Author Archive
Road To Empowerment- Episode 45
Posted on: February 10, 2011
Episode 45 features Perla Ernest who hails from Mexico, by way of the UK, Saudi Arabia, and Brunei. She is 23 years old, British/Mexican, and has a history of covert stuttering, except when she couldn’t hide it! Today, Perla views herself as a recovering stammerer.
Perla is an ambitious young woman. She wants to use her years of experience abroad to start her own business of cross-culture training. She sees a need to teach multi-cultural norms and differences in a global business world.
Perla and I were introduced by Maria McGrath, featured in Episode 38. Perla shares how the McGuire therapy program changed her life. Perla explains many of the basic tenets of the McGuire program, including breathing and voluntary stuttering.
Listen in as we discuss career goals, communication and covert stuttering. Perla tells some great stories about the elaborate avoidance techniques she used to keep her stuttering hidden. Perla poignantly shares the story of how the mother of an ex-boyfriend who referred to her as “Perla the Stammerer”, and how that jolted her out of her belief that she had hidden her stammering successfully.
We also discuss inspiration, empowerment and leadership. And we talk about rock bottom and acceptance. Perla hopes to bring the McGuire program as an option to people who stutter in Mexico.
Credit for the podcast safe musical clip”Scott Waves to April With Salty Grace” goes to ccMixter.
Feel free to leave comments for Perla (or me). Feedback is a gift!
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Last night I got a call from a professor from an elite university here in my area. She is teaching a graduate level physics class which is just getting underway for the semester. One of her students is from China and is pursuing his graduate degree in engineering.
The professor shared with me that he has a severe stutter. She says she talked with him about it and he told her that there is nothing that can be done for him. She wanted to find some resources to educate herself and to pass on to him, if she senses he would be OK with that.
She told me on the first night of class, she partnered students up in pairs for introductions, and she purposely paired herself with the student who stutters. As she told me this, her tone seemed to imply that she thought she was protecting him. Each person in the pair had to introduce the other.
When the professor introduced this student, she told the class that he stutters, that it is nothing to fear or shy away from, and that it will be an expectation of the class that he participate as often as everyone else and that patient listening would be the norm. She asked me if I thought she did the right thing.
My immediate reaction was, Yes, if he was OK with it. I asked her, “How did he seem to react to that? Was he embarrassed?” She said no – he seemed fine with it, maybe a little even relieved.
I then said that I thought it was great she was taking the initiative to make it OK to talk about. I shared with her how I felt in college, when I was presenting and felt so humiliated, and no one said anything, just didn’t look at me and looked liked they pitied me. I told her I would have much rather been in an open, supportive atmosphere, which she is obviously trying to do for this student.
She asked me for resources, specifically if I had any experience with therapy. I shared with her what was available in the area, and explained my take on fluency shaping and stuttering modification. She asked specific questions about both, and I could hear her writing this information down. (Smile!)
I also gave her some information on self-help and support, and some web resources, again realizing she was writing all of this down. She even asked md if there were any good books that I could recommend, so she could educate herself, and in turn, her student. I gave her information on Van Riper’s and Guitar’s stuttering textbooks and Jezer’s memoir about his life experiences with stuttering.
I was really happy this woman called and I was able to answer some questions. She had seen my name affiliated with a newspaper article I had written and with an upcoming workshop I am doing at our community library.
I was also impressed that a university professor took the time and showed an interest in educating herself to better help a student.
What do you think? Do you think the way she introduced the issue of stuttering to her class was appropriate?
Facing The Monster – Episode 44
Posted on: February 1, 2011
Episode 44 features Anna Margolina, who hails from Redmond, Washington, by way of Russia. Curiousity compelled me to find Anna and “hear” her story. Let me explain!
I found the January 2011 issue of Toastmasters Magazine in my mailbox two weeks ago. The headline “From Stuttering to Public Speaking” on the cover grabbed my attention immediately. I flipped open to the article and saw five people profiled.
They were all successful Toastmasters who also happen to stutter. Four of the five profiles were men, one of which I know – Russ Hicks from Dallas, Texas. That was pretty cool, but I didn’t want to know more about Russ (sorry, friend). I wanted to know about Anna!
I was drawn to “her” story, because women who stutter are practically invisible in media, and here she was a Toastmaster and featured in a magazine. There was no personal contact information provided for Anna, but her Toastmaster club name and city was noted. I knew that was enough for me to find her!
I found her club on the Toastmaster International website and sent an email to the club contact. I asked if they would forward a message along to Anna. They did, Anna responded, and we connected. Anna was happy to share her story and voila, here we are.
Listen in as we chat about acceptance, negative self-talk, and positive change. Anna demonstrates “blocking” and how voluntary stuttering helped her face her monster. We also discuss Toastmasters, of course, John Harrison on Redefining Stuttering and Neurolinguistic Programming.
This episode is an absolute treasure trove. We dive into everything. This is the link to the article on “From Stuttering to Public Speaking” which only scratched the surface and fueled my fire to “meet” her and hear her story.
Anna also happily shares a video of one of her speeches on stuttering. You have to see this! She’s great!
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With all of the media attention and buzz surrounding the movie “The King’s Speech”, I wondered why there was no coverage in my area. We have a local college with a 40 year history of working with people who stutter. And the College of St Rose has an affiliated chapter of the National Stuttering Association as well.
So, I emailed one of the popular local anchor/reporters, told her a bit of my story and shared that I have a unique perspective on the experiences of women who stutter. I asked her if she would be interested in doing a story. She responded the next day, saying she would love to, and we set a date for a week later. Wow!
On Friday morning I welcomed Elaine Houston and her camera technician, Jesse, into my home. It was exciting and surreal at the same time. Elaine and I chatted while Jesse transformed my living room into a studio, complete with bright lights and lots of cameras. And then we got down to the business of talking and stuttering and talking about stuttering.
Turns out, Elaine had not even seen the movie. We were not going to talk about “The King’s Speech”. I wasn’t fully aware of this, but the reason that Elaine jumped at the opportunity to hear this story is that she is passionate about women’s issues. She was excited about the podcast highlighting women who stutter telling their stories. She does a weekly segment called “Today’s Women” which airs on News Channel 13 which is also included on the station’s website.
So, we discussed the “often not talked about” issues of stuttering, including the emotions and vulnerability, and how I have been affected personally and professionally. We talked about my journey,why I started this blog and how the women’s podcast morphed from there. Elaine was really interested in the women I have talked to, their hopes and dreams, and how stuttering does not limit anyone from living life fully.
Elaine had this huge, bright, enthusiastic smile the whole time we were chatting. Her passion is obvious, and she shared with me about her visit to Africa. She is working on a documentary about the lives of women around the world. I was telling the perfect person about my journey. And what I have learned from being brave enough to start talking to women all over the world.
We spent over 90 minutes together, taking lots of pictures and talking about everything. Especially about the powerful stories of women who stutter and how my life has been enriched simply by being part of this. I was grateful to have this opportunity to tell this story, and open up a conversation about stuttering from the women’s perspective.
Funny how things happen, huh? I have been so empowered by inviting women to share their stories. Elaine has had the same experience. Check out the book she wrote, The Friendships Between Women.
Things happen for a reason and usually at just the right time.
Letting Go Of Fear – Episode 43
Posted on: January 27, 2011
Episode 43 features Elaine Saitta, who hails from Seattle, Washington. She has been an active member of the National Stuttering Association (NSA) for many years. She has held several NSA positions such as Chapter Leader, Regional Chapter Coordinator, Board of Directors member, and Executive Director.
Elaine is a SLP in the Seattle school system and also works in private practice with children who stutter. She coordinates a teen support group as well as youth and adult workshops locally and nationally.
She believes in being open about her stuttering and educating others. But that wasn’t always the case! Like many people who stutter, Elaine was covert for a long time. Even though her stutter was mild, she was always very embarrassed and felt shame. She shares that she didn’t have the tools to talk about stuttering and her feelings.
Listen in as we talk about how and what changed for Elaine. Meeting other people who stutter had a profound affect on her perspective and her very sense of self. Elaine also shares “the conversation” she always wanted and needed to have with her dad. And she talks about the journey and how she arrived at acceptance.
We wrap up with how being more open to life’s experiences in general can broaden one’s life. I prompt her to share her recent solo journey to China and how letting go of fear enabled that. How powerful those four words are – letting go of fear!
Speaking of that, Elaine was recently featutred on NPR in Seattle to raise awareness on stuttering! Check it out here!
Feel free to leave comments or just let Elaine know what a great job she did. Feedback is a gift!
Credit for the music clip “Echoed” used in this episode goes to ccMixter.
What Happens When They Forget?
Posted on: January 24, 2011
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I had an interesting conversation Sunday with a friend. She wondered out loud what will happen when the attention surrounding “The King’s Speech” dies down and mainstream forgets about the movie. They will, you know.
By the end of the year, people who don’t stutter won’t even remember the movie. Attention will shift to the slew of movies that are always released at the end of the year, just in time for Academy Award buzz.
My friend mentioned that someone told her that right now, the movie almost makes it “cool to stutter”. A year from now, we will still have to worry about sending the message that it is “OK to stutter”.
In this fast paced world, people’s attentions spans are about as long as my pinkie-finger. We move from one thing to the next at lightening speed. I even have trouble these days recalling what I said an hour ago, unless I write it down. And then I can’t always even read my hand-writing any more. And speech recognition software doesn’t work well if you stutter! I tried it years ago!
So what do we do? How do we keep a reasonable focus on stuttering and remind the world that we are here, competent and able?
Another friend posted on Face book that the DVD and Blue Ray for “The King’s Speech” will be available on April 29, 2011. Who needs to know that? Who will buy the DVD? My bet is that most sales will be to us – people who stutter and people who care about people who stutter.
So we will need to continue educating others, raising awareness, talking about stuttering openly and advocating for ourselves. That includes keeping our blogs and podcasts alive and current, encouraging people who stutter to step out from behind the shadows and do everything we can to eliminate bullying of kids who stutter and workplace discrimination of adults who stutter.
That stuff will still happen. Kids will be teased and adults will be passed over for opportunities because people just don’t understand something outside of their “own world” realm.
Reminds me of a comment I saw posted on one of the stuttering email groups a few months ago. A woman asked, “are there any women who stutter in high power, visible,management positions?” Like CEO or Executive Director of known businesses?
We hear about Jack Welch of GE (20 minutes from me) and John Stoessel of 20-20 News (but he records his broadcasts and edits out stuttering). And here in my community, we have a male Mayor who stutters. But where are the women who stutter?
That’s why we will still need to keep talking and making our voices heard long after this movie is forgotten. For the kids who come behind us, and for the women who stutter openly that are not visible in those high level positions.
I recently met a woman who stutters who is her company’s Chief Branding Officer and the company is very successful. Hopefully, we will hear her story soon.
But in the meantime, we can’t complacently ride the coat tails of this movie. We who stutter every day and make room for it in our lives will have to be stronger and louder than ever to keep teaching the world that we are OK and what we have to say is important.
What do you think?
I Am Enough – Episode 42
Posted on: January 21, 2011
Episode 42 features Nora O’Connor, who hails from Los Angeles, California. Nora is a Licensed Clinical Social Worker. She presently works as a therapist in a residential drug treatment program for male parolees.
Nora shares how she always wanted to be in the helping profession. But she thought for a long time that being a social worker with a severe stutter (that she did not accept) was a real oxymoron. It’s a good thing for us that Nora worked this out, because as you will hear, she is a real gift.
Nora shares glimpses of her very personal journey with addiction and the dark depths of hopelessness. She turned to alcohol and other drugs to deal with her stuttering, and has now celebrated 15 years in recovery. She strongly believes that this journey has influenced every aspect of her being. It has also helped her find the beautiful, strong woman Nora always was, just waiting to emerge.
Listen is as Nora talks about what authenticity means to her, and how she discovered that bringing her whole true self to the table is very inviting to others. We also discuss finding acceptance, and how Nora wants to move beyond that, to just “being”. Not being a woman or person who stutters, but just being and breathing. (By the way, check out Nora’s blog, Just Breathe and Stay Human, for more on that).
We also talk about the important people in her life, and how Nora is excited to discover the opportunities that await her in the next decade. I always look for a key phrase or thought that a woman who is telling her story shares with us. This was hard, as Nora shares many gems. But in addition to the apt title of this episode, I loved how Nora refers to stuttering as “humility in disguise.”
Nora also co-wrote a paper on Self-Image Issues as part of a panel presentation on Women Living with Stuttering for the 2002 International Stuttering Awareness Day (ISAD) on-line conference, which can be found on The Stuttering Home Page, an absolute wealth of information on stuttering.
The podcast safe music clip, “Today Then Tomorrow” used in this episode is credited to DanoSongs.
If Nora’s story touches you (as it did me), be sure to leave a comment. Feedback is a gift.
He Too Will Have A Voice
Posted on: January 20, 2011
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I got this letter from a gentleman who read the print newspaper article I had written about The Kings’s Speech movie. I was surprised to hear from someone in Pennsylvania, as I did not know my article had been printed outside of the Albany NY area.
I share this to show that we have no way of knowing that what we do can impact others. And also how touched I was to learn he has a three-year old grandson in therapy for stuttering.
Dear Pam:
The piece that you wrote for the Albany Times Union, “The King’s Speech” Puts Spotlight on Misunderstood Disability: Stuttering, appeared in our local paper, The Sunday News in Lancaster, PA. It caught my attention because I am a stutterer. It brought back some old feelings from the days of my struggle with my speech. I first became aware of my “handicap” when I was 12 and in sixth grade.
Jumping ahead to Penn State at 19, my sophomore year, I met a fellow stutterer in Speech 101, a required course. He introduced me to the Speech Clinic at PSU. I attended therapy sessions through my senior year. The “graduation” effort was to address a large class of students on a topic I had chosen. It was a big step toward liberation. Some people accuse me of not shutting up since.
I still stutter/stammer occasionally but I get past that pretty quickly. I graduated with a degree in forestry (I could live in the woods and hide from people), began a program in rural sociology, served two years in the army, completed additional credits in secondary education and earned a certificate in education and became a science/health teacher. I continued on and got my Masters Degree and became a counselor in secondary education, sometimes call a guidance counselor, a term I dislike.
My experiences and interests led me to become a high school career counselor. I was responsible for establishing career development centers in four schools districts for which I worked in Delaware, New Hampshire and Pennsylvania. I began my career in 1960 and retired after 40 years in 2000. I volunteered as an aid in the Career Development Center in PA after I retired.
This year at 77 I finally hung up my last life and career rainbow.
Three things prompted me to write to you: first, the title of your piece; second, your last name and its similarity to mine; and third, the fact that you are a career counselor. I am interested in hearing how you arrived at your destination.
Coincidently or otherwise, my three-year old grandson is in therapy for stuttering. He too will have a voice.
I wrote back to this gentleman and shared how I arrived at my destination of career counselor, and he shared a little more about himself.
It is always such a nice surprise to hear from someone unexpected that shares stuttering in common and feels comfortable enough to share it with a stranger. Proof that we never know who we may impact on a day-to-day basis. Our words and actions often have a farther reach than we know. It is nice to acknowledge that, and thus, be acknowledged.
Why It Matters – Episode 41
Posted on: January 17, 2011
Episode 41 is a departure from the usual format of this podcast. A woman of strength and courage, Irina, whom we met in episode 16, takes the microphone and the lead and invites me to tell some of my story.
This felt strangely awkward, but I was so glad that Irina was the one asking the inviting questions. We have become friends and share a lot in common. We had to do the Skype session twice, because the first time we had such a poor connection between New York, USA and Burgas, Bulgaria.
I hail from Albany, New York and have been “out” about my stuttering for about four years. My whole life changed in an instant in 2006, when I was fired from a job due to stuttering. That rock bottom moment helped me find resources and support, and my voice. Turns out, I always had a voice, but just didn’t know it.
Listen in as I share what it has been like for me going from “covert to overt”, how stuttering has affected me both personally and professionally, and how I really am not the same person I was just four short years ago. Irina invites me to share how and why I started this unique space for women who stutter, and how this has changed me as well.
I am proud of my journey and have no idea where it may take me next. I look forward to whatever it may be. And I am grateful for what I have learned from the strong, beautiful women from all over the world I have met. My heart and soul has been touched by each of you. Thank you!
Credit for the podcast safe music clip “Fire Babies” goes to ccMixter.
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Women Who Stutter Have Different Brain Connections Than Men Who Stutter; Findings May Help Explain Why More Men Than Women Stutter – – ScienceDaily (Nov. 18, 2010)
I could not resist re-posting this article. My risk-taking friend Lori San Martin posted this link on Facebook and made reference to me in her comment. Lori mentioned that she participated in the clinical research for this study, at NIH in Bethesda, MD. So did I, way back in 2006.
Neither of us knew each other then, so there was no way of knowing this shared connection. Interestingly, Lori chose to post this link on Face book, hoping I would see it and her comment, “Eat your heart out Pam.” When I read the article, I recognized the lead author was the researcher conducting the trial when I flew to Bethesda that summer.
I volunteered for the study because I could. I was available, healthy and willing to help unlock any clues to the mysteries of stuttering, and particularly why women are a “minority within a minority.” Plus, they compensated you, and I had just been fired from my job for stuttering. I felt I could contribute somehow by letting interested researchers study my brain. Lori must have felt the same way.
I even went to Columbia University in 2009 for a similar study of different brain activity. Again, making sacrifices for the good and welfare of the stuttering community. (And it was a sacrifice indeed. I stayed with a friend overnight in his Brooklyn apartment with his wife and two cats. Suffice it to say, I am not a cat person).
Here is the content of the article! As Lori says, “Eat your heart out.” We already know women are special and unique.
According to new research, women who stutter show brain patterns that are distinct from men who stutter. Finding diagnostic brain markers that are unique to people who stutter could help scientists develop treatments that target those areas in the future.
The research was presented at Neuroscience 2010, the annual meeting of the Society for Neuroscience, held in San Diego.
About five percent of young children stutter, but up to 80 percent of them recover. Of those who don’t, most are men; about five times more men than women stutter. These new findings show one difference in brain connections that may explain the striking sex difference in chronic stuttering.
“Girls who continue to stutter past childhood may have greater deficits that are not overcome during development,” said lead author Soo-Eun Chang, PhD, of Michigan State University. “Knowing the sex-based differences in brain development that underlie stuttering may help us find sex-specific neural markers for it.”
Chang and her colleagues mapped participants’ brains using two imaging tools: functional magnetic resonance imaging (fMRI), which showed brain areas active during speech, and diffusion tensor imaging, which provided structural information on connections between brain regions. They tested 18 volunteers who stutter and 14 who don’t.
The images showed that speakers who stutter had fewer connections between the motor planning and execution areas in the left hemisphere of their brains, as well as increased connections between hemispheres. In addition, the women who stutter had distinctly greater connectivity between the motor and sensory regions in both hemispheres than men who stutter. These findings may indicate that the link between motor control and sensory functions may be abnormal in women who stutter.
“These results need to be replicated in young children to examine whether this is the case at stuttering onset or whether it later appears only in adult females who continue to stutter,” Chang said.
Research was supported by the Intramural Research Programs in the National Institute of Neurological Disorders and Stroke and the National Institute on Deafness and other Communication Disorders.
So, what do you think? Comments, thoughts, questions. Come on guys! Can there be discourse about this? Hmm?
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A covert stutterer posted this question on one of the email groups. It generated lots of discussion and opinions. Another covert woman asked how do we actually show our stuttering at a Toastmasters meeting and “let the cat out of the bag”. This is what I shared as a response, not realizing that I had remembered this so clearly.
One of the best topics for a person who stutters to give a speech on is stuttering. That’s how I desensitized myself when I joined 4 years ago. My first speech the – “ice breaker” – I told my stuttering story, complete with how I tried to hide it, faking it, how I pulled it off, how it made me feel, etc.
The “ice-breaker” is supposed to be 4-6 minutes. Mine was 15 minutes, because I got emotional and choked up, and did not think I could finish. There was this huge long pause – a wait, actually – and all eyes were on me. This was the first time I had ever told people I had been hiding stuttering all my life. I was fired on May 4, 2006 and I gave this speech on May 23, 2006.
While the room waited for me to compose myself, a funny thing happened. I could feel the energy in the room shift. No one was annoyed, no one was rolling their eyes, no one was being dis-respectful. In fact, I could feel most of them “willing” me to finish. I don’t think they were going to let me out of the room unless I finished.
No one said a word. It was utter silence for 1-2 minutes, which seemed forever, and I willed myself to plod along and finish. I swear I felt that energy pushing me to finish.
When I was done, they all clapped like they do for everyone as I walked back to my seat. By then, my heart was pounding and tears were streaming down my face. There was more silence, as everybody wrote little comments about how I had done and put them in a basket and passed them to me. Next, the person who had been assigned to be my formal evaluator stood up and gave his opinion of how I delivered my first speech.
As he spoke, fresh tears erupted, as I realized what I had just done. I had just done the scariest thing I could ever have imagined doing to a bunch of strangers. My evaluator, Jim (who became my unofficial mentor) stood at the lectern for a sec, then began his evaluation by uttering one word: “Bravo”.
He said he and every person in the room learned as much as they ever would that night about me, about my courage, my resilience, my desire to communicate, my writing skills and my spirit. He talked of things like wearing my emotions on my sleeve, risking being vulnerable, daring to be so personal in a first effort. He also reminded me of time limits, which I can laugh about now, and how I had started a journey that he hoped I would be compelled to finish.
People came up and hugged me after as the meeting got over, and I did not read the little slips till I got home. All of them said something similar – that is was one of the most inspirational first speeches they had heard.
A year later, I gave my 10th speech, and Jim was my evaluator again. He referred back to that night, and many of the same people were there. I still go over time a lot, I still get emotional when I share personal stuff, but that’s what makes for compelling speeches.
People want to hear things that are interesting. Even people who don’t stutter can relate to identifying fears, working to overcome them, doing things anyway, feeling struggle and triumph at the same time.
Lots of people in my club affectionately refer to “Pam’s first speech” as an example of what Toastmasters can do for a person.
In my remaining 9 speeches of the first level, I talked about stuttering twice.. One objective was to speak on something I had researched. So I spoke about the origins of stuttering, best estimates at causes, resources – including support and therapy. I demonstrated the different ways a person might stutter. That was easy. I knew how to stutter.
The other speech was on Voluntary Stuttering, as related to helping people get over fears. I related fear of water to a person gradually stepping in, getting their face wet, holding their breath, dunking in water, etc, and what a person afraid of heights might do. Then I explained how voluntary stuttering helps to break the fear someone may have of stuttering publicly. I had everyone try it with a partner and had them do repetitions on their names.
Tackling the fears we have at Toastmasters is as easy as talking about what we know best. When we talk about what we know best, its easy. We already know the material.
Sounds easy coming from someone who has already done it, but I will never forget how it felt when I made that first speech. My heart thumped, my chest heaved, my cheeks were warm, my eyes were moist. How it felt walking up to the front, how it felt walking back to my seat, how it felt watching everyone write those little feedback slips – WHICH I STILL HAVE – and how it felt to hear a veteran Toastmaster say in his evaluation that I had inspired him and others.
We all have a first time doing everything. Members of my club tell me all the time they still have their first comments slips, they still remember the anxiety, the fear, the relief, the PRIDE. Everybody feels it – stutter or not. Most people rank public speaking as the greatest fear, even over death. At a funeral, most people would rather be in the coffin than delivering the eulogy.
We all have to communicate in life. Toastmasters gives ALL OF US a place to practice, get feedback, and realize, that everybody has their own sweaty palms, dry throat, pounding heart, nervousness, desire to flee . . . . not just us.
Toastmasters has the potential to change lives. Check it out. Find a meeting near you and visit.
Doors Of Opportunity-Episode 40
Posted on: January 10, 2011
Episode 40 features Mary Rose Sevilla Labandelo, or Mary Lab,as she is known on Facebook, who hails from Vancouver, British Columbia, Canada.
Mary is the founder/coordinator of the Vancouver Support Group for Stutterers and has been a board member of the British Columbia Association for People who Stutter. She is presently a Pre-school teacher.
Mary has always enjoyed being around children, and finds she stutters much less when around children. She finds she has more control, when being in the “role” of teacher, and therefore, has more control over her speech. Mary discusses how she finds that “acting out characters” when reading to children really helps her!
Listen is as we discuss the impact of stuttering on Mary’s childhood and how its been different for her as an adult. We discuss disclosure, acceptance, and the value of using her own experiences to help others.
Mary shares how attending a conference of the Canadian Stuttering Association helped her finally embrace herself and drive her towards acceptance. Mary also discusses how she views her stuttering as different from the “stereotypical” image of stuttering.
The podcast safe music clip, “I’m Gonna Shine” used in this episode is credited to DanoSongs.
Please feel free to leave comments for Mary, or just let her know what a great job she did! Feedback is a gift, as I keep learning!
We Never Know Our Reach
Posted on: January 7, 2011
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I was so surprised and honored to receive a recent message from a woman in Brazil who had sent me a friend request on Facebook. Because I did not know her, I inquired who she was and why she was interested in connecting.
Ignes wrote: “I am the president of the Brazilian Institute of Fluency – IBF. I’m a speech pathologist specializing in the treatment of stuttering, however I’m not a person who stutters. This is my personal website: www.gagueiraonline.com.br. It is written only in Portuguese yet, but I plan to translate it into English and Spanish soon.”
“I really admire your work. Here in Brazil we use a video of you – in lectures and courses to educate teachers about what stuttering is and how to treat a person who stutters. I visited your blog and really enjoyed it. I forwarded the link to several people from the Institute and two colleagues in particular who are also founders of the IBF and women who stutter. They will probably write to you.”
“It is indeed a great pleasure to establish contact with you and be able to exchange knowledge.”
Now maybe I am just getting wimpy in my old age, but this really touched me. I did not even know that somewhere in Brazil, teachers are looking at a video of me talking to kids about stuttering so they would understand it and know how to best work with those children. The kids I talked to that day did not stutter. I was teaching them about it so they would not be afraid when they encounter someone who talks different and not laugh at someone who stutters.
What a powerful message this was for me when I read Ignes’ response. We never know who we might touch. We never know how what we do today may impact someone else tomorrow. I visited that middle school to talk to kids about respect for differences during National Stuttering Awareness Week two years ago and it is making a difference in Brazil today as well. Wow!
Moments like this remind me of why I keep doing this. Sometimes I don’t get any feedback and wonder if I should keep on writing and sharing my journey, my story. Thank you , Ignes, for reminding me that what we do does matter.
What people are saying!