learning and practicing. Guess what? It was fun and I really enjoyed it.

I had disclosed that I stutter in the first week of class, so got that out of the way quickly. Then I just went with the flow and let myself be creative and have fun with my classmates. My worry about making a fool of myself was unfounded because that’s exactly what you’re supposed to do in improv.

Here’s what I learned in improv. You  don’t have to be funny to do improv. You just have to be open to what a partner says and respond and build on what they’ve said. One of the rules of improv is “Yes, And.” This means to agree with your partner and add to what they’ve said, whether or not it makes contextual sense.

I also learned that I have the ability to be a deep listener, which is an essential tool of improv and of life. I think stuttering has taught me to be a great listener, because I used to always prefer listening to talking.

And I learned how to be more mindful and in the present moment, which is also helpful in all aspects of life. Being grounded means we can develop better relationships and we need that more than ever in today’s world.

The performance went great. Our group was called the “Slippery Alligator Udders.” We had a supportive audience who laughed and enjoyed our show. My initial nerves dissipated right away as I relaxed and leaned into the creativity and playfulness of our group.

I never thought I’d say this, but improv was good for me. it helped me get out of my head and enjoy something without worrying about stuttering. I’d recommend it for anyone looking to push out of their comfort zones.

I am looking forward to taking the 201 level class and seeing what I can create next.

 

PamEpisode 164 features Sofia Espinoza, who hails from Atlanta, Georgia, although Sofia is originally from Peru. Sofia works for the Centers for Disease Control (CDC) in Atlanta. She is an engineer and works in IT, implementing systems.

Sofia went into engineering because she thought it would be a field where there wouldn’t be much talking. When she began her Masters program, she saw it was much more interactive and would require talking and class participation. It was at this time that Sofia began researching support opportunities and found the NSA and Toastmasters.

She threw herself into both at the same time, as well as seeing a counselor. All of these things helped Sofia to graduate.

Listen in as we discuss covert stuttering, baby steps, shyness and anxiety, and the pain of stuttering.  We also talk about wearing armor to protect ourselves and how heavy that armor can be to carry around.

Sofia attended her first NSA conference this year, as it was held in Atlanta. We talk about her experiences and her favorite workshop.

The music used in today’s episode is credited to ccMixter.

PamEpisode 163 features Chani Markel, who hails from Teaneck, New Jersey. Chani just moved to NYC for a new job as a school-based speech language pathologist (SLP) with the NYC public schools. Chani also keeps busy with yoga and writing.

Listen in as we discuss the transformative experience Chani had with therapy which she sought out on her own when she was a senior in high school. This experience led her to pursue a career in speech language pathology.

We talk about the National Stuttering Association and the impact it has had on her life. The NSA has helped her both personally and professionally.

Chani also shares about her experience with starting a writing group, that combines writing about stuttering, communication and identity.

Chani offers words of wisdom for anyone who stutters thinking about becoming a SLP and offers to talk with anyone who’d like to explore this with her.

The music used in today’s episode is credited to ccMixter.

 

Well, I took a big risk and joined an improv class. I had heard improv was a great way to get out of your comfort zone, practice being in the moment and have fun.

My first class was this week. I had googled a few articles on improv so had a general idea as to what it was, but really had no idea what to expect when I walked into the classroom. I was nervous and excited at the same time. I was nervous about looking foolish in front of others and about how to handle the fact I stutter.

It was important for me to find a way to let my classmates know that I stutter so they wouldn’t be surprised when they heard me stuttering.

We started out with doing some warm-up exercises to get to know each other. They were a combination of saying our names and doing a fun action. Before we knew it, everyone was laughing and seemed somewhat comfortable. Turns out, I wasn’t the only one who was nervous.

We then moved into learning some of the basics of improv, like establishing relationships and places so that onlookers can get a sense of the scene you’re creating. We worked on collaborating with each other, using the improv strategy of “Yes, and.” This strategy has us agreeing with what our partner gives us and adding to it, forging onward with what we are given. In other words, much of improv is going with the flow.

At one point, the teachers wanted all of us to get to know one another, as our selves, not characters we were creating. We paired up and just talked to each other, asking questions to get to learn about each other.

My partner asked me how my summer was and if I had done any thing fun. Here was my opening to talk about stuttering. I mentioned that I had gone to Atlanta for a conference and naturally she asked what type of conference.

I told her it was the annual NSA conference for people who stutter and that I stuttered. She went with the flow and said that was very interesting. Everyone was watching our “introduction piece” so I advertised it to the group as well. After that, I felt more comfortable letting my stuttering out and just going with the flow.

I am really looking forward to seeing how this class goes. I’ve been looking for something to challenge me since finishing with Toastmasters and this definitely will be a challenge. I’ve been worried about the fact that I am not naturally funny and I’ve read that I don’t have to try and be funny. I can just be natural and work with classmates and think in the moment and work as a team and funny will naturally happen. I’m hopeful that’s true.

Wish me luck. We do a performance in front of an audience at the end of the class, live on stage. I’ll really be stepping out of my comfort zone and hopefully having a blast!

 

He-StuttersEpisode 22 of the very occasional male series features Chaz Bonnar who hails from Glasgow, Scotland. Chaz is 24 years old and is a dancer and freelance creative artist. He works with young kids building their confidence and self-esteem through dance.

Chaz believes that dance has helped him to express himself without words. He has been dancing – specifically breakdancing – since he was 15. Now he works with kids with the hope of offering them the same opportunities for self expression.

Listen in as Chaz shares what has helped him overcome his stuttering. He is a strong believer in the laws of attraction and feels that we have more control over our lives than we have been led to believe.

Chaz also talks about the importance of being completely honest with ourselves with regards to our speech and other areas of our life. And finally, we hit on social anxiety, which has many parallels to stuttering.

Chaz encourages listeners to reach out to him on social media if they’d like to talk with him about his ideas. Instagram: @chazbonnar Snapchat: @chazbonnar Twitter: @ChazB

The music clip used in todays episode is credited to Dano Songs.

PamEpisode 162 features Alexandra D’Agostino who hails from London, Ontario, Canada. Alex is 23 years old and is going into her last year of university where she is pursuing a double major of psychology and anthropology.

Alex is considering a Master’s degree in either music therapy or nursing when she completes her undergraduate work. She loves traveling and music, playing seven instruments and singing in her university choir.

Alex is very actively involved in the stuttering community. She is a member of the Board of Directors of the Canadian Stuttering Association (CSA) where she is part of the social media team. She runs the CSA’s Facebook page. The CSA is holding their annual One Day conference on October 22, 2016. Both Alex and her mom are running workshops.

Alex has also attended conferences of the National Stuttering Association (NSA) since 2011 when she was 18. Her parents have come with her to the annual NSA conferences. Alex served on the NSA’s Teen Advisory Council for three years.

Listen in as we discuss growing up with a stutter, being bullied and speech therapy experiences. We discuss how cyclical stuttering really is and how it affects our life differently depending on what stage of life we are in. Right now, Alex is happy with her speech and feels she has accepted her stuttering.

This was a wonderful conversation with a wonderful young woman who wants everyone who stutters to know that they are not alone. Music used in today’s episode is credited to ccMixter.

 

Stuttering_Pride5-300x160Every year, the stuttering community celebrates International Stuttering Awareness Day on October 22. It’s a day for people across the world to recognize stuttering, educate others who don’t stutter and raise awareness of an often isolating difference.

For the last 12 years, the community has further celebrated by participating in a three week online conference about stuttering, hosted by the International Stuttering Association (ISA.) The conference is held from Oct 1-Oct.22 and can be found linked to the ISA site.

This year, the theme of the conference is stuttering pride. Yes, we can take pride in the fact that we stutter, that we’re part of a huge community that empowers each other and that can take responsibility for educating others about stuttering.

The conference needs to hear from you, people who stutter, loved ones of people who stutter and people generally interested in the stuttering community. The conference is seeking submissions of papers, audio or video around the theme of stuttering pride. Specific information can be found here at the ISAD section of the ISA site.

Won’t you consider writing something about your stuttering experience? Or sharing an audio or video message? It can go a long way towards the goal of educating others and creating a world that better understands stuttering.

Last week I had a wonderful opportunity to speak to kids who stutter at a stuttering camp. The director had invited me to meet with the kids, ages 8-12, via Skype. Before my talk, the kids explored this blog and my podcast and prepared some questions.

The goal of the week was to get the kids talking about stuttering, to gain confidence and to learn how to create their own podcast.

My chat with the kids was great. They asked about how I feel when I stutter, if I ever get nervous when talking in front of people and what I’ve done to get comfortable talking. We had a real back and forth conversation and we all learned from each other. The kids had never met an adult who stutters. I think they thought it was cool!

Later in the day, the director emailed me. The kids were asked to reflect on their day and several said my talk was a highlight. One kid drew a picture to illustrate what the room looked like when I was talking to them via the computer.kids listening to Pam

Later in the week, the kids learned how to create a podcast and they did several, on all kinds of creative topics. They also presented on the last day to their parents and SLP students about facts on stuttering, what they learned during the week and what they’re thinking about for the new school year.

This was a unique opportunity for these children. They focused on talking and having fun and gaining skills and confidence. I was happy to have a small part in the week.

I just recently had the below post published as an article on The Mighty, which is a site that features stories about all kinds of disabilities and differences. I am pleased to have my writing featured on another site, as hopefully it will raise awareness about stuttering to people who don’t stutter. You can see the article here, titled “Why It’s Important To hear Other People Who Sound Like Me.”

For the longest time, I hated the sound of stuttering. I hated to hear myself stutter. I thought I sounded choppy and unnatural, and always imagined the bad things a listener was thinking about me. I hated to have to leave a voicemail, as I didn’t want someone to have a recording of me stuttering. And I hated to have to record my own outgoing voicemail message. I remember re-recording my voicemail message about 20 times until it was perfect, without one syllable of stuttered speech.

I did not want to hear other people who stuttered because it reminded me of me and how I sounded.

I hated to hear characters who stuttered in movies. I remember getting red-faced and cringing when I heard the stuttering lawyer in the movie “My Cousin Vinny.” The character seemed to be created to get a laugh and it was a demeaning and demoralizing role. I did not identify with this character, nor the characters in “Primal Fear” and “A Fish Called Wanda.”

But when the movie “The King’s Speech” came along in 2010, I felt a little differently. By then, I had come out of the covert closet and stuttering openly. I was OK with it. I was actually kind of proud to hear a main character in a movie who stuttered realistically and wasn’t solely there for comic relief. I could relate to the stuttering in this movie, even though it was a male (as have been most of the characters who stutter in movies).

Something was changing within me. I was reaching the point where I enjoyed the sounds of stuttering. In 2010, I started a podcast called “Women Who Stutter: Our Stories.” I created this to give women who stutter a place to share their story and hear other women who sound like them stuttering naturally and openly. I made it a goal to interview women from all over the world, and have so far spoken with women who stutter from 32 different countries.

I like hearing the stuttering with different accents. I like hearing the cadence of a woman’s voice that stutters. I like how I sound on the podcast – something I never believed would be possible. How could I like something I had so vehemently hated for such a long time?

I have heard from friends that have heard me on the podcasts that I have a “radio voice.” Me, who stutters, actually has a nice voice. They’ve said it’s easy to listen to, even with the stuttering.

I have heard from listeners to the podcast that many feel grateful to listen to other women who stutter because it helps them feel less isolated. Stuttering can be lonely, especially when you don’t know someone else in person who stutters. That was me until about 10 years ago. I had never met another person who sounded like me. I grew up thinking I was the only one who stuttered and spoke with broken speech.

I just recently returned from the annual conference of the National Stuttering Association, which was held in Atlanta in early July. There were over 800 people who stuttered at the conference, from all walks of life and different parts of the world. The event was a joint venture with the International Stuttering Association. During the day at workshops and at night in the hotel lobby, I heard so many stuttered voices blending together into a wonderful symphony of sounds. It was music to my ears.

Finally, I have realized I like the sound of stuttering. It reminds me of me, that I am not alone and together our voices are strong.

PamEpisode 161 features Lynne Mackie, who hails from Edinburgh, Scotland. She presently resides in Newcastle, England where she is doing an internship for a mobile application for people who stutter. Lynne is a student who is finishing up her Master’s degree in Information and Library Studies. She also loves drama and all sorts of media.

Listen in as we talk about advertising, covert stuttering, taking strength from other people, the recent joint NSA/ISA conference and so much more.

Lynne talks about how successful advertising has been for her in university and with friends. She talks about letting listeners know what she prefers, and that what she says will be worth the wait.

We talk about the situation for people who stammer in Scotland and the rather new Scottish Stammering Network, of which Lynne is Vice Chair. Lynne also runs the Edinburgh support group.

Lynne applied for an internship for people with disabilities. She learned that Newcastle University had wanted to develop a mobile app for people with speech impediments and Lynne was asked to head up the research into the app for stammering. The goal of the app is to help people boost their confidence in everyday speaking situations.

We wrap up this great conversation talking about Lynne’s experience at the recent conference. Music used in today’s episode is credited to ccMixter.


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© Pamela A Mertz and Make Room For The Stuttering, 2009 - 2025. Unauthorized use and/or duplication of this material without express and written permission from this blog’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to Pamela A Mertz and Make Room For The Stuttering with appropriate and specific direction to the original content. Same protection applies to the podcasts linked to this blog, "Women Who Stutter: Our Stories" and "He Stutters: She Asks Him." Please give credit to owner/author Pamela A Mertz 2025.
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