Podcasts about Fetal alcohol spectrum disorder

Send us a textWelcome back to headfirst: A Concussion Podcast. Today we have the honour and privilege to be hosting Nick Rushworth. Nick Rushworth is the Executive Officer of Brain Injury Australia, a position he has held since 2008. Before joining Brain Injury Australia, Nick worked for the Northern Territory Government setting up their Office of Disability whilst also formerly a producer with the Nine Television Network's “Sunday” program and ABC Radio National, where Nick's journalism has won a number of awards, including a Silver World Medal at the 2003 New York Festival, a National Press Club and TV Week Logie Award. Nick's current primary focus is facilitating a national “community of practice” in brain injury for the National Disability Insurance Agency.  Furthermore, Nick serves as a consumer representative for numerous organisations some of these include but not limited to: Mission for traumatic brain injury: A medial research future fund-initiative providing $50 million in federal government funding over 10 years), the Australian Trauma Quality Improvement Program Steering Committee; the Victorian Neurotrauma Advisory Council;  the Executive of the Brain Injury Rehabilitation Directorate of New South Wales Health; the Victorian Transport Accident Commission/ Monash University Institute for Safety, Compensation and Recovery Research Behaviours of Concern Project; the Monash Epworth Rehabilitation Research Centre Advisory Board; the Disability Advisory Committee of the Australian Electoral Commission; Nick is also a Director of the Australian Federation of Disability Organisations, and is an Ambassador for the National Organisation for Fetal Alcohol Spectrum Disorders and the Queensland Brain Institute's concussion research.In April 2024 Nick was appointed to the Australia Government Medical Research Traumatic Brain Injury Mission Expert Advisory Panel. - How Nick Become Involved in the Brain Injury and Concussion Space? (02:30)- Ways the mTBI/ concussion space has change since late 1990's to now? (04:10)- Differences in Mild, Moderate and Severe Traumatic Brain Injury (06:37)- Raising Awareness of mild Traumatic Brain Injury outside of Sports-Related Concussion (12:05)- Indigenous Australian's and Concussion/mTBI (17:02)- Incidences Rates of mTBI (20:30)- Language Around mTBI (22:30)- Falls in the Elderly (23:51)- Difficulties When Talking About Policy Changes and Research Grants? (27:34) - Brain Injury Australia (33:00)  Brain Injury Australia: https://www.braininjuryaustralia.org.au Subscribe, review and share for new episodes which will drop fortnightlySocial media:Twitter: @first concussionFacebook: Headfirst: A concussion podcastInstagram: Headfirst_ Concussion  Email: headfirstconcussion@gmail.com

Booze industry lobbyists have been given input into the development of alcohol policies, including how to deal with Fetal Alcohol Spectrum Disorder. Guyon Espiner spoke to Ingrid Hipkiss.

In today's episode, a new Pope has been found, Cardinal Robert Francis Prevost becomes Pope Leo XIV, booze industry lobbyists have been given input into the development of alcohol policies, including how to deal with Fetal Alcohol Spectrum Disorder, huge numbers of predatory feral cats are endangering our native birds populations as well as killing other wildlife, we have our weekly political panel and we cross the Tasman to get the latest from Kerry-Anne Walsh.

Listen to expert guest, Dr. Kathryn Page in this just released podcast on Fetal Alcohol Spectrum Disorder and FASD-WISE Parenting for practical strategies to support your child with FASD, from hard places.Trauma and attachment experts share the latest information specifically related to adoptive, foster and kinship parenting. In every episode, you will find helpful insights and practical parenting tips.Bio of Guest: Kathryn Page earned a PhD from the Center for Psychological Studies in Berkeley and an internship in addiction recovery at Stanford, a few highlights of Kathryn Page's career include: Disabilities Specialist for the Santa Clara County Juvenile Drug Treatment Court; bilingual School Psychologist in San Lorenzo; 504 Coordinator in the Santa Clara Juvenile Hall; and teacher of social workers with UC Davis Extension.Dr. Page has been working on FASD for 30 years. She founded and directed the diagnostic clinic in Santa Clara County, CA, and is the co-chair of that county's 5-year plan. She provides the mandatory FASD training for Los Angeles County's mental health providers, and advocates for legislation at the state and federal levels. Kathryn consults, writes, teaches, and lives with this condition in her son as well as herself.

In this episode, Jessica Birch speaks to clinical social worker Prue Walker and shares her lived experience with Fetal Alcohol Spectrum Disorders (FASD). She reflects on her personal journey, the stigma encountered surrounding FASD, and how an accurate diagnosis can be life-changing, offering hope and access to essential services.Liked this episode? Stay tuned for future episodes of In the First Person…  by following MHPN Presents.Visit the MHPN website for episode host and guest bios, recommended resources and a self-directed CPD form.Share your comments, questions and feedback about In the First Person or any of MHPN's podcast series here: https://mhpn.org.au/podcast-feedback/ 

Fetal Alcohol Spectrum Disorders (FASD) is a condition that often goes undiagnosed, yet understanding it is vital for providing the right support.  In this episode, Dr Hester Wilson, GP and addiction specialist, speaks to clinical psychologist Dr Vanessa Spiller and parent advocate Angelene Bruce to explore the complexities of identifying and supporting people with FASD. Both Vanessa and Angelene, mothers of children with FASD, offer honest insights into the challenges of diagnosis and raising children with FASD. They discuss the gaps in professional education, early intervention strategies, and the importance of appropriate support systems.Liked this episode? Stay tuned for future episodes of A Conversation About … by following MHPN Presents.Visit the MHPN website for episode host and guest bios, recommended resources and a self-directed CPD form.Share your comments, questions and feedback about A Conversation About …  or any of MHPN's podcast series here: https://mhpn.org.au/podcast-feedback/ 

Send us a textSophie Harrington is our guest for this episode. Sophie is the CEO of NOFASD Australia, the nation's peak body supporting people and families living with Fetal Alcohol Spectrum Disorders.NOFASD presented at the Complex Needs Conference 2025 on the complexities of this hidden disability, sharing research, therapeutic strategies and resources, in particular for health care professionals and support workers.NOFASD Helpline 1800 860 613ermha365 co-hosted the conference with ACSO Australia on behalf of Victoria Government's Department of Families, Fairness and Housing (DFFH), which funded the 2-day conference.ermha365 provides mental health and disability support for people in Victoria and the Northern Territory. Find out more about our services at our website.Helplines (Australia):Lifeline 13 11 14QLIFE 1800 184 52713 YARN 13 92 76Suicide Callback Service 1300 659 467ermha365 acknowledges that our work in the community takes place on the Traditional Lands of many Aboriginal and Torres Strait Islander Peoples and therefore respectfully recognise their Elders, past and present, and the ongoing Custodianship of the Land and Water by all Members of these Communities.We recognise people with lived experience who contribute to GET REAL podcast, and those who love, support and care for them. We recognise their strength, courage and unique perspective as a vital contribution so that we can learn, grow and achieve better outcomes together.

In this episode of the A&F podcast we speak to adoptive parent and Neurodiversity Coaching Psychologist Anna Webster. She shares her experience of parenting a child with a diagnosis of Fetal Alcohol Spectrum Disorder and the development of the Neurowise Programme on Therapeutic Caregiving for FASD.  It is a genuinely fascinating chat and we both drew lots of new information and thinking about the role of parents and the specific challenges parents and carers of children with FASD face.  Anna is on X here and Linkedin 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   Listen/subscribe on iTunes here Spotify here

Self-advocate and author Rebecca Tillou shares the realities of life with FASD, and her journey towards getting a diagnosis at age 33. Rebecca Tillou is a self-advocate of Fetal Alcohol Syndrome, which is under the umbrella Fetal Alcohol Spectrum Disorders. Since being diagnosed at the age of 33, she has become a tireless advocate raising awareness of this often misunderstood condition. She is the author of the auto-biographical book “Tenacity”, and the founder of the virtual 5K for FASD United. For more about Rebecca and FASD, visit: https://adultingwithfasdcoms.com/ https://fasdunited.org/ http://www.runfasd.org/ Follow Different Brains on social media: https://twitter.com/diffbrains https://www.facebook.com/different.brains/ https://www.instagram.com/diffbrains/ Check out more episodes of Exploring Different Brains! http://differentbrains.org/category/edb/

About one to five percent of school-age children in the United States are living with fetal alcohol spectrum disorders — known as FASDs — developmental challenges caused by drinking alcohol during pregnancy. The numbers are higher for children in foster care.  A Minnesota-based organization called Proof Alliance is working around the country to raise awareness of FASDs and support people who are impacted by them. DaKota Morgan, a participant in the organization's youth programs who has an FASD, and Proof Alliance's Executive Director, Mollie O'Brien joined Minnesota Now to talk about their work to raise awareness about FASDs.

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. 

I realized after posting yesterday's podcast episode that I missed Witness Wednesday. I was away for the weekend, and coming back on Monday must have thrown me off. However, I didn't want you to miss out on Witness Wednesday, so I am just doing it a day late this week.  Today's witnesses are from Matthew West's website called popwe.org. If you don't know who Matthew West is, he is a singer, songwriter, and storyteller. This website is for the non-profit that he has with his father, a pastor. Matthew and his father encourage people to share their stories. They have various categories of stories. Today, I chose two testimonies from the Salvation Category. Often, we can hear our own story in someone else's story. When we listen to others tell their story, it helps us see that we are not alone. When we hear how God worked in their situation, it gives us hope that He will work in ours, too! I pray when you hear these testimonies, you get the faith and hope to believe that miracles can happen in your situation, also. I pray you know that God is there with you, and if you invite Him into your situation, He can help. I hope you enjoy these testimonies.My name is Cyndi. My broken story started before I was even born. I was the last of my bio mom's seven kids.  Unfortunately, she was an alcoholic who drank during her pregnancy, so I have Fetal Alcohol Spectrum Disorder.When I was born in 1971, I weighed about 3 lbs. I was adopted at age 1. Unfortunately, the family I was adopted into was dysfunctional. I suffered all manner of abuse, including sexual abuse. This hurt me so bad that I wanted to die for many years.I was diagnosed at twenty with Bipolar Disorder. But I didn't take the medication because I just didn't want to. I got pregnant at twenty-one.  I literally had my son on my twenty second birthday.  I married his dad four months later.But my husband was abusive, mentally, emotionally, and verbally.  And because I had never dealt with my previous abuse, I believed his abuse was my fault. Not only did I stay with him and raise my son, but I also had another child, a daughter, when my son was six years old.Even though I thought our problems were my fault, I still knew how ridiculous that sounded because I knew I didn't really want to live like that. I separated from him when my daughter was three and tried to take the kids.He used lies and insinuation to get them back. I ended up being divorced and having visitation with my kids. It wasn't easy, but we managed to survive. You may wonder about my faith throughout all of this. Don't worry, I'm getting there!  I was raised Catholic but got into the Jehovah's Witnesses in 1996. I stayed that in that group until November of 2022, when I learned it wasn't what I had been led to believe.I was a lost soul for a little while but came back to Christianity the next November and have been loving it since. I'm quite happy these days. I do take meds. I have two spectacular kids and a wonderful granddaughter. I've been through more therapy than I care to admit and I'm still in it. But I've learned that it's okay to not be okay sometimes.Because I spent twenty-seven years not doing any holidays or birthdays, I take care to do them all and really celebrate them.  I really appreciate and enjoy my friends and family. So, I guess I have a pretty good ending to my broken story.But it's all because of Jesus. I do wish that my kids would love Jesus like I do, but they have to get to know him from a different perspective now. Just like I did.Ben:  I grew up in a Christian home going to church every Sunday, being involved in AWANA and Youth Group, and going to Bible camps based on the Bible. The broken chapters of my life started before age 14. I was a Christian then. I believed hard on God, He was my Savior and He loved me. In 2017, when I was in the 6th grade, the garage of my house went up in flames. That was really tough for me and my whole family to go through. I hated God through that. It was about a year of moving around, and not being in my own neighborhood.
Further into my life starting around age fourteen is when I fell apart from God.  I got introduced into pornography. That was my biggest struggle. A lot of changes happened. I hated God and felt like I didn't belong with Him. Satan took me over and I felt what he could do to me. Just to be living through that, though, is how I saw God. I became an addict to pornography and that was really harsh. Going though that, plus still going to church was a struggle. I believed that God didn't want me and that He left me. I hated God for writing my life like this. And yet, I prayed almost every day for Him to bring me out of this hell, out of Satan's world.Skipping forward in my life, I am now two months from my 16th birthday. In late February 2021, I moved from my hometown of Naperville, IL to South Nashville, TN. This was the biggest move of my entire life. I was confused and scared of moving so far away, but during this time I was doing better with God. I felt Him closer to me and with me more often. As life moved on during February, I came to realize that God has made my life for a purpose and He has drawn my path. So I just had to trust God that He knew what He was doing in my life. In June 2021, me and my family took a trip back up to my hometown to see friends and family and the community. About halfway through the trip, I was fishing at one of my favorite lakes and started to talk to God. I fished there that day for about 2 1/2 hours and during that time I was having a conversation with God. I felt really close to Him and loved Him. I poured out my fears and thoughts.During week three of the trip, I was in bed one night thinking of my strong fear of death. It scared me so bad, something happened between me and the Lord that I fell apart again. That time was one of the closest times I came to taking my own life, but I never did because of God. He came into my thoughts and blocked that idea. I was so scared of death, I couldn't do it.In week 4 of June, my family and I made our way to Gull Lake Ministries, in Hickory Corners, Michigan. The Friday of that week, I was out on the fishing dock at night about 10:30pm and was listening to my Christian music playlist and the song ‘Way Maker' came on. I poured out my heart to The Lord Jesus Christ asking for forgiveness. After that night, I asked God to come back to my heart.  I prayed and I cried happy tears knowing I had been saved.The week before school started, I joined my school's marching band…lots of hard work balancing that with my studies and with God. A month later, I was greatly in line with God. A month after that I met this girl who was in my instrument section for marching band. She is a very strong believer and a true Christian. She is one of the main people that brought me back to Christ. We prayed together and we both shared music, verses and Bible plans to know Jesus more. Finding a church is one of the harder struggles along with finding a youth group that can be of fit for me to be more connected.
One week, she invited me to her youth group and I liked it. I was able to become closer to the Lord and know that community.Two days later, the thought of killing myself and hurting myself came back. I fell apart from God again. I talked to my friend about this, and she seemed really worried. She tried to talk me out of it. She talked to her parents and gave me music and Bible verses about how God wants me, loves me, and knows me. This lasted about two weeks which is the longest I have had in my life yet. The struggle with the aftermath –going through that was the hardest. Reconnecting myself with God, I found this song by Matthew West called ‘The God Who Stays.' I put this song on repeat and listened to it about 100+ times. The lyrics of the song are really powerful and meaningful. After about a week, I grew closer to Christ, and during worship in a church service, I poured my heart out to the Lord. I felt him right next to me and knew that He was with me. Over the last couple months, I have been in line with Jesus, asking for forgiveness, talking openly to friends about Him, and being involved with church leaders. Now I see and consider myself a Christian, after three years of on/off with God. I am back.I got baptized on February 18, 2022. I love Jesus and I never want to lose Him again.  Amen!Thank you so much to both of you for sharing your stories. You have both had such a hard journey. I appreciate you being vulnerable and sharing your story so that others know they are not alone. It also shows them that if God got you through it, he will get them through it too! Thank you so much for sharing!  www.findingtruenorthcoaching.comCLICK HERE TO DONATECLICK HERE to sign up for Mentoring CLICK HERE to sign up for Daily "Word from the Lord" emailsCLICK HERE to sign up for my newsletter & receive a free audio training about inviting Jesus into your daily lifeCLICK HERE to buy my book Total Trust in God's Safe Embrace

“Every child has the capacity to heal and grow, but it starts with meeting them where they are—with respect, curiosity, and an understanding of their unique needs.” – Natascha Lawrence 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.

"Jesus said, 'The thief comes only to steal and kill and destroy; I have come that they may have life, and have it to the full.'” -John 10:10   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 and FASD advocate, Jodee Kulp.   Jodee is a tireless advocate for those affected by Fetal Alcohol Spectrum Disorders. She has authored 12 books on FASD, is the co-founder of the international Red Shoes Rock FASD awareness campaign, and mother to the late Liz Kulp who lived with FASD.   Jodee provides invaluable wisdom for families, communities, educators, and healthcare providers in her desire to create supportive environments that allow individuals with FASD to thrive.   Tune in to Sandra's conversation with Jodee Kulp on Episode 464.   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 Orphans No More—A Journey Back to the Father on amazon.com Embracing Zak by Jodee Kulp can be purchased on Amazon.com

For many, spending time with family during the holidays is joyful and fulfilling. For others, spending time with family is emotionally challenging as they navigate varying degrees of disease, disinformation and dysfunction. Guida Brown talks about how we can take care of ourselves, set healthy boundaries, and handle relationship dysfunction with honesty and respect. Guida is the Principal for Guided by Guida and serves as the Community Relations Consultant for the US Drug Testing Laboratories in Des Plaines, Illinois. She has been an adjunct faculty member for Carthage College, University of Wisconsin -- Parkside, Concordia University, and Gateway Technical College. Guida is certified by the State of Wisconsin as a Substance Abuse Counselor, a Fetal Alcohol Spectrum Disorder trainer, and an Intoxicated Driver Program Assessor. She is also a Kenosha (Wisconsin) County Board Supervisor. She can be reached at https://guidedbyguida.guide/ The views and opinions of the guests on this podcast are theirs and theirs alone and do not necessarily represent those of the host, Westwords Consulting or the Kenosha County Substance Abuse Coalition. 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!

In this episode, Dr. Kenneth Lyons Jones, one of the pioneers who first identified Fetal Alcohol Spectrum Disorders (FASD) in the United States in 1973, and Dr. Christina Chambers, a renowned epidemiologist who has conducted groundbreaking research on the prevalence of FASD, join host Chris Stallman, CGC, to discuss the discovery of FASD, its common physical and cognitive traits, and its prevalence today. BONUS: Earn continuing education credits for listening to our entire FASD 3-part series. Scroll down to learn more. Resources Mentioned in This Episode: Dr. Kenneth Lyons Jones on the History of Fetal Alcohol Syndrome - FASD  Prevalence of Fetal Alcohol Spectrum Disorders in 4 US Communities | Antenatal Exposures and Child Outcomes | JAMA | JAMA Network  Fetal Alcohol Spectrum Disorders – American Academy of Pediatrics Types of Treatment for FASDs | Fetal Alcohol Spectrum Disorders | CDC Choline supplements in young children with fetal alcohol spectrum disorder have lasting cognitive benefits | National Institute on Alcohol Abuse and Alcoholism (NIAAA)  _______________________________________________________________________________________________________ MotherToBaby: FASD Podcast SCPD4929     PROGRAM DESCRIPTION: This podcast series is intended to reach various audiences, including healthcare professionals, who can use the information presented to inform their practice and their interaction with clients/patients. The podcast episodes will educate participants on 1) the discovery, prevalence, and newest research on the topic of fetal alcohol spectrum disorders (FASDs), 2) CDC's work in addressing prenatal alcohol and other substance use and FASDs, and 3) the experiences of people living with FASDs. OBJECTIVES: After completing this course, the learner will be able to: 1.      Describe Fetal Alcohol Spectrum Disorders (FASDs). 2.      Describe the National Center of Birth Defects and Developmental Disabilities' (NCBDDD) approach to addressing FASDs. 3.      Describe the impact on people who are living with FASDs. 4.      Describe how interprofessional collaboration addresses FASDs. 5. Describe how interprofessional teams can help people living with FASDs transition from pediatric to adult healthcare.   FACULTY/                                                   CREDENTIALS: Laura Bousquet, Family Navigator/Self-Advocate, FASD United Christina Chambers, PhD, MPH, Distinguished Professor of Pediatrics, University of California, San Diego Elizabeth Dang, MPH, Behavioral Scientist, Centers for Disease Control and Prevention Nicholas Deputy, PhD, MPH, Health Scientist, Centers for Disease Control and Prevention Kenneth Jones, MD, Distinguished Professor of Pediatrics, University of California, San Diego  Chris Stallman, MLS, MS, CGC, Director,    MotherToBaby Arizona, University of Arizona  Jennifer Wisdahl, Chief Operating Officer, FASD   United   CE ORIGINATION DATE: CE EXPIRATION DATE:   January 9, 2025 January 9, 2027     URL   https://momtobaby.org/FASDep81youtube   INTENDED AUDIENCE:   Advanced Practice Nurses, Certified Health Educators, Medical Assistants, Licensed Practical/Vocational Nurses, Physicians, Physician Assistants, Registered Nurses, and Social Workers   PREREQUISITES:   Learners will have a basic understanding of what fetal alcohol spectrum disorders are.   FORMAT: This activity is Web on Demand   CONTACT INFORMATION: CDC's CE Accreditation Team has a policy for grievances that is available upon request.   Division of Birth Defects and Infant Disorders cdcinfo@cdc.gov    ACCREDITATION STATEMENTS:     In support of improving patient care, this activity has been planned and implemented by the Centers for Disease Control and Prevention and MotherToBaby. The Centers for Disease Control and Prevention is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team   CME: The Centers for Disease Control and Prevention designates this enduring activity for a maximum of 0.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. CNE: The Centers for Disease Control and Prevention designates this activity for 0.5 nursing contact hours. CEU: The Centers for Disease Control and Prevention is authorized by IACET to offer 0.1 CEU's for this program. CECH: Sponsored by the Centers for Disease Control and Prevention, a designated provider of continuing education contact hours (CECH) in health education by the National Commission for Health Education Credentialing, Inc. This program is designated for Certified Health Education Specialists (CHES®) and/or Master Certified Health Education Specialists (MCHES®) to receive up to 0.5 total Category I continuing education contact hours. Maximum advanced level continuing education contact hours available are 0. Continuing Competency credits available are 0.5. CDC provider number 98614. DISCLOSURE: In compliance with continuing education requirements, all planners and presenters must disclose all financial relationships, in any amount, with ineligible companies during the previous 24 months as well as any use of unlabeled product(s) or products under investigational use.    CDC, our planners, and content experts wish to disclose they have no financial relationship(s) with ineligible companies with the exception of Dr. Christina Chambers, PhD, MPH and she wishes to disclose she receives research funding from Amgen, AstraZeneca, GlaxoSmithKline, Janssen Pharmaceuticals, Pfizer, Inc., Regeneron, Hoffman La-Roche-Genentech, Genzyme Sanofi-Aventis, Takeda Pharmaceutical Company Limited, Sanofi, UCB Pharma, USA, Leo Pharma, Sun Pharma Global FZE, Gilead, Novartis, and the Gerber Foundation.  All relevant financial relationships listed for this individual have been mitigated. Content will not include any discussion of the unlabeled use of a product or a product under investigational use. CDC did not accept financial or in-kind support from ineligible companies for this continuing education activity. The Centers for Disease Control and Prevention (CDC) complies with applicable Federal civil rights laws and does not discriminate based on race, color, national origin, age, disability, religion, or sex (including pregnancy, sexual orientation, and gender identity). To learn more visit: https://www.hhs.gov/civil-rights/for-individuals/nondiscrimination/index.html. Instructions for Obtaining Continuing Education (CE) To receive continuing education (CE) for SCPD4929 – MotherToBaby: FASD Podcast, please visit CDC TRAIN and search for the course in the Course Catalog using SCPD4929 Follow the steps below by January 9, 2027. Register for and complete the course. Pass the post-assessment at 75 %. Complete the evaluation. Visit Your Learning to access your certificates and transcript.   FEES: No fees are charged for CDC's CE activities.   ______________________________________________________________________ Looking for even more education about FASD? Don't miss a special free Birth Defects Awareness Month webinar January 31, 2025 at 9a PT/12p ET. The webinar will be presented by Dr. Noemi Spinazzi of the American Academy of Pediatrics. It is a free webinar, but advanced registration is required at the following link: https://momtobaby.org/FASDwebinar2025

Dr Vanessa Spiller explains the history of Fetal Alcohol Spectrum Disorder, offers tools to diagnose FASD and helpful pathways for Clinical Psychologists offering therapy. She explains why it is so easily overlooked in comparison with other commonly co-occurring diagnoses, and reveals FASD's alarmingly high rates of involvement with the criminal justice system.

Addressing mental health in college is extremely important. Today we're talking to Chris Troutt, LMFT, a Christian family therapist who brings a unique background to her clients. She and her late husband, Burt, are parents to twelve children and have twenty-five grandchildren. Chris is a biological mother, an adoptive mother, a stepmother, and a foster mother; she brings both education and personal perspective into the therapy session. Chris believes strongly in systems theory and in the power of God working in a person's life. It is her desire to help others during their journey. Chris specializes in Prenatal Exposure to Alcohol and Drugs, Trauma and Attachment Disorders. Her work with Fetal Alcohol Spectrum Disorders is especially meaningful to her as a parent of a child diagnosed with Fetal Alcohol Syndrome. Chris has a Master's Degree in Marriage and Family Therapy from Trevecca Nazarene University, Nashville, Tennessee. Chris is the co-founder and CEO of the Papillion Center for FASD with offices in Gallatin, Tennessee and Paducah, Kentucky. She speaks nationally and internationally on Understanding Children and Families from Hard Places, including Fetal Alcohol Spectrum Disorders. In episode 517 of the Fraternity Foodie Podcast, we find out what are Fetal Alcohol Spectrum Disorders and why Chris is so passionate about it, what are the realities of neuro-biological outcomes for trauma in a child's life, what opportunities there are to heal after that trauma at a young age, common signs that a college student might need to seek help for their mental health, how students can manage the pressure of social media while maintaining a healthy self-image, how students can develop resilience and cope with rejection, advice on dealing with imposter syndrome, tips for managing test anxiety or performance stress, and how students learn to set boundaries with friends, family, and professors to protect their mental health. Enjoy!

Click here to send us a topic idea or question for Weekend Wisdom.Do you wonder if your child was prenatally exposed to alcohol or drugs? There may be nothing in the files, but something feels not right? We talk about diagnosing and treating these kids with Dr. Larry Burd, a professor of pediatrics at the University of North Dakota School of Medicine and the Director of the North Dakota Fetal Alcohol Syndrome Center.In this episode, we cover:Most of our audience is foster, adoptive, and kinship parents and professionals. Often they don't know for sure if a child has been exposed. The US government estimates that about 10% of all children in the US have been prenatally exposed to alcohol or drugs. Do you have a feel for the percentage of children in foster care or who have been involved with the child welfare system? International adoption? Domestic infant adoption?Does prenatal exposure increase the likelihood of a disruption to a foster or adoptive placement?How is prenatal exposure to alcohol detected or diagnosed?What type of training do pediatricians receive during their education or residency on prenatal exposure and on how to diagnose?Can you tell at birth or in infancy if a baby has been exposed to alcohol in utero?How is prenatal exposure to drugs detected or diagnosed?How does birth order change the likelihood that a child who is at risk has been exposed during pregnancy?What are the long-term impacts of alcohol exposure? What are the symptoms that are most noticeable to parents, teachers, and other professionals working with these children?Alcohol exposure affects multiple systems in the body.Does it matter what type of alcohol was consumed?Who can diagnose a child with Fetal Alcohol Spectrum Disorder?What are the long-term impacts of the following drugs?OpioidsHeroin and FentanylDepressants (benzodiazepines, such as Valium, Xanax)-Prescribed and unprescribedStimulants-Prescribed and unprescribedMethamphetaminesMarijuanaTobacco/NicotineDo pediatricians have a body of resources to offer parents regarding raising a child with prenatal exposure?Tips for parents.Tronick's Still Face ExperimentSupport 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

Episode Summary:  In this thought provoking episode, host Joseph Arvidson sits down with Dr. Jerrod Brown to explore the complex factors contributing to false confessions and wrongful convictions. Dr. Brown, an expert in neurocriminology, offers insights into how various mental and physical health factors-such as untreated nutritional deficiencies and cognitive impairments-impact behavior, decision making, and the reliability of client interviews.  Together, Joseph and Dr. Brown unpack the vulnerabilities that can make certain individuals more susceptible to false confessions, from neurodevelopmental disorders and high levels of suggestibility to external pressures in the interview room. This episode challenges justice professionals to broaden their perspectives, looking beyond traditional frameworks like risk-needs-responsivity, to embrace a holistic view of client behavior. With practical implications for probation officers, correctional staff, and all who interact with justice-involved individuals, Dr. Brown's insights offer a pathway toward more effective, informed, and compassionate practices in the field. What You'll Learn:  The types and causes of false confessions: Voluntary, Coerced, and Internalized. How cognitive impairments, neurodevelopmental disorders, and high suggestibility influence client statements and behaviors. The impact of nutritional deficiencies and physical health on mental well being and behavior in justice contexts. Practical strategies to improve client interactions, including accommodating neurodevelopmental needs and promoting a sensory friendly environment. Why a broader, interdisciplinary approach to justice work is essential for improving outcomes.      Resources mentioned in this episode:  Neurocriminology Informed Professional Certificate Program For those interested in deepening their understanding of the brain-behavior connection and its application in justice settings, Dr. Brown's certificate program offers a comprehensive look at neurocriminology's impact on criminal behavior.  Learn more here Research paper: Fetal Alcohol Syndrome and the Risk-Needs-Responsivity Model. A guide for Criminal Justice and forensic mental health professionals: Co-Authored by Dr. Brown, and Joseph Arvidson, this paper dives into the complexities of working with clients affected by FASD and how the R-N-R model can be adapted to meet their unique needs.  Read their paper here!  Contact Dr. Jerrod Brown: Connect with Dr. Brown for more information on neurocriminology, false confession, and training opportunities.  Dr. Brown's email address Stay Connected: Make sure you subscribe to The Criminologist podcast to keep up with the latest conversations aimed at advancing your knowledge and practice in the criminal justice field.We will be back soon with more expert insights and transformative solutions! Key words: False Confessions, Neurocriminology, Fetal Alcohol Spectrum Disorder, Wrongful Convictions, Risk-Needs-Responsivity, Cognitive Impairments, Nutrition in Criminal Justice, Joseph Arvidson, Dr. Jerrod Brown.  Credits: Joseph Arvidson Dr. Jerrod Brown             

“God is our refuge and strength, a very present help in trouble.” -Psalm 46:1   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 discusses the primary, secondary and tertiary symptoms of Fetal Alcohol Spectrum Disorder. She also unpacks how she provides accommodations for her nineteen year-old son with FASD.    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.

In this episode, Geoff Marsh speaks to Dr. Stephanie Ford about our Collection on Fetal Alcohol Spectrum Disorder.Read the collection here: https://www.nature.com/collections/fccidiefbi Hosted on Acast. See acast.com/privacy for more information.

This is FASD Awareness Month, to teach people about Fetal Alcohol Spectrum Disorder. On Thursday, we heard from retired physician, now Senator, Mohamed Ravalia of Twillingate. He has proposed legislation to bring in a national framework on FASD. Today, we spoke with the organization in this province that is focused on education, awareness and support related to Fetal Alcohol Spectrum Disorder. Katharine Dunbar Winsor is executive director of FASD NL.

Families and caregivers of children with fetal alcohol spectrum disorder are welcoming an announcement from the Health Minister that for the first time ever, the prevalence of the neurodisability is to be measured.

A senator from Newfoundland and Labrador is continuing his work to try to improve how Canada deals with fetal alcohol spectrum disorder, or FASD. Senator Mohamed Ravalia of Twillingate is a retired physician. His bill, S-253, is a proposed piece of legislation that would bring in a national framework for fetal alcohol spectrum disorder. This is FASD Awareness Month. Senator Ravalia spoke with the CBC's Bernice Hillier.

In this episode, Vicki Atkinson and Wynne Leon are with blogger, parent, FASD advocate and amazing human, Ab from the My Life with T blog. Ab tells us of the moment both his advocacy and blogging started. When a program supporting kids like his young son was canceled, it lit both fires. The writing practice is part of Ab's self-care. It helps him process the events that need to be noted, held onto, learned from, and cherished. It's a great tool in his wonderful resource kit for parenting well. And then his writing helps to raise awareness about people living with FASD. Ab shares the definition of Fetal Alcohol Spectrum Disorder and we discuss how building awareness and understanding is so important. Ab makes such great connections about different blogs and the way our writing unites us. It was so much fun to be able to talk with Ab. It feels as if we are old friends after interacting nearly every day for 4 years on one blog or another. He is so passionate, funny and articulate and we could have talked for hours. Vicki and I are so lucky to have the great fun of being able to talk with people who are dear blog friends. This in an incredible conversation about how moments of disappointment and frustration can blossom into something fruitful when you follow the threads as Ab did. We're confident you'll love the scenic and beautiful places we explore as we share the power of storytelling. We know you'll love it! Links for this episode: Episode 85 show notes My Life with T blog by Ab In Canada: What is FASD? - CanFASD In the United States: FASDUnited.Org A great resource for caregivers trying to understand and support a loved one with FASD: Trying Differently Rather Than Harder: Fetal Alcohol Spectrum Disorders - Third Edition: 9780972953207: Books - Amazon.ca A book by recognized FASD educator Nate Sheets: Essential FASD Supports: Understanding and Supporting People with Fetal Alcohol Spectrum Disorders: Sheets, Nate: 9781977245083: Books - Amazon.ca From the Hosts: Vicki's recently released book: Surviving Sue Wynne's book about her beloved father: Finding My Father's Faith

"There is no difference between Jew and Gentile, for all have sinned and fall short of the glory of God, and all are justified freely by His grace through the redemption that came by Christ Jesus." -Romans 3:22-24   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.   September is FASD Awareness Month and our special guest today is JJ Dunham Reed. JJ is a strong coffee-drinking, homeschooling, Jesus-seeking mama. A happily married wife to a wonderful God-fearing man, a strong FASD Advocate creating FASD-informed resources and services in her community, and one of many primary care providing biological mothers of children with FASD. In 2021 she boldly stepped onto the stage of FASD Advocacy after years of knowing something was going on with one of her younger sons, there was confirmation of prenatal alcohol exposure and still, there were no answers, resources, or services to turn to. Finding this great deficit unacceptable, JJ founded Our Families Are FASDtastic Families: Fetal Alcohol Spectrum Disorder(s) Education, Caregiver Peer Support & FASD Awareness Advocacy. JJ boldly stands up to stop the shame, blame, and stigmas associated with Fetal Alcohol Spectrum Disorders so that all families of individuals with an FASD can be confident in seeking wrap-around support and so that the support will be there when they need it most.   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 www.DunhamReed.com Email:  jj@dunhamreed.com   Social Media: Facebook and Instagram @JJDunhamReed, @FASDtasticFamilies and @FASDtasticKidJJ

When it comes to fetal alcohol spectrum disorder (FASD), understanding is key, but misconceptions often get in the way. In this episode, Sickboy sits down with Judy Heilik to shed light on the realities of living with FASD. They tackle the stigma and blame that often surround the condition, emphasizing the need for empathy and support. Judy explains how alcohol consumption during pregnancy can impact brain development, leading to a range of challenges from emotional regulation to social interactions. She also delve into the barriers that make accessing resources difficult and highlight the importance of a holistic approach to care. This conversation is a call to action for increased awareness and a more compassionate perspective on FASD.Catch the full video version of this episode on YouTube.Follow Sickboy on Instagram, TikTok and Discord!

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

When it comes to fetal alcohol spectrum disorder (FASD), understanding is key, but misconceptions often get in the way. In this episode, Sickboy sits down with Judy Heilik to shed light on the realities of living with FASD. They tackle the stigma and blame that often surround the condition, emphasizing the need for empathy and support. Judy explains how alcohol consumption during pregnancy can impact brain development, leading to a range of challenges from emotional regulation to social interactions. She also delve into the barriers that make accessing resources difficult and highlight the importance of a holistic approach to care. This conversation is a call to action for increased awareness and a more compassionate perspective on FASD.Catch the full video version of this episode on YouTube.Follow Sickboy on Instagram, TikTok and Discord!

CW: Mentions of suicide and experiences with the criminal justice system as it relates to FASD. Patti Kasper is a Neurobehavioral Coach and Trainer who provides staff development training and coaching services to support people affected by Fetal Alcohol Spectrum Disorders (FASD). With over thirty years of experience in the fields of addiction, mental health, and child welfare, Patti draws on her personal experience with FASD, her degrees in social work and psychology, and her training as a Certified Facilitator of FASCETS Neurobehavioral Model.   Patti hosts a weekly podcast called Living with FASD. The second edition of her book, “Sip by Sip: Candid Conversations with People Diagnosed as Adults with Fetal Alcohol Spectrum Disorders (FASD),” was recently released with additional interviews and updated research. During this episode, Patti talks about: ●    What FASD is, and why it's more common than most people realize ●    How she discovered in her 50s that she has FASD  ●    Some of the struggles that people with FASD may experience ●    How she supports families and individuals impacted by FASD Find links to Patti's website, book, podcast and more. 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.*

Người mẹ uống bia rượu ở bất cứ thời điểm nào của thai kỳ đều có thể gây rối loạn phát triển của thai nhi cũng như ảnh hưởng đến suốt quá trình sinh trưởng của con sau này. Điều cần thiết là trẻ được chẩn đoán sớm và hỗ trợ trong môi trường phù hợp.

A drug is a drug is a drug, unless that drug is alcohol, in which case it is, or is not, considered a drug, depending on where you live, how you grew up, and what part of the family you come from. Guida Brown discusses the difficulty in diagnosing Alcohol Use Disorder and the ongoing efforts to treat it as a disease. Guida is the Principal for Guided by Guida and serves as the Community Relations Consultant for the US Drug Testing Laboratories in Des Plaines Illinois. She has served as adjunct faculty for Carthage College, University of Wisconsin-Parkside, Concordia University, and Gateway Technical College. Guida is certified by the State of Wisconsin as a Substance Abuse Counselor, a Fetal Alcohol Spectrum Disorder trainer, and an Intoxicated Driver Program Assessor. She is also a Kenosha, Wisconsin, County Board Supervisor. Guided by Guida The views and opinions of the guests on this podcast are theirs and theirs alone and do not necessarily represent those of the host, Westwords Consulting or the Kenosha County Substance Abuse Coalition. 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!

This episode originally aired April 16th, 2022 Robbie Seale is a mother to multiple children with FASD. Over the last 20 years of parenting, she has gained priceless knowledge on the subject. Not only does the stigma and misdiagnosis affect children with FASD, but after speaking with Robbie, it clearly affects the mental health of parents and care givers. Robbie has a podcast dedicated to supporting those who are affected by FASD and educate those who educating. Her podcast FASD Family Life is available on most podcasts platforms. listen to FASD Family Life on Apple here https://podcasts.apple.com/ca/podcast/fasd-family-life/id1561078669 Topics include FASD, fetal alcohol spectrum disorder, addiction, trauma, depression, anxiety Please consider buying me a coffee here!  Check out the podcast merch store here! Purchase my children's book Sometimes Daddy Cries here! FOLLOW BUNNY HUGS AND MENTAL HEALTH ON SOCIAL MEDIA Facebook, Instagram, TikTok   Bunny Hugs and Mental Health is currently on the Top Ten Best Canadian Mental Health Podcasts list!  And the Top 100 Best Mental Health Podcasts on the internet! Follow this other great Canadian podcast Hard Knox Talks  Please donate to Cornwall Alternative School here This episode is brought to you by Co-op Follow Co-op on social media @CoopCRS on Facebook, Instagram, Twitter and @wearecoop on TikTok

Professor Soraya Seedat weighs in on research into fathers' alcohol consumption and its impact on fetal alcohol disorder syndrome. See omnystudio.com/listener for privacy information.

An AWHONN Board Member joins this panel of changemakers from the Collaborative for Alcohol‐Free Pregnancy, NP's, Midwives, and Nurses partnering to prevent FASDs at the 2024 AWHONN Convention. Together, we learn more about neurodiversity, living with FASD, and implementing evidence-based care practices that reduce stigma and educate about the risks of substance and alcohol [...] The post Understanding Fetal Alcohol Spectrum Disorder – The Nurse's Role appeared first on AWHONN.

An AWHONN Board Member joins this panel of changemakers from the Collaborative for Alcohol‐Free Pregnancy, NP's, Midwives, and Nurses partnering to prevent FASDs at the 2024 AWHONN Convention. Together, we learn more about neurodiversity, living with FASD, and implementing evidence-based care practices that reduce stigma and educate about the risks of substance and alcohol [...] The post Understanding Fetal Alcohol Spectrum Disorder – The Nurse's Role appeared first on AWHONN.

"I have been crucified with Christ and I no longer live, but Christ lives in me. The life I now live in the body, I live by faith in the son of God, who loved me and gave himself for me." -Galatians 2:20   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.   Throughout the month of June, we're focusing on dads! To kick us off, this week host Sandra Flach talks with Joshua Legg. Joshua is passionate about helping men grow in Christ and seeing marriages healed. He understands the complexities of families parenting children with special needs and is well versed in Fetal Alcohol Spectrum Disorders—both professionally and as a brother of an adopted sibling with FAS.    Joshua pursues his passion for dads and families as a pastor, and through discipleship mentoring, and coaching. He and his wife Heather offer marriage intensives, drawing from their own journey and walking beside couples as they heal.   Listen in as Joshua offers encouragement and hope to foster and adoptive parents—especially dads.   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 joshualeggcoaching.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.

On today's episode, Sandra shares about her own experiences with FASD and how she came to the place she is now, which is speaking and advocating for those affected by FASD. We talk about the school systems and ways to support our kids in the educational setting. Finally, Sandra gives us a better understanding of FASD and ways that we, as a community, can do a better job of supporting our kids with invisible disabilities. This is a must-listen for everyone! Sandra is a mom of 8, 5 through adoption (2 with FASD). She is the Executive Director of Justice For Orphans, host of the Adoption & Foster Care Journey Podcast, and a certified facilitator of the FASCETS neurobehavioral model. She is passionate about serving adoptive & foster families. You can find her on Instagram or on Facebook. Where to find Mending Families: Instagram - @mendingfamilieswa TikTok - @mendingfamilieswa Facebook - @mendingfamilieswa YouTube - @mendingfamilies1594 https://www.mendingfamilieswa.com --- Send in a voice message: https://podcasters.spotify.com/pod/show/melissa-pemberton/message Support this podcast: https://podcasters.spotify.com/pod/show/melissa-pemberton/support

Are you unwittingly overlooking a silent epidemic affecting newborns right under your nose? This game-changing episode of Pediatric Meltdown will redefine everything you thought you knew about molding young minds. We delve deep into the world of FASD (Fetal Alcohol Spectrum Disorders) and the critical need for timely screening at newborn visits. Hosted by Dr. Lia Gaggino, we dive into the transformative world of the oft-missed signs of fetal alcohol spectrum disorders and the life-altering implications they hold. Uncover the resources every parent and pediatrician should have at their fingertips, the surprising truth about the plasticity of the brain, and the lifeline that support groups offer to families navigating this challenging journey. It's clear that understanding and addressing ND PAE requires ongoing effort and awareness. The valuable insights shared in this episode are bolstered by the wealth of resources and guidance provided by organizations such as the American Academy of Pediatrics (AAP). Through Pediatric Meltdown, we aim to bring this critical information to the forefront, equipping practitioners and families with the know-how to usher in positive change. Tune in to hear how this episode promises to reveal a groundbreaking approach recommended by the AAP that could turn the tide in the ongoing battle against pediatric mental health challenges. Don't miss out – your next step in pediatric care innovation could be just one listen away! [05:30-12:44] Understanding FASD and Its ImpactDefinition and prevalence of FASD, including the sobering statistic that it affects 1 in 40 children.Prenatal alcohol exposure significantly affects the brain, especially the hippocampus and amygdala, causing developmental challenges.A look at the physical features associated with FAS, highlighting the preventability of this condition.Recognizing FASD early is crucial for intervention and leveraging the brain's adaptability for better outcomes with help.[12:45-22:14] Screening and Prevention Strategies The necessity of nonjudgmental surveillance questions at newborn visits to screen for ND PAE.discussing alcohol use with patients before and during pregnancy to avoid guilt and stigma affecting truthful disclosure.The roles of obstetricians and pediatricians in fostering ongoing dialogues about the risks of alcohol consumption.Prevention measures and education for adolescents and women of fertility age, aiming to mitigate the prevalence of FASD.[22:15-34:09] Resources for Clinicians and ParentsInformation on available resources from AAP, NOFAS, CDC, and NIMH for diagnosis and parental support.Recommendations for referring to developmental behavioral pediatricians or child psychiatry access programs.The utility of early intervention services for children with suspected ND PAE.Advocation for parent support groups as a means of providing guidance and comfort[34:10 - 50:48] Medications and InterventionsDiscussion on medications used for FASD, with particular emphasis on ADHD and mood-stabilizing medications.The debated effectiveness of non-stimulant medications like alpha agonists for children with ND PAE.Tips on prescribing medications appropriately, with support from programs like ECHO.Insights into the specific challenges faced by children with FASD, including attention to detail issues and difficulty with self-soothing.[50:49 - 59:11] Closing segment TakeawayLinks to resources mentioned on the showAAP Toolkit:

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

“But Moses' hands grew weary, so they took a stone and put it under him and he sat on it, while Aaron & Hur held up his hands, one on one side, and the other on the other side. So, his hands were steady until the going down of the sun.” Exodus 17:12   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 speaks with adoptive mom and FASD Family Navigator, Kristen Eriksen.   Kristen is mom to teenage twins with Fetal Alcohol Spectrum Disorder. She's also a Family Navigator with FASD United and works with family's in Massachusetts through massFAS.   Listen in to Sandra and Kristen's conversation and be encouraged for 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: sandraflach.com justicefororphansny.org sandraflach@justicefororphansny.org Focus on the Family FASD Resource massFAS.org https://fasdunited.org/family-navigator/

Hour 1: Jason asks listeners if it's okay to just enjoy the warmth? Then Mollie O'Brien from Proof Alliance joins him to spread the word about Fetal Alcohol Spectrum Disorders.

Mollie O'Brien is the Executive Director of Proof Alliance and as we wrap up "Dry January" she joins Jason to spread the word about Fetal Alcohol Spectrum Disorders (FASD). 

“Therefore, encourage one another and build each other up, just as in fact you are doing.” Thessalonians 5:11   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 episode host Sandra Flach speaks with FASD mentor and coach, Laurie Anderson. Laurie shares from her years of experience as a Big Sister and now guardian of a young woman with Fetal Alcohol Spectrum Disorder.    As Laurie advocated for her daughter she committed herself to learning all she could about FASD. Today, she's a sought after mentor and coach and an asset to the FASD community.   Listen in as Laurie shares her story and encourages our listeners.   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 sandraflach@justicefororphansny.org Focus on the Family FASD Resource fasdsuccess.com

On today's episode, Eileen gives us more insight into Fetal Alcohol Spectrum Disorders, what they are and how we can support those in our lives living with FASD. She talks about Brain First Parenting and explains how she uses this approach in her private practice to help support families affected by FASD.  If you want to learn more about Brain First Parenting and all that Eileen is involved in, you can go to her website www.eileendevine.com, her Instagram page or her Facebook page. Where to find Mending Families: Instagram - @mendingfamilieswa TikTok - @mendingfamilieswa Facebook - @mendingfamilieswa YouTube - @mendingfamilies1594 https://www.mendingfamilieswa.com --- Support this podcast: https://podcasters.spotify.com/pod/show/melissa-pemberton/support

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