The FASD Success Show

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

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

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

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

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

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

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

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

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

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

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

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

Embark on an enlightening journey through the multifaceted world of FASD caregiving with a special focus on mental health, as we welcome Emma Jewell to Episode #141 of the FASD Success Show. I'm your host, Jeff Noble, and in this pivotal episode, we're weaving together a tapestry of knowledge, experience, and the drive for change, underscored by the innovative work on the Mental Health Toolkit from the Canada FASD Research Network (CanFASD), created in collaboration with the Canada Northwest FASD Partnership. Emma lends her expertise and insights, illuminating the path for caregivers and mental health professionals alike. As we delve into the depths of FASD care, we illuminate the often-unseen challenges and triumphs encountered by those who navigate this complex landscape. Our conversation explores the delicate balance of managing mental health within the FASD community and the critical importance of dismantling implicit biases that can hinder progress. By the end of this episode, you'll be armed with newfound understanding and practical tools designed to elevate the support provided to individuals with FASD. This episode is a clarion call to foster a more informed and empathetic approach to mental health care, highlighting the strength found in knowledge and advocacy. If you're set on a course to deepen your impact and harness the collective wisdom of experts and caregivers, this episode is your beacon. Don't miss out on these insights: Tune in for an episode that promises to not only inform but also transform your approach to FASD caregiving. Hit subscribe, join our heartfelt conversation, and become part of a movement towards a brighter, more understanding future for the FASD community. Show Notes: Click for Mental Health Toolkit Support the show

Welcome to Episode #140 of The FASD Success Show, where we're kicking off the new year with renewed energy and unwavering commitment to the FASD community. Join us as we dive into an enlightening conversation with Audrey McFarlane, Executive Director of the Canada FASD Research Network, and explore the groundbreaking developments shaping the future of FASD advocacy and support. In this episode, Audrey shares insights on the evolution of FASD discussions, emphasizing a holistic approach beyond prevention and addressing the diverse needs of individuals with FASD and their families. We unveil the much-anticipated Mental Health Toolkit, a vital resource for professionals eager to make a difference in the lives of those affected by FASD. We also discuss the importance of the Family Advisory Committee and how your unique perspectives can influence pivotal research projects. Audrey sheds light on the challenges and opportunities in FASD diagnosis and policy, highlighting the need for collective action to drive progress. Moreover, we talk about the international efforts to recognize FASD as a priority on the global stage and the upcoming 2025 FASD conference in Toronto, which promises to be a catalyst for innovation and collaboration. Audrey's call to action is clear for caregivers: your participation in initiatives like the Family Advisory Committee and caregiver surveys can spearhead transformative policies tailored to your experiences. Celebrate with us as we reflect on a recent successful conference and the recognition of Audrey's tireless work with a prestigious award. This is a testament to the passion and dedication that fuels our journey towards FASD success. Whether you're a caregiver, frontline worker, or an individual on the spectrum, this episode is a treasure trove of inspiration, information, and a call to action. Be part of the movement, share in our collective triumphs, and help us shape a world where every individual with FASD is supported and understood. Connect with us and continue the conversation on our Facebook page at www.facebook.com/fasdsuccess and our free group at www.facebook.com/groups/fasdforever. Your voice, your involvement, and your advocacy are the cornerstones of the incredible strides we're making together. Tune in, get engaged, and let's embark on this year's journey with determination, hope, and the shared vision of creating everyday success for the FASD community. Because together, we're unstoppable. Support the show

Prepare for a journey into the heart of FASD caregiving with a twist of inspiration and a dose of real-world wisdom. I'm your host, Jeff Noble, and in this must-listen episode, I'm bringing together a dynamic team of coaches from the Caregiver Kickstart coaching program. These remarkable individuals are not only experts in their fields but also share their lives with individuals with FASD, offering a perspective that's as authentic as it gets. As we navigate the complexities and celebrate the triumphs of FASD caregiving, each coach offers a piece of their story, shedding light on the power of connection, understanding, and resilience. Their shared experiences are a beacon for those navigating similar waters, providing solace and solidarity. By the close of our chat, you'll be loaded with strategies, bolstered by expert insights, and touched by stories that echo your own. If you're ready for a surge of motivation and community, don't hesitate to hit subscribe. Key Takeaways: Show Notes: 🌟 Special Feature: Breaking Through Burnout Workshop 🌟 Battling caregiver burnout? Step into the light with us. The unrelenting pace, the high-intensity moments, and the quest for effective strategies can overshadow even the brightest days. If this rings true, then our FREE 3-day workshop, "Breaking Through Burnout," is your sanctuary. It's time to shift from survival mode to a thriving life. This workshop isn't just about coping – it's about thriving. We're ready to equip you with the tools to manage challenging behaviors, simplify complex decisions about medications, and refine your therapeutic tactics. With live, interactive coaching, evidence-based methods, and a community that embraces your struggles and victories alike, you'll emerge from burnout with a fresh perspective and renewed vigor. 👉 Don't miss out! Registration for the Breaking Through Burnout Workshop is LIVE: Click here to REGISTER! Support the show

Hold onto your seats, folks! This episode is a rollercoaster of emotions, insights, and 'aha' moments that you won't want to miss. I'm Jeff Noble, and today I'm joined by Stacia Stribling, an alumni of my online coaching program. Stacia transitioned from being a professor of early childhood development to working in the nonprofit sector, and she's here to share her transformative approach to FASD caregiving. Stacia and I get down to the nitty-gritty of FASD caregiving. We talk meltdowns, navigating the maze-like educational system, and the emotional toll that caregiving can take. Stacia shares her philosophy of "connection before correction," and how she's unlearning conventional caregiving norms to better support her loved ones. By the end of this episode, you'll walk away with actionable strategies and a newfound sense of hope. So, if Stacia's journey feels a lot like your own, hit that subscribe button for more 'aha' moments. Key Takeaways: The power of "unlearning" in caregiving Emotional self-care tips for caregivers Navigating the educational system with FASD in mind Show Notes: 🔥 Special Announcement: Breaking Through Burnout Workshop 🔥 Are you on the brink of caregiver burnout? You're not alone. The daily chaos, managing meltdowns, and navigating the education maze can take a toll on even the most resilient caregivers. If you are feeling burnt out and overwhelmed, then don't miss our FREE 3-day workshop, "Breaking Through Burnout." This is your chance to turn that fatigue into fuel for a better tomorrow. This workshop is designed to empower you with the skills to manage aggressive and impulsive behaviors, understand medication options, and establish effective therapy strategies. With live coaching, evidence-based strategies, and a supportive community, you can break the cycle of burnout, rewrite your parenting story and reclaim your life —one practical step at a time. 👉 Registration is now OPEN for the Breaking Through Burnout Workshop: Click here to REGISTER! Support the show

Get ready for an episode that will leave you inspired and hopeful! Meet Angela, a remarkable birth mom, who takes us on her life-changing journey of raising a child with FASD. If you've ever felt like you're running on fumes in this FASD rollercoaster, don't skip out early—we've got a game-changing update that you'll seriously kick yourself for missing. Angela and I get real about the wild ride of FASD caregiving—the meltdowns, the small victories, and the moments of utter exhaustion and isolation. Trust me, Angela's been through the wringer, and she's got wisdom to share. By the end of this episode, you'll walk away with actionable strategies to better manage day-to-day challenges, understand the impact of being a birth mom in the FASD community, and feel invigorated by Angela's testament to human strength and endurance So, if Angela's rollercoaster feels a lot like your own, hit that subscribe button for more 'aha' moments. And hey, listen up because we've got an exciting announcement about a free workshop that might just be your FASD game-changer. Seriously, you won't want to miss this. Show Notes: Follow our Facebook Page for daily tips and inspiration: FASD Success If you are a parent or caregiver and need some virtual support, join us in our: FASD Caregiver Support Facebook Group. Support the show

Tired of feeling like you're talking to a brick wall when you're trying to get educators to understand your child's unique needs? You're not alone. In this no-holds-barred episode of the FASD Success Show, host Jeff Noble cuts through the fluff and gets real about what it takes to build a bridge between home and school. With firsthand stories, expert insights, and actionable strategies, this is the guide you've been waiting for. Whether you're feeling unheard or just downright frustrated, this episode is your rallying cry for change. And whatever you do, don't miss the end—we've got an exclusive offer that promises to redefine your approach to FASD and education. Don't forget to subscribe to the FASD Success Show for more insightful episodes that will help you navigate the FASD journey with knowledge, compassion, and actionable strategies. Your subscription helps us reach more caregivers like you, spreading awareness and fostering success in the FASD community. Show Notes: Follow our Facebook Page for daily tips and inspiration: FASD Success If you are a parent or caregiver and need some virtual support, join us in our: FASD Caregiver Support Facebook Group. Support the show

Hey there, amazing caregivers! Ever felt like you're constantly treading water, even after soaking up all there is about FASD? There's a big leap between knowing FASD and truly grasping its essence. In this episode, we're going to explore why, despite all the knowledge we pack in, finding genuine empathy and understanding for our loved ones with FASD can still be tricky. Here's the bright side: I'm rolling out my top 3 'AHA' moments that flipped the script for me, and I bet they'll do wonders for you too. So, whether you're a seasoned listener or it's your maiden voyage here, join me, Jeff Noble, as we bridge the gap between 'knowing' and 'living it'. If this episode resonated with you, and you're curious to dive deeper into the world of FASD, be sure to check out our YouTube channel or website for more insights, stories, and discussions. Here's to having more 'AHA' moments together! Jeff- Support the show

In this eye-opening episode of the FASD Success Show, host Jeff Noble delves into the intricacies of Fetal Alcohol Spectrum Disorder (FASD). From breaking down the official definition to tackling the stigma and misunderstandings surrounding FASD, this episode is a must-listen for caregivers and anyone looking to deepen their understanding of this complex condition. Jeff also shares his own experiences and insights, offering a holistic view that combines scientific facts with lived experiences. Whether you're a seasoned caregiver or new to the FASD community, this episode will equip you with the tools and knowledge to better support your loved ones and advocate for FASD awareness. Don't forget to subscribe to the FASD Success Show for more insightful episodes that will help you navigate the FASD journey with knowledge, compassion, and actionable strategies. Your subscription helps us reach more caregivers like you, spreading awareness and fostering success in the FASD community. Show notes FASD Caregiver Support Facebook Group: www.facebook.com/groups/fasdforever FASD Definition: www.canfasd.ca Support the show