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Jessica Birch is a national advocate and speaker living on the South East Coast of Australia. Since her late diagnosis of Fetal Alcohol Spectrum Disorder (FASD) at the age of 33, she has turned her attention to awareness building and education to create a better understanding of the prevalence and consequences of prenatal alcohol exposure in Australia. Jessica shares her lived expertise in an effort to equip individuals, parents/carers, educators and health professionals with the information they need to create successful interventions and support. She believes awareness and action are key to minimizing the rate of prenatal alcohol exposure globally and works closely with organizations, stakeholders and government on alcohol policy and regulatory reform. During this episode, you will hear Jessica talk about: Her life growing up with undiagnosed FASD How she learned what FASD is and how it applies to her  Her concerns about doctors being unaware and minimizing the effects of FASD  How receiving the diagnosis changed her outlook on life Types of outside support that she receives for FASD To find out more about Jessica and her work, check out her website at www.jbtalksfasd.com.au, email her at jessicabirch.fasd at gmail dot com, and follow her on Instagram @jb_talksfasd and Twitter/X at @JB_TalksFASD. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Welcome to "Ditch the Lab Coat," the podcast where we break down complex medical topics with leading experts shaping the future of healthcare. In today's episode, we're diving into the nuanced and critical conversation surrounding Fetal Alcohol Spectrum Disorder (FASD) with our distinguished guest, Dr. Susan Rich. With a career spanning decades, Dr. Rich is a trailblazer in child and adolescent psychiatry and an ardent advocate for public health. She's here to shine a light on prenatal alcohol exposure's often overlooked impacts on brain development. Did you know that not only alcohol consumed during pregnancy but even prior to conception can lead to multigenerational health issues? Dr. Rich unpacks how prevalent this is, affecting 1 in 20 children, yet remains largely unrecognized. Throughout our discussion, we'll explore systemic challenges, the myths perpetuated by the alcoholic beverage industry, and most importantly, the critical steps we need to take for prevention and support. Whether you're a healthcare professional, a parent, or just intrigued by one of public health's hidden crises, this episode promises to be both enlightening and empowering. Get ready for a thought-provoking journey as we seek a healthier future for the generations to come.Key Takeaways :The Hidden Impact of Alcohol on Fetal Development Dr. Susan Rich explains that fetal alcohol spectrum disorder affects approximately 1 in 20 children (5% of the population), with far-reaching consequences beyond the commonly known physical characteristics.Early Pregnancy Vulnerability Critical developmental impacts occur as early as the third to fourth week post-conception, often before women know they're pregnant. About 13.5% of childbearing age women in America binge drink, and approximately 50% of pregnancies are unplanned.Beyond Traditional Understanding While medical education traditionally focused on severe cases with facial deformities and intellectual disabilities, Dr. Rich reveals that only 10-15% of affected children show these classic features. The majority have neurodevelopmental issues without obvious physical signs.Male Factor Contribution Alcohol consumption by men up to three months before conception can affect sperm quality through epigenetic modifications, potentially making the embryo more susceptible to alcohol exposure during pregnancy.Economic and Social Impact The alcohol industry generates approximately $220 billion annually, while the cost of caring for just those with full fetal alcohol syndrome (not including the entire spectrum) was estimated at $5.4 billion as of 2003 data.Prevention and Treatment Approaches Dr. Rich advocates for better public health messaging, comprehensive support systems for affected children, and the need for healthcare providers to better understand and recognize the full spectrum of alcohol-related developmental disorders.03:14 - Alcohol's multigenerational impact explained.08:27 - Alcohol's epigenetic effects on offspring.13:17 - Unplanned pregnancies and fetal alcohol syndrome.15:33 - Neural crest and facial development.19:18 - Fetal alcohol, nutrition, and growth.23:04 - Dr. Kathleen Sulick's contributions.25:26 - Alcohol's impact on family events.28:38 - Alcohol's cultural role and societal effects.30:57 - Alcohol's toxicity and informed consent.34:05 - Liquor profits and education funding.37:35 - Rethinking alcohol's role in society.42:56 - Global epidemic: Fetal alcohol impact.45:05 - Supporting neurodivergent youth transitions.47:50 - Taxing alcohol to aid impoverished children.51:01 - Alcohol's Hidden Health Impacts.54:12 - Rethinking alcohol's impact on children.DISCLAMER >>>>>>    The Ditch Lab Coat podcast serves solely for general informational purposes and does not serve as a substitute for professional medical services such as medicine or nursing. It does not establish a doctor/patient relationship, and the use of information from the podcast or linked materials is at the user's own risk. The content does not aim to replace professional medical advice, diagnosis, or treatment, and users should promptly seek guidance from healthcare professionals for any medical conditions.   >>>>>> The expressed opinions belong solely to the hosts and guests, and they do not necessarily reflect the views or opinions of the Hospitals, Clinics, Universities, or any other organization associated with the host or guests.       Disclosures: Ditch The Lab Coat podcast is produced by (Podkind.co) and is independent of Dr. Bonta's teaching and research roles at McMaster University, Temerty Faculty of Medicine and Queens University. 

Chris, Kayla, and Ryan sit down with their friend Sandra Flach, Founder and Executive Director of Justice for Orphans and host of The Adoption and Foster Care Journey Podcast. They discuss the myths and realities of Fetal Alcohol Spectrum Disorder (FASD) and offer some ways to help. Sandra is an FASD Educator and Coach. Links Justice for Orphans The Adoption and Foster Care Journey Podcast FASD Resources One Big Happy Home Web | Facebook | Instagram | YouTube | TikTok | Email Produced by Dallas Stacy

"The LORD is my strength and shield. I trust Him with all my heart. He helps me, and my heart is filled with joy." -Psalm 28:7   Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you as you care for children in crisis through adoption, foster care and kinship care.   This week we welcome back returning guest, Dr. Jerrod Brown. Dr. Brown is a professor, trainer, researcher, and consultant with multiple years of experience teaching collegiate courses. He has provided consultation services to caregivers, professionals, and organizations pertaining to Autism Spectrum Disorder (ASD), Fetal Alcohol Spectrum Disorder (FASD), confabulation, suggestibility, Traumatic Brain Injury (TBI), youth fire-setting, trauma and other life adversities.   Jerrod has completed 4 separate master's degree programs and holds graduate certificates in Neuropsychology, ASD, Other Health Disabilities (OHD), and TBI. In 2021, Dr. Brown completed a post-doctoral certificate in Leadership and Organizational Strategy and a Professional Certificate in Forensic Psychology. Jerrod has published several articles and book chapters and is regularly featured on several national and international podcasts.    Listen in today as Sandra Flach and Dr. Brown discuss FASD and Addictive Behaviors.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media. Links mentioned in this episode: justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Hope For the FASD Journey Support Group

The third annual Fetal Alcohol Spectrum Disorder (FASD) conference is taking place next month. The event will take place at the Halifax Tower Hotel on November 8th and will feature talks from people with lived experience and ways we can address FASD in Nova Scotia. The conference is put on by the organization Fetal Alcohol Nova Scotia, which was founded by Allan Mountford and Rochelle Howlett. Allan is a retired educator, and Rochelle is a parent and advocate for families with FASD. Mainstreet's Alex Guye gave them both a call and she began by asking Allan to explain how FANS was founded.

Kurt is joined by Dr David Junior Gilbert from the University of Salford in the UK. He is a University Fellow researching the intersection of FASD and the criminal justice system. His research focuses on factors that make individuals with FASD more vulnerable to involvement in the criminal justice system, such as confabulation, suggestibility, compliance, and acquiescence. Dr. Gilbert is leading a larger international study examining these issues in multiple countries, aiming to provide scientific evidence to support decision-making in the justice system. For more information about FASD, please go to: https://www.nofasd.org.au/ If you are interested in the international study on Fetal Alcohol Spectrum Disorder (FASD) and the justice system, at the time of the release of this podcast Dr Gilbert is still recruiting research participants. To express your interest in being involved please see: https://app.onlinesurveys.jisc.ac.uk/s/salford/international-fasd-and-justice-system-study Producers: Kurt Lewis, Louise Gray and Julie Flanagan Interviewer: Kurt Lewis Interviewees: Dr David Junior Gilbert Narrator: Frances Price The copyright is owned by NOFASD Australia. All rights reserved – No reproduction or use of this content without written consent of Kurt Lewis and NOFASD Australia. The views expressed in this podcast are those of the interviewee. NOFASD makes every effort to ensure all content is free from judgement and stigma. NOFASD's mission includes reducing stigma for families and individuals impacted by FASD.

In this episode of The Defender Podcast, we welcome Sandra Flach, a devoted mom of eight, including five adopted children—one through kinship and four internationally. With over 30 years of parenting experience, Sandra shares her journey of raising children with trauma histories, particularly her two youngest who have Fetal Alcohol Spectrum Disorder (FASD). As the co-founder of Justice For Orphans and host of the Adoption & Foster Care Journey podcast, Sandra offers valuable insights into the challenges of FASD, the importance of awareness, and practical strategies for parents and caregivers. Tune in to hear Sandra's story of faith, resilience, and her mission to support vulnerable children and families.GUESTSandra Flach is a mom of eight, with five adopted children—one through kinship and four internationally. With over 30 years of parenting experience, she understands the challenges of raising children with trauma histories, especially her two youngest who have Fetal Alcohol Spectrum Disorder (FASD).In 2011, Sandra co-founded Justice For Orphans, a nonprofit ministry supporting orphans and foster children. She hosts the Adoption & Foster Care Journey podcast, offering encouragement and insights to foster and adoptive parents. Her book, Orphans No More—A Journey Back to the Father, shares her family's story and her spiritual journey as an adoptive parent. Sandra lives in upstate New York with her husband, Wayne, where they continue to parent their teenage sons and enjoy time with their grandchildren.HOSTDr. Rick Morton is the Vice President of Engagement at Lifeline Children's Services.LIFELINE CHILDREN'S SERVICESThe mission of Lifeline Children's Services is to equip the Body of Christ to manifest the gospel to vulnerable children. Our vision is for vulnerable children and their communities to be transformed by the gospel and to make disciples. FOLLOW USFacebook, Instagram, TwitterThe Defender Podcast: Subscribe on iTunes | Transistor | SpotifyThe Defender Bible Study: Subscribe on iTunes | Transistor | Spotify

Send us a Text Message.What does it take to transform life's most challenging seasons into a story of hope and inspiration?In this episode, we delve into the extraordinary journey of Patricia Morgan, author of "Love Her as She Is." Patricia's story is a testament to the unpredictable, heartwarming, and often heartbreaking journey of motherhood. When Patricia and her husband adopted their daughter Kelly at 6, they embarked on a journey of profound love, unique challenges and endless fears. After years of facing the peaks and valleys together things became more clear when Kelly was diagnosed with Fetal Alcohol Spectrum Disorder (FASD).As a mother, coach, clinical counsellor and author, Patricia is no stranger to adversity.  Both a student and teacher of life, Patricia shares her inspiration for writing this book for Kelly, what Kelly taught her and what feeds the limitless love and strength that resides within us. Patricia identifies some of the adversities that informed her resilience journey and lets us in on her "secret sauce" for maintaining such extraordinary energy and drive.  Currently battling cancer, Patricia's spirit remains unshaken and her light shines bright. Website: https://www.solutionsforresilience.com

I have the incredible opportunity this episode to discuss the intricacies of Fetal Alcohol Spectrum Disorder (FASD) with Barb Clark, an esteemed expert in the field. As someone who works closely with children, exploring this topic was eye-opening for me, resonating deeply with the struggles and challenges many young ones face. Barb, a mother of five, shares her personal journey and insights gained from her eldest daughter's FASD diagnosis, offering a wealth of knowledge and perspective. Throughout our conversation, she sheds light on the complexities of FASD, emphasizing its profound impact on brain function and behavior. We discuss the misconceptions surrounding alcohol use during pregnancy and the urgent need for early recognition and support for affected individuals. One of the most powerful aspects of our discussion is Barb's advocacy for a paradigm shift in parenting and caregiving approaches, highlighting the limitations of traditional disciplinary methods and sharing strategies for fostering understanding, empathy, and connection with children affected by FASD. From navigating transitions to building supportive relationships, Barb provides invaluable advice for professionals and caregivers alike. Through her expertise and personal anecdotes, she underscores the importance of advocacy, empathy, and resilience in supporting individuals and families affected by FASD. Our conversation sheds light on a topic that is often overlooked and misunderstood, empowering listeners to advocate for greater awareness and support for those living with FASD.   Highlights: [2:19] - Barb explains what FASD is. [4:08] - Barb advocates against moderate alcohol use during pregnancy due to the limitations of flawed research. [5:34] - Barb highlights the prevalence of unplanned pregnancies, stressing the need for improved FASD awareness. [8:36] - Hear about Barb's journey from working with at-risk youth to parenting and the challenges that she faced. [11:29] - Barb recounts escalating efforts to address her daughter's behavior, leading to a pivotal discovery about FASD. [13:42] - Learn about Barb's daughter's FASD diagnosis and the transformative impact of expert training. [16:32] - Consequence-based parenting exacerbates anxiety and hinders learning, especially for children with FASD and/or histories of trauma. [18:38] - Barb argues that parenting children with FASD or trauma requires a relational approach, moving beyond traditional consequences. [20:21] - Shifting from consequences to understanding, Barb fostered open dialogue with her daughter. [23:58] - Barb recounts a humorous church incident, having noticed the similarities between FASD and Alzheimer's behavior. [26:46] - Barb expresses that teaching her daughter the concept of confabulation helps her understand her brain's unique workings and builds self-awareness. [29:25] - Barb explains why adults often struggle to understand FASD. [31:56] - Incorporating preferred activities at neutral locations before returning home eases transitions for children. [33:14] - Barb points out how inserting fun and creativity into activities eases transitions for children and reduces resistance. [36:52] - Talk-based therapies often inadequately address FASD, but sensory-focused interventions like occupational therapy are even more effective. [39:41] - Barb asserts that we need to stop stigmatizing birth moms and understand FASD's brain-based nature for effective support. [42:26] - Barb adds that it's also important to understand that children with FASD usually function at half their physical age. [43:53] - Barb credits one of her closest friends, Julie Martindale, for having taught her a great deal about FASD.

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 #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

Patti is committed to improving children's lives by providing practical tools to parents and professionals who care for children with brain-based differences, whose behaviors are reflective of either brain changes that resulted from exposure to prenatal toxins and/or from trauma, or reflective of the poor fit between their cognitive abilities and the world's expectations of them. Patti has worked in the fields of mental health and child welfare for over thirty years and has worked with hundreds of foster and adoptive families. She has led workshops in the areas of adoption, trauma and resiliency, attachmend and neurobehavior for several years. Patti's other work, as a hospice chaplain, has fueled her fire of helping others to live life well and end the cycle of intergenerational trauma. Patricia Kasper, MA, MTh, is a Neurobehavioral Coach and Trainer, who is passionate about supporting those affected by Fetal Alcohol Spectrum Disorder (FASD). With over thirty years of experience in the fields of addiction, mental health, and child welfare, Patricia recognized a need for greater outreach to help those impacted by FASD. Patricia hosts a weekly podcast, Living with FASD: Candid Conversations with Patti Kasper. Her first book, Sip by Sip: Candid Conversations with People Diagnosed as Adults with Fetal Alcohol Spectrum Disorders (FASD) launched in late August 2023. Patricia Kasper, MA, MTh, Training Services, LLC provides staff development training and coaching services, serving not only parents of children with brain-based differences but neurodivergent adults as well. Because traditional therapeutic approaches generally fail those with FASD or other neurobehavioral conditions, Patricia is passionate about helping others in the helping professions (social workers, therapists, coaches, and recovery specialists) to adopt a more effective paradigm to better support those who are neurodivergent. Out of her wealth of experience, Patricia has also created training packages addressing intergenerational trauma and adoption preparation. @healing Learn more about your ad choices. Visit megaphone.fm/adchoices

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

Co-host: Tom Druke, Balchem Corporation & Dr. Eric Ciappio, Balchem CorporationGuests: Dr. Stephen Hursting & Dr. Susan Smith, University of North Carolina Nutrition Research Institute; Dr. Steven Zeisel, University of North Carolina; Dr. Kevin Klatt, University of California, Berkeley; Dr. Richard Canfield, Cornell University; Dr. Colin Carter, Columbia University; Dr. Joe McFadden, Cornell UniversityToday's episode was filmed at the Future Directions in Choline Symposium put on by the University of North Carolina Nutrition Research Institute.Our first guests are Dr. Stephen Hursting and Dr. Susan Smith, the director and deputy director of the UNC Nutrition Research Institute. Steve and Susan give some background regarding the inspiration behind the conference as well as what will be covered during the symposium. The gathering is an opportunity to get the leading choline researchers together to update each other and build the momentum of choline research. The last time choline researchers gathered was in 1998, when requirements were set. (0:50)The next guest on our roster is Dr. Mark Manary, a professor of pediatrics at the Washington University School of Medicine. Mark's symposium talk discusses choline and food aid. Food aid products are specially designed to address needs from crisis situations. These specialized food aid products are standardized to meet great deficiency or inadequacy needs. On the most extreme side, there is a product called ready-to-eat therapeutic food for children who are starving to death. Other food aid products include those for children who are severely underweight. Dr. Manary's research consists of clinical trials in sub-Saharan Africa that include different nutrients in food aid to see if there are improvements in children's responses. One trial with the inclusion of DHA found a 6-15 IQ point difference by adding fish oil or DHA. Mark hypothesizes that a doubling of that effect will be observed when choline is added. (6:52)Next up is Dr. Kevin Klatt with the University of California - Berkeley. His symposium talk consisted of choline and DHA, focusing on two areas of his work. The first is dietary choline's impact on the production of phosphatidylcholine species enriched in the omega-three DHA, specifically in pregnancy. The second is interactions between lauric acid and choline, where a phosphatidylcholine species can actually bind to proteins that turn genes on and off. In one experiment, Kevin's group hypothesized that inadequate choline intake during pregnancy compromises the efficient handling of DHA by the liver. They showed in a randomized controlled trial that supplementation with choline dramatically improved the status indicators of DHA status. (17:33)Our fourth segment features Dr. Richard Canfield from Cornell University, whose symposium talk focused on choline and neurodevelopment. Rick is a developmental psychologist by training who works in infant and early child cognition. He has researched visual cognition and speed of information processing with babies in the first year of life for women who received a diet containing the recommended intake of choline and those who received double the recommended intake during pregnancy. They found that cognition improved for babies in the high choline group over their first year of age, which was maintained until seven years of age. The cohort is now 14 years old, and additional testing is being conducted to see if in utero exposure to choline still impacts the children 14 years later. (29:51)Dr. Robert Colin Carter from Columbia University is our next guest. His talk focused on choline and Fetal Alcohol Spectrum Disorder (FASD). His research has mainly been fetal alcohol spectrum disorders, with a particular interest in how both maternal and child nutrition might impact the teratogenic effects of alcohol. Prenatal alcohol exposure is the most common preventable cause of developmental delay worldwide, and a common view might be that women should just stop drinking. Dr. Carter argues that view is shortsighted because alcohol use is a really complicated problem for a lot of people. Asking someone who has an alcohol use disorder to stop drinking is probably not realistic for a lot of women. In animal models, supplementing a pregnant dam with choline seems to ameliorate at least some of the teratogenic effects of alcohol. Dr. Carter has completed a pilot study of 70 women from South Africa where beneficial effects of choline treatment during pregnancy were observed for growth, neurobehavior, and memory in their children. Another clinical study with 300 participants is now underway.  (51:38)We end our day one episode with a wrap-up from Dr. Dr. Susan Smith with the University of North Carolina Nutrition Research Institute and Dr. Joe McFadden with Cornell University. Susan emphasized the recurring message that choline is so important in prenatal health and in early postnatal periods. Pregnant and lactating women generally don't take enough choline, and choline is so important for healthy brain development in the fetus and the infant. Joe's takeaways from the livestock side of things include the impact of choline on colostrum production in animals and early-life supplementation in young livestock. (1:08:42)Be sure to subscribe so you don't miss day two highlights from the Future Directions in Choline Symposium in future episodes. If you want one of our new Real Science Exchange t-shirts, screenshot your rating, review, or subscription, and email a picture to anh.marketing@balchem.com. Include your size and mailing address, and we'll get a shirt in the mail to you. 

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

"Finally, brothers & sisters, rejoice! Strive for full restoration, encourage one another, be of one mind, live in peace. And the God of love and peace will be with you." 2 Corinthians 13:11   Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you to care for children in crisis through adoption, foster care and kinship care.   On this final FASD Awareness Month episode host Sandra Flach speaks with Eileen Devine, LCSW, founder of Brain First Parenting and the Resilience Room Community. She is also an adoptive mom of a daughter who lives with Fetal Alcohol Spectrum Disorder FASD.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media. Links mentioned in this episode: sandraflach.com justicefororphansny.org runfasd.org FASCETS.org FASDUnited.org EileenDevine.com

Discover the groundbreaking FASCETS Neurobehavioral Model and its profound impact on understanding Fetal Alcohol Spectrum Disorder (FASD) within child welfare - essential listening for anyone passionate about improving the lives of children and families. In this episode, Patti Kasper and I delved into a profound discussion centered around the FASCETS Neurobehavioral Model, Fetal Alcohol Spectrum Disorder (FASD), and its implications in child welfare. The conversation was enlightening and touched on various critical aspects of these complex subjects. Patti began by highlighting her extensive background in child welfare and her journey through different academic disciplines, including social work and psychology. Her diverse experiences led her to develop a deep passion for understanding and assisting children with FASD, a condition caused by prenatal exposure to alcohol. One of the key takeaways from the conversation was the emphasis on viewing FASD as a developmental disorder that persists beyond childhood. Patti pointed out that this condition doesn't simply disappear when a child reaches a certain age, challenging the prevailing perception of FASD as a childhood disability. This understanding is crucial in ensuring that individuals with FASD receive adequate support throughout their lives. The heart of the discussion revolved around the FASCETS Neurobehavioral Model, a tool that helps parents and caregivers understand and support children with FASD. Patti explained how this model focuses on identifying brain tasks, assessing what is easy and difficult for the child and tailoring support accordingly. This approach allows caregivers to provide individualized care and accommodations, helping children with FASD thrive. Throughout the conversation, Patti passionately addressed the misconceptions and stigmas associated with FASD. She emphasized the need for a shift in societal perception, particularly regarding behavioral challenges. Patti urged parents and caregivers to consider that behaviors in children with FASD are not intentional choices but often the result of how their brains are wired. We also discussed the parallel between FASD and other neurobehavioral conditions. Patti highlighted the importance of recognizing the unique wiring of each child's brain and advocated for the application of the FASCETS model to support children with various neurobehavioral conditions, whether diagnosed or not. Our conversation also touched on the challenges faced by parents and caregivers, including the immense mental load of caregiving and the toll it takes on their own mental and physical health. Patti shared her own experiences as a caregiver for her mother, and the importance of self-care and support for caregivers. Patti highlighted the urgent need to dispel the assumption that behaviors in individuals with neurobehavioral conditions are intentional choices. She stressed the importance of considering the role of their brains in shaping their behavior. This conversation with Patti Kasper provided a comprehensive and insightful exploration of the FASCETS Neurobehavioral Model, FASD, and their broader implications in child welfare. We underscored the need for a shift in perception, increased understanding and tailored support to help individuals with FASD lead fulfilling lives. Patti's extensive knowledge and passionate advocacy for this cause made for a captivating and enlightening conversation. More about Patti: https://www.tacosfallapart.com/podcast-live-show/podcast-guests/patricia-kasper --- Send in a voice message: https://podcasters.spotify.com/pod/show/mommafoxfire/message Support this podcast: https://podcasters.spotify.com/pod/show/mommafoxfire/support

Laura Hernandez is the CEO and founder of Mama Systems, a coaching business that helps moms create peace in their homes through systems. So many of us are simply reacting to life and surviving motherhood that we are missing out on the people we love and the things we want to be doing. In this episode, Laura discusses Fetal Alcohol Spectrum Disorder (FASD), Reactive Attachment Disorder (RAD), and other forms of neurodiversity. Laura's family story of fostering, adopting, and special needs has shaped not only her life but has also brought about this company that has coached hundreds of moms to peace in their homes. https://www.mamasystems.net/ https://www.mamasystems.net/creating-chores The Autistic Me: Blog: https://www.tameri.com/autisticme/ Podcast: https://autisticme.libsyn.com/ Facebook: https://www.facebook.com/autisticme/ Twitter: https://twitter.com/autisticme YouTube: https://www.youtube.com/c/CSWyatt LinkedIn: https://www.linkedin.com/company/autisticme

The FASD journey can be very defeating and very frustrating. Mostly because, we are constantly dismissed by providers, or made to feel like we're a bit crazy when we try to get answers. How do you break through this?  We're glad you're here for this episode as we dive into the topic of advocacy, especially as it relates to parenting a child with a Fetal Alcohol Spectrum Disorder (FASD).  We're joined by Laura Hernandez, from Mama Systems, who is an adoptive mama, but also the caregiver to children on the spectrum. She knows first hand what it looks like and feels like to be dismissed, but she also shares some valuable insight we can. take home as caregivers, when it comes to advocacy!  How To Connect With Laura:  Get her FREE resource (especially for being a listener of this show!). Click Here!  Connect with her on Facebook Follow her on Instagram Also On The Show... Insight Virtual Conference is coming soon! Get free access to our latest round of Fast-Action Bonuses when you register by April 1st! Click Here to learn more! Thanks for stopping by this week ;-) 

The Lord is compassionate and gracious, slow to anger and abounding in lovingkindness.  Psalm 103:8 Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you to care for children in crisis through adoption, foster care and kinship care.   On this episode, host Sandra Flach continues her series on the Primary Characteristics of Fetal Alcohol Spectrum Disorder (FASD). Listen in as Sandra shares how prenatal alcohol exposure affects the individual's ability to generalize information, how it might present in our kids, and offers some helpful strategies for accommodations.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media. Links mentioned in this episode: sandraflach.com justicefororphansny.org

Welcome to Season 4, episode 22 of the FASD Family Life Podcast. This is the only show about FASD hosted by an FASD Specialist and parent with 30 years lived experience.  I am Robbie Seale, your host and mom to five incredible people; including three teens diagnosed with Fetal Alcohol Spectrum Disorder.  It is my passion to help families thrive.  To learn more about me and my work check out my website,  https://fasdfamilylife.ca/Fetal Alcohol Spectrum Disorder (FASD) refers to a constellation of disorders resulting from prenatal exposure to alcohol; the manifestations include birth defects, developmental disabilities, and neurological and behavioral problems. Fetal Alcohol Spectrum Disorder is a common disability impacting 1 in 20 people in the general population in the US, which is nearly 3 times more common than Autism.This week I am in the Netherlands where it is estimated that 2000 babies annually are born with FASD.I am speaking with Nienke Peters and Luke Schut to learn about an innovative photo book project that they have been involved in to raise awareness of Fetal Alcohol Spectrum Disorder in Holland.Luke Schut is the Project coordinator of the FAS-project. Her background is in pedagogics. She came in contact with the FAS-project through her Masters program.  Luke says "I am the most inspired by all these parents and caregivers, and the warm and caring FASD community. Let's keep sharing stories with each other to make FASD more visible."Nienke Peters is mother of 4 bio kids and grandmother of 4. Fostered 12 children with FASD and still fostering a boy with FASD and NAS. Met Allard de Witte in 2014 when he photographed one of our foster sons. Her family has been part of the Buddy Project of Witte Bos for over 4 years now.‘Het Witte Bos' is a non-profit organization, which initiates transmedia project on the cutting edge of journalism, art and society. The FAS-project started as a journalistic initiative, but eventually developed into a big multimedia awareness campaign, showing the potentially dangerous consequences of alcohol consumption during pregnancy. By storytelling, the project raises attention to a relatively unknown problem in a personal way. The FAS-project started in 2013 and launched with the book FAS-kinderen (Children with FAS). After this the fas-project continued under the name FAS2025. In the past years the project developed and gained a wider reach & more impact. FAS2025 tells the story of Isiah, Lorenzo, Marcella, Mila and Jasmijn, following their journey towards adulthood for ten years. Their stories are told by a collection of stories, portraits and mini-documentaries. To give children with FAS(D) a face, make FAS(D) less abstract and to tell what FAS(D) means to them and how it impacts their lives. The project also consists of expositions, books, a podcast, a college tour to inform future professionals about FAS, readings at professional organizations who (may) come in contact with FAS(D), and a buddy project in which children/youngsters with FAS(D) are matched to a buddy to have a nice time together.Link to purchase the book Children with FAS/Kinder mit FAShttps://fasproject.nl/en/product/children-with-fasd/The English website: https://fasproject.nl/enHave a comment or question about the show, email me at fasdfamilylife@gmail.comSupport the show

"Love is patient and kind.  love does not envy or boast. is not arrogant or rude. It does not insist on its own way; it is not irritable or resentful. it does not rejoice in wrongdoing but rejoices with the truth. Love bears all things, believes all things, hopes all things, endures all things….Love never ends."  1 Corinthians 13:4-7 Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you to care for children in crisis through adoption, foster care and kinship care.   On this episode, host Sandra Flach continues her series on the Primary Characteristics of Fetal Alcohol Spectrum Disorder (FASD). Listen in as Sandra shares how prenatal alcohol exposure affects the senses, how it might present in our kids, and offers some helpful strategies for accommodations.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media. Links mentioned in this episode: sandraflach.com justicefororphansny.org

This week, we preview our recently published paper highlighting  FASD and the implications for those operating under the Risk-Need-Responsivity framework.  Fetal Alcohol Spectrum Disorder (FASD) is an umbrella term used to describe a range of significant, neurodevelopmental, brain based disorders that result from prenatal alcohol exposure. FASD is a high prevalence, but under diagnosed group of disorders affecting individuals within the criminal justice system.  Our article proposes a renewed focus on applying and adapting the RNR approach to individuals with FASD in criminal justice settings. Listen for a summary and some thought provoking insights!!! Paper available below!   FASD and the RNR Model: A guide for criminal justice and forensic mental health professionals The Paragon Group The Criminologist YouTube channel!      

"Plans fail for lack of counsel, but with many advisers they succeed." -Proverbs 15:22 Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you to care for children in crisis through adoption, foster care and kinship care.   On this episode, host Sandra Flach breaks down the Primary Characteristics of Fetal Alcohol Spectrum Disorder (FASD) and focuses on difficulties with abstract concepts—like time and money.    “Abstract reasoning deficits like problems with time management, math, or money matters can actually be a symptom of an FASD”    Please be sure to subscribe to the podcast, leave a review, and share it on your social media. Links mentioned in this episode: sandraflach.com justicefororphansny.org

"I lift up my eyes to the mountains—where does my help come from? My help comes from the LORD, the Maker of heaven and earth." Psalm 121:1-2 Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you to care for children in crisis through adoption, foster care and kinship care.   On this episode, host Sandra Flach breaks down the Primary Characteristics of Fetal Alcohol Spectrum Disorder (FASD) and focuses on memory problems—a common symptom.    “Memory problems can look like disobedience, defiance or even laziness if we don't understand the brain and how it's impacted by prenatal exposure to alcohol.”   Please be sure to subscribe to the podcast, leave a review, and share it on your social media. Links mentioned in this episode: sandraflach.com justicefororphansny.org

“Be joyful in hope, patient in affliction, faithful in prayer.” Romans 12:12 Welcome to The Adoption & Foster Care Journey—a podcast to encourage, educate and equip you to care for children in crisis through adoption, foster care and kinship care.   On this episode, host Sandra Flach discusses impulsivity—a primary characteristic of Fetal Alcohol Spectrum Disorder—FASD. Listen in as Sandra explains impulsivity and shares what it looks like at her house. She also offers accommodation suggestions such as prevention and preparation.    Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: sandraflach.com justicefororphansny.org proofalliance.org fasdunited.org

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. Episode 163 is our FINAL episode of FASD Hope. For over two years, we have been blessed to be a voice for giving IMPORTANT guests a platform to share their journeys, experience, research, clinical work, legislative activity, philanthropy and inspiration for the FASD Community!  Thank you for listening to our small but mighty family podcast about FASD. We're certainly not experts and we're still on this journey, too. It's now time for us to focus even more on our family, navigate what lies ahead, and face uncertainty with faith and fortitude.  We're SO thankful to be ending this amazing journey by leaving over 160+ episodes of FASD Hope! Thank you for listening, take care and always have HOPE! "The LORD will fight for you; you need only to be still." - Exodus 14:14 Sincerely, Natalie and John Vecchione FASD Hope     

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. November is National Adoption Month and FASD Hope is honored to highlight Andrew Bridge in Episode 162.  Leaving foster care at eighteen, Andrew Bridge attended Wesleyan University, then graduated from Harvard Law School and he was awarded a Fulbright Fellowship. He began his legal career representing children in mental health facilities across Alabama. His work as an attorney and an advocate enforced children's constitutional rights to be free from staff abuse and to receive meaningful psychiatric care. Andrew returned home to Los Angeles as the CEO of The Alliance for Children's Rights. He defended children at MacLaren Hall, where he was once confined. He won the right for Los Angeles' 60,000 foster children to speak publicly about their treatment. He investigated the excessive removal of African-American babies from their parents, which led to one of the first government initiatives to stop it. Andrew is the Co-Founder of National Adoption Day. He went on to lead one of California's largest recruiters of foster and adoptive parents. Called to address the unjustified placement of foster children in mental institutions, Andrew has served as a Senior Advisor to the State of Illinois. His educational work resulted in the creation of New Village Girls Academy, California's first all-girls high school for parenting teens. Andrew serves on Arizona's Foster Care Review Board and he consults with child welfare systems and foundations. Andrew is also the author of the New York Times AND Los Angeles Times BEST SELLER book, "Hope's Boy: A Memoir". The Washington Post named "Hope's Boy" one of it's Best Books of the Year, with a review that called it "filled with vivid scenes and empathetic description...compulsively readable". In this THOUGHT-PROVOKING episode, Andrew shares: his personal journey and lived experience as a foster child in the Los Angeles Foster Care System, his journey in becoming an attorney and child rights advocate, insights and discussion points from "Hope's Boy", the punitive nature that was / still exists in child welfare systems, his thoughts on how to educate those in the child welfare system about FASD and other brain-based diagnoses, the beginnings of "National Adoption Day" in 2000 and how it's grown, his current work and initiatives and words of hope and encouragement. EPISODE RESOURCES - Andrew Bridge -  Hope's Boy - https://hopesboy.com  LinkedIn - https://www.linkedin.com/in/andrew-bridge-667860210/   FASD Hope Resources - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ “HOPE FOR THE FASD JOURNEY COMMUNITY”, CO-LEAD BY NATALIE VECCHIONE AND SANDRA FLACH TO LEARN MORE ABOUT “HOPE FOR THE FASD JOURNEY” COMMUNITY OR TO SIGN UP, VISIT THE BELOW LINK -  https://www.justicefororphansny.org/hope-community   Check out our book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. Episode 161 is the FINAL FASCETS Friday Episode in which Episode 81 Guest, Lynn Alsup of FASCETS and her daughter, Clare, share how their family was transformed by the FASCETS Neurobehavioral Model. Lynn was our first "FASCETS Friday" guest in Episode 81 - airdate September 14, 2021.  In this ENLIGHTENING episode, Lynn and Clare share the following:  Lynn's work in FASCETS and the progress of her upcoming memoir, their family's FASD journey / life before Clare's FASD diagnosis, learning about the FASCETS Neurobehavioral Model and how it TRANSFORMED their family, how their family is doing now, Clare's accomplishments / important insight and words of hope and encouragement. FASCETS RESOURCES - FASCETS Website - https://fascets.org/ Facebook - https://www.facebook.com/FASCETS Instagram - https://www.instagram.com/fascets_inc/ Twitter - https://twitter.com/FASCETS2   FASD Hope Resources - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ “HOPE FOR THE FASD JOURNEY COMMUNITY”, CO-LEAD BY NATALIE VECCHIONE AND SANDRA FLACH TO LEARN MORE ABOUT “HOPE FOR THE FASD JOURNEY” COMMUNITY OR TO SIGN UP, VISIT THE BELOW LINK -  https://www.justicefororphansny.org/hope-community   Check out our book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. Episode 160 celebrates the AMAZING advocacy, work and fellowship of the Rural FASD Support Network (Ontario, CA). The Rural FASD Support Network was founded by a small group of volunteers with personal knowledge of & lived experience with FASD in rural Ontario (Canada). Today's conversation is with Rob More, Secretary of Rural FASD. Rob and his wife Shelley are proud parents of three amazing young adult children impacted by FASD. Rob, Shelley and four other dedicated volunteers are the co-founders of the Rural FASD Support Network of Eastern Ontario, which is currently the largest, nonprofit, lived disability experience in Canada following "Nothing For Us Without Us". In this HOPE-FILLED EPISODE, Rob shares the following:  the history of the Rural FASD Support Network, the exponential growth & key developments of Rural FASD, the diversity & representation of Rural FASD, the exciting legislative update of the National FASD Framework Legislation in Canada (and how Rural FASD and others advocated on Parliament Hill on October 20th), the blessings (and challenges) of living in a rural area as a family of those with FASD and words of hope and encouragement. "As you have therefore have received Christ Jesus the Lord, so walk in Him, rooted and built up in Him and established in the faith, as you have been taught, abounding in it with thanksgiving."  - Colossians 2: 6-7   EPISODE RESOURCES -  Rural FASD - https://ruralfasd.ca/ email - ruralfasd@gmail.com Instagram - https://www.instagram.com/ruralfasd/ Twitter - https://twitter.com/FasdRural   FASD Hope Resources - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ “HOPE FOR THE FASD JOURNEY COMMUNITY”, CO-LEAD BY NATALIE VECCHIONE AND SANDRA FLACH TO LEARN MORE ABOUT “HOPE FOR THE FASD JOURNEY” COMMUNITY OR TO SIGN UP, VISIT THE BELOW LINK -  https://www.justicefororphansny.org/hope-community   Check out our book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. Returning to FASD Hope is regular guest and friend in FASD advocacy, Dr. Jerrod Brown in Episode 159 - "All About FASD - FASD and Bullying Part 2". Jerrod Brown, Ph.D., M.A., M.S., M.S., M.S. is a professor, trainer, researcher and consultant with multiple years of experience teaching collegiate courses. Jerrod is also the founder and CEO of the American Institute for the Advancement of Forensic  Studies (AIAFS) and the Editor in Chief of Forensic Scholar Today (FST).  In this second episode about FASD and Bullying, Jerrod further explores the following topics: why it's critical to have a good knowledge of FASD / bullying, the links between bullying and self-destructive actions, cyberbullying, how bullying erodes mental health in individuals with FASD (and why they are already susceptible with mental health diagnoses), the further implications of bullying to already existing trauma and attachment issues, where to look for resources and words of encouragement and hope. EPISODE 159 RESOURCES - Dr. Jerrod Brown - jerrod01234brown@live.com American Institute for the Advancement of Forensic Studies (AIAFS) - https://aiafs.com Facebook - https://www.facebook.com/AIAFSAssoc Twitter - https://twitter.com/AIAFS2011   FASD Hope Resources - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Check out our book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. Episode 158 of FASD Hope explores a controversial topic: the School to Prison Pipeline (STPP).  The STPP or SPP is the significantly increased tendency of students from disadvantaged backgrounds, students with brain-based diagnoses, developmental disabilities and BIPOC students to become involved in the juvenile justice system. In today's episode, discussing the STPP and it's implications for students with brain-based diagnoses (including FASD, Autism, ADHD, etc.) is Dr. Deanna Westedt. Dr. Deanna Westedt received a doctorate in curriculum and instruction and spent 22 years in education. Currently, she homeschools and provides guidance for families, both homeschooled and traditionally schooled.  She has a special passion for twice-exceptional students and providing learning that goes outside of a classroom box. Her insights into twice-exceptionality have been featured in publications and venues such as Psychology Today, Future First Education, and CABE. Dr. Westedt's research was featured in AERA 2020. However, her best accomplishment is that of the growth her boys made during their time in homeschooling so far, where her ideas on how to accommodate their special combination of giftedness and learning disabilities paid off. She currently provides coaching and writing sessions, as well as specializes in early literacy that can be blended into any type of setting. Additionally, she provides parent sessions, diagnostics, and flexible differentiation training for homeschool/ educational organizations. In this highly informative and thought-provoking episode, Dr. Westedt shares the following: her professional background, her family's journey, her passion for creating academic equity for all students, how she became aware of the STPP, how students with brain-based diagnoses (including FASD) become even more susceptible to getting involved in the STPP, addressing how the traditional cycle of discipline reinforces the STPP (especially for students with developmental disabilities & brain-based diagnoses), how a systemic shift is required to break this cycle, how to better support those students involved in the STPP / JJ systems and her words of hope for listeners.  "Trust in the LORD with all your heart, And lean not on your own understanding; In all your ways acknowledge Him, And He shall direct your paths." - Proverbs: 5-6   EPISODE RESOURCES - Dr. Deanna Westedt - https://deannawestedt.com/ info@deannawestedt.com Facebook - https://www.facebook.com/drwestedt Instagram - https://www.instagram.com/dr.deannawestedt/ LinkedIn - https://www.linkedin.com/in/deanna-westedt-ed-d-64a2741b1/   FASD Hope Resources - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/   HOPE FOR THE FASD JOURNEY ONLINE COMMUNITY - Co-Lead By Natalie Vecchione and Sandra Flach -  Hope for the FASD Journey is a faith-based, membership support community for parents and caregivers of individuals prenatally exposed to alcohol and other substances. Led by Natalie Vecchione of the FASD Hope Podcast and Sandra Flach of the Adoption & Foster Care Journey Podcast— 2 moms living the FASD experience. With more than 20 years of adoptive parenting each, Natalie & Sandra offer abundant knowledge and resources to provide hope to families on this journey. “ TO LEARN MORE ABOUT THE “HOPE FOR THE FASD JOURNEY COMMUNITY” OR TO SIGN UP, VISIT THE BELOW LINK -  https://www.justicefororphansny.org/hope-community   Check out our book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. October is National Bullying Prevention Month. Episode 157 welcomes back Candice Dugger (Season 1, Episode 39, Feb. 25, 2021) to highlight her CRITICAL work in bullying awareness / prevention / education  through "Bullied, Broken,  Redeemed". Candice is a nationally-recognized anti-bullying expert, author, speaker and trainer. Candice and her team at Bullied, Broken, Redeemed specialize in equipping leaders, parents and youth on all aspects of Gen-Z Bullying. Candice also is the co-founder of "Reimagine Education Conference", which specializes in helping families transition to homeschool. Finally, Candice is the founder of Kids Business Academy, an organization that comes alongside parents to teach the essentials of entrepreneurship. In this INFORMATIONAL and INSPIRATIONAL episode, Candice explores the following: Candice's family's journey with bullying / starting BBR, statistics, facts about bullying & kids / teens with neurodiversity, myths about bullying, how bullying is a cultural epidemic, key points about bullying, how BBR and her other initiatives support and help heal children / teens who have been through bullying and her words of hope and inspiration for listeners. "Therefore comfort each other and edify one another, just as you also are doing."  - 1 Thessalonians 5:11   EPISODE RESOURCES - Candice Dugger - https://candicedugger.com/index.html Instagram - https://www.instagram.com/cedugger/ Bullied, Broken and Redeemed Facebook - https://www.facebook.com/bulliedbrokenredeemed LinkedIn - https://www.linkedin.com/in/candice-dugger-1a606952/   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!  

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. FASD Hope Podcast is celebrating it's 2 year anniversary ( aka "Podversary")! FASD Hope launched on October 1, 2020. We are airing this milestone episode (a day early) on Friday, September 30th - International Podcasting Day. FASD Hope is thrilled to be active and embraced in both the FASD and Podcasting Communities!  Episode 156 is also a first for FASD Hope, in that our "Most Frequent Guest", Jennifer Wisdahl of FASD United is this episode's GUEST HOST.  Jennifer and Natalie have a heart to heart conversation with much warmth, hope and joy! EPISODE RESOURCES - FASD United -  https://www.fasdunited.org Jennifer Wisdahl of FASD United - wisdahl@fasdunited.org FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience.  Episode 155 welcomes back the AMAZING mother / daughter team of Maryelen and Paula McPhail of Oshays Brain Domain (formerly Oshays FASD). Maryelen is a FASD parent advocate and Paula is an FASD Self-Advocate. Together, they are the leadership behind Oshays Brain Domain - a Social Enterprise based in Ayr, Scotland with a mission of supporting families / children with FASD. Since their previous episode (#66 - airdate July 13, 2021), Maryelen and Paula have wonderful updates about: their global expansion, supports, programs and FASD advocacy initiatives through Oshays Brain Domain!    EPISODE RESOURCES -  Oshays Brain Domain / FASD - https://www.oshaysfasd.org/ Facebook - https://www.facebook.com/oshaysbraindomain Instagram - https://www.instagram.com/oshays_fasd/ Twitter - https://twitter.com/OshaysFASD LinkedIn - https://www.linkedin.com/in/maryelen-mcphail-fasd-969663165/ Email - info@oshays.org Phone - +44 (0) 01292 261094  (Scotland) The FASD Article that Paula wrote / shared - https://metro.co.uk/2022/09/09/my-mums-pregnancy-drinking-caused-me-lasting-damage-17307228/   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. September is FASD Awareness Month!  FASD Hope is thrilled to welcome back previous guest (Episodes 89, 112) and FASCETS Facilitator, Suzanne Emery for FASCETS Friday! Suzanne Emery has a Master in Leadership Nursing and she is a Family Nurse Practitioner. She is a Certified Facilitator of the FASCETS Neurobehavioral Model and she is a FASCETS Program Director. Today's FASCETS Friday episode topic is "FASD in Spouses". Suzanne has experience working with couples where one of the spouses or partners has a Fetal Alcohol or Neurobehavioral Diagnosis. Given the prevalence of FASD and Other Brain Based Diagnoses, Suzanne shares how determining a suspected FASD or other Neurobehavioral Diagnosis is critical with couples who are encountering tension and unresolvable challenges in their relationships.  Suzanne also discusses the following topics: exploring FASD/NB as the root if there are difficulties in a marriage / relationship, how to know if a spouse were on the FASD spectrum, why seeking a diagnosis (or ruling out an FASD) would be critical in a marriage / relationship, what to do if you suspect your spouse has an FASD, support or training that can help and stories of hope. NOTE - If you are interested in learning more about an online support group for spouses of those adults with FASD, email Suzanne at suzemery28@gmail.com EPISODE RESOURCES- FASCETS - https://fascets.org/ Facebook - https://www.facebook.com/FASCETS Instagram - https://www.instagram.com/fascets_inc/ Twitter -https://twitter.com/FASCETS2 To learn more about the online workshop opportunities given by FASCETS, click on the below link for more information or to register.  https://fascets.org/workshops/ Note - If you decide to sign up for a FASCETS training, please let FASCETS know that you were referred by FASD Hope (as this helps in supporting FASD Hope as an organization).   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. It's September- FASD Awareness Month! Episode 153 of FASD Hope jumps into the ring of AWESOME FASD Advocacy with Jeremy Elliott and William G. of "Embrace Our Journey".  Jeremy Elliott is a martial arts teacher, champion and owner of United Family Martial Arts in Niagara Falls, Ontario (Canada). He is also a Top 500 Pro Wrestler.  Jeremy created the "Embrace Our Journey" FASD Advocacy campaign with his teen godson, William G, an FASD self-advocate. Together, Jeremy and Will are champion FASD advocates! In this MOTIVATIONAL episode, Jeremy and William discuss: the beginnings of "Embrace Our Journey", the MANY FASD Advocacy events they have for September and October, how martial arts and wrestling has made such a powerful impact (and support) in William's life, the benefits of finding a martial arts school that can be a good fit for students with FASD (or other brain based diagnoses) and their words of hope for listeners. EPISODE RESOURCES - United Family Martial Arts (Canada) - https://www.ufmaniagara.com/ Jeremy Elliott - ufmaniagarafalls1@gmail.com Facebook - https://www.facebook.com/UFMANiagara https://www.facebook.com/JeremyNickVickersElliott Instagram - https://www.instagram.com/jeremyelliottnf/   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with more than twenty years of lived experience. Episode 152 welcomes back two-time guest, Shannon Iacobacci of "Embracing the Brain". Shannon is a mom of multiple children with varying developmental disabilities, including Fetal Alcohol Spectrum Disorder (FASD). As an FASD specialist, Shannon helps families living with FASD. She also helps students with executive functioning struggles, attention, behaviors, memory, social & adaptive skills, and mental health needs.  Shannon's in-depth experience includes being a FASD Specialist, FASD Public Speaker/Trainer for multiple organizations, school districts, Child and Family Services, foster family agencies, & universities, a Certified facilitator - FASCETS Neurobehavioral Model, 18 + years IEP experience. In this RESOURCEFUL and HELPFUL episode, Shannon explores the following topics: her business / services through "Embracing the Brain", IEP / 504 basics, the differences in IEP's for students with FASD vs. other brain based diagnoses, top accommodations that are seen on 504s/IEPs of students with FASD, tips for parents / caregivers when going into 504 / IEP meetings and her words of hope and encouragement (especially for the new school year). "Now may the God of hope fill you with all joy and peace in believing, that you may abound in hope by the power of the Holy Spirit." - Romans 15:13   Shannon's previous episodes on FASD Hope were - Episode 5 -"FASD and Teens" Episode 26 - Climbing Down Holiday Mountain"   EPISODE RESOURCES -  Embracing the Brain website - www.EmbracingTheBrain.com  Email - Shannon@EmbracingTheBrain.com  Instagram - https://www.instagram.com/shannon.iacobacci/ LinkedIn - https://www.linkedin.com/in/shannon-iacobacci-92982016a/  Facebook - https://www.facebook.com/EmbracingTheBrain    FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!      

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through he lens of parent advocates with over twenty years of lived experience.  Episode 151 is airing on September 9th - International FASD Awareness Day titled "FASD at 50" with Dr. Kenneth Lyons Jones and Andrea "Andy" Torzon, LMFT of the University of California San Diego School of Medicine's Institute for Fetal Alcohol Spectrum Disorders Discovery. This important episode highlights returning guest, Dr. Kenneth Lyons Jones, who is considered the leading expert in FASD and who was one of two doctors at the University of Washington, who first identified Fetal Alcohol Syndrome (FAS) in the United States in early 1973. Dr. Jones is joined by Andrea Torzon, LMFT, a family therapist who works with Dr. Jones at the UC San Diego's Institute for FASD Discovery. As the 50 year anniversary of the first identification of FAS approaches, this special episode is titled "FASD at 50" and shares highlights from Dr. Jones' Keynote presentation "FASD at 50" from NOFASD Australia's "The FASD Forum '22 Virtual Conference". In addition to Dr. Jones' highlights from this important presentation, Andrea "Andy" Torzon shares her work and professional perspective of working with families at the UC San Diego Institute for FASD Discovery and through her nonprofit organization "Twinkle, Twinkle LIttle Farm".  Together, Dr. Jones and Andy discuss the following topics: the stigma that continues to surround FASD 50 years after the identification of FAS, the "4 Critical Issues" in understanding and moving forward in the FASD community, the importance of reframing wording and discussions to reduce stigma associated with FASD,  the importance of establishing FASD Centers of Excellence in each state and their words of hope and encouragement.   EPISODE RESOURCES - Dr. Kenneth Lyons Jones -https://www.rchsd.org/doctors/kenneth-lyons-jones-md/ https://betterbeginnings.org/who-we-are/leadership/ https://betterbeginnings.org/who-we-are/leadership/dr-kenneth-lyons-jones-md/ https://medschool.ucsd.edu/som/pediatrics/Divisions/dysmorphology/about/Pages/Dysmorphology_Teratology_Division_Members.aspx https://pediatrics.med.ubc.ca/2018/03/20/a-retrospective-look-at-43-years-of-fetal-alcohol-spectrum-disorder-fasd-how-did-we-get-here-from-where-we-started/ https://www.facebook.com/UCSDcbb/ https://twitter.com/ucsdcbb https://www.instagram.com/ucsdcbb/ Andrea "Andy" Torzon - https://betterbeginnings.org/what-we-do/patient-care/fetal-alcohol-spectrum-disorder-clinic/programs/ Twinkle, Twinkle Little Farm Nonprofit - LinkedIn - https://www.linkedin.com/in/andrea-andy-torzon-576b2283/ Facebook - https://www.facebook.com/twinkletwinklelittlefarm Instagram - https://www.instagram.com/twinkletwinklelittlefarm/ YouTube - https://www.youtube.com/channel/UCNPSUMYBTDDObZvdXhZ_mdQ   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. FASD Hope is HONORED to be a part of TEAM RUN FASD 2022, which is Coach Rebecca Tillou, Jenn Wisdahl, Susan Elsworth and Natalie Vecchione. Episode 150 is “Let's Go”,  an update, important information & the official launch for this 2nd Annual Virtual 5K for FASD! The Run FASD Virtual 5K will be held September 9th - 25th, 2022. It's not too late to register, registration is open until September 14th, 2022. Listen to this final update of Run FASD 2022 Virtual 5K and learn how you can participate, promote and support this 2nd Annual Virtual 5K for FASD! EPISODE RESOURCES - Run FASD Virtual 5K website - https://runfasd.org/ Instagram - https://www.instagram.com/runfasd/?hl=en Facebook - https://www.facebook.com/groups/runfasd FASD United - https://fasdunited.org/ FASD HOPE RESOURCES -FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast series about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. September is FASD Awareness Month!  Episode 149 highlights Kristen Eriksen and Laura Bedard of MASS FAS, an FASD United Affiliate. Kristen and Laura are both moms of children with FASD and united in their advocacy in their leadership of MASS FAS. In this ENCOURAGING episode, Kristen and Laura share: how they became parent advocates (from their respective families' journeys), how MASS FAS has grown in the past year, what they have learned as FASD parent advocates, their advice for parents who want to take that leap into FASD parent advocacy, the many offerings of MASS FAS for Massachusetts (and beyond), their upcoming work for MASS FAS and their words of encouragement and hope.   EPISODE RESOURCES -  MASS FAS website - https://www.massfas.org/ Facebook - https://www.facebook.com/massfetalalcoholsyndrome Instagram - https://www.instagram.com/massfas1/ Twitter - https://twitter.com/massfas1   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. It's September, which is FASD Awareness Month!  Episode 149 welcomes back Dr. Jerrod Brown to continue our series within the series “All About FASD Special Edition- A Panel Discussion". This month, Jerrod will be answering a variety of questions / subtopics within FASD. Jerrod Brown, Ph.D., M.A., M.S., M.S., M.S. is a professor, trainer, researcher and consultant with multiple years of experience teaching collegiate courses. Jerrod is also the founder and CEO of the American Institute for the Advancement of Forensic Studies (AIAFS) and the Editor-in-Chief of Forensic Scholars Today (FST). In this FASD RESOURCE AND INFORMATION PACKED episode, Jerrod answers questions from FASD podcasters around the world! Our FASD Podcast Panelists include: Kurt Lewis, Pregnancy and Alcohol, The Surprising Reality Podcast Gilberto Spencer-Wired Differently - Rewire Your Brain Podcast Robbie Seale, FASD Family Life Podcast Sandra Flach - The Adoption and Foster Care Journey Podcast Natalie Vecchione- FASD Hope Podcast Episode 148 Resources - Dr. Jerrod Brown - jerrod1234brown@live.com American Institute for the Advancement of Forensic Studies (AIAFS) - https://aiafs.com/ Facebook - https://www.facebook.com/AIAFStraining Instagram - https://www.instagram.com/aiafsassoc/ Twitter - https://twitter.com/AIAFS2011 LinkedIn - https://www.linkedin.com/in/aiafs/?miniProfileUrn=urn%3Ali%3Afs_miniProfile%3AACoAABntPzUB2qCg_fmbOMKXQbRSlzI9pSfdRG4   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience.  Episode 146 is the first of a two part episode special in preparing for "Back to School / Back to Homeschool" - FASD and Friendship Skills with regular guest, Dr. Jerrod Brown.  Jerrod Brown, Ph.D., M.A., M.S., M.S., M.S. is a professor, trainer, researcher and consultant with multiple years of experience teaching collegiate courses. Jerrod is also the founder and CEO of the American Institute for the Advancement of Forensic  Studies (AIAFS) and the Editor in Chief of Forensic Scholar Today (FST).  In this episode, Jerrod explores the following topics: the basics of friendship skills, what skills are required in making and maintaining friends, the risk factors that individuals with FASD (and other brain based diagnoses) have in not having healthy friendships, the protective factors for helping individuals with FASD make and maintain friendships, advice and words of encouragement and hope. Episode 146 Resources - Dr. Jerrod Brown - jeffod1234brown@live.come American Institute for the Advancement of Forensic Studies (AIAFA) - https://aiafs.com/ 612-250-5432 Facebook - https://www.facebook.com/AIAFSAssoc Twitter- https://twitter.com/aiafs2011 LinkedIn - https://www.linkedin.com/in/aiafs/   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!  

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience.  Episode 147 is the second of a two part episode special in preparing for "Back to School / Back to Homeschool" - FASD and Bullying - Part 1 with regular guest, Dr. Jerrod Brown.  Jerrod Brown, Ph.D., M.A., M.S., M.S., M.S. is a professor, trainer, researcher and consultant with multiple years of experience teaching collegiate courses. Jerrod is also the founder and CEO of the American Institute for the Advancement of Forensic  Studies (AIAFS) and the Editor in Chief of Forensic Scholar Today (FST).  In this episode, Jerrod discusses the following topics: the basics of bullying, risk factors that cause individuals with FASD (and other brain based diagnoses) to be more susceptible to bullying, the protective factors, what to know when helping individuals with FASD who are being bullied, symptoms and traumatic effects of bullying, where to look for resources and words of encouragement and hope. Note - the second Bullying episode with Dr. Jerrod Brown will be aired in October. Episode 146 Resources - Dr. Jerrod Brown - jeffod1234brown@live.come American Institute for the Advancement of Forensic Studies (AIAFA) - https://aiafs.com/ 612-250-5432 Facebook - https://www.facebook.com/AIAFSAssoc Twitter- https://twitter.com/aiafs2011 LinkedIn - https://www.linkedin.com/in/aiafs/   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our  book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

FASD Hope is a podcast about Fetal Alcohol Spectrum Disorder (FASD), through the lens of parent advocates with over twenty years of lived experience. Welcome to the official book launch of "It's OK to Be You - Living Well with FASD or Other Disabilities" by Kenny LaJoy!  Episode 145 celebrates new author, Kenny LaJoy and his new book, which is a valuable resource for ANYONE in the FASD community, neurodiversity community...and many more! Episode 145 is the "story behind the book". Kenny shares: his adoption journey, his FASD journey, his journey in becoming an independently published author, his faith, his hopes for his new book and how "It's OK to Be You" is an affirmation and resource for those with FASD, their families / loved ones or anyone wanting to learn more through the lens of a FASD self-advocate. EPISODE RESOURCES -  "It's OK to Be You - Living Well with FASD or Other Disabilities" by Kenny LaJoy Available now on Amazon https://www.amazon.com/dp/B0B7QP8PFC/ref=cm_sw_em_r_mt_dp_3FZJ6DAVTV6JJF2YEFEH Contact Kenny at itsoktobeyoubook@gmail.com Blue Collar Homeschool - https://www.bluecollarhomeschool.com/ Buckaroos Slices and Scoops - https://www.buckaroosmontrose.com/   FASD Hope - https://www.fasdhope.com/ natalie@fasdhope.com Instagram - https://www.instagram.com/fasdhope/ Facebook - https://www.facebook.com/fasdhope1 Twitter - https://twitter.com/fasdhope LinkedIn- https://www.linkedin.com/in/natalie-vecchione-17212160/ Racket - @fasdhope Clubhouse - @natalievecc Check out our book “Blazing New Homeschool Trails: Educating and Launching Teens with Developmental Disabilities” by Natalie Vecchione & Cindy LaJoy  BUY IT NOW!

As we conclude our special series, FASD Expert Spotlight, we are pleased to share an interview we had the pleasure of doing with our good friend Jeff Noble from The FASD Success Podcast.  Jeff is an FASD caregiver turned educator and a highly sought-after speaker, leader, and parent coach.  On this episode we dove into how to overcome shame and disappointment on this journey, as well as what it means to transform from trauma, build healthy attachments with our children, and so much more!  A little more about Jeff... Jeff Noble is the Founder and CEO of, an organization that provides hope and education to people caring for someone living with Fetal Alcohol Spectrum Disorder (FASD) through online applications and in-person training sessions, demonstrations and consultations. Jeff is a helper, a leader and an innovator. His focus is FASD, but his expertise is building community through social media. Using an interactive, yet personal approach, Jeff delivers relevant, useful and need-to-know information to help and support front line workers, educators and caregivers of those living with FASD. How to connect with Jeff... Listen to the podcast Visit The FASD Success website Connect with him on Instagram Also on the show... Dads! Join us for Road Trip 2022 in the mountains of Colorado this coming October. Register by September 1st and receive some amazing bonuses. Click Here. Join us for Replanted Conference this coming October 13-15 in Chicago! Use the promo code OASIS to get $20 off in-person price, and $10 off simulcast price. Thanks for stopping by this week ;-) 

My guest this week is Eileen Devine In this episode, Eileen and I discuss parenting through behavior and developmental challenges, with a spotlight on Fetal Alcohol Spectrum Disorder (FASD). Whether you have a child diagnosed with FASD or not, I encourage you to listen to this conversation as the content and tips can be applied to parenting kids with or without any behavioral or developmental challenges, at any stage of life.  We talk about why a brain-based parenting lens is so much more effective than a behavior-based approach, especially for kids with behavior challenges or developmental delays.  Eileen's personal and professional experience with FASD is incredibly insightful, where she shares what FASD does and does not look like, diagnoses, what research shows, and many realistic tips and tools to not just support a child in improving brain development and function, but also helping the parents in the process. Eileen Devine is a licensed clinical social worker living in Portland, Oregon and has over 20 years of clinical experience. She's also the mother of a teenager with Fetal Alcohol Spectrum Disorder, a serious brain based disability that has challenging behavioral symptoms. She believes that when we understand the way a child's brain works, we then understand the meaning behind challenging behaviors and begin to see them as symptoms of a child's differences. Through her work with parents, Eileen has created the Resilience Room membership community and the Brain First Parenting Program, both designed to support parents in their unique parenting journey. In addition to her one on one and group work with parents, she also facilitates dozens of workshops and trainings a year and is an instructor for the CASE Institute's Training for Adoption Competency Post-masters certification program.     Connect with Eileen Devine: Insta: @eileen.devine_brain.first Facebook: https://www.facebook.com/EileenDevineBrain Website: www.eileendevine.com     Episode Takeaways   Introduction to Eileen Devine & FASD … 00:01:45 What is Fetal Alcohol Spectrum Disorder and Diagnostic Process … 00:05:52 Outdated Assumptions of FASD Presentation … 00:11:20 FASD, Toxic Stress, & Other Prenatal Substance Exposures … 00:15:40 Common Behavioral Challenges Seen on the Spectrum … 00:18:15  Parenting Children Who are Physically, Behaviorally or Cognitively Impulsive … 00:26:42 Consequences Aren't Working: Better Behavioral Techniques … 00:30:15  Parenting Tips: A Brain-Based Reframe Rather Than a Behavior-Based Lens … 00:35:09 The Gap Between Expectations and What They are Capable of Doing … 00:40:42 Tips & Where to Start for FASD & Behavioral Challenges … 00:47:15  Resources & Episode Wrap Up … 00:50:10         Need help with improving your child's behavior naturally? My book Life Will Get Better is available for purchase, click here to learn more. Looking for more? Check out my Blog and Workshops. Interested in becoming a patient? Contact us here. Instagram Facebook Drbeurkens.com