Jeff Noble thought he knew all about FASD... until he became a full time FASD Foster Parent. Fast forward to now. Jeff has been coast to coast and from one side of the earth to the other talking, teaching and learning about FASD with other Caregivers, Fro
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The FASD Success Show podcast is an incredibly impactful and informative resource for anyone impacted by Fetal Alcohol Spectrum Disorder (FASD). Every episode provides valuable insights from caregivers, doctors, and individuals with FASD that can greatly benefit those affected by this condition. The host, Jeff, has a deep understanding of FASD and expertly chooses guests who provide the most compelling and relatable information. The compassion I have gained from listening to this podcast is a testament to its effectiveness.
One of the best aspects of The FASD Success Show is the range of perspectives it offers. The variety of guests interviewed allows listeners to gain insights into different aspects of FASD and how it can affect individuals in various ways. This diversity helps to paint a comprehensive picture of the condition and fosters a deeper understanding for both caregivers and those with FASD. Additionally, the real-life suggestions provided in each episode give practical advice that listeners can implement in their own lives.
Another positive aspect of this podcast is Jeff's interviewing style. He stays focused on the positive aspects, providing hope and encouragement to parents and caregivers who may feel overwhelmed or isolated. His ability to draw out valuable information from his guests creates an engaging listening experience that leaves listeners feeling empowered and motivated to advocate for those with FASD.
Unfortunately, one downside of The FASD Success Show podcast is that it may not be accessible to everyone who could benefit from it. While podcasts are increasingly popular, there are still individuals who may not have access or be familiar with this platform. It would be beneficial if the show could expand its reach through other mediums such as social media or written resources.
In conclusion, The FASD Success Show podcast is an invaluable resource for anyone impacted by Fetal Alcohol Spectrum Disorder. It provides hope, empathy, education, and practical suggestions that can greatly enhance the quality of life for individuals with FASD and their caregivers. Jeff's expertise and ability to draw out impactful information make this podcast a must-listen for anyone seeking a deeper understanding of FASD.
Send us a textIn 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: Crystal's raw honesty about feeling like she might leave it all behind—and how she turned things around.Creating Peace in the Chaos: How Mike and Crystal learned to manage behaviors and meltdowns without letting their home spiral out of control.From Survival to Thriving: Discover how understanding FASD on a deeper level allowed them to parent with compassion and less stress.The Power of Community: Why finding others who get what you're going through can be a game-changer for caregivers.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: Our free, once-a-year workshop is happening on September 14th, 15th, and 17th! Gain the confidence and tools you need to create more peace and structure for your loved one with FASD. Register here.Support the show
Send us a textWelcome 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: How a chance encounter at a foster care training changed everything for Ryan and her family, leading to an FASD diagnosis.Managing Explosive Behaviors: Ryan shares her strategies for handling the unpredictable and overwhelming moments with her kids and how she learned to stop feeling alone in the fight.Building a Support Network: Discover how connecting with a community of FASD caregivers helped Ryan shift from isolation to empowerment.Shifting the Mindset: How Ryan went from seeing her kids' actions as defiance to understanding them as symptoms of FASD—and how that changed her whole approach.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: Our free, once-a-year workshop is happening on September 14th, 15th, and 17th! Gain the confidence and tools you need to create more peace and structure for your loved one with FASD. Register here.Support the show
Send us a textJoin 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: How Ray and Jen learned to stop blowups before spiraling out of control and found more peace in their daily lives.Working as a Team: Discover how getting on the same page as caregivers transformed their ability to parent effectively, even when emotions run high.Understanding FASD Behaviors: Hear how they shifted from seeing their kids' actions as defiance to recognizing the brain-based challenges of FASD—and how that changed everything.Finding Community and Support: Learn how connecting with others on the same journey brought them the understanding and validation they needed to thrive.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: Our free, once-a-year workshop is happening on September 14th, 15th, and 17th! Gain the confidence and tools you need to create more peace and structure for your loved one with FASD. Register here: www.fasdsuccess.com/fasdworkshopSupport the show
Send us a Text Message.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: Hear my personal journey through grief and how it's reshaped my perspective on life and work.Lessons in Acceptance: Discover how letting go of control can actually empower you in your caregiving journey.What's Next for You: Get the inside scoop on the exciting new resources and events we've been working on, including the return of the Caregiver Kick Start Workshop.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: If you're dealing with school anxiety or feeling like nobody understands your loved one with FASD, get our free, fillable PDF guide to help educators and others understand your child's unique needs. Download Here: https://www.fasdsuccess.com/understandingmeRegister for the Caregiver Kick Start Workshop: Don't miss our free, once-a-year workshop happening on September 14th, 15th, and 17th. This is your chance to gain the confidence and tools you need to create stability and success for your loved one with FASD. Register Here: https://www.fasdsuccess.com/fasdworkshopJoin Our Online Community: Connect with other caregivers and find support in our FASD Forever Facebook Group. Join Here: https://www.facebook.com/groups/FASDFOREVERSupport the Show.
Send us a Text Message.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: Discover how to keep your child's day structured even without the school routine, reducing anxiety and behavioral issues.Engaging Activities: Get ideas for activities that keep kids occupied and stimulated, from camps to at-home projects.Managing Sibling Dynamics: Learn tips for balancing the needs of multiple children and minimizing conflicts.Self-Sanity for Caregivers: Hear essential strategies for taking care of yourself amidst the summer chaos, ensuring you have the energy to support your family.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: Connect with other caregivers and find support at FASD Forever Facebook Group.Support the Show.
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 SyndromeSupport the Show.
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.
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:How Demi carved out her path to independence and what this means for your loved ones with FASD.Real talk on navigating life's curveballs, from shifting living situations to personal loss, and finding stability amidst it all.The ins and outs of managing finances when the numbers just don't add up, and strategies that actually stick.Cracking the code on workplace accommodations – because thriving in a job with FASD is more than possible.Plus, we dabble in:Demi's real-life success, serving as a beacon of what's possible with the right support and a dash of courage.Building your tribe: the significance of community and how it's a game-changer for the journey ahead.Everyday life tips that you can bank on – from the nitty-gritty of budgeting to the self-care routines that keep the ship sailing smoothly.Finding joy and purpose in hobbies and interests that go beyond just filling time – they're about enriching life.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.
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.A deep dive into Aaron's personal struggles and achievements, offering a mirror to many of our own experiences with FASD.Insightful discussions on the transformative role of support and acceptance in navigating FASD.Practical advice and strategies drawn from Aaron's life, providing guidance for those in similar situations.A dose of inspiration from Aaron's journey to advocacy, proving that individuals with FASD can drive awareness and positive change.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 Off: Alex had this killer sense of humor that could make the rough patches feel a bit smoother. Find out how his laughter became our best medicine.Stronger Together: Alex was all about pulling us closer, making sure everyone felt part of this big, sometimes messy FASD family.Leaving Marks on Hearts: Get ready for some stories that'll make you smile and maybe tear up a bit, as folks from our gang share how Alex made life a little brighter for all of us.Why 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/3wLtnzcThis 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:Empowering Peer Connections: Discover the mentorship program's role in fostering vital relationships that inspire confidence, mutual understanding, and support among individuals with FASD.The Importance of Asking for Help: Hear from Nicole about the significance of seeking assistance as a step towards greater self-reliance and personal development.Collaboratively Creating Meaningful Resources: Learn about the process behind Adopt4Life's resource development, ensuring that every tool and initiative is reflective of the real needs and voices of the FASD community.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: How to scout for a lawyer who's not only willing to take on your case but eager to understand the unique challenges of FASD.Educating to Advocate: We're talking about the game-changing power of making sure everyone from the judge to the prosecutor gets FASD. It's about building a team that's on your side.The Importance of the Right Tests: Why getting comprehensive evaluations can make or break your case and how to go about securing them for your loved one.Fighting for a Fair Shot: Kyle shares why we should push for treatment and understanding over punishment, and how this approach can lead to better outcomes for everyone involved.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 living 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 showSupport 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 Longval, 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:The power of collaboration in creating impactful FASD conferences and events.How to sustain momentum and learn from past advocacy efforts to build a stronger future.Insights into mobilizing community support and engaging government stakeholders.Allan and Rochelle's inspiring journey, demonstrating that with resilience, even setbacks can be springboards to greater achievements.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:Learn more about Allan and Rochelle's advocacy work and how to start your own FASD initiative in your area.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.- Explore resources and strategies for effective caregiving and self-advocacy in the context of FASD.- Learn more about the role of Personal Support Workers and the challenges faced in caregiving environments.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:A deep dive into the Mental Health Toolkit for FASD, a pioneering resource by CanFASD.Understanding and overcoming implicit biases in the realm of FASD caregiving and mental health support.Strategies to empower mental health professionals and caregivers in their roles as advocates and allies for those with FASD.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 ToolkitSupport 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:Unveiling the transformative journey of FASD caregiving through the lens of experienced coachesHarnessing the collective strength of a community that truly understands the FASD journeyReal-life stories from caregivers that inspire and educateShow Notes:
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 caregivingEmotional self-care tips for caregiversNavigating the educational system with FASD in mindShow Notes:
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 enduranceSo, 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 SuccessIf 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.Show Notes:If you are a caregiver and need some support, join us at: FASD Caregiver Support Facebook Group.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.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 notesFASD Caregiver Support Facebook Group: www.facebook.com/groups/fasdforeverFASD Definition: www.canfasd.ca Support the show
After a hiatus, Jeff Noble returns to the FASD Success Show with a tale that's been waiting in the wings. Dive into an episode filled with unexpected twists, raw emotions, and the resilience that defines every journey. Why did Jeff step away? And what brought him back to the microphone? More importantly, there's an announcement on the horizon that promises to reshape the FASD landscape. You won't want to miss this triumphant return, where every revelation leads to a brighter path forward. Tune in, lean in, and discover what's been unfolding behind the scenes.As we draw our journey to a close, we delve into the realm of emotional wellness and learn how to cope during challenging times. I'll share how I lean on my tribe for support and express my gratitude to those who've been there for me. So, are you ready for this emotional rollercoaster? Join me on this epic journey and let's face life's ups and downs together, turning every challenge into a success story.Show Notes:Check out our blog for all the links at FASD SuccessSupport the show
"The End of a Chapter: Navigating Life After Loss"In this episode, I delve into the complicated and emotional process of moving forward after the loss of my sister. As we navigate the loss of my sister's passing, I reflect on the ups and downs of grieving and how it has changed me. Join me as I share my experiences and the eulogy I never got to say. In this episode it is you helping me cope with grief and honor the memory of my sister Jennifer. I also give an update on the future of the show. Despite this difficult time, I am still passionate about sharing my story and connecting with others. I talk about the new topics I plan to cover and the ways I will be evolving the show moving forward.This is was really hard to do so I appreciate you taking the time to listen. We'll be back soon...better than ever! Support the show
We are back! What a whirlwind the last couple of months has been! In this return episode, I let you know where we have been, what we have been doing, and what the future of the show is, but more importantly for right now for you I am giving a mini-coaching session all about how to navigate not only this season but anytime there is a holiday or shift in routine and structure.How are you holding up? Many of the caregivers in our Facebook Group and Coaching Course are feeling the strain. You may be burnt out but so are our kids. Even my daughter, who is neurotypical. Add in the disability, seasonal depression, or trauma (for you or your kids) and we have an assault on our nervous systems. Tune in to hear the collective wisdom from my team and the families I work with on how to navigate this season. I dig deep and share:questions to ask and prompts to center yourself if you are strugglingquick suggestions to help ease transitions and changesa new way to respond to the negative voices when you or others think our kids are missing outI also share how my family shifted to create new traditions that reduced anxiety and pressure on everyone in our celebrations. Some of our kids can manage the season (and that's great), and some only require minor tweaks to traditions and routines (fantastic) … but for others, to survive this season, you really need to ask yourself some tough questions. Because can we ask our kids to extend their functioning beyond their current ability and expect traditional outcomes? I don't have all the answers, but I do have ideas and questions you can ask yourself to find answers that work for your family.Oh, and about the Show and where it's going? I will give you all the details on that, so you are going to want to tune in!From all of us at FASD Success, whatever you are or are not celebrating during this time of year, I hope you find more good days and success. Thank you for tuning in this year and making The FASD Success Show one of the top 5% most shared globally (according to Spotify)! That is all down to you, the listener! Thank you for sharing your time with us and The Show with others!Support the show
When Michelle and her husband adopted their son, they were told he may have issues in school due to international adoption-related issues – but no one mentioned FASD. Despite hitting all his early milestones, his challenges escalated as he got older. Their life was chaotic and stressful. They tried everything and saw all the professionals. Even the Occupational Therapist, who was on track with accommodations, didn't mention FASD. Even with a Master's in Social Work, Michelle didn't think FASD.Eventually, things escalated to the point where there was involvement with the juvenile justice system, placement in a therapeutic day school, and residential treatment. We talk about how that left her feeling like she failed as a mom and a professional. She shares what led her to make a significant shift that helped her son, her family, and herself, and how she has gone from not wanting to share her story for fear of judgment to advocating with various systems and even having her Congresswoman phoning her to talk about FASD!While each journey is unique, I hope hearing others helps you not feel alone, understand that success comes in many forms, and be inspired for your future!Show Notes:FASD Workshop: Learn what's working now from Jeff and other FASD parents and caregivers with 800+ years of experience. Click: Free Virtual Workshop. Once you register, you will get support, encouragement, strategies, and tips to deal with everyday challenges at home or school. Check out our website: FASD SuccessSupport the show
Anne and Jeff Munson are parents to four teenagers on the Spectrum. They were living in a hormone hurricane of constant dysregulation (theirs and the kids), police involvement, and challenges at school. Anne was talking back to her kids talking back to her and Jeff was trying to hold on and shore up the dam from bursting. They felt judged. They felt they were horrible parents. Their kids weren't listening to them. The teachers didn't understand them. After 17 years of trying everything, one of their kids told Anne they needed to go to parenting school. And they did.In this episode, you will find out where they went, what they discovered, what changes they made, and what results they have seen in themselves and in their kids. They also talk about their proudest moment when the school went from not listening to Anne to inviting her to train their special education staff!They still have challenges, but they are better equipped to manage them. And you can find that balance too. Check out this episode for details.Show Notes:FASD Workshop: Learn what's working now from Jeff and other FASD parents and caregivers with 800+ years of experience. Click: Free Virtual Workshop. Once you register, you will get support, encouragement, strategies, and tips to deal with everyday challenges at home or school. Check out our blog at FASD SuccessSupport the show
Brad and Sara Evans went from a loud, outgoing family involved in their community, to question why they ever left the house. Everybody knew them and loved them. Until they adopted their young great-niece and nephew. They anticipated challenges, because of the children's background, but because they didn't know about fetal alcohol spectrum disorder, they were not prepared for the challenges they faced.In the beginning, it was like walking on eggshells every day. They expected their niece and nephew to function like their 5 bio kids, including their 3 and 5-year-olds, and respond to the same parenting strategies, but they did nor could not.If you are like Sara was, yelling to be heard, and Brad thinking discipline is all you need, then check out their story and find out what they did to turn things around and you can learn what's working now from Jeff and other FASD parents and caregivers with 800+ years experience. For more information, click: Free Virtual Workshop. Once you register, you will get support, encouragement, strategies, and tips to deal with everyday challenges at home or school.Show Notes: Check out our blog for all the links at FASD SuccessSupport the show
In this episode of The FASD Success Show I am talk to entrepreneur, pizza store manager and now author – Kenny LaJoy about his recently released book: It's OK to Be You. Living Well with FASD or Other Disabilities. We talk about his journey toward acceptance and how others can better live with disabilities. He shares his motivation for the book, as well as key advice he has for individuals and the people who support them. This is an uplifting episode that doesn't paint a picture of unrealistic achievement, but it does provide encouragement on how you can accept who you are, build on your strengths and find ways to achieve realistic goals. And that it is ok to be who you are.Show Notes: Check out our blog for all the links at FASD SuccessSupport the show
Our first AMA episode (#112) was so successful I am back for Round 2 of the Q and Ehs! As with last time, I answer questions submitted by caregivers. And these six are real and raw.Please note: I am not a doctor, lawyer or social worker. I do have lived experience, education and have interviewed many individuals with FASD, researchers, professionals in the field and coached hundreds of families. I like to say, I'm an advisor. You are the expert on your child.In this episode you will get answers to questions about: responding to judgement about parenting choices with respect to accommodating symptoms or preparing our kids for ‘real' life, is the wool being pulled over my eyes when they can do one thing but not another, do all kids exhibit big behaviour, will delays be permanent or limit his future, and how to provide supervision to teens.So grab whatever you need to take notes, get comfy and get ready to get some answers. Thank you to everyone who sent in these very personal questions.If listening to this episode, created a question in your mind, feel free to reach out and you just may get it answered in the next round.Show Notes: Check out our blog for all the links at FASD SuccessSupport the show
Have you heard the phrase, nothing about us without us? A lot of self-advocates use the phrase to remind us that we need to keep people with experience in the conversations. We've had quite a few individuals with FASD on the Show and I thought a great way to wrap up FASD Month was to hear from someone who openly shares her experience with many caregivers to help them understand their kids.Heather Vickers received her diagnosis seven years ago when she was 44. She has been married since 2005, has a stepson with Autism, and is a cat mom and self-advocate. She candidly shares her before and after journey. The before is filled with difficult challenges trying to make it on her own without a diagnosis, understanding, and support. But she has an incredible story of transformation that occurred through sheer determination. She now shares her journey and insights to help other individuals with FASD and those that support them.Show Notes: Check out our blog for all the links at FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Caregivers ask me all the time … how can I teach my loved ones skills to soothe themselves, stop a meltdown, or regulate themselves. Understanding the sensory system is key to answering those questions and you can get some ideas on how to do that with my guest this week, Jessica Sinarski. We first met Jessica in episode #099, Insight on Trauma, Attachment, and Sensory Systems. She returns to talk about her upcoming book aimed at normalizing sensory processing differences and helping kids understand their sensory systems.We talk about her beginnings in work with trauma and resilience, the sensory system and why our kids get big feelings, how Riley the Brave came to be, and why stories are effective as teaching tools.While this book isn't about kids with FASD, it is a book that will help kids with FASD and their parents and caregivers. I think you will find Jessica has taken a subject that many adults don't understand and put it in a format that will reach kids and their parents. Be sure to check out the Show Notes for a link to our blog to order a copy and follow Jessica.Show Notes: Check out our blog for all the links at FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
It's September 9 and that means it's International FASD Awareness Day! In honour of that, we have a unique and special treat for you today! What started out as a quick promo video for a new song, turned into a BONUS podcast episode because it was so great!I am talking to Joanne Garofalo from Voice in a Million & FASD Hub Scotland and Darren Day, an actor and singer from the UK, about the release of a new song – You Are My Story – written by James Hawkins.The cool part is that while this version is launched today - FASDay - a bigger project is in the works that anyone can participate in. You will get all those details, plus:Why Joanne wanted to broaden the Voice In A Million to include this songWhy Darren became involved and how he will navigate any negative pushbackTheir hope for this song and for those who listen and shareAn incredible opportunity we have when we work in this field is to witness the realization people have about how prenatal alcohol exposure may have touched their lives. I went into this interview thinking it would be a 5-minute video promo about a song and soon realized it was much more. Especially for Darren, who is now a champion for FASD. As he said, he is “eager like an athlete on the starting line.”Check out the links below. I hope whatever you do today has meaning for you. Together we will bring awareness to light about prenatal alcohol exposure, the strengths and brilliance of people with fetal alcohol spectrum disorder and the amazing support and advocacy of parents and caregivers.Show Notes:“You Are My Song”. Written by James Hawkins, performed by Darren Day, and supported by a choir of children with FASD and other neurodevelopmental conditions and their families. Download the song here: https://www.adoptionuk.org/fasd-month-22 Previous Podcast with Jo:#082 Jo Garofalo: FASD The Hidden DisabilityHistory Notes of FASDay: Day 50 OF 99 Days: The Birth of FASDayCheck out our website: FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Even if the school has started, there is still time to set the tone to help you and your child have the best year and relationship with school personnel. I brought this week's guest back after seeing her last episode is in the top 7 downloads. This tells me you like what she is saying, and I know you will love her back-to-school tips!Danna is the Director of the Foothills Fetal Alcohol Society and an FASD Instructional Coach with the Wrap2FASD program. We know back-to-school season is a tough transition for everyone. You are thinking about last year and wondering how this year is going to go. Danna shares her insights using an easy-to-remember analogy: T.I.P.S.In addition, she reflects on her work in the early days of the growth of the Autism Community and offers her thoughts on how to get out of our “stinking thinking.” She leaves us with an invitation to get in touch with the person we are underneath the advocate. Let me know if you use any of these T.I.P.S. and how they worked! I would also love to hear from the teachers – what are your tips?Check out our website: FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
One of my goals with The FASD Success Show podcast is to bring you a wide variety of guests, including those who are leading experts in the FASD community. Today's guest, Audrey McFarlane, the Canada FASD Research Network Executive Director, is no exception. She returns to the Show for the third time and brings updates on research and some exciting announcements of interest to our listeners from anywhere in the world.Tune in to find out details about how you can get involved in a caregiver survey, and FASD Month, as well as announcements on a national FASD strategy, an international prevention series, as well as details about projects on substance use, housing, and mentoring new researchers.If you want to know about some exciting new developments and projects and how to get involved, be sure to tune in and check out our blog for all the links.Show Notes: Check out our blog for all the links at FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Today's episode is a heavy topic that might make some people uncomfortable, but it is one that we should be prepared for – because it is inevitable at some point our children will be faced with a death – whether that is a pet, family member or friend. We reached out to Marj Wingrove who is a parent to an individual with FASD but also a Death Doula and producer and host of the Death Happens podcast.We talk about her experiences as a caregiver, thoughts on why adults are uncomfortable with the topic, when to talk about it and five tips on how to talk to children with FASD about it. She also gives suggestions for parents on how to balance their own grief while trying to support their child(ren).Be sure to check out the link in the Show Notes to find resources to help as well as to Marj's podcast.Show Notes: Check out our blog for all the links at FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Have you ever wished you could understand how your loved one experiences the world? What do they think about their disability and what do they want others to understand? Today's guest is going to help us do that. Last year, Miranda Eodanable was on The FASD Success Show to talk about a Photovoice Research Project she was about to undertake, asking young people to document their experience in pictures. In this episode, she shares the results from the group of eight individuals with FASD (ages 12 – 19 years old) who participated.Miranda is an Educational Psychologist in Scotland responsible for neurodevelopmental assessment pathways with health services in areas of FASD and Intellectual Disabilities. She has worked in education systems for the last 20 years and has guest lectured on the Scottish Masters in Educational Psychology courses. Currently, she is working on a Ph.D. at the University of Edinburgh on the value and impact of an FASD diagnosis.This project asked individuals with FASD to photograph their lives. Through these photographs, they shared what is essential in their lives at home, and school and what the diagnosis and disability of FASD mean to them.Miranda also tells us about the next two research projects she will be undertaking with health and then educational professionals. This project certainly unearthed some fascinating research. While some of the themes and words that emerged confirm what prior research tells us, there are some interesting opposites. Make sure you stay tuned until the end when Miranda lets us know about an emotional response from an individual with FASD after he saw the results. Check the Show Notes for a link to the Project.Show Notes: Check out our blog for all the links at FASD Success.Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
It's back-to-school season, and with that comes IEPs, IPRC, 504s, and education plans! If the terms or process are confusing and frustrating, we have covered you in this week's podcast with Mark Courtepatte – one of the most popular Insider Experts in our CKS Coaching Program. But you don't have to be in the program now to hear his expertise!We talk about how Mark met Savanna, his partner who has FASD, how they became involved with the Hamilton Parents and Caregivers Support group that he co-chair, and how his interest in the education sector developed.This episode is full of insight on how to work collaboratively with teachers and the school board. Mark is just as comfortable talking to the Minister of Children and Community Services as he is too overwhelmed by caregivers or children with FASD. You will find out why he thinks 99% of IEPs are not worth the paper they are written and gives you some concrete steps to follow from being confused and not sure how to proceed to become the confident advocate for your child. He provides some suggested rebuttals to resistance and gives you a gauge to know if the plan is working. You are going to find out why his workshops are one of the most popular in our CKS program.Be sure to check out the show notes for a link to our blog where you can find his awesome support group website.Show Notes: Check out our blog for all the links at FASD Success.Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Tigger Warning: Incarceration, Suicide, Trauma, and Sexual Assault This unique episode has some critical information about how systemic barriers and failures can result in adverse outcomes for individuals with FASD. We will leave the detail for the episode, but we want to give you a general idea about the content. First up, I want to thank Shawn for being brave and vulnerable in sharing his story. Rhonda also has my deep respect for supporting and loving him through this process, while also recognizing the impact and harm on the victim. Rhonda has worked in the child welfare system for 30 years. She was first introduced to FASD in her personal life when she provided respite for Debbie and Bill Michaud (both former podcast guests). Eventually, she raised 8 individuals (most with FASD) and supported a variety of their friends and family along the way, which is how she came to know Shawn. My hope in sharing Rhonda and Shawn's story is that caregivers will gain valuable tips for supporting vulnerable individuals. I also hope it shines a light for professionals on what can happen where there is no diagnosis and no access to informed services. When we assume a person “looks normal and talks normal”, we put them into situations where they can fail. When they fail, someone gets hurt. They get charged and the charges can be serious. Now we are left with families in ruins where the failure was in fact not the individual, but systemic from years and years ago. There have been some hard lessons in Shawn's story but there have been some silver linings. No matter what happens in Court, we hope that Shawn and his victim find healing. Show Notes: Check out our blog for all the links at FASD Success Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
When I ask caregivers what the one thing they'd like to change is – physical health is at the top of that list for many. That is why I invited Stephanie Burns onto the Show. Stephanie has a degree in Physical and Health Education and runs Burns Fitness. She and her husband have 4 kids, 2 with neurodiverse needs. On top of that, she undertook a program to lose 100 pounds and get fit. So she gets it. Stephanie also talks about the reality of having kids and the effect not being in good health can have on caregiving. She gives ideas on incorporating all this with a busy household and kids with neurodiverse needs. She also gives you a five-point plan to follow and a piece of wise advice on what to say when you are in the trenches and might be hard on yourself. I know she is good at what she does because Tara and I are in her program. And because she has been in the trenches, I wanted her to share her knowledge with you. Show Notes: Check out our blog for all the links at FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
If you've attended any of my presentations, taken my CKS Coaching Course or followed me for a while you will know one of my sayings is “I'm not a doctor, a lawyer or a social worker,” but my guest today is a social worker and she just happens to be my wife and business partner – Tara Soucie-Noble. Tara does much of the behind-the-scenes work - with our daughter and our business - but she had a long career working with individuals with FASD, was a foster parent with me, and has worked with a variety of populations who have intensive housing support needs. In this episode you will hear her perspective on our marriage, time as foster parents and on how incredibly lucky we are to share what we know with other caregivers. She is also going to share her insight how caregivers can support each other, how to survive in the moment and what individuals with FASD need for successful interdependent living. I want to acknowledge that Tara is a big part of our community. Without her, there would be no business and no Show. In fact, she will be taking on a bigger role come September and I can't wait for more awesomeness she will bring to help caregivers. I hope you enjoy getting to know her a bit more and enjoy our banter back and forth! Show Notes: Check out our blog for all the links at FASD Success Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Today's show is a show of firsts. You will learn how Tristan and Scott Casson-Rennie first met, how they became the first same-sex couple to adopt through the agency they used, their trials and tribulations as they navigated parenthood with first a sibling group and then a third child added to the mix, how they created their first organization together called FASD Ireland, and what the first item Scott asked for after coming out of surgery. You will also learn about their partnership with the Hidden Disabilities Sunflower, the barriers to starting a new venture in a culture of alcohol acceptance, Scott's involvement with the Adoption and Fostering Podcast, and a recent serious health condition that changed their perceptions on life and created an unexpected change in one of their sons. This was a fun interview as well as an enlightening one. I love to hear what is going on in different parts of the world. Despite cultural differences caregivers around the world have so much in common. While you may not be able to start your own organization, I hope you will be inspired by Scott and Tristan and find something you can take into your everyday caregiving that helps you meet with more success. Be sure to check out the Show Notes for a link to our blog if you want to give them a follow or get in touch. Show Notes: Check out our blog for all the links at FASD SuccessSmells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
You may have heard talk in the FASD world about a new documentary in the making, Embraced: Truth about Fetal Alcohol Spectrum Disorder. I wanted to find out the details so invited the three principals on the project to talk about it. Joel Sheagren is the Director with Jodee Kulp and Justen Overlander co-producing. Joel has a 30-year background in advertising and is a parent to a young man on the Spectrum. Jodee is an author, advocate, both an individual with and parent of a loved one with FASD, co-founder of the Red Shoes Rock movement, and returning guest. Justen is a former teacher who also works in the film industry.You will find out what the project is all about, how it will be different from other films about FASD and how you can help support Embraced. And if you stay until the end of the Show, you will find out what challenge Jeff issues to Joel! You can find all the links on our blog. Link in the Show Notes below.Show Notes: Check out our blog for all the links at FASD Success Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Another first for The FASD Success Show – You Asked and Jeff Answers! I contacted caregivers in our private Facebook Group and Email Newsletter to find out what questions they wanted answers to. I received so many that I couldn't decide which to feature, so I randomly picked eight and will save the rest for a future episode. It's important to recognize I am not a doctor, lawyer, or social worker. I have lived experience, and education, and have interviewed many individuals with FASD, researchers, and professionals in the field, and coached hundreds of families. I like to say, you are the expert on your child, I'm an advisor. In this episode you will find out more information on the importance of a diagnosis, neurofeedback, my top 2 takeaways from interviewing adults on the Spectrum and why understanding FASD as a Spectrum is important, toileting, swearing, plans for workshops or gatherings, survivor guilt for siblings, and regression in young adults. So grab a pen and paper, get comfy, and get some answers. Thank you to everyone who sent in the questions. Let me know if you like this format. Cause if you do, we will definitely do it again. Show Notes: Check out our blog for all the links at FASD Success Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
Have you ever wanted to share your story and experience with the world? Let others in on your lessons learned and hope they find comfort knowing they aren't alone in their journey? That's exactly what my guest, Jillana Goble has done – for a second time, with her new book: A Love Stretched Life, Stories on Wrangling Hope, Embracing the Unexpected and Discovering the Meaning of Family. In this episode, Jillana reflects on her journey to fostering, and what she learned along the way, including the difference between how children are presented in the foster system versus the reality and how shifting their expectations allowed them to thrive, survive and grow as a family. We wrap up talking about the critical conversations and shift in mindset she feels needs to happen in the foster care system to better prepare foster and adoptive parents, along with her best advice for prospective and adoptive parents. We also touch on how she self-regulates and why she stays off social media. Jillana has crafted a collection of personal stories that will serve as a guidepost for caregivers who need to navigate the often-tumultuous terrain of fostering, adoption, and raising a neurodiverse child in a world that doesn't quite understand. Show Notes: Check out our blog for all the links at FASD Success Smells Like HumansLike spending time with funny friends talking about curious human behavior. Listen on: Apple Podcasts SpotifySupport the show
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