Description:What happens when a speech-language pathologist also stutters? Some Stutter, luh! Welcomes Robert Kurliand, a trilingual SLP, neuroscience enthusiast and a person who stutters, who brings a mix of clinical expertise and personal insight on STUTTERING! Join us to know more about Robert’s refreshing perspective on stuttering treatment, emphasizing authentic communication, personalized therapy, and stuttering appreciation rather than just acceptance!Notes:In this thoughtful conversation, Robert talks about therapy that should focus on helping people who stutter become effective communicators, not necessarily fluent speakers. He values authentic communication and stuttering appreciation, suggesting PWS should celebrate the personal growth that comes from the journey. He also offers deep insight into the real-life emotional and psychological challenges faced by people who stutter. Robert emphasizes that PWS shouldn’t let their stutter define or limit their career choices. Robert believes the field of speech therapy is broad, so deep specialization in stuttering is rare but needed. He also highlights the emotional aspect of stuttering—fear, shame, avoidance—that is often more impactful than the physical symptoms and SLPs need better tools, frameworks, and support to address these emotional layers effectively.As the conversation follows, we see a deeper reflection on acceptance vs. appreciation, and how changing the language we use to describe our stuttering journey can lead to greater authenticity and peace. While "acceptance" is often framed as the ultimate goal in therapy, the word "appreciation," is more empowering and less pressure-filled.Many people who stutter develop ingrained habits of avoiding difficult words, situations, or speaking altogether. He points to the concept of "avoiding avoidance" that encourage confronting these strategies only when they interfere with saying something important or meaningful. Because when core identity or values are at stake, avoidance can cost more than the stutter itself. He also has powerful reflections on self-disclosure, authenticity, and why owning our stutter can bring us closer to others.Mary Wood Episode: https://www.youtube.com/watch?v=3sgj6jrZaMA#Stuttering #SpeechTherapy #Neurodiversity #SomeStutterLuh #SLP #MentalHealth #Communication #fluency #acceptance #stutteringacceptance #stutteringawareness #stutteringappreciation #authenticity
In this eye-opening episode of 'Some Stutter Luh!', hosts Paul, Laura and Greg welcome Molly Clarke, a speech language pathologist, to discuss the critical shortage of publicly funded speech language pathology (SLP) services in Newfoundland and Labrador. Molly shares her journey from starting her own clinic to becoming an advocate for more SLP positions in the public sector. She highlights the challenges faced by families and clinicians alike, such as long wait times, lack of resources, and the financial constraints on new graduates. Molly's advocacy work, sparked by hearing parents struggle with wait times on CBC radio, has rapidly gained media attention. The discussion also emphasizes the importance of public awareness, parental advocacy, and the need for systemic change to ensure children receive necessary support. The episode calls for action, inviting listeners to join in advocacy efforts, possibly through writing to MHAs (Members of the House of Assembly) or public protests, to bring lasting change to the SLP services in the province.00:00 Introduction and Host Introductions00:20 Meet Molly Clarke: Speech Language Pathologist00:56 Advocating for Publicly Funded SLP Positions01:52 Challenges in the Public System05:31 The Reality of Casual Employment07:50 Starting a Private Practice15:13 Ethical Dilemmas in Private Practice23:05 The Need for More Public SLP Positions30:14 Survey Results on SLP Services30:53 Challenges Faced by SLPs and Caregivers31:29 Restrictions on Public Criticism33:44 Union and Political Advocacy38:29 Parental Advocacy and Government Response41:54 Communication Disorders and Their Impact48:52 Call to Action for Change54:57 Upcoming Events and Final Thoughts#speechlanguagepathology #therapy #newfoundland #labrador #crisis #healthcare #stuttering #stammering #language #disabilitypride #disabilityawareness #advocacy #government #publicgoods #funding #currentaffairs #politics Original news storyN.L. speech therapist says she can't get a job, despite 2-year waitlists for kids needing helphttps://www.cbc.ca/news/canada/newfoundland-labrador/speech-language-pathology-nl-1.7551750CBC interviewhttps://www.cbc.ca/listen/live-radio/1-47-on-the-go/clip/16150836-speech-therapists-working-remotely-due-local-hiringReddit DiscussionN.L. speech therapist says she can't get a job, despite 2-year waitlists for kids needing helphttps://www.reddit.com/r/newfoundland/comments/1l53bwt/nl_speech_therapist_says_she_canx27t_get_a_job/
Description:When life blocks you, do you break or build? In this episode, SSL! Welcomes Dr. Satyendra Srivastava who has built a community of courage! His journey started as a four-year-old who was bewildered by his first stammer, to a covert teenager hiding behind English synonyms, and ultimately a visionary who turned private struggle into global advocacy. His decision to blog in 2008 sparked the Indian Stammering Association (TISA), a volunteer-driven movement teaching self-help techniques and transformed stammering from shame into shared strength. Tune in now and be inspired!Notes:Dr. Srivastava’s story begins at age 4, when he was unable to utter “half past three,” he discovered the bewildering reality of stammering. Over time, his sensitivity to criticism turned him into a “covert stutterer,” using English synonyms or withdrawing entirely to avoid the shame of blocks and repetitions.In adolescence, the emotional weight of a stammer—shame, guilt, fear—left him feeling alien to himself. He describes a “loss of self” when his primary identity hinged on fluency. Seeking solace, he immersed himself in solitary pursuits—reading, trekking, nature walks—only to emerge years later with renewed purpose. Dr. Srivastava believes true healing starts with radical acceptance—embracing life’s gains and losses, blocks and fluency, without ever resigning yourself.His decision in 2008 to write about his experiences marked the start of his recovery, transforming private struggle into public advocacy. TISA, the Indian Stammering Association, was born from Dr. Srivastava’s conviction that stammerers cannot wait for external solutions. TISA’s self-help groups teach core techniques—bouncing, prolongation, voluntary stammering, pausing—and encourage open sharing of stuttering stories to foster community and laughter rather than shame. Supported by volunteer coordinators and allied therapists, TISA offers an accessible, no-fee alternative that complements professional services. Recalling his first encounter with a professional fluency specialist in 2003—at a cost he deemed prohibitive—Dr. Srivastava investigated the real expectations and guarantees of therapy. He concluded that no one can promise a cure for stammering, unlike medical procedures such as cataract surgery. This led him to champion self-help: individuals can learn and apply many therapy techniques themselves, without incurring unaffordable costs or waiting for scarce specialists. By turning stammering into a “portal” for self-discovery and spiritual growth, TISA’s volunteer-driven network proves that collective courage and creativity can reshape vulnerability into strength!TISA website: https://stammer.in/home/#stuttering #stammering #disabilitypride #interview #stutteringacceptance #stutteringawareness #stammeringawareness @indianstammering
What if your greatest challenge became your greatest asset? In this compelling episode of "Some Stutter Luh!", David, a medical student at Queen’s University, shares how stuttering has shaped his path in medicine. He candidly discusses his journey through medical school interviews, learning to self-disclose with confidence, and adapting to new environments through trial and error. Let’s listen to David, who didn’t let his stutter choose his future!
David’s journey is a bold reminder that stuttering is not a barrier to excellence. He shares how owning his stutter helped him connect more meaningfully with patients and peers, and how it shaped his understanding of identity and empathy. David offers thoughtful commentary on the intersection of disability, performance, and professional identity. He describes how interactions with patients became a source of confidence and growth, and how embracing vulnerability can lead to personal empowerment. This episode highlights the power of resilience, self-awareness, and advocacy in navigating high-pressure environments. It serves as a meaningful resource for students, educators, healthcare professionals, and anyone interested in stuttering, inclusion, and communication diversity.
#stutteringawareness #stuttering #stammering #fluencyisnotaprerequisiteforsuccess#medschool #stutteringacceptance #disabilitypride #stutteringpride
Description:
In our third Persian episode in Some Stutter, Luh! podcast we welcome Ali Akbar Afzhuland, a 25-year-old engineer from Iran who has stuttered since middle school. He discusses societal misconceptions, the importance of awareness, and his experiences with different types of treatments. For anyone navigating a similar journey or seeking greater understanding of stuttering, this episode offers invaluable insights and encouragement. Join us in creating a more informed and accepting society where everyone’s voice is valued!
Notes:
In this episode, Ali Akbar reflects on how stuttering affected his life, especially in school and university, where a lack of awareness often made the situation worse. Ali Akbar recounts his initial attempts at self-treatment using traditional methods before discovering the Iran Stuttering Association. He emphasizes the importance of professional speech therapy, highlighting that he has seen significant improvements through this approach, despite still experiencing some stuttering. He emphasizes the need for society to treat people who stutter normally and highlights the impact of raising awareness to foster a more inclusive and supportive environment. He believes that stuttering has helped him become a reader, build meaningful friendships, and develop a more social life.
#newfoundlandandlabrador #iran #persian #podcast #stuttering #stutteringawareness #support #stammering
Description:
In this special episode, Carolina and Sang, a long-distance couple in their mid-40s who both stutter, return to Some Stutter, Luh! for their fifth episode and third Valentine's special. As they celebrate nearly six years together, they reflect on the importance of communication, trust, and mutual support in their relationship. They share insights into navigating love and life with a stutter, inspiring confidence and openness in others. Join us to explore how their six-year journey proves that love speaks louder than words, no matter how we communicate!
Notes:
Carolina and Sang, returning guests to Some Stutter, Luh! podcast, discuss how they nurture their relationship through honesty, emotional support, and choosing trusted confidants. Carolina shares how Sang became her rock during her father’s hospitalization, while Sang emphasizes frequent check-ins and humility in strengthening their bond. Their love story began at a National Stuttering Association conference, where years of crossing paths led to a meaningful connection. They go on to speak about love, trust, and emotional security in relationships, particularly in long-distance partnerships, highlighting the role of strong communication and sentimental keepsakes in maintaining closeness. They also differentiate between dating and commitment, emphasizing personal growth, patience, and mutual support. They encourage others not to give up on finding the right partner and to step beyond their comfort zones. Their story proves that love transcends words and speaks louder than any challenge!
Description:In this episode of Some Stutter, Luh! podcast, Ben Pahl shares his journey with stuttering—from childhood speech therapy to fully embracing his speech today. He highlights the role of community, humour, and self-acceptance in overcoming stigma. Let’s listen to Ben who considers his stutter as part of his identity that has made him more confident and even memorable!Please "Like" and "Share" our videos with others who might be interested in, or feel supported by our content. Thank you so much for your support!Notes:28-year-old Ben shares his experiences growing up with stuttering and undergoing speech therapy from elementary to high school. He reflects on the challenges of speech therapy, including limited resources and ineffective techniques, and the long journey toward self-acceptance. Ben emphasizes that stuttering is not something to be "fixed" but rather embraced, and fluency is not everything! Ben shares how finding a supportive community and embracing humour as a tool that lightens the situations have been transformative in his journey. His message is one of resilience and self-acceptance, inspiring others to see stuttering as a unique part of their identity.
Description: This episode of “Some Stutter, Luh!” podcast welcomes Alex Delgado, a writer and a person who stutters shares his story of transitioning from being a covert stutterer to embracing open stuttering. Listen to Alex’s story that highlights the importance of community, creativity, and a mindset shift in overcoming the stigma associated with stuttering. In this episode: 00:00 Intro 01:05 About Alex Delgado 05:06 Stuttering Support Group 08:27 The Interview! 12:38 Why did you decide to become an open stutterer? 20:55 Train Wreck vs Wonderful Experience of Stuttering 23:40 Alex and the Stuttering Support Group 25:59 Alex is a writer 30:03 Thank you! Notes: Alex discusses his ambition to be influencer on YouTube, where he provides advice and share experiences with other stutterers. Through self-discovery and connecting with others, Alex realized the importance of authenticity and made a conscious effort to embrace open stuttering. He now openly discloses his stutter in conversations and has found that this not only reduces his anxiety but also empowers him to face challenges with greater confidence. Alex advocates for reframing stuttering as a unique trait rather than a limitation. Referring to the book Beyond the Fear of Stuttering by Mary Wood, it is emphasized how a mindset shift, such as reframing "train wreck speaking experiences" as "wonderful moments of stuttering," can help transform one's perspective. Alex delved into the psychological dimensions of stuttering, emphasizing how emotional states like stress and anxiety can exacerbate fluency issues. He stresses the importance of building a supportive community and shifting the narrative around stuttering from one of struggle to one of strength and uniqueness. Alex considers his participation in the Stuttering Support Group on Discord a significant aid in embracing and accepting his stutter. He also shares his passion for writing, mentioning his current projects, including a mystery novel and an anthology of short stories. He has published some of his short stories online on Inkitt. Alex Delgado: https://youtube.com/@iamthenight2024 “Beyond the fear of stuttering” by Mary Wood: https://www.amazon.co.uk/Beyond-Fear-Stuttering-Journey-Self-Acceptance/dp/B09WLGHL2Q Shuttering Support Group: https://discord.com/channels/583077735212122114/@home https://www.reddit.com/r/stutter Alex's Writings: https://www.inkitt.com/alexdelgado
This is Part 2 of a two-part interview.
This episode of Some Stutter, Luh! podcast continues the conversation with Daniel Allen Cox, exploring his journey as writer of “I Felt the End Before it Came: Memoirs of a Queer Ex-Jehovah’s Witness.” and also a person who stutters. Daniel discusses his life experiences, including leaving the Jehovah's Witness community, his struggles with substance use, and finding his authentic self.
Notes: Daniel discusses leaving the Jehovah’s Witnesses, elaborating on the varied experiences of those who drift in and out of the religion. His journey was more definitive, marked by rejection due to his sexuality, which contrasts with others. He also critiques how certain groups, including Jehovah's Witnesses and Alcoholics Anonymous, use language to manipulate and control individuals, particularly through the concept of reliance on higher powers. He refers to “Cultish: The Language of Fanaticism” written by Amanda Montell to point out how different groups use cultish language. Initially hesitant to publicly read his work due to his stutter, Daniel overcame his fear with encouragement from friends, realizing that his authentic voice, including his stutter, is integral to his story. He prefers the term "queer" over "gay," as it better represents his identity and relationships. Daniel is touring his memoir, engaging in workshops, and editing books for others. He aims to continue writing, mentoring, and advocating for marginalized communities while merging activism with his art. Cultish: The Language of Fanaticism with Amanda Montel: • Cultish: The Language of Fanaticism w... You can buy her book here: https://www.amazon.com/Cultish-Langua... This podcast is brought to you with help from Memorial University of Newfoundland, the Newfoundland and Labrador Stuttering Association, and a whole team of volunteers behind the scenes. Additionally, thank you to @Student Linguists at MUN for their ongoing support of the stuttering community. We're always looking for exciting ideas and engaging guests, so if you or anyone you know has a great idea or would like to appear on the podcast, send us a message: info at somestutterluh.ca. As always, don't forget to hit the "Like" button, "Share" with people you know, and "Subscribe" so you don't miss any of our upcoming episodes. Interacting with the video in these ways helps YouTube know that you think our content is important and should be shared with people who stutter, the people who love them, and all the other allies to the stuttering community. #stuttering #stutteringawareness #podcast #stutteringsupport#newfoundland #newfoundlandandlabrador #communicationskills #communication #stutter
Episode Description In this first episode of Season 6, Some Stutter, Luh! welcomes Richard Holmes, a person who stutters and a speech-language pathologist. In this episode, Richard talks about his journey from his childhood speech therapy, to becoming a speech-language pathologist (SLP) himself. Richard reflects on how stuttering affected his self-perception, interactions, professional development, support groups, and speech therapy programs. Richard and Greg also question the word “fluency” - as known as the "f" word. Are you ready to learn more about how to “dance with a tiger”? This is Part 1 of a 2-part interview. Part 2 will air on November 5, 2024. Notes Greg and Richard explore the complexities of stuttering, including the psychological and emotional challenges that come with it. Richard shares personal experiences in therapy and his thoughts on the relationship between stuttering and self-acceptance. He stresses that most of the challenges related to stuttering are not visible or audible, but emotional and psychological. Richard believes fluency doesn't necessarily mean the absence of stuttering, but rather a smoother, more comfortable way of communicating. He appreciates the role stuttering played in shaping who he is and encourages others to live harmoniously with it, using it as a tool for self-awareness. As an SLP, Richard believes speech therapists should focus on the entire person rather than just the mechanics of speech. He advocates for a balanced approach that combines speech therapy with emotional acceptance and personal growth. - Check out Richard on YouTube: @walktalkforstutteringaware3080 - Check out Richard’s TedxUW talk: Stuttering and the Art of Mountain Biking: https://youtu.be/CQrZgsPsiRA?si=IuqCgQf5q4zLBm2V - Our website: https://somestutterluh.ca/ - International Stuttering Awareness Day(ISAD) is October 22, 2024. For more information, check out their website: https://isad.live/ This video has been brought to you with help from Memorial University of Newfoundland, the Newfoundland and Labrador Stuttering Association, and a whole team of volunteers behind the scenes, without whom this video would not have been possible. We're always looking for exciting ideas and engaging guests, so if you or anyone you know has a great idea or would like to appear on the podcast, send us a message: info at somestutterluh.ca. As always, don't forget to hit the "Like" button, "Share" with people you know, and "Subscribe" so you don't miss any of our upcoming episodes. Interacting with the video in these ways helps YouTube know that you think our content is important and should be shared with people who stutter, the people who love them, and all the other allies to the stuttering community. Happy International Stuttering Awareness Day!
Description:
This episode of Some Stutter, Luh! podcast welcomes Dr. Kelly Wright, an experimental social linguist and scholar-activist, who identifies as a Black, biracial, queer woman. She discusses her work on linguistic justice, focusing on how language ideologies impact marginalized communities, particularly Black individuals. Dr. Wright's key message is that language reflects our whole selves, and acknowledging this can foster more inclusive and understanding environments.
Notes:
Dr. Wright delves into how societal expectations around "standard" language use often exclude and stigmatize individuals who communicate differently. Her research examines how these biases manifest in various contexts, from professional settings to sports journalism, where Black athletes, for instance, are often described in animalistic or stereotypical terms compared to their white counterparts.
She believes individuals navigate multiple marginalized identities, such as being Black, queer, or a person with a disability, and these identities impact their daily interactions and opportunities. She highlights the importance of creating safe spaces where people can express their authentic selves without fear of judgment or exclusion. She advocates for recognizing and celebrating linguistic diversity, emphasizing that language is deeply tied to identity and should not be constrained by rigid standards. Dr. Wright emphasizes the importance of policy-driven research aimed at identifying and dismantling linguistic barriers, advocating for more inclusive practices at institutional and governmental levels.
Description: Some Stutter, Luh! Welcomes Dr. Hazel Price, a lecturer in English language at the University of Salford, and author of "The Language of Mental Illness: Corpus Linguistics and the Construction of Mental Illness in the Press". She shares her insights about the intersection of language, media, and mental health, emphasizing the critical role of linguistics in understanding and addressing stigma. Let’s listen! Notes: In her book, "The Language of Mental Illness: Corpus Linguistics and the Construction of Mental Illness in the Press," published in 2022, Dr. Price examined how UK news reports have shaped public perceptions of mental health over 30 years using a corpus of 45 million words. She aimed to bridge the gap between linguistic research and practical guidelines for language use in mental health contexts. In her book, she used methods from corpus linguistics and critical discourse analysis to analyze public perceptions and stigma related to mental illness. She discusses the importance of accurate language in media and its impact on public understanding and stigma. Dr. Price emphasizes that all health experiences are mediated through language, from recognizing symptoms to communicating with healthcare providers. She discusses the role of language in perpetuating stigma and the importance of linguistic research in health communication.
Description: Some Stutter, Luh! welcomes Kris Conlin who shares her personal experience with dyscalculia. She emphasizes the importance of raising awareness about dyscalculia and the need for better support systems in education. Kris recommends others to follow their passion to maintain mental wellbeing! Notes: Kris explains her challenges with dyscalculia, a branch of dyslexia that affects the brain's processing of numbers and data, making math challenging. She faced difficulties at school due to dyscalculia, but she was lucky to receive help from supportive teachers, and specialized programs. Dyscalculia significantly affected Kris's self-esteem and mental health. Despite her condition, she successfully navigates her job by coping strategies like focusing on her love for plants and gardening to manage stress. Emphasizing the need for increased awareness and support for dyscalculia, Kris advocates for more resources and training for teachers and mental health professionals. She highlights the vital role of her support systems, including therapy and family, in managing her condition. Additionally, she advises others with dyscalculia to engage in activities they are passionate about to help manage their condition and maintain mental well-being. About Kris: My name is Kris and I’m honored to be a guest on this radio podcast to share my personal journey with Dyscalculia. I believe that by sharing my experiences, we can raise awareness about this learning disability and inspire others to overcome its challenges. I realized I had Dyscalculia roughly around Grade 8 when one of my best friends mentioned the condition as they were recently diagnosed. It made perfect sense; I struggled with mathematics and trying to practice the concepts were marked by frustration and self-doubt. However, I was determined not to let this learning disability define my potential. Challenges: Dyscalculia presented a range of challenges in my academic and personal life. Tasks that involved numbers, such as basic calculations and mental math seemed insurmountable at the time. I often felt isolated and struggled to keep up with my peers. Thankfully, I wasn’t alone as there were a group of kids in my grade that all needed some extra help. The Turning Point: My turning point came when I met a couple supportive teachers in middle school (Ms. N. Elias and Ms. L. Cusak) who recognized my struggles and provided alternative teaching methods. With their help, I started building a foundation of numerical understanding step by step. It was a slow and often frustrating process, but I remained committed. Overcoming Dyscalculia: Through years of hard work, determination, and the support of dedicated educators and loved ones, I began to gain confidence in my mathematical abilities. I discovered strategies and tools that worked for me, such as visual aids, specialized tutoring, and assistive technology. Today, I can proudly say that I’ve overcome many of the challenges associated with Dyscalculia. I’ve not only improved my math skills but also learned to embrace my unique way of thinking. My journey has led me to become an advocate for individuals with learning disabilities and to inspire others to never give up on their dreams. Message to Others: To anyone struggling with Dyscalculia or any learning disability, I want to emphasize that you are not alone, and it’s okay to seek help. With the right support and determination, you can overcome the challenges posed by Discalculia and achieve your goals. Remember, your journey is unique, and your strengths are immeasurable. I’m grateful for the opportunity to share my story on this podcast, and I hope it encourages conversations about Dyscalculia and the importance of inclusive education. Together, we can create a world where everyone, regardless of their learning differences, can thrive and reach their full potential.
This episode of SSL! presents Helme’s journey from misdiagnosis to proper treatment of Wilson's disease, which can cause various symptoms including speech difficulties like dysarthria and dysphasia. Let’s learn about his challenges and coping strategies. Notes: Helme discusses how Wilson's disease, a condition affecting copper metabolism, affects daily activities, work, and relationships, highlighting the importance of support systems and managing stress. The disease's complexity and variability contribute to under diagnosis, necessitating awareness and consideration for alternative diagnoses, such as multiple sclerosis. This episode highlights the significance of recognizing personal limits and the need for greater support for people with conditions like Wilson's disease. It emphasizes the importance of awareness and understanding among medical professionals about the diverse manifestations of the disease. Despite ongoing struggles, Helme emphasizes gratitude for his recovery and aims to raise awareness about Wilson's disease.
About Steff: I am a speech-language pathologist who stutters in the United States. My brother has stuttered since the age of six (child-onset) and me since the age of 36 due to a brain injury. I am also a person that lives with chronic lung disease- and stuttering support groups helped me find myself and navigate this lung disease journey as a young career woman, wife and mother- more than lung support groups. I have been an SLP for almost 15 years, and now own a private practice solely focusing on the treatment of stuttering. I LOVE to talk about the shift in treatment to a very holistically-based model focused on autonomy of the person who stutters in the therapy room. Additionally, I am an adjunct professor at four universities! Website: https://somestutterluh.ca/ Anchor: https://anchor.fm/somestutterluh Instagram: https://www.instagram.com/somestutterpodcast Facebook: https://www.facebook.com/somestutterluhpod/ Google Podcasts: https://podcasts.google.com/feed/aHR0cHM6Ly9hbmNob3IuZm0vcy80ZDk5ZjhhYy9wb2RjYXN0L3Jzcw== Breaker: https://www.breaker.audio/some-stutter-luh Pocket Casts: https://pca.st/f104pr7u Radiopublic: https://radiopublic.com/some-stutter-luh-Ww7lXa Spotify: https://open.spotify.com/show/5f9V7PkdfcPPOBSc7WNsBf #stuttering #podcast #newfoundland #labrador #speech #therapy #therapist #disability #communication
This episode was recorded in Persian. An English translation is provided on our Youtube channel: https://www.youtube.com/@somestutterluh
This special episode of SSL! podcast presents the cultural perceptions of stuttering in Iran. As a person who stutter, a speech therapist and the founder of the first stuttering-focused startup in Iran, GREEN SPEECH, Amir covers various aspects of stuttering, including personal experiences, societal perceptions, treatment approaches, the role of awareness, and the importance of self-acceptance. Let’s listen to someone who made his stuttering to a stepping stone to success! Notes: Amir Hossein, as a PWS, a speech therapist and founder of Green Speech, discusses his personal journey with stuttering. He shares his experiences with stuttering from childhood through adulthood, detailing the reactions of family, peers, and professors. Amir emphasizes the importance of self-acceptance and open communication about stuttering to reduce stigma and improve quality of life. As student of speech therapy at University of Michigan, he also addresses the differences in cultural attitudes towards stuttering between Iran and America, highlighting the need for awareness and support for people who stutter. In his role as a speech therapist and startup founder, Amir aims to provide resources, support, and education to both individuals who stutter and professionals in the field and he emphasizes on the importance of early intervention. He encourages those who stutter to seek help and take action towards improving their speech, stressing that stuttering does not define one's worth or capabilities. Website: https://somestutterluh.ca/ Anchor: https://anchor.fm/somestutterluh Instagram: https://www.instagram.com/somestutterpodcast Facebook: https://www.facebook.com/somestutterluhpod/ Google Podcasts: https://podcasts.google.com/feed/aHR0cHM6Ly9hbmNob3IuZm0vcy80ZDk5ZjhhYy9wb2RjYXN0L3Jzcw== Breaker: https://www.breaker.audio/some-stutter-luh Pocket Casts: https://pca.st/f104pr7u Radiopublic: https://radiopublic.com/some-stutter-luh-Ww7lXa Spotify: https://open.spotify.com/show/5f9V7PkdfcPPOBSc7WNsBf #stuttering #podcast #speech #language #disability #Iran #Persian #Newfoundland #Labrador #Communication
