Podcasts about intellectual disabilities

Send us a textWhy are so many girls with ADHD still being overlooked?In this episode of The Fully Mindful, I sit down with licensed psychologist Dr. Hila Pazner to explore the hidden side of ADHD—particularly in girls and young women. Drawing on her years of experience as a school psychologist and her current private practice where she specializes in assessing and working with children and adolescents with learning disabilities (such as Dyslexia, Dysgraphia, Dyscalculia), Intellectual Disabilities, giftedness, ADHD, autism, and behavioral and social-emotional difficulties, Dr. Pazner shares how outdated systems, subtle masking behaviors, and gender bias contribute to underdiagnosis and missed opportunities for support.Together, we dive into:How ADHD presents differently in girls vs. boys—and why that mattersThe long-term consequences of undiagnosed ADHD in girlsWhy a diagnosis isn't just a label—it's a launchpad for understanding, support, and growthHow psychoeducational testing can uncover hidden learning differences, executive function challenges, and emotional strugglesThe hopeful evolution of school psychology toward strength-based, neurodiversity-affirming modelsReal talk on masking, stigma, and what parents can do when something “just feels off” with their childWhether you're a parent, educator, or someone with lived experience, this episode is a must-listen. It's an invitation to rethink how we see neurodivergence—not as a deficit, but as a different and powerful way of being in the world.

Listen in to our latest episode as Kristin chats with Chelsea Felkai about being a healthcare provider for patients with intellectual disability. Chelsea is a community pharmacist who is completing her PhD at the University of Newcastle. You can find resources relating to the provision of inclusive healthcare and the NSQHS Standards User Guide for the Health Care of People with Intellectual Disability that Chelsea refers to in the podcast here. Other resources include: PSA Medicine safety: disability care report https://www.psa.org.au/advocacy/working-for-our-profession/medicine-safety/disability-care/  Australian Commission on Safety and Quality in Health Care - https://www.safetyandquality.gov.au/our-work/intellectual-disability-and-inclusive-health-care  Australia's Disability Strategy 2021-2031 - https://www.disabilitygateway.gov.au/ads/strategy  NDIS - https://www.ndis.gov.au/ NDIS – Consumables - https://ourguidelines.ndis.gov.au/would-we-fund-it/consumables  Guardianship Division - https://ncat.nsw.gov.au/how-ncat-works/ncat-divisions-and-appeal-panel/guardianship-division.html  Behaviour Support Plans - https://www.ndiscommission.gov.au/rules-and-standards/behaviour-support-and-restrictive-practices  Easy Read - https://pwd.org.au/resources/easy-read-info/  Ten Principles of Good Prescribing (British Pharmacological Society's Principles for Good Prescribing 2010) Maudsley deprescribing guidelines for antidepressants, benzodiazepines, Gabapentinoids, and Z-drugs. PHARMACISTS OPTIMISING MEDICINES IN PEOPLE WITH INTELLECTUAL DISABILITY AND AUTISM (POMPIDA) – Facebook group Public Hearing Report – Hearing 6 (Royal Commission into Violence, Abuse, Neglect and Exploitation of People with Disability)

In this conversation, Arthur Hairston shares his journey in the behavioral health field, focusing on group homes and the challenges faced in providing care for at-risk Autistic youth. He discusses the complexities of Medicaid, the importance of family involvement in business, and the dynamics of running a group home. The conversation also touches on the challenges of educational rights for children in care, navigating parental rights, and the significance of staff retention in providing quality care. Arthur emphasizes the need for community services and plans to expand their impact. Watch the video of this conversation here! https://youtu.be/qji4Aign8_M   Continuing Education Credits (https://www.cbiconsultants.com/shop) BACB: 1.5 Learning IBAO:  1.5 Learning QABA: 1.5 General We also offer certificates of attendance! Follow us! Instagram: https://www.instagram.com/behaviourspeak/ Bluesky: https://bsky.app/profile/benreiman.bsky.social.bsky.social LinkedIn:  https://www.linkedin.com/in/behaviourspeak/ Contact: Arthur Hairston Strive Youth and Family Services https://striveyfs.org/ Arthur on LinkedIn https://www.linkedin.com/in/arthurhairston/ Links: Dr, Shane Spiker https://www.linkedin.com/in/shane-t-spiker-phd-bcba-d-5bb34b50/ Dr. Nandi Nelson https://www.linkedin.com/in/nandi-nelson-phd-lcsw-bcba-d-a5a31b11a/ Behaviour Speak Podcast Episodes on Related Topics Episode  20 Consulting in Group Homes Using ACT with Monica Peters  https://www.behaviourspeak.com/e/episode-20-consulting-in-group-homes-using-act-with-monica-peters-mads-bcba/ Episode 40  Applications of Behavior Science to Foster Care, Runways The Homless and Bullying with Dr. Kim Crosalnd https://www.behaviourspeak.com/e/episode-40-applications-of-behaviour-science-to-foster-care-runaways-the-homeless-and-bullying-with-kimberly-crosland-phd-bcba-d/ Episode 48: Group Homes For People with Intellectual Disabilities with Dr. Christine Bigby https://www.behaviourspeak.com/e/episode-48-group-homes-for-people-with-intellectual-disabilities-with-christine-bigby-msw-phd/  

Brandon Franklin returns to the podcast after a very long hiatus. You'll have to go back to Session 36 to hear his first appearance as a matter of fact. It turns out that he's been doing a lot of innovative clinical work in that time. Currently, he is the Chief Behavior Analyst for the Lee Specialty Clinic and a Behavioral Consultant at Kramer Behavioral Health. In these roles, Brandon has implemented various interventions to help individuals with intellectual disabilities access routine medical and dental care. If you're not familiar with this topic, it might sound pretty mundane, but as you'll hear, these populations really struggle to attend and participate in routine medical appointments, which, not surprisingly, has downstream negative health consequences. As such, interventions that improve on the current statistics can truly be considered life-saving. In this podcast, we get into the following: Common phobias associated with medical treatments. Brandon's personal experience with aerophobia (the fear of flying), and what he did to improve it. The basics of desensitization strategies. How he and his team members use these strategies to improve the rate of successful medical appointment visits. And finally, the research on this topic that he is doing for his dissertation. Brandon has generously compiled a list of references, which you can find here. He's passionate about this topic and is willing to talk with anyone about it, so feel free to hit him up on LinkedIn. Here's all of Brandon's contact info. Here's all the desensitization resources you could ask for. This podcast is brought to you by: Frontera. Consider taking a demo of Frontera's Assessment Builder and see how the ethical application of AI technologies can help you serve clients and save you time! Your first assessment report is free. And if you use code BOP25 you'll get an additional five assessments for just $100. So head to fronterahealth.com to check it out! The Profound Autism Summit. The Profound Autism Summit is a two-day conference taking place on April 10th and 11th in Boston, MA. Following on the massive success of the 2024 Summit, the 2025 event brings together leaders from the areas of research, medicine, treatment, advocacy, and education to discuss the needs and support of those with Profound Autism across disciplines and throughout the lifespan. HRIC Recruting. Cut out the middleman and speak directly with Barbara Voss, who's been placing BCBAs in great jobs all across the US for 15 years.  CEUs from Behavioral Observations. Learn from your favorite podcast guests while you're commuting, walking the dog, or whatever else you do while listening to podcasts. New events are being added all the time, so check them out here.  The Behavioral Toolbox. Check out our courses for school-based and other behavioral professionals, including our newest one, Motivational Interviewing: Getting Educator Buy-In.

In this episode of IDD Health Matters, Dr. Craig Escudé sits down with Richard Chapman, Assistant Director for Disability Leadership at the Partnership for People with Disabilities in Richmond, Virginia. With a background in mental health counseling and a deep commitment to advancing equity, Richard shares his journey and current work at the intersection of mental health and self-determination for people with intellectual and developmental disabilities (IDD). Richard dives into how increasing self-determination—the ability for individuals to make their own life choices—can lead to better mental health outcomes and an improved quality of life. He discusses his current research, supported by the National Research Consortium on Intellectual Disability and Mental Health, which aims to show a causal relationship between self-determination and reduced psychopathology. Throughout the conversation, Richard highlights the importance of inclusion, cautions against the overuse of polypharmacy, and advocates for restraint-free support systems. He emphasizes that people with IDD not only deserve access to psychotherapy but also thrive when they're empowered to make their own decisions. Don't miss this powerful discussion on redefining support systems, challenging outdated models, and building a more equitable future for people with IDD.

In this episode of IDD Health Matters, Dr. Craig Escudé sits down with Richard Chapman, Assistant Director for Disability Leadership at the Partnership for People with Disabilities in Richmond, Virginia. With a background in mental health counseling and a deep commitment to advancing equity, Richard shares his journey and current work at the intersection of mental health and self-determination for people with intellectual and developmental disabilities (IDD). Richard dives into how increasing self-determination—the ability for individuals to make their own life choices—can lead to better mental health outcomes and an improved quality of life. He discusses his current research, supported by the National Research Consortium on Intellectual Disability and Mental Health, which aims to show a causal relationship between self-determination and reduced psychopathology. Throughout the conversation, Richard highlights the importance of inclusion, cautions against the overuse of polypharmacy, and advocates for restraint-free support systems. He emphasizes that people with IDD not only deserve access to psychotherapy but also thrive when they're empowered to make their own decisions. Don't miss this powerful discussion on redefining support systems, challenging outdated models, and building a more equitable future for people with IDD.

Our guest this week is Rady Johnson of Westport, CT, a recently retired senior executive at Pfizer and a father of three including one with intellectual disabilities.Rady and his wife, Diane, have been married for 38 years and are the proud parents of three children: Katherine (36), Bridget (30) and Michael (34) who was adopted from Romania as a one year old and who has intellectual disabilities.Despite a wide range of challenges, Michael has lead a pretty remarkable life.  Through organizations like Special Olympics, Best Buddies and church youth groups, Michael has grown and developed.  Remarkably, Michael holds down three jobs; one as an office aid a Tauck, the world-wide travel agency, another on the maintenance crew at a Long Island beach, and a third at Marshall's the department store.  The Johnson family story is a shing example about commitment and the importance of communityall on this episode of the SFN Dad to Dad Podcast.Show LinksPhone – (917) 545-3090Email – Rady.Johnson@outlook.comLinkedIn –  https://www.linkedin.com/in/rady-johnson-0ab46a7/MIRA Usa Guide Dogs For The Blind https://www.mirausa.orgRegister for the 6th Annual SFN Dads Virthual Conference on May 10, 2025: https://us02web.zoom.us/meeting/register/TLkN_ViJTTqnaK-M8pHPNA After registering, you will receive a confirmation email containing information about joining the meeting.Special Fathers Network -SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/  

We’re getting an update on Jesus Clubs - Ministering to People with Intellectual Disabilities.Your support sends the gospel to every corner of Australia through broadcast, online and print media: https://vision.org.au/donateSee omnystudio.com/listener for privacy information.

Click here to send us a topic idea or question for Weekend Wisdom.Are your child's birth parents struggling with addiction, mental illness, or intellectual disability? If so, join us for this discussion with Teresa Bradley, a psychotherapist with over 17 years of experience in addiction counseling and mental health. She is a Master Addiction Counselor, Trauma-Focused Cognitive Behavioral Therapist, and clinical trainer at Amerigroup.In this episode, we discuss:Substance Abuse DisordersWhat are some of the challenges that adoptive or foster parents might expect to see when a birth parent is struggling with a substance abuse disorder (SAD) and not able to raise this child?How are those issues different for relative caregivers, like grandparents raising grandchildren? At what age should we start talking to the kids in our care about their parents' challenges with substance abuse? How do we bring it up? How do we decide what to share and when?How can parents address that emotional fallout and deal with their own expectations, triggers, or negative feelings about the birth parents' SAD?For relative caregivers, especially grandparents raising grandchildren, adding layers of guilt, shame, and disappointment.How might an open adoption relationship change across a birth parents' journey through SAD? How should adoptive parents approach openness in their adoption when SAD is a known issue?What do you suggest parents or relatives do to process their feelings? Mental Health Challenges or Intellectual DisabilitiesWhat are some of the specific challenges that adoptive or foster parents might expect when they are trying to support a child of parents with mental illness or intellectual difficulties?How can parents explain a birth parent's challenges to children? When? How?What are some of the questions kids might have but cannot voice?  How do we address a child's concern that they will “get” this mental illness without scaring the child?Is this a good reason to limit contact with birth parents?How might an adoptive or foster parent talk to children and youth about the birth parents' ability to connect or maintain a relationship? When a kinship caregiver has a pre-existing relationship with this birth parent, how do they talk about the challenges and how their relationship changes in light of their struggles? What other issues do we need to consider to maintain a relationship with the birth parents while keeping the child safe and feeling cherished and supported?Resources:How Do You Manage Relationships with Birth Parents with Substance Use Disorders? Open AdoptionSupport 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

In this episode of Dimensions of Diversity, host Lloyd Freeman examines the changing landscape of disability rights with Robert Dinerstein, Professor Emeritus at American University's Washington College of Law. With over forty years of experience, Robert has been a prominent advocate for disability rights, serving on the President's Committee on People with Intellectual Disabilities and consulting with the World Health Organization.Lloyd and Robert engage in a detailed discussion about the ongoing movement for disability rights, examining the impact of landmark legislation such as the Americans with Disabilities Act (ADA) and the persistent challenges that still exist. They explore how disability intersects with other dimensions of diversity, the evolving perception of intellectual and mental disabilities, and the importance of building cultures of belonging. Robert shares insights on how organizations, particularly in the legal profession, can promote inclusivity through practical actions—many of which require little to no financial investment.The conversation also highlights the American Bar Association's (ABA) Pledge for Change initiative, which encourages law firms, law schools, and other organizations to actively support disability inclusion. Robert emphasizes the importance of systemic changes, such as making workplaces more accessible, adopting universal design principles, and ensuring that accommodations are treated as standard rather than exceptions.To view a full transcript of this episode visit: https://share.transistor.fm/s/a84e18a4 Dimensions of Diversity is a podcast created by Buchanan Ingersoll & Rooney, highlighting diversity in the workplace. Hosted by Lloyd Freeman, Chief Diversity & Inclusion Officer, the podcast features meaningful conversations with industry and community leaders working to advance D&I. 

On this episode of Today's Your Day Podcast, Tedi welcomes special guest Cathy Blatnik, who serves on the Mid-Michigan Autism Association's Board of Directors as its Treasurer and co-owns a business with her son Dominic called Baked Goods by Dominic.  Cathy shares with us how she and her husband Larry persevered when learning their 20-year-old son, Dominic, was diagnosed with Autism, ADHD, Anxiety Disorder, Epilepsy along with an Intellectual Disability.  Cathy tells Tedi it was a lot of trial and error, as 20-years ago there was not much information available about Autism and ADHD.  Cathy shares with us why her role as a board member and community activist are so important to her and how it can help make a difference for so many. This is a great conversation, one you def do not want to miss. Contact Information for Cathy Blatnik:Website: Mid-Michigan Autism Association Baked Goods by Dominic (Facebook Page)Email: BakedGoodsByDominic@mail.comEpisode Sponsor: Graze Craze, Okemos, MIhttps://www.grazecraze.com/okemos-miThe opinions and statements made on the Today's Your Day Podcast are/or do not necessarily reflect those of the Today's Your Podcast Podcast or Tedi Parsons. To learn more, please visit: https://owningtheday.comThe music used for this podcast was provided by: total-happy-up-and-sunny by sascha-ende-from-filmmusic-io. https://filmmusic.io/standard-license. License (CC BY 4.0):

Send us a textAndrew Radford lives in New South Wales and is a long-time advocate for people with intellectual disability and autism.Andrew himself has autism and a mild intellectual disability and has recently taken his advocacy to the next level with his appointment to the board of The Disability Trust. The trust is not-for-profit registered NDIS provider of supports and services and  last year it celebrated its 50 years!The Disability Trust has been part of Andrew's life for more than 20 years in many ways, including education and employment support.Andrew was also a part of the ABC series The Assembly where one of Australia's most renowned interviewers, Leigh Sales, mentors Autistic journalism students as they learn their craft and interview well known Australian personalities.Andrew is making history with The Disability Trust, which is the first major not-for-profit organisation in Australia to appoint a person with an intellectual disability to its Board.More info:VALID - the Victorian peak advocacy organisation for adults with intellectual disability.The Assembly (ABC)Andrew Radford Joins TDT Boardermha365 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.

Dr. Michael Puente joins host Dr. Ben Young to share his experience founding the first eye clinic specifically for adult and pediatric patients with intellectual developmental delay. Dr. Puente provides practical tips for all ophthalmologists to improve their care for this vulnerable population. For all episodes or to claim CME credit for selected episodes, visit www.aao.org/podcasts.

Most people would like to have a Government that is representative of the population, but there are some groups with very little representation.Dr Vivian Rath, Research Fellow at the Trinity Centre for People with Intellectual Disabilities at TCD was part of a group that looked into the difficulties that people with disabilities face when trying to enter politics. He joins Seán to discuss.

Most people would like to have a Government that is representative of the population, but there are some groups with very little representation.Dr Vivian Rath, Research Fellow at the Trinity Centre for People with Intellectual Disabilities at TCD was part of a group that looked into the difficulties that people with disabilities face when trying to enter politics. He joins Seán to discuss.

On this rebroadcast episode of the Special Chronicles Podcast: Daniel Smrokowski sits down with Soeren Palumbo, co-founder of Spread The Word, to talk about the Spread the Word Day of Activation this week on March 5th. This Week, our focus is on derogatory language. Tune in to a rebroadcast conversation with Soeren as he talks about: his backstory of growing up with his sister who has intellectual disabilities; why he co-founded this campaign; how he met Timbo Shriver; Importance of the r-word campaign; Backstory of article he and Tim co-authored entitled “Spread This: Be Good to People with Intellectual Disabilities”; Soeren's thoughts on this year's awareness day; Future of the r-word campaign; and much more! We think the world would be better if everyone were included. Around the world, exclusion and discrimination continue to divide people with and without intellectual and developmental disabilities. We are changing that with grassroots action for inclusion. That's Spread the Word. This year, you can engage and activate in multiple ways by choosing your focus: derogatory language, bullying or inclusive action. Visit SpreadTheWord.Global to access resources, sign the pledge, and grab your official gear. Together, let's create a more inclusive world! This episode originally aired on March 8, 2015 Episode 757 ShowNotes & Links:

Adults with an intellectual disability and an epilepsy have many of the same needs as those without the former - but things can take longer to figure out - hence, care and patience are crucial from clinicians! Neuropsychiatrist Mike Kerr shares how what to many may seem like small gains can have huge, positive impacts on the Quality of Life of people with an ID and an epilepsy. This is part 2 of 2 with Mike. -----------------------------------------

Neuropsychiatrist Mike Kerr talks about the intersection of epilepsy and Intellectual Disability, the complexities of communication, the need for tailored communication strategies, the needs of individuals and caregivers, and the importance of building relationships in healthcare! Mike and Torie also touch on new treatments and the overall quality of life for the people affected. -----------------------------------------

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. 

Description: Susanna Miller-Raines, MSW, Program Manager with Think College at the Institute for Community Inclusion at the University of Massachusetts Boston, discusses post-secondary education for students with intellectual disabilities. Interviewer: Bethany Chase, DSW, LSW, CESP, Training and Consultation Specialist at The Boggs Center on Disability and Human Development Click for Full Transcript of Episode 34

Buttons and magnets with the perfect message for your special someone? Sounds like the best Valentines' gift to me! The Button Shop is an enterprise of the Vera Perlin Society, and it employs people with intellectual disabilities -- and they can make you just about anything you like, for any occasion. Mary Ann Oakley is the CFO of the group, and she joined us in studio this morning.

Special Olympics' Chief of Global Youth & Education, Jackie Jodl, joins Raj Kumar for a podcast episode looking at how sports and education can drive societal change, the state of social inclusion for people with intellectual and learning disabilities, and the opportunities and risks presented by AI. This episode is sponsored by Special Olympics.

Pippa speaks to Carien Human, a social worker at Camphill Village West Coast, about the facility where adults with intellectual disabilities can lead happy and productive lives in a secure environment.See omnystudio.com/listener for privacy information.

Today we're buzzing about Masterpiece Alliance, a Roanoke, Virginia nonprofit with a mission of building community for adults with intellectual disabilities. BUZZ creator Michael Hemphill speaks with Scott Habeeb, who founded Masterpiece AlliancA in part to help people like his daughter who struggle to make friends and find social connections once they graduate from high school. One place where assume they can find community is the church. But as Scott shares, that's often not the case for a variety of reasons, and his organization has created an upcoming conference designed to fix that. Are you a nonprofit with an event that we could help promote? Or a marketing problem we could help fix? Contact us and we'll share on an upcoming episode.- - - - - - - - - - - - - - - - FOLLOW US:F A C E B O O K ➜ http://facebook.com/buzz4good​​I N S T A G R A M ➜ http://instagram.com/buzz4good​​L I N K E D I N ➜ https://www.linkedin.com/company/buzz4goodY O U T U B E ➜ http://youtube.com/c/buzz4goodW E B S I T E ➜ http://buzz4good.com​​- - - - - - - - - - - - - - - - The United States has more than 1.5 million nonprofits — from homeless shelters, food banks and rescue squads to children's choirs, science museums and animal refuges — that employ one out of every 10 Americans. Like any company, nonprofits have salaries and bills to pay, a budget to balance. They require money. And if enough people don't know about them, don't believe in them, don't support them — in short, if they lack BUZZ — they suffer and die.

BUZZ creator Michael Hemphill buzzes about coffee in today's Buzz4Good! Specifically, coffee from a Roanoke, Virginia, establishment that is brewed and served by adults with intellectual disabilities. A few years ago, Beth Woodrum founded Chris' Coffee and Custard to help individuals like her son, Chris, who has Down Syndrome, find meaningful employment and community. Beth recently announced an exciting new venture for Chris' Coffee and Custard – and her nonprofit that operates it, LovABLE Services – and so on today's show we share our inspiring conversation with Beth!Are you a nonprofit with an event that we could help promote? Or a marketing problem we could help fix? Contact us and we'll share on an upcoming episode.- - - - - - - - - - - - - - - - FOLLOW US:F A C E B O O K ➜ http://facebook.com/buzz4good​​I N S T A G R A M ➜ http://instagram.com/buzz4good​​L I N K E D I N ➜ https://www.linkedin.com/company/buzz4goodY O U T U B E ➜ http://youtube.com/c/buzz4goodW E B S I T E ➜ http://buzz4good.com​​- - - - - - - - - - - - - - - - The United States has more than 1.5 million nonprofits — from homeless shelters, food banks and rescue squads to children's choirs, science museums and animal refuges — that employ one out of every 10 Americans. Like any company, nonprofits have salaries and bills to pay, a budget to balance. They require money. And if enough people don't know about them, don't believe in them, don't support them — in short, if they lack BUZZ — they suffer and die.

In this episode of Better Thinking, Nesh Nikolic speaks with Dr. Stefan Carlo Michalski about using an AI-powered VR application to build life skills and improve healthcare access for people with intellectual disabilities. Dr. Stefan Michalski is a Research Fellow in the National Centre of Excellence in Intellectual Disability Health at the University of New South Wales. His research has focused on the use of immersive virtual reality (VR) to improve real-world outcomes for clinical populations, with a particular focus on intellectual disability. Stefan holds a PhD in Psychology, where he explored how immersive VR could assist people with intellectual disability in developing life skills. Currently, Stefan is leading research aimed at addressing significant healthcare disparities faced by people with intellectual disability. He has highlighted that fear, anxiety, and communication challenges often act as barriers for people with intellectual disability when seeking healthcare. His ongoing VR research incorporates generative AI-powered intelligent agents to support and prepare people with intellectual disability to navigate healthcare environments. These tools are designed to reduce anxiety during appointments, increase healthcare engagement, and foster better health outcomes. Through his work, Stefan seeks to transform the role of technology in promoting participation, independence, and improved health outcomes for people with intellectual disability. Episode link at https://neshnikolic.com/podcast/stefan-carlo-michalskiSee omnystudio.com/listener for privacy information.

We humans, typically, have 23 pairs of chromosomes. Sometimes, for a variety of reasons, we have an extra chromosome or we are missing one. Down syndrome, also known as Trisomy 21, is a genetic disorder that occurs when an individual has a full or partial extra copy of their 21st chromosome. Down syndrome is the most frequent of the chromosomal disorders in humans, occurring in approximately 1 in 700 births in the US. With improved care of often life-threatening clinical challenges, individuals with Down syndrome are living much longer. In this month's podcast of Your Child's Brain we are going to talk about Down Syndrome and especially focus on how the increased lifespan of those with Down syndrome is impacting treatment and research for people living with this diagnosis.   Resources · Down Syndrome Association of Maryland (dsamd.org) · National Down Syndrome Society (ndss.org) · National Down Syndrome Congress (ndsccenter.org) · Global Down Syndrome Foundation (https://www.globaldownsyndrome.org) · LuMind IDSC Foundation (https://lumindidsc.org) · NIH – research plan across the LifeSpan - Project INCLUDE for co-occurring medical conditions (www.nih.gov/include-project) · Eunice Kennedy Shriver National Institute of Child Health and Human Development (nih.gov) · National Task Group on Intellectual Disabilities and Dementia Practices - Intellectual Disabilities and Dementia Resources | The NTG (the-ntg.org)See omnystudio.com/listener for privacy information.

This Week on the Special Chronicles Podcast: Comedian and Podcaster Dustin Nickerson sits down with Award-winning Podcaster Daniel Smrokowski for an entertaining conversation about his Backstory in Comedy, Funny Podcast about Family, Comedy at Disability Camp, Inclusive Comedy, Non-Offensive Jokes to Intellectual Disability, How To Be Married To Melissa Book, Amazon and YouTube Specials, and we highly recommend you see him on tour! Episode 604 ShowNotes & Links:

John Paizis is the creative force behind Performing Arts Studio West whose focus is elevating the talents of performers with intellectual and physical disabilities. Together with friends of the studio, Mindy Sterling and Debra Wilson, John joins us to talk about their latest project, a storybook which puts a dark, new twist on age old fairytales, Mother Goose Reanimated. John shares his extensive experience in the non-profit space and how the seeds for this project were planted decades ago when he began working with autistic adults and fostering their potential. John, a performer and musician, founded PASW 26 years ago, providing hands-on individualized training, career management, and on-location support for performers with disabilities working in film, television and commercials. They've conquered most media but this is their first book!John shares the themes and inspirations behind the reimagined stories, how the creative team came together, and the collaborative process of writing, casting, costuming, set designing, and shooting a picture book. We also hear about Mindy's personal journey with her autistic son and the challenges that he has encountered. Debra shares how she got her big break and talks about her successful voice acting career (she's the current voice of Daisy Duck AND Ursula!), John tells us about working with Frank Oz and Jim Henson and everyone gushes about their recent experience launching the book at Los Angeles Comic Con!Plus, Fritz is recommending the doc, Maestra on Netflix, Weezy read and loved The Women by Kristin Hannah. And, tasked with sampling and recommending content from our generation, our Gen Z tech, Mason is binging and loving Cheers!Path Points of Interest:Mother Goose ReanimatedPerforming Arts Studio WestPASW on FacebookPASW on YouTubeMother Goose Reanimated WebsiteMindy Sterling on IMDBMindy Sterling on WikipediaMindy Sterling on X/TwitterDebra Wilson on IMDBDebra Wilson on WikipediaJohn Paizis on IMDBJohn Paizis on FacebookThe Women by Kristin HannahMaestra - NetflixGift of DemocracyMedia Path PodcastYoutubehttps://youtu.be/4xp9xEoFQN8

We explore the unique challenges faced by patients with intellectual and developmental disabilities (IDD) during dental appointments. Our guests, Brian Jones, a health care executive, and Tina Saw, a dentist and health care leader, share insights on how sensory sensitivities, higher oral care needs, and barriers to care impact these patients. They'll discuss innovative approaches like chair-side salivary testing and the critical role of medical-dental integration in improving health outcomes. Brian Jones is a health care executive. Tina Saw is a dentist and health care executive. They discuss the KevinMD article, "Is saliva the key to early disease detection and better oral health outcomes for patients with intellectual and developmental disabilities?" Our presenting sponsor is DAX Copilot by Microsoft. Do you spend more time on administrative tasks like clinical documentation than you do with patients? You're not alone. Clinicians report spending up to two hours on administrative tasks for each hour of patient care. Microsoft is committed to helping clinicians restore the balance with DAX Copilot, an AI-powered, voice-enabled solution that automates clinical documentation and workflows. 70 percent of physicians who use DAX Copilot say it improves their work-life balance while reducing feelings of burnout and fatigue. Patients love it too! 93 percent of patients say their physician is more personable and conversational, and 75 percent of physicians say it improves patient experiences. Help restore your work-life balance with DAX Copilot, your AI assistant for automated clinical documentation and workflows. VISIT SPONSOR → https://aka.ms/kevinmd SUBSCRIBE TO THE PODCAST → https://www.kevinmd.com/podcast RECOMMENDED BY KEVINMD → https://www.kevinmd.com/recommended GET CME FOR THIS EPISODE → https://www.kevinmd.com/cme I'm partnering with Learner+ to offer clinicians access to an AI-powered reflective portfolio that rewards CME/CE credits from meaningful reflections. Find out more: https://www.kevinmd.com/learnerplus

Send us a textWhat does it mean to be human? Who counts as a human being and why? Anthropologist Tom Pearson has been asking these questions for a living for a long time, and then his daughter was born and diagnosed with Down syndrome, prompting him to ask the questions all over again in his book An Ordinary Future. Amy Julia and Tom discuss:Normalcy, disability, and the human experienceCultural perceptions of disability and the historical context of eugenics and institutionalization How prenatal testing influences societal views of disabilityInterdependence and its relationship to the human experienceThe ways disability is a source of innovation and community, not just an inevitabilityFREE RESOURCE: 10 Ways to Move Toward a Good Future {especially for families with disability}Guest Bio:Tom Pearson is a cultural anthropologist with wide-ranging interests in the fields of environmental justice and disability studies. He teaches at the University of Wisconsin-Stout, where he also chairs the social science department. His writing has appeared in numerous scholarly journals and other public outlets. The birth of his daughter Michaela and her diagnosis with Down syndrome thrust him into an unfamiliar world of disability and difference. His book An Ordinary Future: Margaret Mead, the Problem of Disability, and a Child Born Different examines this experience in relation to Margaret Mead's path to disability rights activism. It confronts the dominant ideas, disturbing contradictions, and dramatic transformations that have shaped our perspectives on disability over the last century. Connect Online:Website | TwitterOn the Podcast:Washington Post: A mystery illness stole their kids' personalities. These moms fought for answers.An Ordinary Future: Margaret Mead, the Problem of Disability, and a Child Born Different by Thomas PearsonTRANSCRIPT: amyjuliabecker.com/tom-pearson/YouTube Channel: video with closed captionsLet's Reimagine the Good Life together. Find out more at amyjuliabecker.com.Connect with me: Instagram Facebook YouTube Website Thanks for listening!

Dr. Carl Tyler is a leading figure in the field of healthcare for individuals with intellectual and developmental disabilities (IDD). He is the current president of the American Academy of Developmental Medicine and Dentistry (AADMD), an organization dedicated to improving healthcare for people with IDD through education, advocacy, and policy efforts. Dr. Tyler is also a professor of family medicine at the Cleveland Clinic, where he plays a key role in training healthcare providers, including residents, on how to care for individuals with IDD. His career began during the deinstitutionalization movement in Ohio, and over time, he became a strong advocate for improving healthcare systems and training physicians to meet the specific needs of this population. Dr. Tyler's work includes research, scholarship, and contributions to medical literature, and he has helped integrate specialized care for individuals with IDD into mainstream medical training programs. In addition to his clinical and educational work, Dr. Tyler has authored several key resources, including the book Intellectual Disability at Your Fingertips, which provides practical guidance for healthcare providers working with this population.

Dr. Carl Tyler is a leading figure in the field of healthcare for individuals with intellectual and developmental disabilities (IDD). He is the current president of the American Academy of Developmental Medicine and Dentistry (AADMD), an organization dedicated to improving healthcare for people with IDD through education, advocacy, and policy efforts. Dr. Tyler is also a professor of family medicine at the Cleveland Clinic, where he plays a key role in training healthcare providers, including residents, on how to care for individuals with IDD. His career began during the deinstitutionalization movement in Ohio, and over time, he became a strong advocate for improving healthcare systems and training physicians to meet the specific needs of this population. Dr. Tyler's work includes research, scholarship, and contributions to medical literature, and he has helped integrate specialized care for individuals with IDD into mainstream medical training programs. In addition to his clinical and educational work, Dr. Tyler has authored several key resources, including the book Intellectual Disability at Your Fingertips, which provides practical guidance for healthcare providers working with this population.

Craig Juffer with Pella Christian Schools discusses the impact of the Knights of Columbus' Annual Campaign for Persons with Intellectual Disabilities. Donations can be made here.

Kelsie Parton with the Pella Community School District and Launching Arrows discusses the impact of the Annual Campaign for Persons with Intellectual Disabilities. Donations can be made here.

If you're looking for support in figuring out the “now what” after diagnosis, you've gotta know Yetta Myrick. Yetta has been in the trenches, supporting her son for 21 years, who was diagnosed early with Autism, ADHD, and intellectual disability.When it came to finding stellar support for her child with cognitive and developmental challenges, Yetta had no quit!This often felt like an uphill battle in a confusing and uncaring system. She is an Erin Brockovitch level Mama Bear - inspiring like an instant bestie who has your back. If you've felt overwhelmed trying to make sense of a diagnosis and on a quest to curate an excellent care team for your kiddo…don't miss this convo.In this episode, you'll learn:How a fierce love and determination to do right for her son helped Yetta become a resource for other families that have been touched by neurodiveristy.Why it's so important for the home environment to reinforce the support your child gets from their other caregivers.How frustrating it can be to find compassionate help for kids who need extra care, and how you can learn from the experiences of mamas like Yetta who've been there.And much more! As always, thanks for listening. Head over to Facebook, where you can join my free group Mastermind Parenting Community. We post tips and tools and do pop-up Live conversations where I do extra teaching and coaching to support you in helping your strong-willed children so that they can FEEL better and DO better. If you enjoyed this episode and think that others could benefit from listening, please share it!Get all the links, resources, and transcripts here: https://mastermindparenting.com/podcast-298About Randi RubensteinRandi Rubenstein helps parents with a strong-willed kiddo become a happier family and enjoy the simple things again like bike rides and beach vacays.She's the founder of Mastermind Parenting, host of the Mastermind Parenting podcast, and author of The Parent Gap. Randi works with parents across the U.S.At Mastermind Parenting, we believe every human deserves to have a family that gets along.Randi's Web and Social LinksWebsite: https://mastermindparenting.com/Facebook: https://www.facebook.com/mastermindparentingInstagram: https://www.instagram.com/mastermind_parenting/ About Yetta MyrickYetta Myrick is the mother of a young adult son diagnosed with Autism, ADHD, and Intellectual Disability. Yetta is the Founder and President of the nonprofit DC Autism Parents, and author of the book Mr. Marshall's Block Party. She has served as an advocate in roles with the Centers for Disease Control, Children's National Hospital, the Department of Health and Human Services, the DC Developmental Disablities Council, and many others. In 2024 she received the Advocate in Equity Award from the DC Developmental Disability Awareness Month Planning Committee.Resources Discussed/LinksDC Autism Parents https://dcautismparents.org/ Our 12-week Basics Bootcamp program is now available as a 100% online self-study course! https://mastermindparenting.com/minimasters/Live assessment:

Ava Leavitt joins Utah's First Lady, Abby Cox, to discuss how vital dancing has been throughout her life, how she’s navigated some of the most complex challenges she’s faced in high school, and her solution to how teenagers negatively engage with social media.  Then, Ava shares how losing her identity inspired her to create Dancers Without Limits, a dance program designed for individuals with intellectual disabilities, and how the organization is helping connect everyone passionate about dance. Colton Hyde also joins us to talk about how volunteering for Dancers Without Limits has taught him to be himself after working with the other dancers. Tammy Leavitt then shares how Dancers Without Limits has changed those participating in the program. Lastly, Ava discusses the program's future as she approaches high school graduation and college.

There's a new tool created by the Pennsylvania State Police for individuals with autism to enhance interactions with law enforcement officers. The cards, which include a person's name, contact information and emergency contacts, state that the cardholder has autism and urge officers to be patient and direct in their interactions. Lieutenant Adam Reed with the Pennsylvania State Police and Mark Davis, President and CEO of Pennsylvania Advocacy and Resources for Autism and Intellectual Disability joined The Spark to offer how the new informational cards will impact those living with autism. Listen to the podcast to hear the conversation.Support WITF: https://www.witf.org/support/give-now/See omnystudio.com/listener for privacy information.

Because there is no constitutional guarantee, every state in the country has different regulations about who is allowed to vote. But in many states, people with intellectual disabilities are denied the right to vote. Paul Collins, an English professor at Portland State University, wonders why his 25 year-old son with Autism Spectrum Disorder can’t vote … or can he? Collins explores this issue in a new article he wrote  for The Believer magazine. He joins us to talk about who votes and why it matters. 

Jesus invites those with intellectual disability to meet Him in His Word. But churches aren't always as equipped to lay out a feast for them, as they are for those without obvious disabilities. Paul and Jill Miller's journey with their daughter, Kim, led to creating interactive Bible studies for individuals with disabilities. Join hosts Dave and Ann Wilson as they hear about the impact disability ministry can have on churches and families. Will they be fed at your church? Show Notes and Resources Learn more about Paul and Jill Miller, their ministry, and their books at seeJesus.net. You can find the See Jesus Interactive Bible Studies here. You can find Jill Miller's devotional for families, Finding Jesus on Upside Down Days: Family Devotions from the Barnyard, in our shop. Finding Joy in the Hard Places with Autism, a conversation with Paul and Jill Miller. His book, 5 Traits of a Healthy Family, is out now! We'll send it at no cost to you with a donation of any size this week, as our way of saying a huge "Thank you!" for partnering with us toward stronger families around the world. Find resources from this podcast at shop.familylife.com. See resources from our past podcasts. Find more content and resources on the FamilyLife's app! Help others find FamilyLife. Leave a review on Apple Podcast or Spotify. Check out all the FamilyLife's podcasts on the FamilyLife Podcast Network

English Version - In April 2023, our host David Hirsch traveled to Cuba with Joni and Friends, as one of 12 U.S. volunteers participating in a Wheels For The World Program, to fit and distribute 200+ wheelchairs to youth and adults, who might not otherwise experience mobility.   This week's guest is Leonardo Cespedes of Bayamo, Cuba, a Baptist Preacher and father of two including a son with intellectual and physical disabilities.  Leonardo and his wife, Mairelis, have been married for 26 years and are the proud parents of two; daughter Reveca (23) who is a teacher, and son Marko (20) who has undiagnosed intellectual disabilities, suffers from seizures and is hard of hearing.   Marko was one of the recipients of a wheelchair. During his visit, David spoke with and recorded interviews with two Cubans connected to the disability community in Cuba.  Special thanks to Dairy Hernandez, the young Cuban woman that served as one of David's translators during the week and for her help translating today's episode in English and Spanish.  That's all on this episode of the SFN Dad to Dad Podcast.  Show Notes - WhatsApp - 53 58 01 426 627 Email – leobayamo@nauta.cuJoni & Friends -  https://joniandfriends.org/ACLIFIM (Asociación Cubana de Personas con Discapacidad Físico - Motora -  https://www.aclifim.cu/Special Fathers Network - SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 700+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/SFN Dads Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/Find out about Horizon Therapeutics – Science and Compassion Working Together To Transform Lives. https://www.horizontherapeutics.com/Versión en Español - En abril de 2023, nuestro anfitrión David Hirsch viajó a Cuba con Joni y sus amigos, como uno de los 12 voluntarios estadounidenses que participan en un programa de Wheels For The World, para instalar y distribuir 200+ sillas de ruedas a jóvenes y adultos, que de otro modo no experimentarían movilidad.El invitado de esta semana es Leonardo Céspedes de Bayamo, Cuba, un predicador bautista y padre de dos hijos, incluyendo un hijo con discapacidades intelectuales y físicas.   Leonardo y su esposa, Mairelis, han estado casados durante 26 años y son los orgullosos padres de dos hijos; su hija Reveca (23), que es profesora, y su hijo Marko (20), que tiene discapacidades intelectuales no diagnosticadas, sufre convulsiones y tiene problemas de audición.  Marko fue uno de los destinatarios de una silla de ruedas.Durante su visita, David habló y grabó entrevistas con dos cubanos conectados con la comunidad de discapacitados en Cuba.  Un agradecimiento especial a Dairy Hernández, la joven cubana que sirvió como una de las traductoras de David durante la semana y por su ayuda para traducir el episodio de hoy en inglés y español.  Eso es todo en este episodio del podcast Dad to Dad de SFN.  Mostrar Notas - WhatsApp - 53 58 01 426 627Correo electrónico - Correo electrónico - leobayamo@nauta.cuJoni y sus amigos - https://joniandfriends.org/ACLIFIM (Asociación Cubana de Personas con Discapacidad Física - Motora - https://www.aclifim.cu/Red de Padres Especiales - SFN es un programa de tutoría de padre a padre para padres que crían niños con necesidades especiales. Muchos de los 700+ Padres Mentores de SFN, que están criando niños con necesidades especiales, han dicho: "Ojalá hubiera algo así cuando recibimos por primera vez el diagnóstico de nuestro hijo. Me sentí tan aislada.  No había nadie dentro de mi familia, en el trabajo, en la iglesia o dentro de mi grupo de amigos que entendiera o pudiera relacionarse con lo que estaba pasando".Los padres mentores de SFN comparten sus experiencias con los padres más jóvenes más cerca del comienzo de su viaje criando a un niño con las mismas o similares necesidades especiales. Los Padres Mentores de SFN NO ofrecen asesoramiento legal o médico, eso es lo que hacen los abogados y los médicos. Simplemente comparten sus experiencias y cómo han aprovechado al máximo las situaciones difíciles.Echa un vistazo al canal de YouTube de 21CD con docenas de videos sobre temas relevantes para los padres que crían niños con necesidades especiales: https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videos Por favor, apoye a la SFN. Haga clic aquí para donar: https://21stcenturydads.org/donate/Red Especial de Padres: https://21stcenturydads.org/Grupo de Mentes Maestras de Papás de SFN - https://21stcenturydads.org/sfn-mastermind-group/Obtenga más información sobre Horizon Therapeutics: la ciencia y la compasión trabajan juntas para transformar vidas. https://www.horizontherapeutics.com/

In today's episode, Yakov sits down with Mike Seidl to talk about the world of capital raising as it relates to human behavior and relationship-building. Mike, a seasoned private money lender since 2017, shares insights into his journey from starting as a lender in residential fix and flips to raising nearly 20 million dollars. Drawing from his diverse background in human services, including roles in residential facilities and psychiatric hospitals, Mike emphasizes the importance of understanding human behavior in both personal relationships and business. Key Takeaways: Mike's career spans from working with abused children to managing group homes and mental health facilities, which shaped his deep understanding of human behavior. Mike shares the benefits of using private capital during economic downturns when institutional capital tends to retract. He breaks down exactly how and why it's so important to build personal connections before discussing business opportunities Mike makes his interest rate prediction and how he will react economically Mike's take on why human interaction is more fruitful than AI automation   More about Mike: Mike Seidl has been a successful private money lender since 2017 when he started partnering with and lending his personal capital on projects to experienced residential fix-and-flip real estate operators. In 2021, Mike was approached by a good friend and fellow business owner about deploying his money for him. He was looking for a safe, reliable return on his capital. Since then, the company has placed investor capital in loans as small as $15,000 and as large as $2,400,000. Mike's first job after studying economics at New York University was at a residential facility for sexually and physically abused kids. He has also managed a group home for adults with Intellectual Disabilities. As well as serving as a mental health worker at a psychiatric hospital. This experience helped him gain a good understanding of human behavior. That, in turn, helped him start, with a partner, grow and build his first company, providing medical alert systems, which they sold to a public company ten years later. After taking five years off, Mike started his second business in the construction industry, focusing on property damage repair. This company was sold in 2017 after being built into one that completed 300 +/- yearly jobs. Mike's goal is to start and self-fund a nonprofit focused on kids who "age out" of foster care and government facilities. The emphasis will be on experience-based training in mindset and how the brain works physically and psychologically, as well as hands-on training in finance, banking, nutrition, exercise, and entrepreneurship.   Ways to connect with Mike: https://www.linkedin.com/in/mike-seidl-reicapitalguys/   Useful links and resources: Yakov Smart's new book 'Attracting Investors' on Amazon https://findmoreinvestors.com/apply   Join our new capital raising community group here: https://www.facebook.com/groups/capitalraisingtalkwithcapitalraisingprosgroup   Free Trainings on “How To Raise More Capital & Find High Net-Worth Investors on Auto-Pilot”: http://findmoreinvestors.com/capital   Enter our monthly raffle by leaving a 5-star review and emailing a screenshot to: reviews@findmoreinvestors.com   Connect with Yakov: https://www.linkedin.com/in/yakovsavitskiy/ https://www.facebook.com/yakov.smart3   The following music was used for this media project: Music: Positive Fat Bass Intro Loop by WinnieTheMoog Free download: https://filmmusic.io/song/6093-positive-fat-bass-intro-loop License (CC BY 4.0): https://filmmusic.io/standard-license Artist website: https://linktr.ee/taigasoundprod   The following music was used for this media project: Music: Just Keep Going (Loopable) by chilledmusic Free download: https://filmmusic.io/song/7245-just-keep-going-loopable License (CC BY 4.0): https://filmmusic.io/standard-license   The following music was used for this media project: Music: Business Of Dreams by MusicLFiles Free download: https://filmmusic.io/song/9392-business-of-dreams License (CC BY 4.0): https://filmmusic.io/standard-license Artist website: https://cemmusicproject.wixsite.com/musiclibraryfiles   #realestateinvesting #capitalraising #realestate #passiveinvesting   

Credits: 0.25 AMA PRA Category 1 Credit™   CME/CE Information and Claim Credit: https://www.pri-med.com/online-education/podcast/frankly-speaking-cme-384 Overview: This episode investigates the inaccurate correlation made between acetaminophen use during pregnancy and an increased risk of developmental disorders, including autism spectrum disorder, in children. Expert faculty discuss the history of these claims, followed by a study evaluating outcomes in children, and emphasize the importance of evidence-based decision-making for patients and clinicians. Episode resource links: Ahlqvist VH, Sjöqvist H, Dalman C, et al. Acetaminophen Use During Pregnancy and Children's Risk of Autism, ADHD, and Intellectual Disability. JAMA. 2024;331(14):1205–1214. doi:10.1001/jama.2024.3172 Nat Rev Endocrinol. 2021 Dec;17(12):757-766. doi: 10.1038/s41574-021-00553-7 Guest: Aylin Madore, MD, MEd   Music Credit: Richard Onorato

Credits: 0.25 AMA PRA Category 1 Credit™   CME/CE Information and Claim Credit: https://www.pri-med.com/online-education/podcast/frankly-speaking-cme-384 Overview: This episode investigates the inaccurate correlation made between acetaminophen use during pregnancy and an increased risk of developmental disorders, including autism spectrum disorder, in children. Expert faculty discuss the history of these claims, followed by a study evaluating outcomes in children, and emphasize the importance of evidence-based decision-making for patients and clinicians. Episode resource links: Ahlqvist VH, Sjöqvist H, Dalman C, et al. Acetaminophen Use During Pregnancy and Children's Risk of Autism, ADHD, and Intellectual Disability. JAMA. 2024;331(14):1205–1214. doi:10.1001/jama.2024.3172 Nat Rev Endocrinol. 2021 Dec;17(12):757-766. doi: 10.1038/s41574-021-00553-7 Guest: Aylin Madore, MD, MEd   Music Credit: Richard Onorato

Send us a Text Message.In a society often obsessed with intelligence, can we reimagine a good life that encompasses joy, meaning, and respect for all? What does it mean to respect and support individuals with profound intellectual disabilities? What role do those most intimately involved in providing care have in advocacy? Professor Amy Lutz, Ph.D., author of Chasing the Intact Mind, joins Amy Julia Becker to discuss:How the severely autistic and intellectually disabled were excluded from the debates that affect them mostControversy and misconceptions about sheltered workshops/14(c) programsThe importance of meaningful relationships and communityBuilding a caring and committed workforce of caregiversListening to caregivers and families_FREE RESOURCE: 10 Ways to Move Toward a Good Future (especially for families affected by disability)_GUEST BIOProfessor Amy Lutz, Ph.D., is a historian of medicine at the University of Pennsylvania. Her research locates at the intersection of disability history and bioethics. She is a founding board member of the National Council on Severe Autism (NCSA) and the author of Chasing the Intact Mind and several other books. She lives outside Philadelphia with her husband and five children, including Jonah, her 25-year-old son with profound autism. _CONNECT ONLINEWebsite: amysflutz.com/_ON THE PODCASTChasing the Intact Mind: How the Severely Autistic and Intellectually Disabled Were Excluded from the Debates That Affect Them Most by Amy Lutz, Ph.D.The Lancet Commission on the future of care and clinical research in autismSection 14(c) of the Fair Labor Standards ActUnited States Commission on Civil Rights 2020John SwintonAmy Julia's essay about the spiritual lives of people with intellectual disabilities_TRANSCRIPT: amyjuliabecker.com/amy-lutz/_YouTube Channel: video with closed captionsLet's Reimagine the Good Life together. Find out more at amyjuliabecker.com and subscribe here to receive my weekly thoughts and reflections.Connect with me: Instagram Facebook YouTube Website Thanks for listening!

A listener named Darby asks Father Dave if those with mental or intellectual disabilities are permitted to receive the Eucharist. She says, “I was told it's up to the priest to make that decision…I have also been told that [those with low cognitive ability could be denied] because of their non-understanding of the concept and importance.”

Mandy and Kate talk to Sonja, a self proclaimed Norwegian princess and introduces us to her gorgeous daughter Emmy who lives with Patau Syndrome or Trisomy 13. Emmy was born 7 weeks prematurely, in a dramatic entrance which has paved the way for Emmy's life so far. Sonja shares the story of Emmys birth, her time in SCN and the genetic testing and diagnosis of Patau Syndrome and the mosaic nature of the results. This time was gut wrenching whilst Emmy was in hospital and they couldn't be together.She came home at 6.5 weeks and was healthy and growing beautifully. Sonja began the journey of hip dysplasia and microcephaly initially and had a hip brace and avoided a head brace. Emmy then got her nickname as baby Elton John with her first pair of glasses.Sonja grew up in America, and lives in Melbourne, so her family came to Australia with their family heirloom gown for Emmy to wear at her christening. It was a very special time.Sonja was told to google Patau Syndrome/Trisomy 13 by her Doctor and she found it affects one in 4000 - 20,000 people. Emmy's geneticist told Sonja that her results had not been found in anyone else in the world and now that Emmy is older, they have met another little boy from QLD.Emmy has had some significant respiratory illness in her life and at age 3, she was extremely unwell and had a cardiac arrest in the ambulance on the way to RCH and thankfully was resuscitated and recovered. She had many respiratory admissions to hospital for many years.Emmy began schooling in mainstream, and then moved to a specialist school in grade one which coincided by covid 2020. Emmy enjoys school and is now in grade 6.Emmy is dramatic, friendly, be anyones best friend, she is a storyteller with a terrific memory. She is a Special Olympics athlete and loves being a part of it. She is now heading into the secondary school with a new diagnosis of Autism and Intellectual Disability and the tours for the schools have began.Sonja is a florist and loves using the creative part of her brain. She is pausing her florist business at the moment, but follow her for when she returns.Thank you for sharing your story Sonja.You can find and follow Sonja on Instagram @sonjabarrettgibbons and @sonjagibbonsfloraldesignPlus: Listen to our Spotify playlist –Too Peas: Songs Our Guest Peas LoveJoin our Facebook HangoutFind us on YouTubeBuy our book The Invisible Life Of Us!Leave us a speakpipe Help spread the love for Too Peas by rating and reviewing us!Melbourne forecast for Thursday April 25 - Shower or two, 16 degrees Hosted on Acast. See acast.com/privacy for more information.

Not many got close to the ruthless, sharp-tongued Sue Sylvester, except Becky Jackson! Lauren Potter joins Jenna and Kevin to discuss her iconic role as Becky, including how she got the role, what it was really like working with Jane Lynch, one of her favorite days on the set involving Cory Monteith, and, of course, Becky and Artie's date at Breadstix!  Plus, Lauren reveals what it was like being appointed to the President's Committee for People with Intellectual Disabilities, going to the White House, and meeting Michelle Obama!See omnystudio.com/listener for privacy information.

Yetta Myrick is the mother of a young adult son diagnosed with Autism, ADHD, and Intellectual Disability. She is the Founder and President of DC Autism Parents (DCAP), a 501(c)(3) non-profit organization in the District of Columbia. Ms. Myrick has served as the CDC's Act Early Ambassador to the District of Columbia since 2016, led the DC COVID-19 Response Team from 2020-2022, and is currently leading the DC Act Early Team. In 2022, she co-authored and self-published, "Mr. Marshall's Block Party". Ms. Myrick leads the DC Autism Collaborative's Developmental Monitoring, Screening, and Evaluation Subgroup, co-leads the Family Advisory Group, Outreach and Education Subgroup, and the Community Resources and Support Subgroup. She serves as the Parent Educator/Advocate on the ECHO Autism HUB Team at Children's National Hospital. Ms. Myrick co-leads the “Family Voices United to End Racism Against CYSHCN and Families” Project and served as the Co-Investigator for the “Building Capacity in the African American ASD Community for Patient-Centered Outcomes Research” Project funded through the Patient-Centered Outcomes Research Institute Eugene Washington PCORI Engagement Award. In 2021, she was appointed to the Interagency Autism Coordinating Committee by Secretary of Health and Human Services, Xavier Becerra, J.D. Additionally, Ms. Myrick is a member of the DC Developmental Disabilities Council and was awarded the 2024 Advocate in Equity Award by the DC Developmental Disability Awareness Month Planning Committee. She holds a Bachelor of Arts Degree in Communication Studies from The Catholic University of America.In this special episode, we discuss:PracticeTaking care of yourself to know yourselfBenefits of restResting practicesYoga off the matSelf-studyBoth/AndPurposeSystems of marginalizationNormalizing disabilityConnect with Yetta on her nonprofit's website and download the Rest to Create Change Toolkit.Podcast music by Charles Kurtz+ Read transcript

- Cold weather, financial collapse, and disability hiring. (0:29) - Hiring people with disabilities in the FAA. (6:26) - US Secretary of Defense's disappearance. (12:29) - Lloyd Austin's death and potential cover-up. (17:37) - Disability hiring in government. (21:47) - Financial collapse, Bitcoin ETFs, and scams. (27:17) - Financial collapse, gold, and cryptocurrency. (42:30) - Autism, biomedical intervention, and healing. (53:08) - Vaccine-induced autism and medical establishment denial. (1:05:09) - Vaccine safety and autism. (1:09:28) - Parenting, health, and autism awareness. (1:14:45) - Vaccine safety and autism prevention. (1:24:52) - Parenting and autism, with a focus on decision-making and medical care. (1:35:07) - Autism awareness and empowerment. (1:39:08) For more updates, visit: http://www.brighteon.com/channel/hrreport NaturalNews videos would not be possible without you, as always we remain passionately dedicated to our mission of educating people all over the world on the subject of natural healing remedies and personal liberty (food freedom, medical freedom, the freedom of speech, etc.). Together, we're helping create a better world, with more honest food labeling, reduced chemical contamination, the avoidance of toxic heavy metals and vastly increased scientific transparency. ▶️ Every dollar you spend at the Health Ranger Store goes toward helping us achieve important science and content goals for humanity: https://www.healthrangerstore.com/ ▶️ Sign Up For Our Newsletter: https://www.naturalnews.com/Readerregistration.html ▶️ Brighteon: https://www.brighteon.com/channels/hrreport ▶️ Join Our Social Network: https://brighteon.social/@HealthRanger ▶️ Check In Stock Products at: https://PrepWithMike.com