The FASD Success Show

Send us a text Join us for a raw and real episode of The FASD Success Show. I’m your host, Jeff Noble, and in this episode, I chat with Ray and Jen, parents of five kids—four of whom are on the FASD spectrum. Before joining our community, they were constantly overwhelmed by daily blowups, meltdowns, and behaviors that left them walking on eggshells. But through training and education, they found the tools to stop engaging in the chaos and create more peace at home. Ray and Jen share their honest and inspiring journey from being stuck in survival mode to finally getting on the same page as a parenting team. If you’ve ever felt like you’re on the brink, this episode will give you the hope and practical tools to help you take back control. Tune in to learn about: Turning Conflict into Calm:Working as a Team:Understanding FASD Behaviors:Finding Community and Support:Whether you’re feeling burnt out or just looking for new strategies, this episode will give you actionable tips and a renewed sense of hope for your FASD journey. Show Notes: Register for the Free Caregiver Kickstart Workshop:www.fasdsuccess.com/fasdworkshopSupport the show

Send us a text Welcome to another inspiring episode of The FASD Success Show! In this episode, I sit down with Ryan Jolly, an incredible single mom of four, two of whom have FASD. Ryan's story is one of resilience, determination, and the transformation that comes from finding the right support. Ryan opens up about her toughest moments—like dealing with explosive behaviors and feeling completely overwhelmed. However, she also shares how she shifted her mindset through training and community support and found new ways to navigate the challenges. Her journey proves that, no matter how tough things get, there’s always hope. Tune in to learn about: The Turning Point:Managing Explosive Behaviors:Building a Support Network:Shifting the Mindset:Whether you’re feeling isolated, exhausted, or in need of encouragement, Ryan’s story will inspire you and offer practical advice to help you on your FASD journey. Show Notes: Register for the Free Caregiver Kickstart Workshop:Register hereSupport the show

Send us a text In this episode of The FASD Success Show, I sit down with Mike and Crystal, a couple who have been through the wringer raising four kids—all on the FASD spectrum. They open up about their darkest moments and the journey that brought them from surviving on the edge to finding peace and understanding. Crystal shares how she was on the verge of running away, feeling overwhelmed and without support. But through education and connection, they found the tools to change their family dynamics. Now, their home feels calmer, and they have the confidence to tackle even the toughest days. Tune in to learn about: The Breaking Point:Creating Peace in the Chaos:From Survival to Thriving:The Power of Community:This episode is packed with hope, real-life strategies, and inspiration. If you’re feeling burnt out or stuck, Mike and Crystal’s story will show you that change is possible. Show Notes: Register for the Free Caregiver Kickstart Workshop:Register hereSupport the show

Send us a text Join us for a raw and real episode of The FASD Success Show. I’m your host, Jeff Noble, and in Episode 158, I’m coming back after an unexpected hiatus with a deeply personal story that’s changed my life. But it’s not just about the challenges—I’m here to share what’s in store for you as we move forward. In this episode, I’m pulling back the curtain on what’s been happening behind the scenes, and I’m spilling the tea on some big changes, powerful lessons, and exciting plans that you won’t want to miss. This isn’t just my story—it’s about how we keep pushing forward, even when life throws us some wild curveballs. Tune in to learn about: Navigating Loss and Resilience:Lessons in Acceptance:What’s Next for You:Whether you’re a seasoned caregiver or new to the journey, this episode offers heartfelt reflections, practical advice, and a renewed focus on supporting you through the ups and downs of FASD caregiving. Show Notes: Download the Understanding Me Guide:https://www.fasdsuccess.com/understandingmeRegister for the Caregiver Kick Start Workshop:Register Here: https://www.fasdsuccess.com/fasdworkshopJoin Our Online Community:Join Here: https://www.facebook.com/groups/FASDFOREVERSupport the show

Send us a text Welcome to "Summer Sanity: How FASD Caregivers Make It Work" Summer break is upon us, and if you're feeling the heat, you're not alone. In this episode, Jeff Noble is joined by the Caregiver Council—a group of seasoned parents from our online coaching programs. They're here to share their tried-and-true strategies to help you navigate the summer months with your FASD kiddos. From maintaining structure and handling behavioral challenges to managing sibling dynamics and sneaking in some self-sanity, we've got it all covered. Tune in to hear practical tips, relatable stories, and a healthy dose of humor to get you through the summer chaos. Tune in to learn about: Maintaining Structure and Routine:Engaging Activities:Managing Sibling Dynamics:Self-Sanity for Caregivers:Whether you're a seasoned caregiver or new to the journey, this episode offers practical advice, relatable stories, and a supportive community to help you navigate the summer months. Show Notes: Join Our Online Community:FASD Forever Facebook GroupSupport the show

Send us a text Join us for an insightful and inspiring episode of The #FetalAlcoholSyndrome(FASD) Success Show. I'm your host, Jeff Noble, and in Episode #156, we welcome Dr. Jeffrey Wozniak and Dr. Blake Gimbel to discuss the latest in FASD research, focusing on choline and brain imaging studies. In this episode, Dr. Wozniak and Dr. Gimbel provide updates on their groundbreaking follow-up study on the effects of choline in children with prenatal alcohol exposure (PAE). They delve into how choline can help optimize brain development and share the promising results from their initial studies. Tune in to learn about: Choline's Role in Brain Development: Discover how choline supplementation can aid in memory and cognitive development in children with PAE and why early intervention is key. -Long-Term Study Findings Dr. Wozniak discusses the lasting impacts observed in children years after the initial choline study, highlighting improvements in nonverbal intelligence and memory. - Brain Imaging Insights: Dr. Gimbel explains their innovative brain imaging study, revealing how differences in brain structure correlate with cognitive and executive function challenges in youth with FASD. - New Research Opportunities: Learn about their latest study using a novel web-based brain assessment tool, BRAIN-online, aimed at making diagnostic assessments more accessible and efficient. Whether you're a seasoned caregiver or new to the journey, this episode offers practical advice, cutting-edge research, and hopeful insights into managing and understanding FASD. Show Notes -Participate in the Brain-Online Study If you have a child aged 8 to 16 with a history of prenatal alcohol exposure or a diagnosis of FASD, you can help advance this crucial research. Learn more and sign up here https://fasd.umn.edu - Explore the role of choline in brain development and the implications of early intervention. - Understand how brain imaging can reveal structural differences that impact cognitive functions in children with FASD. - Discover the benefits of the BRAIN-online assessment tool and how it aims to improve diagnostic accessibility. Don't forget to subscribe to The FASD Success Show for more episodes that inspire, inform, and empower the FASD community. Join us in fostering a more supportive, empathetic, and resilient future for everyone impacted by Fetal Alcohol Syndrome Support the show

Send us a text Join us for an insightful and inspiring episode of The #FetalAlcoholSyndrome(FASD) Success Show. I'm your host, Jeff Noble. In Episode #155, we are thrilled to welcome Alicia Munn, a dedicated advocate and pioneer in the FASD community. Alicia brings a wealth of knowledge and practical experience, offering invaluable tips for creating an FASD-friendly environment and navigating the complexities of FASD advocacy. In this episode, Alicia shares her journey from working in healthcare to becoming a key figure in FASD support and education. Her story is a testament to the power of empathy, persistence, and innovative thinking in transforming the lives of individuals with FASD and their caregivers. Tune in to learn about: Creating an FASD-Friendly Home: Practical tips and strategies for adapting your home environment to meet the unique needs of individuals with FASD, promoting independence and reducing daily stress. -Advocacy and System Navigation: Alicia’s strategies for dealing with healthcare, education, and social services to secure the necessary resources and support for loved ones with FASD. Community Building and Support: The importance of building a supportive network and the role of community activities in fostering a sense of belonging and mutual aid. Empathy and Changing Expectations: Understanding that behaviors are responses to unmet needs can transform your approach to caregiving, making interactions smoother and more supportive. Alicia’s experiences provide a roadmap for managing the complexities of FASD with empathy and resilience. Whether you're a seasoned caregiver or new to the journey, this episode offers practical advice and inspiring stories that will resonate deeply with you. Show Notes: - Connect with Alicia Munn and learn more about her advocacy work through her participation in our private Facebook group, FASD Forever. - Explore resources and strategies for creating FASD-friendly environments and effective advocacy in caregiving. - Discover how community involvement and support groups can make a significant difference in the lives of individuals with FASD. Don't forget to subscribe to The FASD Success Show for more episodes that inspire, inform, and empower the FASD community. Join us in fostering a more supportive, empathetic, and resilient future for everyone impacted by FASD. Support the show

Send us a text Do you need some HOPE? Wondering if all this effort is worth it in the end? Well, I'm here to say it is, and in this episode, I'm bringing you Exhibit (A) in the case for hope: Demi Forsyth – a young woman who embodies resilience. With heartfelt candor, Demi shares her day-to-day triumphs and trials, offering a dose of reality mixed with a surge of optimism for caregivers and individuals alike. Here's what you'll uncover: Plus, we dabble in: In the face of so many challenges, it's hard not to lose sight of hope. The path isn't always clear, and the stakes are high – not just for us, but for our kids. It can feel like a relentless uphill battle, with every step forward met with two steps back. But take heart. This episode isn't just about sharing a story; it's about reaffirming that you're not alone on this voyage and every effort you make counts. It's about real experiences that shed light on the possibilities that lie ahead, even when the night seems darkest. Don't miss out on this episode. Hit play, get comfortable, and let's reinforce that sense of purpose and focus. Because here at The FASD Success Show, we're not just talking about the difficulties; we're actively turning them into stepping stones for success. Join us, and let's keep the hope alive – together. Stay Connected with The FASD Success Show: - Connect with fellow caregivers in our Facebook community https://www.facebook.com/groups/fasdforever, where shared experiences forge a path to understanding and support. - Follow [FASD Caregiver Success on Facebook](https://www.facebook.com/fasdsuccess) for continuous insights and resources tailored for the FASD journey. Jeff Noble on [Instagram](https://www.instagram.com/fasdsuccess) - Visit [The FASD Success Show website](https://www.fasdsuccess.com/podcast) for comprehensive episode breakdowns and a treasure trove of FASD resources. Support the show

Send us a text Join us on a compelling journey in Episode 153 of The FASD Success Show as we delve into the often-overlooked struggles that fathers face in the world of FASD caregiving. Host Jeff Noble sits down with Dr. Mike Howlett, who not only navigates the complexities of FASD at home with his family but also balances a demanding career as a veterinarian. In this heartfelt conversation, Dr. Howlett opens up about: The Real Struggles of FASD Dads: Explore the emotional and practical challenges dads encounter in a caregiving role that is traditionally viewed as maternal. Discover how societal expectations shape their responses and strategies for more effective involvement. Balancing Acts: Learn how Mike juggles his professional responsibilities with his family's needs, providing insights into the emotional resilience required to manage such a dual-demanding role. Championing Advocacy: Dr. Howlett provides practical tips for other dads to effectively advocate for their children within their home and school systems. This episode isn't just a conversation; it’s a guide for fathers and families striving for success in the challenging journey of FASD caregiving. Tune in to gain valuable strategies that can help your family navigate the challenging waters of FASD with greater success and less stress. Stay Connected with The FASD Success Show: Join Our Community: Connect with fellow caregivers in our Facebook community at FASD Forever, where we share experiences and support each other on this unique journey. Follow Us for More Insights: Keep up with ongoing FASD insights and resources at FASD Caregiver Success on Facebook. Instagram Updates: Follow Jeff Noble on Instagram for more updates and inspiration. Dig Deeper: Visit The FASD Success Show website for comprehensive episode breakdowns and access to a wealth of FASD resources. Support the show

Send us a text Embark on a journey of resilience and hope in Episode 152 of The FASD Success Show, "How to Live with Less Fear and Frustration about the Future." Join host Jeff Noble as he explores the transformative insights of Kim Driscoll, whose experiences shine a light on navigating the complexities of FASD with unwavering love and strategic advocacy. In this episode, Kim Driscoll, a seasoned FASD caregiver and advocate, unveils her roadmap for managing the unpredictable waves of FASD. Her narrative is a testament to the power of compassionate caregiving, structured routines, and relentless advocacy in crafting a hopeful path for families grappling with FASD. Discover key takeaways from Kim’s journey: - The art of emotional regulation and how to transform chaotic moments into opportunities for bonding and understanding. - Navigating the educational landscape to secure the support and accommodations essential for your child’s success. - The strength found in community: learning how peer support can alleviate the loneliness of the FASD caregiving journey. This episode is more than a guide; it’s a lifeline for caregivers seeking to diminish the shadow of fear and frustration that often accompanies FASD. Tune in to uncover the strategies that can lead to a future where love, understanding, and advocacy prevail in the face of FASD. Stay Connected with The FASD Success Show: - Connect with fellow caregivers in our Facebook community https://www.facebook.com/groups/fasdforever, where shared experiences forge a path to understanding and support. - Follow [FASD Caregiver Success on Facebook](https://www.facebook.com/fasdsuccess) for continuous insights and resources tailored for the FASD journey. Jeff Noble on [Instagram](https://www.instagram.com/fasdsuccess) - Visit [The FASD Success Show website](https://www.fasdsuccess.com/podcast) for comprehensive episode breakdowns and a treasure trove of FASD resources. Support the show

Send us a text Step into Episode 151 of The FASD Success Show, where we uncover Aaron Howlett's heartfelt story, a narrative that many in our community will find intimately relatable. Witness Aaron's evolution from confronting daily FASD hurdles to stepping up as a beacon for advocacy and enlightenment within the FASD realm. Join Jeff Noble and Aaron in a conversation that delves into the trenches of living with FASD. Aaron articulates the journey from initial confusion and struggle to the empowering realization of the importance of support and self-advocacy. This episode offers an authentic and hopeful perspective on how receiving and accepting help can pave the way for personal development and a wider impact on the FASD community. Stay Connected with The FASD Success Show: - Join our dedicated Facebook group, https://www.facebook.com/groups/fasdforever, to connect with a community that gets it. - Check out our Instagram https://www.instagram.com/fasdsuccess for inspiring stories and tips. - Visit https://www.fasdsuccess.com/podcast for comprehensive resources and in-depth episode breakdowns. Tune in for an episode that’s not just about facing the challenges of FASD but transforming them into stepping stones for advocacy and awareness. Be part of Aaron's journey and get inspired to make a difference in the FASD community. Support the show

Send us a text Welcome back to the FASD Success Show, where we transform despair into hope and isolation into community. I'm Jeff Noble, and today we're diving deep into the heart of transformation with Mary Byrnes. Her story is not just a journey; it's a battle cry for change and empowerment in the FASD world. Mary's tale begins on the brink, where frustration and fear loomed large, threatening to shatter her family's spirit. But through the storm, a leader emerged. Join us as Mary shares her raw, unfiltered path from nearly hitting rock bottom with her son Harrison's aggressive FASD challenges to founding Harrison’s Hope, a lighthouse for families navigating the FASD storm. In this episode, we'll explore Mary's journey, its gritty realities and golden triumphs. You'll hear how she transformed personal agony into a public advocacy powerhouse, creating a support network that breathes life and hope into the FASD community. It's a story of breaking barriers, building bridges, and lighting the way for others to follow. Here's what you'll uncover in this inspiring episode: - Mary's relentless fight from facing her darkest fears to becoming a beacon of hope for the FASD community. - The birth and vision of Harrison’s Hope, a sanctuary of support, education, and advocacy for families touched by FASD. - Practical wisdom and life lessons from Mary's expedition that will illuminate your path, whether you're a caregiver or a professional in the FASD realm. So, grab your headphones and join us for an episode that's more than a conversation—it's a journey from despair to community care in the FASD universe. Subscribe now, be part of our heartfelt discussion, and step into a community where transformation is not just a dream, but a reality. Show Notes: Support the show

Send us a text Today on The FASD Success Show, we’re rolling out something special: a tribute to our very own Alex Duthie. Alex wasn't just a moderator around here; he was the heart and soul of our community, a true friend who recently passed away. Alex, known for his infectious humor and unwavering compassion, left a lasting legacy within the FASD world. Alex was a giant in our world, not just for keeping the peace but for lighting up the place with his quick wit and endless kindness. He tackled life and the challenges of Fetal Alcohol Spectrum Disorder (FASD) with a laugh and a smile, showing us all the way. Dive in as we explore his journey, honor his impact, and soak in the wisdom he dished out so generously. What We’re Talking About: Laugh It OffStronger TogetherLeaving Marks on HeartsWhy You Gotta Listen: It’s more than a tribute; it’s a reminder of the power of sticking together, sharing a good laugh, and spreading a little kindness, just like Alex showed us. His way of rolling with life’s punches, always with a joke at the ready, is something we could all learn from. To keep Alex’s laughter echoing and support his family, swing by the GoFundMe we’ve set up: https://www.gofundme.com/f/alex-duthie. Every bit helps. And don’t miss out on the “Virtual Celebration of Alex's Life.” It’s a chance for us to come together, swap stories, and honor the legend that Alex was. Sign up here: https://bit.ly/3wLtnzc This episode's for you, buddy. Let’s do Alex proud by keeping the laughs loud, the support strong, and the community closer than ever. Support the show

Send us a text Welcome to Episode #148 of The FASD Success Show: Discover the Impact: Transforming FASD with Peer Mentorship. This week, host Jeff Noble brings you an enlightening conversation centered on the transformative effects of connection, understanding, and peer support within the FASD community. We're excited to showcase how Adopt4Life's pioneering mentorship program is making significant strides, offering new hope, and facilitating positive change. Join us for an engaging discussion with Nicole, one of the six project mentors (Christina, Connor, Monica, Nicole, Sabrina and Shelby) who shares her firsthand experience as an individual on the Spectrum and one of the mentors, alongside Project Co-Leads, Tracy Moisan and Catherine McIntyre from Adopt4Life. Together, we explore the critical role of peer mentorship and its profound impact on both mentors and mentees navigating the challenges of FASD. Listeners will be inspired by stories of empowerment, personal growth, and the collaborative creation of resources that resonate with individuals with FASD. This episode is a journey through: You will also get first hand knowledge of the second phase of the project - Until Next Time | FASD & Me: For Teens & Youth video series where each of the mentors share insight for other teens and youth with FASD on topics such as school, work, community and family. This episode stands as a powerful showcase of how peer mentorship can serve as a catalyst for positive change in the lives of individuals with FASD and their caregivers. Nicole, Tracy, and Catherine don't just share their expertise; they share their passion, offering a narrative that highlights the importance of empathy, connection, and informed support in navigating FASD. Show Notes: Visit the Podcast Blog Post for links to the Adopt 4 Life ASD & Me Program and Until Now Video Series for Youth as well as Links to all the FASD Success Socials. Support the show

Send us a text Welcome to Episode #147 of The FASD Success Show: This week, host Jeff Noble takes on a topic that hits close to home for many: "Legal Lifelines: Advocating for FASD in the Justice System." It's all about standing up for our loved ones with Fetal Alcohol Spectrum Disorder (FASD) when they face legal challenges. We're cutting through the legal jargon and shining a light on how to navigate the system with confidence and compassion. Join us as we dive into the nitty-gritty of finding a lawyer who doesn't just see another case but sees the person behind it – someone who's ready to learn about FASD and fight the good fight. We're unpacking everything you need to know to be the best advocate for your loved one, from the importance of getting the right evaluations to understanding how the legal process works. Listeners will walk away with real-world advice on: Finding Your Legal Champion:Educating to Advocate:The Importance of the Right Tests:Fighting for a Fair Shot:This episode isn't just a talk; it's a toolbox for anyone facing the daunting world of legal challenges with FASD. With Kyle White's expert insights and Jeff's passion for the cause, you're in for an empowering listen that'll leave you ready to take on the world, or at least the courtroom. Show Notes: So, whether you're knee-deep in legal battles or just want to be prepared, Episode #147 is your go-to guide for navigating the justice system with FASD by your side. Let's get informed, get inspired, and get going! Support the show

Send us a text Tune in to Episode 146 of The FASD Success Show, where host Jeff Noble tackles a topic that's as loaded as a baked potato at a steakhouse – swearing in individuals with Fetal Alcohol Spectrum Disorder (FASD). "Unpacking the 'Why' Behind the Words: A Caregiver's Guide to Turning 'F*&* OFF' into Understanding" takes you on a deep dive into the reasons behind the raw and unfiltered verbal expressions that can leave caregivers feeling like they're walking a tightrope without a net. With the same tenacity and heart that has made him the guide for countless FASD caregivers, Jeff dissects the brain's complex wiring and why those with FASD may reach for expletives in moments of stress or high emotion. This episode isn't about finger-wagging or brow-beating; it's about providing a life jacket in the sea of FASD caregiving, empowering you with knowledge and empathy to transform those cringe-worthy moments into opportunities for connection and growth. Listeners will discover: The neurological underpinnings of swearing in individuals with FASD and why it's often a reflex, not a choice. How emotional regulation, or the lack thereof, can lead to outbursts and what caregivers can do to help navigate these stormy waters. Practical strategies for responding to swearing in a way that maintains dignity and respect for both caregiver and child, turning potential conflicts into teachable moments. The importance of understanding and respecting the unique challenges faced by individuals with FASD, reframing our approach from one of frustration to one of advocacy and support. This episode is a masterclass in shifting from conflict to comprehension, equipping caregivers with the strategies necessary to guide their loved ones towards expressing their emotions more constructively. It's an opportunity to reframe the experience of swearing not as an intentional slight, but as an indicator of underlying needs and challenges, offering a blueprint for empathetic and impactful caregiving. Support the show

Send us a text Join host Jeff Noble in this uplifting episode of The FASD Success Show, where we turn the spotlight on the incredible achievements and milestones of individuals with Fetal Alcohol Spectrum Disorder (FASD) and their families. In "The Shout-Out Special," we share heartwarming stories submitted by our listeners, ranging from academic accomplishments and vocational successes to personal triumphs and strengthened family bonds. This episode is not just a celebration but also a powerful reminder of the resilience, potential, and diverse talents within the FASD community. Through these stories, we highlight the positive impact of understanding, support, and appropriate accommodations in enabling individuals with FASD to thrive in various aspects of their lives. Listeners will be inspired by: Real-life accounts of overcoming challenges and achieving goals, demonstrate the wide range of abilities and interests among individuals with FASD. The crucial role of supportive relationships, whether it's family, educators, or mentors, in fostering success and personal growth. Strategies and insights from caregivers who have navigated the journey of supporting a loved one with FASD, sharing lessons learned and strategies that made a difference. The importance of celebrating every win, big or small, and how these moments of recognition contribute to building confidence and a positive self-image. This special episode is a celebration of hope, progress, and the strength of the FASD community. It serves as a testament to the incredible achievements possible with the right support, understanding, and love. Join us as we share these inspiring stories, offering encouragement and motivation to families, caregivers, and individuals with FASD everywhere. Let's celebrate the successes and continue to work together towards a brighter future for all those affected by FASD. Show Notes: Support the show

Send us a text In this pivotal episode of The FASD Success Show, host Jeff Noble is joined by Dr. Catherine Lebel, a leading researcher in the field of brain development in individuals with Fetal Alcohol Spectrum Disorder (FASD). Together, they unravel the complexities of the FASD brain, shedding light on its unique growth patterns and the profound impact of caregiving on this development. Dr. Lebel shares groundbreaking findings from her latest research, offering hope and actionable insights to caregivers dedicated to supporting individuals with FASD. This conversation is a deep dive into the dynamic nature of brain connectivity, the factors influencing brain development, and the critical periods for intervention. Listeners will gain invaluable knowledge on: The latest scientific discoveries regarding how the FASD brain develops over time. The role of early intervention and environmental factors in promoting optimal brain growth and functionality. The importance of understanding and adapting caregiving strategies to meet the evolving needs of individuals with FASD. Real-life implications of the research for caregivers, educators, and healthcare professionals. This episode is a testament to the power of persistence, love, and informed support in the lives of individuals with FASD. Dr. Lebel's expertise, combined with Jeff's passion for the FASD community, creates a compelling narrative that underscores why every effort matters in the quest to understand and support brain development in FASD. Show Notes: Support the show

Send us a text Episode #143 of The FASD Success Show. Your host, Jeff Noble, invites you into a narrative of transformation and tenacity, as we sit down with Allan Mountford and Rochelle Howlett, two extraordinary figures who've taken FASD awareness and support in Nova Scotia from a whisper to a roar. This episode is a masterclass in determination, uniting the quiet strength of Rochelle, a mother on a mission, with the enduring passion of Allan, a teacher-turned-advocate. Together, they've harnessed their collective fire to create an FASD conference that's not just an event, but a beacon of hope, learning, and connection. As Allan and Rochelle share their blueprint for sparking change in your city, they'll reveal the steps, the stumbles, and the unwavering spirit required to elevate FASD into the public consciousness. From rallying community support to engaging policymakers, their story is one of unrelenting advocacy that's rewriting the narrative of FASD in their province – and beyond. In this episode, you'll discover: This episode is a call to action for anyone dreaming of making a difference in the world of FASD advocacy. It's proof that no voice is too quiet, no effort too small, and no dream too big. Subscribe, tune in, and let's embark on this inspiring journey of advocacy together. Show Notes: Don't forget to subscribe to The FASD Success Show for more stories of courage, connection, and community in the world of FASD. Support the show

Send us a text Join us on a compelling journey into the heart of FASD caregiving and advocacy in Episode #142 of The FASD Success Show. I'm your host, Jeff Noble, and in this insightful episode, we welcome Amanda Burley, a dedicated Personal Support Worker trainee and a passionate advocate for the FASD community. This episode is a tapestry of personal stories, professional experiences, and the resilience required to navigate the complexities of FASD. Amanda brings her unique perspective to the show, sharing valuable lessons from her own life as someone living with FASD. We delve into the critical aspects of making and maintaining meaningful friendships, facing and overcoming workplace challenges, and the enduring power of resilience in daily life. Her experiences shed light on the nuanced realities faced by individuals with FASD and those who care for them. This episode is not just a conversation; it's a journey into the core of what it means to advocate for oneself and others in the face of adversity. Amanda's story is a testament to the strength and perseverance inherent in the FASD community. In this episode, you'll gain insight into: - Navigating the nuances of building and sustaining friendships when living with FASD. - Overcoming workplace challenges with resilience and self-advocacy, especially in caregiving roles. - Strategies and experiences in managing stress and emotional challenges, essential for caregivers and individuals with FASD. - Amanda's inspiring journey in her PSW training and her aspirations in healthcare, highlighting the importance of ambition and continuous personal growth. This episode is a must-listen for anyone seeking to deepen their understanding of FASD and the resilience required to thrive within this landscape. Subscribe, tune in, and join us in this heartfelt exploration of the challenges and triumphs in FASD caregiving. Be part of our mission to foster a more supportive, empathetic, and resilient future for the FASD community. Show Notes: - Connect with Amanda Burley and her advocacy work through her TikTok profile @AmandaBurley2. Don't forget to subscribe to The FASD Success Show for more episodes that inspire, inform, and empower the FASD community. Support the show