Archive for July 2015
Don’t Ever Give Up – Episode 143
Posted on: July 23, 2015
Episode 143 features Samantha Temme-Raberding, who hails from Toledo, Ohio, where she lives with her husband and one “fur-child.” Samantha is a SLP, currently working in a skilled nursing home.
Listen in as Samantha shares how she chose her profession and acknowledges that she considered careers that would require the least amount of communication. Samantha also discusses her years of avoidance and the anxieties and fears that had to be later undone.
The majority of this episode focuses on Samantha’s journey toward becoming a SLP and the lack of support and even negativity she faced in graduate school because she stutters. She chose speech pathology because she thought she’d be more accepted than other careers, but found that not to be the case.
Samantha shares that it was “highly suggested” that she participate in intensive therapy while in grad school, which interfered with her clinical work. Comments were made to her such as, “It’s a shame this career requires so much talking. Have you ever thought of going the research route?”
She was also told that her disfluency would take away time needed to spend with clients, and that she ranked in the top 5 of most severe stutterers a professor had ever heard.
Samantha’s story of perseverance is compelling and inspiring. She wants to shout out Marilee Fini who was an amazing mentor and support through her grad school experience.
The podcast safe music used in this episode is credited to ccMixter.
Being Outed As A Stutterer
Posted on: July 13, 2015
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I’ll never forget the time at a Toastmasters meeting where we had a visiting “dignitary” with us to install new officers. It was the beginning of a new Toastmaster year and it is tradition in Toastmasters that a leader performs an induction ceremony.
I was so surprised when our Area Governor, whom I had not previously met, started speaking and I realized he stutters. In a way, I was kind of excited to realize there was another person in the room and in Toastmasters that stutters like I do.
I have often heard that people who stutter have a sense of radar when we hear other people who stutter. We can hear the repetitions, the breaks in speech, the blocks, all signs that a person stutters. I found myself hanging on this person’s every word as he completed the induction. He spoke slowly, deliberately, with repetitions and blocks.
After the meeting, I went up to introduce myself and congratulate him for a job well done. I also decided to disclose that I stuttered too, and that I was pleased to see a fellow stutterer do so well in Toastmasters.
Well, he became quite defensive and denied that he stutters. I remember this like it was yesterday. He got a little red in the face and adamantly let me know that he does not stutter. I felt foolish, as I had “outed” him when he clearly did not wish to be identified as a stutterer. I remember apologizing quietly and hurrying away, feeling embarrassed that I had embarrassed him.
Has this ever happened to you? How did you handle it?
Another time, I was at a networking meeting and heard a woman talking about her organization and clearly stuttering. I remember having self-talk with myself, again excited to hear another person who stutters in a professional environment and feeling conflicted if I should say anything to her.
The negative experience I had at the Toastmasters meeting still hung over me and I felt it was best that I not “out” another person. Disclosing that you are a person who stutters is a personal choice that needs to be respected, despite the overwhelming inside urge to yell, “hey, over here, me too. I stutter too.”
I remember being introduced at a Toastmaster meeting where I was to be a featured speaker. A fellow Toastmaster was responsible for introducing me and I thought he would share my usual bio which I had provided to the club, as we were all asked to. He ad-libbed a bit and added some extra things to his introduction of me.
He included that I was a proud stutterer and an inspiration to the club. I remember feeling embarrassed that he said that about me. There were people in the audience who were new and didn’t know me and now knew something about me that was very personal. It didn’t bother me that I stutter because I do and am open about it in Toastmasters. What bothered me was not being able to disclose it myself – I felt like I had been “outed.”
Now I knew what I felt like to be outed, even in a very well-intentioned manner and in a moment of pride. Ever since then, I have been very cautious about going up to anyone I hear stutter and saying anything, even the “I stutter too.”
It’s a slippery slope, outing someone as a stutterer or being outed yourself in a way you didn’t expect.
What do you think?
Where Stuttering Is Normal
Posted on: July 7, 2015
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I just returned from the annual National Stuttering Association conference, held in Baltimore, Maryland this year. I spent a week at the conference site, catching up with friends for a few days before the actual conference started.
To say I had an outstanding experience would be an understatement. It is hard to put into words what it is like to be immersed in the stuttering community for 5+ days. It is a time filled with connection, bonding, laughter and tears. Even though it had been a year since I had seen most people, we picked up as if it had only been a week. That’s the beauty of community.
It is also the time each year where stuttering is normalized. It is freeing to stutter openly with hundreds of people who share and get the otherwise isolating experience.
I was very involved in first timer activities at this conference, hosting the first timer’s orientation workshop and welcome luncheon. It was great to meet new people just coming into the community who have not been in an environment where stuttering is the norm.
Everywhere I turned, I heard people stuttering. It is almost magical to hear the different types of stuttering and to see people thrive in a patient, non-judgemental environment.
One first timer I met in person after having “met” him online in Stutter Social hangouts was Shane. He kept looking around in wonder and exclaiming how unbelievable it was for him to be there and to hear so much stuttering. He kept saying “thank you” to us “old timers” he met, as he was so grateful for the experience to be in a normalized, inclusive stuttering environment.
The sense of community at a stuttering conference picks you up, holds you up and surrounds you with love and support. People meeting each other for the first time hugged in greeting, as if they were old friends. Sharing something as personal as stuttering is an almost instant bond. Lifelong friendships are made at conferences and people eagerly look forward to the next one before the current one is even finished.
On my last day, I became overwhelmed with emotion as I was saying goodbye to new and old friends. As I hugged people, tears flowed and I got choked with emotion so strong it surprised me.
I guess I figured after 10 years of attending stuttering conferences, saying goodbye would be easier. Not true. I felt sadness and a yearning to stay with the community rush over me like waves crashing against a shore. It will be another year before I see most of these people and get to experience the magic of the stuttering community again.
Now, I am transitioning back into a world where fluency is the norm and I am in the minority. But I take the love and support of my stuttering family with me and I will remember the power of support and community. I can’t help but remember – it flows through my veins.
What people are saying!