Podcasts about fasd

"How beautiful on the mountains are the feet of those who bring good news, who proclaim peace, who bring good tidings, who proclaim salvation, who say to Zion, 'Your God reigns!'” -Isaiah 52:7   This episode continues our  FASD Awareness Month series with our special guest, Kathrin Hui Gregorovic. Kathrin grew up in Switzerland and now lives in Austria with her family. She and her husband are foster parents to two neurodivergent kiddos. Kathrin is also an artist. As a child she loved drawing and that passion was rekindled as she learned about FASD and started drawing again for self-care. Kathrin calls herself an ‘advocartoonist'—using her illustrations and cartoons to advocate for people with FASD.   Listen in as Kathrin Hui Gregorovic shares her family's FASD story and how she uses her talents on behalf of the FASD community worldwide.   Links mentioned in this episode: https://redshoesrock.com/ FASDUnited.org Free Breath Prayer Download See Available Trainings AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

FASD specialist and adoptive mom Sandra Flach joins Jesse to break down fetal alcohol spectrum disorder: what it actually is, why it hides behind behavior nobody understands, and why it's one of the most common and least discussed disabilities in foster care and adoption. Sandra shares her own family's diagnosis journey and the accommodations-based approach that finally helped her understand her sons instead of just managing their behavior. It's a conversation for anyone parenting a child whose brain might be working differently than expected, diagnosed or not. Sandra Flach is co-founder of Justice for Orphans and an adoptive and kinship parent of six. After her own sons were diagnosed with fetal alcohol syndrome, she became a national voice on FASD, offering training, coaching, and a peer support community for foster and adoptive families. Website: Justice for Orphans: FASD Training & Support Key Takeaways FASD is far more common than most people realize (one in twenty people prenatally exposed to alcohol, up to seventy percent of kids in foster care), yet true diagnosis is rare because doctors are trained to look for facial features present in fewer than ten percent of cases. FASD symptoms overlap heavily with trauma and can look like willful defiance, but the brain difference is real: what looks like "won't" is usually "can't," especially around executive function, auditory processing, and daily living skills. The path forward is accommodation, not consequence: understanding a child's specific struggles (memory, impulse control, sensory processing) and adjusting expectations the same way we already do for visible disabilities. Timestamped Outline 00:00 – Introduction: meet Sandra Flach, adoptive and kinship mom, FASD specialist and advocate 00:01 – FASD 101: how common it actually is, and why it's called an invisible disability 00:08 – Getting a diagnosis: who can diagnose FASD, and why so few doctors do 00:13 – Why the standard diagnostic criteria miss 90% of cases 00:19 – Not a straight line: the "scribble" and FASD's scattered developmental profile 00:28 – Why it's not that they won't, it's that they can't: executive function and the brain 00:36 – The neurobehavioral approach: accommodations instead of consequences 00:40 – "A child with brain damage": the reframe that changed how Sandra saw her sons 00:46 – Grief, interdependence, and redefining what success looks like 00:52 – Untangling shame, for parents, kids, and birth parents 01:03 – The long view: daily living skills, connection, and "not yet" instead of "never" 01:07 – Where to find Sandra: her support group, training, podcast, and a free gift Resources Mentioned Justice for Orphans: FASD Training & Support Hope Community (Sandra's online FASD support group) The Adoption & Foster Care Journey podcast Sandra Flach's site (Soul Care Saturday devotional and free breath prayers download) Call to Action (CTA) ETC Shopify ETC Newsletter signup ETC Instagram ETC Facebook Chapters (00:00:00) - Introduction and Sandra's Background(00:01:46) - What Is Fetal Alcohol Spectrum Disorder(00:03:30) - Sandra's Family Journey to Diagnosis(00:07:57) - Challenges Getting an FASD Diagnosis(00:10:36) - Alcohol as a Teratogen and Whole-Body Effects(00:12:58) - Diagnosis Barriers and Facial Features Myth(00:14:17) - Navigating Diagnosis Without Birth History(00:18:48) - Developmental Gaps and Scattered Abilities(00:26:22) - Coping Strategies and Stress Capacity(00:28:21) - Executive Function and Misunderstood Behavior(00:30:28) - Communication Challenges and Real-Life Examples(00:33:55) - Untangling Trauma vs FASD Symptoms(00:35:54) - Accommodations as a Neurobehavioral Approach(00:39:36) - Seeing Brain Differences Instead of Bad Behavior(00:42:19) - Adults with FASD and Lifelong Accommodations(00:44:17) - Grieving Expectations and Celebrating the Child(00:47:58) - Community, Support Groups, and Celebrating Wins(00:52:04) - Addressing Shame and Building Acceptance(00:57:38) - Dispelling Shame Around Alcohol and Pregnancy(01:03:16) - Long-Term Goals and the Power of Connection(01:06:58) - Closing Resources and Farewell

This week, we're hearing from the dads! Shannon and Tash sit down with Joel Sheagren and Carl Young for an honest conversation about fatherhood, fetal alcohol spectrum disorder (FASD), and its overlap with autism. Joel and Carl share what they've learned while raising children with complex needs, how they've adjusted their parenting along the way, and why support and community matter so much. We also talk about the differences between FASD and autism—and why more families need to understand FASD. Website: embracing-neurodiversity.com Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

“For you created my inmost being; you knit me together in my mother's womb. I praise you because I am fearfully and wonderfully made.” -Psalm 139:13-14   This episode continues our  FASD Awareness Month series with our special guest, Patricia Kasper. Patti is an author, podcast host, self-advocate, life coach, social worker, as well as a former therapist and hospice chaplain. With over thirty years of experience in addiction, mental health, and  child welfare, Patti took a deep dive into FASD to better support the children and families on her caseload. In the process, she discovered that she too is on the FASD spectrum. Her self-identification was later confirmed with an FASD diagnosis.    The magnitude of seeing oneself differently, through a truer lens, and understanding the impacts of prenatal brain injury upon one's physical, emotional, and cognitive development, uniquely experienced by everyone, revolutionized both her personal and professional life. Patti's work pivoted to focus solely on FASD in hopes of bringing a monumental shift in understanding and grace to the nearly 15 million adults in the U.S. who have never understood why life was harder for them than for most.   Listen in as Patti Kasper shares from both her professional experience and as an adult diagnosed with FASD.   Links mentioned in this episode: patriciakasper.com FASDUnited.org Free Breath Prayer Download See Available Trainings AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

In this episode of “Pregnancy, Alcohol and FASD: The Surprising Reality”, host Kurt Lewis speaks with Emma McDougall, a FASD-informed occupational therapist and Clinical Advisor at NOFASD Australia. Emma discusses what it truly means to be FASD informed, moving beyond simply knowing about FASD to understanding how it affects each individual's daily life.They explore the importance of a strengths-based and brain-based approach, the value of listening to lived experience, and how professionals can adapt environments, expectations and supports to better meet the needs of people with FASD. Emma also shares practical advice for clinicians working with people with FASD, including considerations for NDIS reports and advocacy.The conversation highlights a key message: awareness is important, but genuine understanding, compassion and action can make a meaningful difference in the lives of people with FASD and their families. For more information about FASD, please go to: https://www.nofasd.org.au/Producers: Kurt Lewis, Julie Flanagan and Sophie HarringtonNarrator: Frances PriceInterviewer: Kurt LewisInterviewees: Emma McDougallThe 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 interviewees. 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.

“For you created my inmost being; you knit me together in my mother's womb. I praise you because I am fearfully and wonderfully made.” -Psalm 139:13-14   This episode continues our  FASD Awareness Month series with our special guest, Jessica Sachs. Jessica is the FASD Specialty Dept. Coordinator & Family Peer Supervisor at Children's Service Center in Wilkes-Barre, PA. She has more than 14 years of experience supporting families and navigating mental and behavioral health systems—with a strong focus on FASD education, advocacy, and family support.   Jessica is also the mom of 5 children. Her FASD journey began personally when she started navigating mental and behavioral health services with her oldest kids. Her passion is bringing greater understanding of FASD to families and professionals, so individuals are better understood and receive the support, accommodation, and treatment they truly need.   Listen in as Jessica shares from both her professional experience and as a birth mom of a child with FASD.   Links mentioned in this episode: Children's Service Center PA FASDUnited.org Free Breath Prayer Download See Available Trainings AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Hello and welcome to the A&F podcast, we recorded this on the 9th September, FASD awareness day.  We speak to Susie Richardson, who is research FASD in the prison population. Susie has a broad range of experience and from running prisons and working with care leavers she has seen the need for a better understanding of the impact and prevalence of FASD in those communities. She shares her journey to this research and what inspires her passion.  You can find out more about Susie here As always if you've experience of adoption, fostering or special guardianship from any perspective personal or professional and would like share that on the podcast please get in touch through the Facebook page, BlueSky or email us at AandFpodcast@gmail.com

Today is International FASD Awareness Day, shining a light on Foetal Alcohol Spectrum Disorder — a lifelong neurodevelopmental disability that can have a profound impact on individuals and families.     There are calls for greater awareness, understanding and support, as well as increased funding for services.     Joining Alan Morrissey earlier was Tristan Casson Rennie, CEO of FASD Ireland, to talk about the campaign and why raising awareness matters. Photo (c) Clare FM

Kurt is joined by Dr Vanessa Spiller; an experienced Clinical Psychologist with around 30 years of practice who is dedicated to supporting individuals with Fetal Alcohol Spectrum Disorder (FASD). She shares her personal and professional journey with FASD - from discovering the condition through parenting her son, to seeing how lived experience has shaped her clinical practice.Dr Spiller explores why FASD can be a “chameleon” condition, often resembling Autism, ADHD, intellectual disability and other diagnoses, and why recognising the brain-based differences behind behaviour is so important. She discusses executive functioning, memory, comprehension, confabulation and suggestibility, and the particular risks these vulnerabilities can create for people with FASD in the justice system.The conversation also offers practical advice for caregivers and professionals, including how to respond to confabulation and perseveration with empathy, regulation and problem-solving rather than confrontation. Dr Spiller highlights the importance of ensuring that people with FASD have appropriate support when interacting with police, medical professionals and the justice system.If you live in Australia and would like to receive some of the free “Police Information Cards” mentioned in this episode, please register your interest and provide your postal address at: https://www.nofasd.org.au/contact-us/ For more information about FASD, please go to: https://www.nofasd.org.au/ Producers: Kurt Lewis, Julie Flanagan and Sophie HarringtonNarrator: Frances PriceInterviewer: Kurt LewisInterviewee: Dr Vanessa SpillerThe 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.

“Speak up for those who cannot speak for themselves; Ensure justice for those being crushed. Yes, speak up of the poor and helpless,  And see that they get justice.” -Proverbs 31:8-9   This episode kicks off FASD Awareness Month with our special guest, Emma Baldwin.  Emma is a sibling of a person with FASD and an autistic self-advocate. Emma's work in the FASD field began with the FASD Network of Southern California and training initiatives at Proof Alliance in Minnesota. While living in Minnesota, Emma served on the advisory council of the Univ. of Minnesota's Institute on Community Integration and chaired St. Paul Mayor's Advisory Committee for People with Disabilities. Today, Emma is the Director of Partnerships at FASD United—leading the FASD United Affiliate Network (which JFO is a member of), supporting the Living Experience track of the International FASD Research Conference, and overseeing the development of the FASD Symposium and White Papers.   Listen in as Emma shares how FASD United, the national organization in the U.S., is empowering people living with FASD, educating systems of care and the public, enacting policy and uniting communities everywhere so that those living with Fetal Alcohol Spectrum Disorder and Prenatal Alcohol Exposure are recognized and supported.   Links mentioned in this episode: FASDUnited.org Free Breath Prayer Download See Available Trainings AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Stündlich wird in Deutschland ein Kind mit FASD geboren. Fetale Alkoholspektrums-Störung ist weltweit die häufigste angeborene Krankheit. Dabei ist sie vermeidbar, wenn die Mutter in der Schwangerschaft keinen Alkohol trinkt. Autorin: Claudia Maschner Von Claudia Maschner.

Nina hat mit dem Trinken aufgehört, als sie mit ihrer Frau ihren ersten Sohn adoptiert hat, der im Alter von drei Jahren mit einer fetalen Alkohol-Spektrum-Störung (FASD) diagnostiziert wurde, eine Behinderung, die weit verbreitet ist, über die aber wenig bekannt ist. Nina erzählt uns vom langen Weg zur Diagnose, den alltäglichen Sorgen und Herausforderungen, wenn man ein Kind mit FASD großzieht, darüber, was hilft und was Eltern für Unterstützung bekommen können. Sie spricht auch über ihren Umgang mit der Wut auf die leibliche Mutter und das Mitgefühl, das sie ihr inzwischen entgegen bringt. Und darüber, was es noch braucht, damit die Gesellschaft besser auf die Bedürfnisse von Kindern mit FASD eingehen kann.Vom 09.09. bis 16.09.2024 findet eine vom FASD Deutschland e.V. initiierte Aktionswoche statt, die viele Veranstaltungen in Präsenz aber auch online anbietet. Informationen auf den Seiten von Los Family und FASD Deutschland e.V.:https://los-family.de/fachleute/2024/08/23/aktionswoche-fasd/https://www.fasd-deutschland.de/SodaKlub Interview über FASD mit Henrike Schecke:https://open.spotify.com/episode/0AWhe9ntlMDmHvFFmEeuby Recovery Walk am 12.09.2026 in DüsseldorfHier findest du uns noch:Abonniere den SodaKlub Newsletter oder werde Mitglied im SodaKlubWerde Mitglied, unterstütze oder informiere dich über Recovery DeutschlandAbonniere Mias Newsletter Romanzen und FinanzenRECOVERY WALK am 12. September in DüsseldorfKontakt für Helfer:innen (keine Vorkenntnisse notwendig): daniela@recoverydeutschland.orgAllgemeiner Kontakt: Info@recoverydeutschland.orgSpendenkampagne: https://www.betterplace.org/de/projects/170427-recovery-walk-2026Mia GatowMias Buch: »Rausch und Klarheit«Mias Newsletter: Romanzen und FinanzenMika DöringRecovery Deutschland e.V. Mikas Kunst Hosted on Acast. See acast.com/privacy for more information.

In dieser Folge von Netzwerk Pflegefamilien – der Podcast spreche ich mit Steffi. Sie führt eine Sozialpädagogische Lebensgemeinschaft und begleitet dort ein neunjähriges Mädchen mit FASD – einer Fetalen Alkoholspektrumstörung. Steffi erzählt von ihrem gemeinsamen Alltag und davon, warum sie manchmal eine Art „Übersetzerin“ sein muss: Denn Verhalten, das für andere zunächst schwer nachzuvollziehen ist, kann einen ganz anderen Hintergrund haben, wenn man genauer hinschaut. Wir sprechen darüber,

“Be Still and know that I am God.” -Psalm 46:10 What happens when the traditional school system simply isn't working for your child? For families raising children impacted by Fetal Alcohol Spectrum Disorder (FASD), finding the right educational environment can require flexibility, creativity, and a willingness to let go of what we thought education was supposed to look like. In this episode of The Adoption & Foster Care Journey, Sandra reconnects with Melissa Dunn Corkum for an honest, informal conversation about their experiences homeschooling children with FASD. Neither approaches the conversation as an educational expert—they're sharing from the perspective of moms who have lived it. Melissa and Sandra talk about the freedom homeschooling can provide to slow down, follow a child's strengths and interests, reduce unnecessary pressure, and create an educational experience around the child's actual needs rather than forcing the child to fit a predetermined curriculum. They also explore the importance of structure, repetition, experiential learning, individualized accommodations, and recognizing that what works for one child may not work for another. From Ninja Warrior and bouldering to learning through everyday routines, their stories demonstrate how strengths-based education can open doors that traditional approaches sometimes miss. But this conversation isn't just about educating our children. Melissa introduces the concept of blocked care and explains why caring for the caregiver's nervous system is essential for long-term parenting. Together, they discuss practical ways parents can recognize stress, reconnect with supportive people, regulate their nervous systems, and give themselves permission to make changes when something isn't working. Whether you're currently homeschooling, considering a change in educational placement, or simply trying to figure out how to help your child learn and thrive, this conversation offers encouragement that there isn't one right way to educate a child—and it's okay to find the way that works for your family.   Links mentioned in this episode: Melissa is also offering a free 10-question Blocked Care Assessment specifically for Justice for Orphans listeners:  risetoregulation.com/jfo Facebook Group: Homeschool the FASD way-a global community Free Breath Prayer Download See Available Trainings AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Hello and welcome to the latest episode of  the AandF podcast.  In this episode we rage across a couple of matters that impact on many families, power dynamics with social workers. After a Tramadol start and Scott's good news we get distracted by the complicated relationship prospective adopters and foster carers can have with their social workers. The power dynamics are often set against applicants and what questions are appropriate and what are not. How do we push back and can we question the questions, it's not simple.  If you want to read the research mentioned you can do that here. If you want to listen to Scott's radio documentary on FASD you can do that here.  As always if you've experience of adoption, fostering or special guardianship from any perspective personal or professional and would like share that on the podcast please get in touch through the Facebook page, BlueSky or email us at AandFpodcast@gmail.com

Foetal Alcohol Spectrum Disorder, it's a condition you might not be too familiar with. But believe it or not, you almost certainly know someone dealing with FASD. Joining Pat is CEO and founder of FASD Ireland, Tristan Casson-Rennie, to tell us about the condition affecting 1 in 10 babies born in Ireland.

“You will keep in perfect peace All who trust in You, All whose thoughts are fixed on you!” -Isaiah 26:3   On this episode, host Sandra Flach, talks with our favorite returning guest, Dr. Jerrod Brown, about Frontal Lobe Impairment and what it means for children impacted by FASD, trauma, and other neuro-developmental differences.   Dr. Brown explains how the frontal lobe plays an important role in: self-regulation, executive functioning, decision making, communication, and adaptive functioning. When these areas of the brain are impaired, what looks like defiance or poor behavior may actually be a sign that a child is struggling with a brain-based difference.   Dr. Brown has 6 PhD's and specializes in topics related to autism spectrum disorder (ASD), fetal alcohol spectrum disorder (FASD), confabulation, suggestibility, trauma and other life adversities, alexithymia, executive dysfunction, criminal recidivism, traumatic brain injury (TBI), and youth fire-setting. You can check out his full bio on our website along with dozens of our bonus episodes featuring Dr Brown.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: Bonus Episodes with Dr. Brown Dr. Brown's email: Jerrod01234Brown@alive.net Free Breath Prayer Download See Available Trainings The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Joshua Legg says his goal is always the same: to equip men with tools that strengthen families and lighten the load for the professionals who serve them. Joshua Legg is the proprietor of Joshua Legg Coaching. He provides pastoral care and mental health coaching and serves as Chair of The Papillion Center for FASD in Tennessee. He is focused on helping men grow into their full potential through a supportive yet challenging approach. With a strong understanding of FASDs and early life adversity, he is committed to fostering healing in men and their families. Joshua can be reached at https://joshualeggcoaching.com/. The State of Wisconsin's Dose of Reality campaign is at Dose of Reality: Opioids in Wisconsin. More information about the federal response to the ongoing opiate crisis can be found at One Pill Can Kill. The views and opinions of the guests on this podcast are theirs and theirs alone and do not necessarily represent those of the host or Westwords Consulting. We're always interested in hearing from individuals or organizations who are working in substance use disorder treatment or prevention, mental health care and other spaces that lift up communities. This includes people living those experiences. If you or someone you know has a story to share or an interesting approach to care, contact us today! Follow us on Facebook, LinkedIn, and YouTube. Subscribe to Our Email List to get new episodes in your inbox every week!

When Rob Scheer entered foster care at twelve, he carried his belongings in a trash bag. Years later, when children arrived at his own home carrying trash bags, he asked a question that became the heart of Comfort Cases: “How about some dignity?”Rob is a former foster youth, U.S. Navy veteran, adoptive dad, author, speaker, and the founder of Comfort Cases. In this conversation, he shares what foster care, homelessness, parenting, and building a family taught him about belonging.Jeff and Rob talk about behaviour as communication, the moments when a child's behaviour hurts even when you understand the why, and the importance of separating the person from what is happening in the moment. They also talk about the danger of letting a diagnosis, a file, or somebody else's prediction become the whole story.This is not a conversation that promises an easy path. It is a conversation about dignity, staying connected, and continuing to see the person when systems only see the problem.Resources mentioned in this episodeComfort Caseshttps://comfortcases.org/Learn about hosting a Comfort Cases packing partyhttps://comfortcases.org/packingparty/Volunteer, host a donation drive, or support Comfort Caseshttps://comfortcases.org/volunteer/Contact Comfort Cases about speaking, partnerships, or bringing the work to your areahttps://comfortcases.org/contact/Rob's memoir, A Forever Family: Fostering Change One Child at a Timehttps://comfortcases.org/more-ways-to-support-us/Listen to Rob's Fostering Change podcasthttps://comfortcases.org/podcasts/Watch Rob and Reece in Somewhat Familiar, Season 1, Episode 5: Foster Familieshttps://tv.apple.com/us/episode/foster-families/umc.cmc.65ir2q0datcn490zoe79z3s02?showId=umc.cmc.1onsp08upednzqqu3esowinwdWatch Rob and Reece in Dads, directed by Bryce Dallas Howardhttps://tv.apple.com/ca/movie/dads/umc.cmc.5voyewgcndqj0a3i9mp7hbloqWant to be around caregivers who understand this world? Join the free FASD Forever Facebook group: https://www.facebook.com/groups/FASDForeverSupport the show

Drop us some Fan Mail. Thanks!Question: Our adopted son is almost 4 months old and perfectly healthy. He eats well, sleeps well, and seems to be hitting his milestones just fine. We know that he was exposed to cocaine during pregnancy, but he was born only three weeks early, which is still full-term. He had a healthy birth weight, he was not suffering from withdrawal in the hospital, and he has checked out as perfectly healthy at all of his pediatrician visits so far. My question is, does the lack of negative effects of cocaine in these early months of his life give us any indication of whether or not he will have learning difficulties or development issues due to the cocaine when he reaches school age? I am curious whether there is any research showing that a lack of symptoms at a young age following prenatal exposure indicates fewer symptoms at an older age. Resources:FASD UnitedPregnancy and Breastfeeding ExposuresRaising a Child with Prenatal Substance ExposurePrenatal Substance Exposure Training for Foster, Adoptive, and Kinship ParentsSupport the showPlease leave us a rating or review.  This podcast is produced by www.CreatingaFamily.org. We are a national non-profit with the mission to strengthen and inspire adoptive, foster & kinship parents and the professionals who support them.Creating a Family brings you the following trauma-informed, expert-based content:Weekly podcastsWeekly articles/blog postsResource pages on all aspects of family building

"Are you tired? Worn out? Burned out on religion? Come to me. Get away with me and you'll recover your life. I'll show you how to take a real rest. Walk with me and work with me—watch how I do it. Learn the unforced rhythms of grace." -Matthew 11:28 & 29 MSG   Children with trauma and Fetal Alcohol Spectrum Disorder (FASD) often aren't choosing challenging behaviors—they're struggling with brain-based differences that affect memory, impulse control, and executive functioning. In this week's episode of The Adoption & Foster Care Journey Podcast, Sandra Flach explores: What confabulation is (and why it's often mistaken for lying) Why consequences and punishment frequently don't work How shifting from consequences to accommodations can transform your relationship with your child   When we recognize the difference between can't and won't, we can replace frustration with compassion and create the supports our children truly need.   Listen now and discover practical, brain-based strategies that can bring more peace and connection to your parenting journey.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: Free Breath Prayer Download See Available Trainings The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Cindy Lee returns to the podcast to talk about how TBRI® intersects with Fetal Alcohol Spectrum Disorders and other forms of neurodivergence such as Autism and ADHD.

Dr. Takon has 23 years of clinical experience assessing children for ADHD, ASD, tics, FASD and epilepsy. She's passionate about helping parents and professionals in communities, understand neurodiversity more clearly. As host of the "Early Intervention Matters" podcast, she regularly creates educational content on child development, early assessment, diagnosis and practical support for neurodivergent children and their families.

Original air date: Jan 28, 2025 In this episode, Lisa reconnects with Natascha Lawrence, a Synergetic Play Therapy Supervisor, EMDR Practitioner, and founder of the FASD Institute, for an essential conversation about supporting children with Fetal Alcohol Spectrum Disorders (FASDs) through play therapy. This is Part 2 of their dialogue, revisiting a topic that rarely gets the attention it deserves in the field of play therapy. Together, Lisa and Natascha dive into: What play therapists need to know about FASD: A holistic understanding of FASD as a whole-body diagnosis and its implications for therapeutic practice. Creating neurodivergent-friendly play spaces: Practical steps to make playrooms sensory-safe and accessible for children with FASD and other neurodiverse conditions. The FASD iceberg analogy: Understanding the layers beneath the surface and how they influence behavior, communication, and regulation. Challenging the stigma: Reframing the narrative for children with FASD and their families, starting with compassion and respect. Supporting caregivers: Why empowering parents and destigmatizing FASD is vital for meaningful therapeutic outcomes. With Natascha's blend of professional expertise and personal insights as a parent of a child with FASD, this conversation provides invaluable tools and perspectives for therapists and caregivers alike. Join Lisa and Natascha for this heartfelt and eye-opening episode, and discover how to make your play therapy practice more inclusive, effective, and empowering for children with FASD.

“And He (Jesus) awoke and rebuked the wind and said to the sea, “Peace! Be still!” And the wind ceased, and there was a great calm.” -Mark 4:39   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.   On this episode host Sandra Flach talks with returning guest favorite, Dr. Jerrod Brown. Dr. Brown has 6 PhD's and specializes in topics related to autism spectrum disorder (ASD), fetal alcohol spectrum disorder (FASD), confabulation, suggestibility, trauma and other life adversities, alexithymia, executive dysfunction, criminal recidivism, traumatic brain injury (TBI), and youth firesetting. You can check out his full bio on our website along with dozens of our bonus episodes feating Dr. Brown.   Here Dr. Brown unpacks the prevalence of migraine headaches among children with adverse childhood experiences (ACEs). Listen in or watch on our YouTube channel to learn risk factors, symptoms, and lifestyle medicine choices to improve outcomes.   You can find episode 539 wherever you get your podcasts!    Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: Dr. Jerrod Brown's Email See Available Trainings The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Drop us some Fan Mail. Thanks!Parenting neurodiverse tweens and teens can feel overwhelming, especially when traditional parenting strategies don't seem to work. In this episode, we talk with Carl Young and Joel Sheagren, co-authors of Embracing Hope: Innovative Strategies to Empower Parents Raising Neurodiverse Teens, about practical, brain-based strategies to reduce conflict, support emotional regulation, strengthen connection, and navigate the hard seasons with more hope.In this episode, we discuss:What are parents of tweens and teens carrying right now that you know they want people to understand?Why do the tween and teen years often become especially hard for neurodiverse kids and their caregivers?One of the themes in your work is “understanding over stigma.” Can you tell us what that means?What are examples of behaviors parents are often blamed for, or blamed on the child, that may actually be rooted in neurodevelopmental differences?Many parents feel confused because traditional parenting advice doesn't seem to work for their child with neurodiversity. Can you explain executive functioning in a way that helps overwhelmed parents understand what their child is actually struggling with day to day? What are some real-life ways those struggles show up at home?What are some common expectations we place on tweens and teens that may not match their developmental abilities? How can parents shift toward more reasonable expectations without giving up on growth?What are some practical strategies to reduce conflict at home while still maintaining structure and boundaries?We understand that self-regulation is a learned skill that comes from years of our own regulation and then sharing it with our kids, called co-regulation.  What does co-regulation actually look like with a tween or teen who is escalating emotionally?How can parents respond differently to behaviors like impulsivity, shutdowns, avoidance, perseveration, or lying?Many caregivers say they feel like they're “walking on eggshells.” It's exhausting and creates so much stress in our homes.Where do you recommend families start when the home has fallen into a state of constant stress or chaos?How can parents introduce and maintain the “calm” in spite of the chaos that our kids' neurodivergence may bring with it?What helps parents hold onto a connection with their child during seasons when everyone feels frustrated or discouraged?Sometimes families need help redefining success. How do you encourage parents to rethink what thriving can look like for neurodiverse tweens and teens?Resources:Embracing NeurodiversityEmbracing Hope: Innovative Strategies to Empower Parents Raising Neurodiverse TeensRaising Kids with Neurodiversity (ADHD, Autism, & Learning Differences)Suggested books for Raising Kids with Learning YouSupport the showPlease leave us a rating or review.  This podcast is produced by www.CreatingaFamily.org. We are a national non-profit with the mission to strengthen and inspire adoptive, foster & kinship parents and the professionals who support them.Creating a Family brings you the following trauma-informed, expert-based content:Weekly podcastsWeekly articles/blog postsResource pages on all aspects of family building

Relebogile Mabotja speaks to Dr Leana Olivier who is the chief executive officer of the Foundation of Alcohol- Related Research (FARR) and Mokebe Thulo who is the chief executive officer of Aware.Org about how families, healthcare professional, educators, and communities can work together to support healthier pregnancies and give every child the best possible start in life. 702 Afternoons with Relebogile Mabotja is broadcast live on Johannesburg based talk radio station 702 every weekday afternoon. Relebogile brings a lighter touch to some of the issues of the day as well as a mix of lifestyle topics and a peak into the worlds of entertainment and leisure. Thank you for listening to a 702 Afternoons with Relebogile Mabotja podcast. Listen live on Primedia+ weekdays from 13:00 to 15:00 (SA Time) to Afternoons with Relebogile Mabotja broadcast on 702 https://buff.ly/gk3y0Kj For more from the show go to https://buff.ly/2qKsEfu or find all the catch-up podcasts here https://buff.ly/DTykncj Subscribe to the 702 Daily and Weekly Newsletters https://buff.ly/v5mfetc Follow us on social media: 702 on Facebook https://www.facebook.com/TalkRadio702 702 on TikTok: https://www.tiktok.com/@talkradio702 702 on Instagram: https://www.instagram.com/talkradio702/ 702 on X: https://x.com/Radio702 702 on YouTube: https://www.youtube.com/@radio702 See omnystudio.com/listener for privacy information.

As a hidden brain injury, FASD can manifest in ways that often lead to challenging behaviors, which can feel overwhelming for caregivers relying on traditional parenting strategies. Making it even more difficult is knowing where to get an accurate diagnosis and help. Barb Clark is the Founder and CEO of FASD Mosaic where she provides coaching, training, and consulting on Fetal Alcohol Spectrum Disorders (FASD), trauma, neurodivergence, and challenging behaviors. Barb is the author of a fabulous book, "Raising Kids and Teens with FASD: Advice and Strategies to Help Your Family to Thrive!" She also serves as the head coach for the international FASD Caregiver Kickstart program. Barb can be contacted at FASD Mosaic. The State of Wisconsin's Dose of Reality campaign is at Dose of Reality: Opioids in Wisconsin. More information about the federal response to the ongoing opiate crisis can be found at One Pill Can Kill. The views and opinions of the guests on this podcast are theirs and theirs alone and do not necessarily represent those of the host or Westwords Consulting. We're always interested in hearing from individuals or organizations who are working in substance use disorder treatment or prevention, mental health care and other spaces that lift up communities. This includes people living those experiences. If you or someone you know has a story to share or an interesting approach to care, contact us today! Follow us on Facebook, LinkedIn, and YouTube. Subscribe to Our Email List to get new episodes in your inbox every week!

“Let me hear in the morning of your steadfast love, for in you I trust. Make me know the way I should go, for to you I lift up my soul.” -Psalm 143:8   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.   On this episode, host Sandra Flach continues her FASD Q & A by answering three questions she is frequently asked:  Is getting an FASD diagnosis important? What about medication? What therapies help with FASD?   Listen in as Sandra unpacks these questions from her personal experience raising two young adult sons with diagnosed Fetal Alcohol Syndrome as well as from her professional experience as a national FASD trainer.   Find Episode 535 wherever you get your podcasts.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: See Available Trainings The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon

Relebogile Mabotja speaks to Dr Leana Olivier who is the Chief Executive Officer of the Foundation of Alcohol-Related Research (FARR) and Mokebe Thulo who is the Chief Executive Officer (CEO) of Aware.org about the realities of Fetal Alcohol Spectrum Disorder (FASD) in South Africa and how families, healthcare professionals, educators, and communities can work together to support healthier pregnancies and give every child the best possible start in life. See omnystudio.com/listener for privacy information.

Fetal alcohol spectrum disorders (FASDs) affect up to 1 in 20 people and is particularly prevalent among young people in the adoption and fostering system. As a hidden brain injury, FASDs can manifest in ways that often lead to challenging behaviors, which makes diagnosis and intervention challenging. Mollie O'Brien, the Executive Director of Proof Alliance in St. Paul, Minnesota, discusses FASDs and how, through community, collaboration, and education, they work to create lasting change and improve outcomes for those impacted by an FASD. Proof Alliance can be contacted at Proof Alliance. The State of Wisconsin's Dose of Reality campaign is at Dose of Reality: Opioids in Wisconsin. More information about the federal response to the ongoing opiate crisis can be found at One Pill Can Kill. The views and opinions of the guests on this podcast are theirs and theirs alone and do not necessarily represent those of the host or Westwords Consulting. We're always interested in hearing from individuals or organizations who are working in substance use disorder treatment or prevention, mental health care and other spaces that lift up communities. This includes people living those experiences. If you or someone you know has a story to share or an interesting approach to care, contact us today! Follow us on Facebook, LinkedIn, and YouTube. Subscribe to Our Email List to get new episodes in your inbox every week!

Hello and welcome to this episode, it's action packed and we reunite after Scott's many travels! We start with a consideration about the recent FASD Ireland conference and the radio documentary that Scott commissioned in Ireland. It's well worth a listen and you can do that here.  Al has been talking to practitioners working with families living with challenging and violent behaviour over the last few weeks and we unpack why there's low confidence in the workforce and nervousness around how to support and help.  As always if you've experience of adoption, fostering or special guardianship from any perspective personal or professional and would like share that on the podcast please get in touch through the Facebook page, BlueSky or email us at AandFpodcast@gmail.com Listen/subscribe on iTunes here Spotify here

Please join us for “Understanding Fetal Alcohol Spectrum Disorder: A Discussion with Jenn Wisdahl and Kristen Eriksen.”Jenn Wisdahl leads strategy and operations at FASD United, the national organization supporting people with Fetal Alcohol Spectrum Disorders (FASD) and promoting healthy pregnancies. With FASD impacting 1 in 20 Americans, a critical part of her role involves the national legislative and policy agenda for this highly prevalent and under-recognized disability. Using a data-driven strategy that keeps people at the forefront, Jenn has supported substantial growth at FASD United, supporting the Family Navigator Program, National FASD Impact Week, and the return of the International FASD Research Conferences, which have moved from Canada to a permanent home in the United States.Kristen Eriksen serves as an FASD United Family Navigator, as well as Caregiver Navigator at MassFASD, and is a nurse with over 35 years of varied experience, including pediatric and obstetrical nursing, early intervention developmental services, with a recent focus on school nursing. Her personal history of raising twins with FASD since infancy has led to a new and different career path.After adopting infant twins in 2007, her entire life trajectory changed. Starting in 2010, she began a long, slow educational process to learn more about the challenges that the twins faced. When they were finally diagnosed with FASD at age 9, her deep dive into FASD began. She began working with MassFASD and began working as a Family Navigator at FASD United in 2022Support the show

This special documentary takes an in-depth look at FASD through the voices of experts, families, and individuals living with the condition. Produced by Clare FM's Programme Director & Head of Operations Padraic Flaherty. Email: pf@clare.fm

Leading international experts, policymakers, advocates and families affected by Foetal Alcohol Spectrum Disorder are gathering in Ennis this week for the 2026 FASD Ireland International Conference. Hosted over three days in Hotel Woodstock, the event will explore the theme of “Justice and FASD” — examining everything from access to services and public awareness to the experiences of people with FASD within social and justice systems. Alan Morrissey was joined by Tristan Casson-Rennie to discuss the conference, the growing conversation around FASD in Ireland, and the importance of awareness, prevention and support. Image © Clare FM

“Then they cried out to the LORD in their trouble, and He brought them out of their distress. He stilled the storm to a whisper, and the waves of the sea were hushed.” -Psalm 107:28-29   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.   On this episode, host Sandra Flach continues the foster care conversation with foster and adoptive mom and FASD expert, Dr. Ryan Jolly.   Dr. Jolly is a Kansas-based psychiatric nurse practitioner and nationally recognized advocate focused on Fetal Alcohol Spectrum Disorders. As the founder of Brain First Family Center, she leads a specialized clinic dedicated to the identification, diagnosis, and treatment of FASD and related neurodevelopment conditions, with a strong commitment to Medicaid access and eliminating long waitlists for vulnerable families.    Ryan's advocacy is grounded in both clinical expertise and lived experience as a single foster and adoptive parent to children with FASD and complex brain-based disabilities. Utilizing her role as a Doctor of Nursing Practice she engages in research to advance understanding  of brain-based differences, trauma-informed systems of care, and increase recognition of FASD within child welfare and education systems. Dr. Jolly strives to reimagine systems of care to ensure all individuals are supported to thrive within families and communities rather than being misunderstood, misdiagnosed, or institutionalized.   Listen in to Sandra's conversation with Dr. Ryan Jolly on Episode 531 wherever you get your podcasts.    Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: See Available Trainings The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon FASD United Brain First Family Center

Drop us some Fan Mail. Thanks!Question: My 2nd grader, adopted domestically, has some pretty big, hard behaviors, like tantrums, clingy whining, and difficulty cooperating or sharing. We know there was prenatal substance exposure. I feel stuck to help them with their big feelings and big behaviors — what do I do to help them day to day?Resources:5 Tips to Save Your Sanity While Raising Kids with Prenatal Substance ExposurePrenatal Exposure, Part 1: Parenting Babies Through Elementary AgesTantrums, Meltdowns, Whining, Oh My! How to Parent Challenging BehaviorsFree E-Guide: Navigating Challenging Behaviors - Practical Strategies for FamiliesSupport the showPlease leave us a rating or review.  This podcast is produced by www.CreatingaFamily.org. We are a national non-profit with the mission to strengthen and inspire adoptive, foster & kinship parents and the professionals who support them.Creating a Family brings you the following trauma-informed, expert-based content:Weekly podcastsWeekly articles/blog postsResource pages on all aspects of family building

Are you a grandparent raising grandchildren while trying to balance compassion with structure in your home? Do you find yourself reverting to “because I said so” parenting, only to meet resistance, trauma triggers, or confusion from the children in your care? Are you yearning for practical guidance, emotional support, and a framework to help you navigate this unexpectedly challenging season of life?I'm Laura Brazan, and like you, I was thrust overnight into the world of kinship caregiving for my grandchildren, suddenly responsible for guiding young hearts through adversity. In this episode, join me as I welcome Dr. Lindsay Emerson, a leading expert in trauma-informed parenting, to unveil the 5C's Framework—an evidence-based approach blending warmth, boundaries, and repair that works for both traditional and modern families. Together, we dissect how to communicate, remain consistent, offer choices, set consequences, and check in with yourself—all essential skills for “amazing parenting." To find out more about, please Send us Fan MailIf you are raising grandchildren who are neurodivergent—or navigating the complexities of an FASD diagnosis—you know that traditional parenting advice often falls short. You aren't just looking for tips; you're looking for a strategy.That's why I want to invite you to a special, FREE conference designed specifically for families like ours.https://www.grandparents-raising-grandchildren.org/ If you had an extra hour of 'found time' tomorrow morning—time that belonged only to you—what is the one thing you'd do that you haven't done in months?Seriously—hit pause, or wait until you're parked, and email me at laurabrazan@grandparents-raising-grandchildren.org. I'm collecting these stories to make sure this book solves the real-world burnout we're all feeling. In this special pre-roll segment, I'm sharing a moving letter from a member of our community, Laurel. Her story of loss, resilience, and raising her grandson after the unthinkable is a raw reminder that none of us are walking this path alone.We want to hear from you. If Laurel's story resonates with you, or if you have a journey of your own to share, join our private community. Your story might be the exact lifeline someone else needs to hear today. Thank you for tuning into today's episode. It's been a journey of shared stories, insights, and invaluable advice from the heart of a community that knows the beauty and challenges of raising grandchildren. Your presence and engagement mean the world to us and to grandparents everywhere stepping up in ways they never imagined.Remember, you're not alone on this journey. For more resources, support, and stories, visit our website and follow us on our social media channels. If today's episode moved you, consider sharing it with someone who might find comfort and connection in our shared experiences.We look forward to bringing more stories and expert advice your way next week. Until then, take care of yourselves and each other.Want to be a guest on Grandparents Raising Grandchildren: Nurturing Through Adversity? Send Laura Brazan a message on PodMatch, here: https://www.podmatch.com/hostdetailpreview/grgLiked this episode? Share it and tag us on Facebook @GrandparentsRaisingGrandchilden Love the show? Leave a review and let us know!CONNECT WITH US: Website | Facebook 

“We will rejoice in our affliction, because affliction produces endurance, and endurance produces character, and character produces hope.” -Romans 5:3   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.   On this episode, host Sandra Flach talks with Johanna Jones. Johanna has worked in the field of disability for over twenty years, serving as a post secondary educator and within the nonprofit sector. Recently, Johanna authored the book, “Inclusion: Building a Framework for Disability,” which is welcoming space that fosters connection and growth and builds upon established research, historical references, and biblical text. The book identifies inclusion as a framework for disability, using the Gospel of Luke, where faith, affliction and disability intersect.   Johanna received her doctorate from Samford University in Birmingham, Alabama, where she completed a mixed methods study that explored factors that impact special needs programming. Johanna's outreach and public service experience includes working as an FASD United Affiliate, presenting information on FASD in the community, as well as within education settings. She's a speaker with nonprofit organizations, schools, foster care workshops, and conferences in Alabama and throughout the US. Additionally, Johanna was awarded the FASD Proclamation by the Governor of Alabama and moderates the FASD Alabama Facebook page which is a clearing house of information on FASD research.   Find Sandra's conversation with Johanna Jones on Episode 527 wherever you get your podcasts.    Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon ReNew Retreat in NC

In this episode, we unpack the surprising reasons why some children experience the world more intensely than others, and why their big emotions are rarely about what they seem to be about. You’ll discover a reframe that just might change the way you see your child’s most challenging moments, including a simple but powerful analogy that explains why your child can hold it together all day and then completely fall apart the moment they walk through your door. If you’ve ever felt frustrated, confused, or just desperate to understand what’s really going on beneath the surface of your child’s behavior, this episode offers the compassionate insight and practical perspective you’ve been looking for. Key Takeaways: Anxiety often hides behind anger. Connection calms a stressed nervous system. Small triggers carry big invisible weight Compassion begins with understanding the “why” Mentioned in this Podcast: Sensitive & Intense Online Course The Table Monthly Giving Program Rocks in the Backpack Video Rocks in the Backpack PDF Check out our website for more resources to support your parenting! This podcast was made possible by members of The Table, whose monthly support creates a ripple effect of change for generations to come. We'd love to have you take a seat at The Table! Love the podcast? Leave a review to help other parents discover the show! Guest Bio: Lynne Jackson is one of the Co-Founders of Connected Families. As a parent coach and mom of three intense kids herself, Lynne has walked alongside hundreds of parents, encouraging and bringing hope. She is also a research enthusiast and loves leaning into brain science to equip parents and caregivers better. Most importantly, as a follower of Christ, she brings biblical wisdom, abundant grace, and a “no shame” policy. Lydia Rex is a registered nurse, wife, and mother of two, and has worked with families in many capacities throughout her career and personal life. She's been a student of Connected Families since 2014 and continues to find it incredibly life-giving for her own family. Areas of her experience/special interest include foster care and adoption, attachment difficulties, developmental and learning disabilities, including FASD. She brings a trauma-informed perspective to the Connected Families Framework and the desire to see families find peace and healing even in the midst of challenges! You’ve seen what the Connected Families Framework can do. What if you could bring that to other families? Join us on May 6 at 12:30 pm CTS for a free one-hour informational webinar on becoming a CF Certified Parent Coach. No pressure. Just real information to help you take your next step. Reserve your spot today! Can’t make it live? A recording will be available through May 14. © 2026 Connected Families .stk-cf6a95f {margin-bottom:39px !important;}.stk-cf6a95f-container{background-color:#e2f4f8 !important;}.stk-cf6a95f-container:before{background-color:#e2f4f8 !important;}.stk-cf6a95f-container:hover{box-shadow:0px 2px 20px #99999933 !important;}@media screen and (max-width:689px){.stk-cf6a95f .stk-block-card__image{width:100% !important;height:250px !important;}} Do you have a child with BIG feelings and BIG needs? The Sensitive & Intense Kids online course is a game changer. It’s for YOU. .stk-7a41d3e .stk-button-group{flex-direction:row !important;}@media screen and (max-width:999px){.stk-7a41d3e .stk-button-group{flex-direction:row !important;}}@media screen and (max-width:689px){.stk-7a41d3e .stk-button-group{flex-direction:row !important;}} .stk-4080859 .stk-button{background:var(--theme-palette-color-1, #ee6c4d) !important;}.stk-4080859 .stk-button:hover:after{background:var(--theme-palette-color-2, #98c1d9) !important;opacity:1 !important;}.stk-4080859 .stk-button__inner-text{font-size:21px !important;font-weight:600 !important;}@media screen and (max-width:999px){.stk-4080859 .stk-button__inner-text{font-size:21px !important;}}LEARN MORE

“Therefore, encourage one another and build one another up, just as you are doing.” -1 Thessalonians 5:11   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.   On this episode, host Sandra Flach shares four commonly asked questions about raising children with FASD (Fetal Alcohol Spectrum Disorder). Listen in as she unpacks: Eating issues Navigating church  Helping teens/young adults with employment How can parents survive each day Find FASD Q & A on Episode 526 wherever you get your podcasts.    Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: FASD Fact Sheet for Educators FASD Face Sheet for Employers The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon ReNew Retreat in NC

Click here to send us a topic idea or question for Weekend Wisdom.Helping young adults in foster or kinship care transition toward adulthood can feel overwhelming for foster parents and relative caregivers. Join us today for a conversation with Vernell Gore of Youth Villages and Nick Sgarlata of Bridge to Brighter, for practical ways to prepare and equip your foster or kin youth for adulthood.In this episode, we discuss:What makes this stage of life uniquely challenging for youth in foster or kinship care compared to their peers?What does a successful transition to adulthood actually look like?What are some common misconceptions that caregivers or professionals have about youth who are nearing adulthood?When you think about a young person leaving care and thriving in adulthood, what key elements need to be in place?Why might a young person leaving foster care or relative care at the same time they are leaving high school feel the weight of this uncertainty more than their peers? How and where can foster parents or kin carers help youth explore different career paths and possibilities?What are some practical ways they can research those options and make informed decisions?What types of programs or pathways will help youth develop skills, discipline, or career direction?What are the most important money skills young people need before they leave care?What are some simple ways to start teaching these skills while the youth are still at home?What are some everyday adult responsibilities that youth may struggle with? What are some of the benefits of mentors for a young person transitioning out of foster care? How can they begin finding mentors or supportive role models?Beyond practical skills, what character traits or skills do young people need to develop to succeed in adulthood?Many youth in foster care or living with a grandparent or relative are carrying trauma from earlier experiences. How important are healing and identity development in preparing them for adulthood?How might a foster parent or relative caregiver support their young person toward healing?What are a few common mistakes adults make when trying to prepare youth for adulthood?What practical steps can foster or kinship carers start today to prepare their youth for adulthood? Resources:Raising Kids with Neurodiversity (ADHD)Maintaining a Healthy Perspective When Parenting Tweens & TeensPrenatal Exposure, Part 2: Parenting Tweens and TeensSupport the showPlease leave us a rating or review.  This podcast is produced by www.CreatingaFamily.org. We are a national non-profit with the mission to strengthen and inspire adoptive, foster & kinship parents and the professionals who support them.Creating a Family brings you the following trauma-informed, expert-based content:Weekly podcastsWeekly articles/blog postsResource pages on all aspects of family building

“But now, O LORD, you are our Father; We are the clay, and you are our potter; We are all the work of your hand.” -Isaiah 64:8   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.   On this episode, host Sandra Flach, talks with Krista LaRock. Kristen and her husband have been married for 30 years and have adopted 14 children including sibling groups. Eight of their children live with FASD—Fetal Alcohol Spectrum Disorder. This led to Kristen to raise dogs to support her children and other individuals. Two years ago she founded FASDogs—a service dog organization to support individuals with developmental disabilities including FASD.   Listen in as Krista shares about her family's adoption journey and how they navigate the challenges of FASD on Episode 524 wherever you get your podcasts.    Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: Krista LaRocque on Facebook Krista LaRocque on Instagram FASDogs.com The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon ReNew Retreat in NC

Click here to send us a topic idea or question for Weekend Wisdom.Are you raising a child with known prenatal exposure to alcohol? Does your child have a diagnosis for Fetal Alcohol Spectrum Disorder? Listen to this conversation with Barb Clark, Founder and CEO of FASD Mosaic. She offers coaching, training, and consulting on Fetal Alcohol Spectrum Disorders (FASD), trauma, neurodivergence, and challenging behaviors, and is the author of Raising Kids and Teens with FASD: Advice and Strategies to Help Your Family to Thrive!In this episode, we discuss:In your experience, what do caregivers most misunderstand about FASD at first?”How does prenatal alcohol exposure impact brain development?What is the difference between FAS and FASD?Do the timing, frequency, and amount of alcohol all matter in the outcomes experienced by the child? Are there other factors at play?Why is FASD still so often missed or misunderstood?Primary neurological impacts on a child who has FASDSecondary behaviors – which, when viewed through that brain-based lens, are adaptive responses that help them process and cope with their environmentWhat are a few practical strategies parents and caregivers can implement to help them reframe how they support their child with FASD?Tantrums or raging as an example of challenging behaviors – how it may look differently across these ages and developmental levelsWhat are a few of the typical strengths seen in individuals with FASD?Why do these strengths often emerge inconsistently?How our home environment and culture set a child with FASD up for successCan you offer practical suggestions for how parents or caregivers would implement a strengths-based approach to raising a child with FASD?Practical strategies that parents and caregivers can implement right away when raising their child with FASDHow do you recommend a parent or caregiver handle the process of repair and reconnection with a child with FASD? What should parents and caregivers consider in planning for the future?Prioritizing self-care and reframing it as interdependence and community care.Resources:Prenatal Substance Exposure Workshops for ParentsPrenatal Substance Exposure resource pageFASD MosaicSupport the showPlease leave us a rating or review. This podcast is produced by www.CreatingaFamily.org. We are a national non-profit with the mission to strengthen and inspire adoptive, foster & kinship parents and the professionals who support them.Creating a Family brings you the following trauma-informed, expert-based content: Weekly podcasts Weekly articles/blog posts Resource pages on all aspects of family building

“A cheerful heart is good medicine, but a crushed spirit dries up the bones.” -Proverbs 17:22   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.   On this episode, host Sandra Flach, talks with Dr. Jerrod Brown about Lego-based interventions and therapy for neurodivergent individuals, including those with FASD, autism, and ADHD. Dr. Brown explains the benefits of using Lego bricks as a therapeutic tool, highlighting their ability to improve cognitive abilities, reduce screen time, and foster social skills. He shares practical tips for implementing Lego-based activities and emphasized the importance of celebrating successes and teaching patience.   Listen to Sandra's conversation with Dr. Brown on Episode 521 wherever you get your podcasts.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: jerrod01234brown@live.com The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon Mobilize Ohio ReNew Retreat in NC

“Behold, I am doing a new thing; now it springs forth, do you not perceive it? I will make a way in the wilderness and rivers in the desert.” -Isaiah 43:19   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.   On this episode, host Sandra Flach, talks with adoptive mom, Kristin Hall. Kristin graduated from Virginia Tech with a degree in Communications and a Master's degree in Public Administration, focusing on nonprofit administration. After school, she got married and started her career as a Program Facilitator for SERVE, an emergency assistance agency, and later worked at the corporate offices of Prison Fellowship Ministries in a similar role.    Kristin stepped away from the workforce in 2003 after adopting her first two children, dedicating herself to family life while also taking on leadership roles in her church. She is also a member of the Hope for the FASD Journey online support community.   Listen to Sandra's encouraging conversation with Kristin Hall on Episode 520 wherever you get your podcasts.   Please be sure to subscribe to the podcast, leave a review, and share it on your social media.   Links mentioned in this episode: The Adoption & Foster Care Journey AFCJ on YouTube justicefororphansny.org justicefororphansny.org/hope-community     Email:  sandraflach@justicefororphansny.org sandraflach.com Soul Care Saturday—52 Devotions for Foster and Adoptive Moms Orphans No More—A Journey Back to the Father book on Amazon Mobilize Ohio ReNew Retreat in NC

Carrie McCarter is a speech-language pathologist with a master's degree who has spent her career working in the birth-to-three world of early intervention. However, when it came to raising her own twins with Fetal Alcohol Spectrum Disorder (FASD), she found that her professional training wasn't enough to navigate the intense dysregulation and sensory challenges at home.In this episode, Carrie opens up about the "professional paradox" of being an expert in child development while feeling like a failure as a parent. She shares the turning point that occurred when she stopped trying to "fix" behaviors and started understanding the unique architecture of the FASD brain.Key Takeaways from the ConversationThe Struggle for Diagnosis: Carrie discusses the two-and-a-half-year journey to secure an FASD diagnosis, which finally came when her twins were 10.5 years old.The 10 Brain Domains: Discover how learning about the brain domains was "gut-wrenching yet freeing," allowing Carrie to move from guilt to effective accommodation.Professional vs. Parent: Carrie explains why her twins would "shut down" at school while displaying acting-out behaviors at home, and why traditional parenting techniques often fail these children.The Power of Yet: A look at how Carrie manages the transition into adulthood and why she remains hopeful about the brain's ability to grow and learn well into the 20s and beyond.Self-Care for the Solo Parent: How Carrie utilizes respite services, online grocery shopping, and "breathing breaks" to stay regulated as a single mother.Resources and LinksFree FASD Workshop Registration Join our upcoming free workshops this February to learn a new brain-body approach to managing aggression and building stability. Register Here: https://www.fasdsuccess.com/fasd-workshop-2026Connect with Carrie McCarter Carrie is a passionate educator and speaker available for training and advocacy sessions. Email: carriemccarterfasd@gmail.com Watch on YouTube See the full video version of this interview: https://www.youtube.com/watch?v=l7UJh3m9ZAAThe FASD Success Show Subscribe on Apple Podcasts or Spotify to never miss an episode.The biggest free training for families is back. We start with a new brain-body approach to aggression that stops the blame. Then, we tackle Advocacy in Action—giving you the tools to talk to professionals and teachers who just don't get this hidden disability. Finally, we build your blueprint for long-term stability and support.Register: https://www.fasdsuccess.com/fasd-workshop-2026Support the show

This episode is a special collaboration between Beyond 6 Seconds and the Living with FASD podcast hosted by Patti Kasper. Fetal alcohol spectrum disorders (FASD) are lifelong conditions caused by prenatal alcohol exposure that can impact physical, cognitive, and behavioral development. FASD is a type of neurodivergence, but it's often left out of conversations about neurodivergence. This episode is part of a series that Patti is doing on her podcast to help bring FASD into those conversations. We discuss what communication differences can feel like for people with certain types of neurodivergence, such as FASD, autism (including apraxia in non-speaking autism), ADHD, and schizophrenia. We also explore why communication challenges can happen, and how friends and loved ones can help provide understanding and support. A quick caveat: This conversation is not medical or diagnostic advice, and it does not speak for every neurodivergent person. Instead, Patti and I are sharing our own experiences and some insights from the people we've interviewed on our podcasts. You can find Living with FASD podcast on Apple, Audible, Patreon, Pocket Casts, Rumble and YouTube, and connect with Patti at dot.cards/yourfasdcoach. Do the things we mention in this episode match your experience as a neurodivergent person? Do you have other experiences? Let me know what you think!  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. *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.*

Episode #187 The FASD Brain and Connectivity with Dr. Raja MukherjeeWhat if many of the struggles we see in FASD are not about behavior at all but about how the brain sends and receives messages?In this episode of The FASD Success Show, Jeff Noble sits down with Dr. Raja Mukherjee, one of the world's leading experts in FASD psychiatry and brain development, to explore what brain connectivity really means for individuals living with FASD across the lifespan.Dr. Mukherjee explains how prenatal alcohol exposure affects the way different parts of the brain communicate with each other and why this can show up as inconsistency, fatigue, emotional overwhelm, and difficulty with daily life tasks even when someone appears capable on the surface.Together, Jeff and Dr. Mukherjee unpack why independence is often the wrong goal, how interdependence supports regulation and mental health, and what caregivers can do differently when they understand the brain through a connectivity lens.In This Episode You'll Hear• What brain connectivity is and why it matters more than IQ or motivation • How miscommunication between brain regions affects regulation, memory, and behavior • Why skills can look “there one day and gone the next” • How stress and overload disrupt already fragile brain networks • Why total independence is not a realistic or healthy end goal for many adults with FASD • How interdependence supports long term success and wellbeing • What caregivers and systems get wrong when they focus on compliance instead of connectionWhy This Episode MattersThis conversation helps caregivers, professionals, and individuals with FASD move away from blame and toward understanding. When you see challenges as connectivity issues rather than character flaws, everything changes including expectations, support strategies, and outcomes.Dr. Mukherjee brings decades of clinical experience and research insight to a topic that caregivers have been living for years. This episode offers clarity, validation, and a brain based framework you can actually use at home and in advocacy conversations.Listen and WatchListen on Apple Podcasts https://podcasts.apple.com/ca/podcast/the-fasd-success-show/id1492499195Listen on Spotify https://open.spotify.com/show/6ntB51glqYnRPmXCh6lOGqWatch on YouTube https://www.youtube.com/@FASDSuccessResources and LinksLearn more about The FASD Success Show https://www.fasdsuccess.com/podcastJoin our free parent and caregiver community https://www.facebook.com/groups/FASDFOREVERFollow Jeff Noble Instagram https://www.instagram.com/FASDSuccess Facebook https://www.facebook.com/FASDSuccessSubscribe to the YouTube Channel https://www.youtube.com/@FASDSuccessYou are not failing. You are responding to a brain that connects differently. And when we understand the brain, we can build better support, better days at home, and a better future.Support the show

What if independence is not the finish line we should be chasing for individuals with FASD?In this episode of The FASD Success Show, Jeff Noble sits down with Chris Fillion, an adult on the FASD spectrum, foster parent, and national advocate, to talk honestly about what adulthood with FASD really looks like when support is done right.Chris shares his lived experience navigating mental health challenges, the justice system, social services, and burnout, and how everything changed when the focus shifted from doing life alone to building the right team around him. Today, Chris is the Vice President of the Manitoba FASD Coalition and the Executive Director of FASD Mentors of Change, helping reshape how systems understand success for adults with FASD.This conversation challenges one of the most exhausting myths caregivers carry, the belief that success means total independence. Instead, Jeff and Chris explore why interdependence, regulation, and community support are the real foundations for long term stability and growth.In This Episode You'll Hear• Why independence is often the wrong goal for adults with FASD • What adulthood with FASD actually looks like beyond the labels • How anxiety treatment and mental health support can unlock capacity • Why having a support team is a strategy, not a failure • How lived experience advocacy is changing systems from the inside • What caregivers can learn about planning for the long gameWhy It MattersSo many caregivers lie awake worrying about the future, wondering if their loved one will ever be okay on their own. This episode offers a powerful reframe.Success is not about doing everything alone. It is about building a life that works with the brain you have, supported by people who understand it.Chris's story is proof that progress is real, timelines are different, and with the right scaffolding, adults with FASD can build meaningful, connected lives.Resources and LinksFASD Mentors of Change https://fasdmentorsofchange.caChris Fillion https://chrisfillion.caManitoba FASD Coalition https://www.fasdcoalition.caNew Directions https://newdirections.mb.caJoin our free FASD Success Facebook Group https://www.facebook.com/groups/fasdforeverWatch full episodes on YouTube https://www.youtube.com/@FASDSuccessFollow Jeff on Instagram https://www.instagram.com/FASDSuccessFull show notes and resources https://www.fasdsuccess.com/podcastSupport the show