Articles

I met Peter Holleley fourteen years ago, when running a Toastmasters Group for People who Stutter in Toronto. In his early 60s, he was older than most people attending the group. He liked to talk, as a lot of people who stutter do.

When Dimitri was a young boy growing up, his stutter prevented him from getting a word into many conversations. He would grunt with frustration and make a fist with his hand anytime his stutter would cut off his sentences.

Hello Canadian Stuttering Association (CSA) members and our wider community. I am your newest Employment Advocacy Coordinator. I am a life-long stutterer. While the severity of my disfluency has improved with the benefit of therapy, my stutter remains.  

My name is David Liu, and I’m joining the Board of Directors as the Conference and Event Planning Coordinator. Once I learn the ropes, I’ll be leading the planning and execution of the CSA’s Let’s Talk Events and annual conferences.

I am a person who stutters, and I’ve stuttered since I could first speak. When I was much younger, I was hardly even aware I had a speech disability. My parents assumed my difficulty speaking was just a phase I would grow out of, and I didn’t really think about my stutter at all.

I’ve been stuttering since I was 2. My mom says that she first noticed it when she got me a pink toy kitchen for Christmas. I was so excited, I couldn’t even speak.

According to the Oxford dictionary, the word “Stutter” is defined as: “talk with continued involuntary repetition of sounds, especially initial consonants.” Prior to 2007, if asked to define the above term, I probably would have replied with a similar re