Posts Tagged ‘International Stuttering Awareness Day’
Episode 169 features Yara who hails from Orange County, Southern California. Yara teaches second grade at a Waldorf school. She kind of happened upon this job, as it was not originally in the plan. Yara has a 12 year old daughter and loves chalkboard art.
Yara says she went from being in a band to now teaching little kids, singing songs every morning.
Listen in as we discuss covert stuttering and how Yara had always worried about stuttering, with everything. She got really good at coming off as fluent. She shares that for a long time she didn’t know that everyone wasn’t struggling to sound fluent.
Yara shares about her “aha” moment, how hard it is to have the conversation when telling someone she stutters and has been hiding it, and how a massive Google search helped her find stuttering resources. We discuss the NSA and how Yara would really like to go to a conference, how that might be easier for her than a small, intimate NSA chapter meeting.
The music used in today’s episode is credited to ccMixter.
Every 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.
My friends in the French stuttering community are launching a campaign to celebrate International Stuttering Awareness Day (ISAD,) which is today, October 22. Their initiative is to portray children who stutter in a positive and casual manner.
The initiative was launched by the mother of a child who stutters and quickly gained momentum with other parents. The French Facebook group plans to feature the children s’ stories on French blogs today and over the next few days.
I think this is a great idea and am so pleased to help “spread the word,” which is the theme of this year’s ISAD. What could be more positive and inspiring than children talking so matter-of-fact about stuttering?
Here is Rose, age 9, and her story.
“My name is Rose. I love drawing. My preferred colour, it’s turquoise. My best friend, it’s Cecilia. My preferred dish, it’s fajitas. And I stutter. It isn’t because I lack self confidence. It is not caused by a trauma. It isn’t my parents’ fault. I just stutter – it’s neurological”.
You’re right, Rose. We just stutter. Rose is beautiful and has so many interests. Help us spread the word.
I had the opportunity to speak on Saturday via Skype at the Irish Stammering Association’s annual National Stammering Awareness Day event in Dublin, Ireland. I was asked to be a keynote speaker during their full day conference style event and speak on the theme of this year’s ISAD, “Spread The Word – Educate, Cooperate, Communicate.”
I wondered what I could speak about that would best convey how I have spread the word about stuttering awareness. Purpose came to mind.
I remember when I attended my first FRIENDS conference in 2008 and I realized that stuttering can actually have purpose. FRIENDS is the association for young people who stutter. It is a parent driven group that is all about support for young people who stutter and their parents.
I learned about purpose after hearing parents tell me how happy they were that I had come to the conference and shared myself and stories with them. For the first time in many years, I realized that my stuttering could be bigger than just me. That I could use it to spread the word and educate others about stuttering, if I dared.
After that FRIENDS conference, I became a real advocate for stuttering awareness. I had articles written in the local newspapers, organized several stuttering events in the community and began visiting middle schools to educate kids who don’t stutter on what stuttering is and tied it into teasing and bullying prevention. Doing these types of awareness activities became bigger for me than my stuttering.
So, that’s what I spoke about at the Irish Stammering Awareness event on Saturday – purpose. How a sense of purpose can be bigger than you and how my desire to help others has kind of transcended my own stuttering.
I shared with the group about the advocacy activities that I do and challenged them to consider doing similar. It was a great experience, even with some technology disruptions. I felt honored to have been asked to share my story and to talk about purpose. Here’s a picture of me as we were just getting started.
The International Stuttering Awareness Day (ISAD) online conference is going on right now and can be found here.
I have a paper in the conference this year addressing the issue of whether stuttering is viewed as a disability. And who gets to make that call, the individual affected by stuttering or society?
I relate some of my experiences with talking with high school students who noted my stuttering as a disability even though I had never articulated it as a disability myself. I find it interesting that I’ve also had a boss who referred to me as having a disability when I don’t really consider myself disabled.
However, I have “ticked off” the disability box on applications and questionnaires because technically, stuttering is covered by the Americans With Disabilities (ADA) Act of 1998 and 2010.
I would love your thoughts on The Disability Question.
What do you think? Do you consider stuttering a disability? Who gets to make that determination?
Every year, International Stuttering Awareness Day (ISAD) is marked on October 22. It is a day when people who stutter all over the world participate in events and activities that raise awareness about stuttering and educate the non-stuttering public.
The International Stuttering Association also sponsors an annual online conference. From October 1 through October 22, a variety of presentations are available for people to read, watch or listen to, all with the goal of learning more about stuttering.
Both people who stutter and speech professionals contribute papers, audio and video that conference attendees can participate in and engage with the author. There is a discussion option where people can leave comments with the authors and get feedback or questions answered.
There is also an “Ask The Expert” section of the conference where speech professionals volunteer their time to respond to specific questions asked by anyone in the stuttering community or general public.
It is always a great conference, with enlightening topics from people who stutter themselves and professionals.
Don’t miss it! There’s something for everyone. The conference starts next week, Thursday October 1, 2015. I will have a paper in the conference this year. I hope you visit, read and leave your feedback.
This year’s International Stuttering Awareness Day (ISAD) online conference begins on October 1, 2013 and runs for three weeks through October 22, 2013.
Authors will present papers on a variety of topics relating to stuttering – attitudes and feelings, therapy techniques, research updates and personal experiences.
Presenters are a mix of people from the international stuttering community – people who stutter, family members of people who stutter, clinical therapists and scientific researchers. This is an exciting conference where different voices from all over the world are heard.
This will be a treasure trove of information on stuttering, and you will have the opportunity to interact with the paper authors and ask questions of professionals in the field.
Plan to check out the conference and plan to learn a lot. Spread the word!