Special Ed Rising; No Parent Left Behind

Mark Ingrassia

This former Special Ed classroom teacher is on his own with a microphone, to share some of the magic he's learned in his 36+ years in the field. Stories, strategies, and a true grasp for what life can be like for parents and caregivers of Disabled children are waiting here! Witnessing, first hand, your challenges in the home has invigorated my desire to share what I know and to be a cheerleader for your lives and the lives of your child using mindfulness as a fulcrum to success. You are not alone and your life matters. Join me as we let go and grow together!

  1. 3d ago

    Beyond the IEP: Planning for Your Child’s Future

    Shellee Howard, a renowned college and education consultant, shares insights on navigating the complex transition from high school to college, especially for students with IEPs and special needs. This episode offers practical guidance for parents to advocate effectively and secure funding and accommodations for their children. keywordscollege planning, IEP, special needs, scholarships, college admissions, advocacy, education consulting, college readiness, financial aid, parent guidance key topics The importance of early IEP evaluation and advocacyStrategies for navigating college admissions with special needsHow to find and secure scholarships for unique student profilesThe role of independent evaluations in college readinessManaging the financial aspects of college for students with disabilitiesBuilding a support team for college successThe impact of social media and self-awareness on college prospectsResources and tools for parents to advocate effectively Sound Bites "Parents need constant reminders and resources""Start the IEP process early in high school""There is a college for everyone, if you know where to look" Chapters 00:00Introduction and episode overview 01:58Shellee Howard's background and expertise 03:48Challenges faced by parents of students with IEPs 05:57The importance of early evaluation and advocacy 09:01Understanding college accommodations and services 11:57The role of independent evaluations in college prep 14:59Starting the transition early in high school 18:11Helping students discover their gifts and passions 20:51Addressing social media and self-identity issues 24:04Choosing the right college environment and support 27:00Exploring career options and undecided students 29:47Financial planning, scholarships, and resources 32:56The importance of advocacy and resourcefulness 35:47Building a support team and community resources 38:53Addressing the future and college alternatives 41:58Encouraging proactive parent involvement 45:09Success stories and scholarship opportunities 46:48Special offers and final advice 48:09Closing remarks and podcast info Shellee Howard links: www.collegereadyplan.info and collegereadyplan.com/resources specialedrising.com Ray's Respite Care Go Fund Me: https://www.gofundme.com/f/join-rays-respite-care-mission

  2. Oct 18

    Beyond Behavior Plans: Connecting Home and School

    When a child experiences significant behavioral challenges, families and educators can find themselves caught in a cycle of incidents, phone calls, meetings, and frustration. But what if we shifted the conversation from blame to understanding, from reacting to preventing, and from simply documenting behavior to teaching skills that help children communicate, participate, and grow? In this episode of Special Ed Rising: No Parent Left Behind, Mark Ingrassia explores how parents, caregivers, teachers, and school teams can work together to understand behavioral patterns, support difficult transitions, teach functional communication, interpret data responsibly, and build more consistent responses across home and school. The episode also examines what research tells us about functional communication training, visual supports, and collaboration during school transitions. The central message is that evidence-informed strategies must be individualized, implemented thoughtfully, and evaluated to determine whether they are helping the child. This is a conversation about accountability with compassion, safety with dignity, and the shared responsibility adults have to help children learn and thrive. Research discussed: Walker, Lyon, Loman, and Sennott (2018), A systematic review of Functional Communication Training (FCT) interventions involving augmentative and alternative communication in school settings, Augmentative and Alternative Communication. Fontil and colleagues (2020), Barriers to and Facilitators of Successful Early School Transitions for Children with Autism Spectrum Disorders and Other Developmental Disabilities: A Systematic Review, Journal of Autism and Developmental Disorders. Mouzakes and colleagues (2025), A Closer Examination of the Visual Schedule Component of Interventions to Improve Transitions, Behavioral Interventions. Listener reflection: What is one change that could help your home-school team move from responding to difficult moments toward preventing them and building skills together? speciledrising.com Ray's Respite Care: https://www.gofundme.com/f/join-rays-respite-care-mission

  3. Oct 5

    When the System Doesn't Fit the Child: Foster Care and Children With Disabilities.

    What happens when a child with a disability enters the foster care system? In this episode of Special Ed Rising: No Parent Left Behind, Mark Ingrassia explores the unique challenges children with disabilities can face in foster care, including longer stays, multiple placement changes, and increased use of group homes or institutional settings. Inspired by NPR reporting by Joseph Shapiro, Mark looks at the impact of trauma, autism, intellectual disabilities, complex medical needs, and behavioral-health challenges—and asks whether the system is equipped to truly understand and support these children. The conversation also examines how families can reach a crisis point when they cannot access the respite, behavioral, medical, and community supports their child needs. Sometimes, “I can't do this anymore” really means, “I've been doing this alone for years, and I desperately need help.” Mark discusses the story of Christian Williams, a 15-year-old with Type 1 diabetes and behavioral-health challenges who died while living in a therapeutic group home, raising important questions about whether children with complex needs are being placed in settings equipped to care for them. The episode explores the importance of family connections, kinship care, better coordination between schools, medical providers, caregivers, and child-welfare agencies, and listening to former foster youth about what children actually experience. Most importantly, this is a conversation about changing the way we think about children with disabilities in foster care. Maybe the goal shouldn't be to make children fit the system. Maybe the goal is to build a system that can fit the child. Because every child deserves to be understood before they're judged, supported before they're punished, and connected before they're corrected. In This Episode: Children with disabilities in foster carePlacement instability and traumaBehavioral-health and complex medical needsFamilies reaching crisis without adequate supportCustody relinquishment and disability-related needsChristian Williams' storyKinship and family connectionsCoordination across schools, healthcare, and child welfareListening to former foster youthBuilding a foster-care system that fits the child Reporting Discussed: Joseph Shapiro, NPR specialedrising.com Ray's Respite Care: What happens when a child with a disability enters the foster care system? In this episode of Special Ed Rising: No Parent Left Behind, Mark Ingrassia explores the unique challenges children with disabilities can face in foster care, including longer stays, multiple placement changes, and increased use of group homes or institutional settings. Inspired by NPR reporting by Joseph Shapiro, Mark looks at the impact of trauma, autism, intellectual disabilities, complex medical needs, and behavioral-health challenges—and asks whether the system is equipped to truly understand and support these children. The conversation also examines how families can reach a crisis point when they cannot access the respite, behavioral, medical, and community supports their child needs. Sometimes, “I can't do this anymore” really means, “I've been doing this alone for years, and I desperately need help.” Mark discusses the story of Christian Williams, a 15-year-old with Type 1 diabetes and behavioral-health challenges who died while living in a therapeutic group home, raising important questions about whether children with complex needs are being placed in settings equipped to care for them. The episode explores the importance of family connections, kinship care, better coordination between schools, medical providers, caregivers, and child-welfare agencies, and listening to former foster youth about what children actually experience. Most importantly, this is a conversation about changing the way we think about children with disabilities in foster care. Maybe the goal shouldn't be to make children fit the system. Maybe the goal is to build a system that can fit the child. Because every child deserves to be understood before they're judged, supported before they're punished, and connected before they're corrected. In This Episode: Children with disabilities in foster carePlacement instability and traumaBehavioral-health and complex medical needsFamilies reaching crisis without adequate supportCustody relinquishment and disability-related needsChristian Williams' storyKinship and family connectionsCoordination across schools, healthcare, and child welfareListening to former foster youthBuilding a foster-care system that fits the child Reporting Discussed: Joseph Shapiro, NPR specialedrising.com Ray's Respite Care: What happens when a child with a disability enters the foster care system? In this episode of Special Ed Rising: No Parent Left Behind, Mark Ingrassia explores the unique challenges children with disabilities can face in foster care, including longer stays, multiple placement changes, and increased use of group homes or institutional settings. Inspired by NPR reporting by Joseph Shapiro, Mark looks at the impact of trauma, autism, intellectual disabilities, complex medical needs, and behavioral-health challenges—and asks whether the system is equipped to truly understand and support these children. The conversation also examines how families can reach a crisis point when they cannot access the respite, behavioral, medical, and community supports their child needs. Sometimes, “I can't do this anymore” really means, “I've been doing this alone for years, and I desperately need help.” Mark discusses the story of Christian Williams, a 15-year-old with Type 1 diabetes and behavioral-health challenges who died while living in a therapeutic group home, raising important questions about whether children with complex needs are being placed in settings equipped to care for them. The episode explores the importance of family connections, kinship care, better coordination between schools, medical providers, caregivers, and child-welfare agencies, and listening to former foster youth about what children actually experience. Most importantly, this is a conversation about changing the way we think about children with disabilities in foster care. Maybe the goal shouldn't be to make children fit the system. Maybe the goal is to build a system that can fit the child. Because every child deserves to be understood before they're judged, supported before they're punished, and connected before they're corrected. In This Episode: Children with disabilities in foster carePlacement instability and traumaBehavioral-health and complex medical needsFamilies reaching crisis without adequate supportCustody relinquishment and disability-related needsChristian Williams' storyKinship and family connectionsCoordination across schools, healthcare, and child welfareListening to former foster youthBuilding a foster-care system that fits the child Reporting Discussed: Joseph Shapiro, NPR specialedrising.com Ray's Respite Care: https://www.gofundme.com/f/join-rays-respite-care-mission

  4. Sep 28

    ArtStream; Performing Beyond Expectations: The Transformative Power of Inclusive Theater

    In this episode of Special Ed Rising: No Parent Left Behind, we explore the transformative power of inclusive theater with ArtStream, a nonprofit creating opportunities for people with intellectual and developmental disabilities to perform, create, collaborate, and tell their own stories. Joining me are Hayley Cutler, MFA, Artistic Director of ArtStream, and Adrian Forsythe, an ArtStream performer since its founding in 2005 who is entering his 21st season. keywords inclusive theater, disability arts, community building, improvisation, original productions, arts and advocacy, peer support, arts education, accessibility in arts, creative collaboration key topics The history and mission of ArtstreamThe process of devising original theater with actors with disabilitiesThe role of improvisation and collaboration in artistic developmentThe impact of inclusive arts on community and confidenceThe integration of families and support networks in arts programsThe importance of authentic representation and 'nothing about us without us'The growth of actors from beginners to professionalsThe benefits of arts for advocacy and self-expression Sound Bites "Every piece is original, every story is unique""Nothing about us without us""Everyone deserves a chance to perform their art" Chapters 00:00Introduction to Artstream and its mission 01:57The process of creating original inclusive theater 09:50The role of improvisation and collaboration 19:56Impact on actors' confidence and community 30:00Family involvement and community support 39:59The growth of actors and the importance of authentic representation 49:56Future aspirations and performances around the world Website: https://art-stream.org/ Specialedrising.com Ray's Respite Care: https://www.gofundme.com/f/join-rays-respite-care-mission

  5. Sep 14

    Team Child: Advocacy Without the Adversarial Approach

    In this episode, January Addison Lare shares her insights on navigating special education, advocating for children, and building collaborative relationships between families and schools. Her personal experiences and professional expertise offer valuable guidance for parents, educators, and advocates. Keywordsspecial education, advocacy, IEP meetings, parent-school collaboration, disability support, education system, guardianship, Medicaid, family advocacy Key TopicsThe importance of relationship building in IEP meetingsStrategies for parents to advocate effectivelyThe role of advocates in special educationImpact of policy changes on families and servicesGuardianship and long-term planning for individuals with disabilitiesThe need for systemic change in education and advocacy GuestJanuary Addison Lare Educational & Family Advocacy Consultant Founder, Empowered to Thrive LLC 📞 785-513-9735 📧 empoweredtothriveconsulting@gmail.com 🌐 empoweredtothriveconsulting.com 📍 811 S 1st Street, Atwood, KS 67730 Sound Bites“Fake it till you make it.”“Parents want someone to listen.”“Treat it accordingly.” Chapters00:00 — Introduction and guest background 324:55:32 — Personal journey and name origin 6388:49:06 — Experience in special education and advocacy 14972:09:33 — Guardianship and long-term planning for loved ones 28555:30:07 — Impact of policy changes on services and families 352777:43:44 — Entering IEP meetings: Building relationships 380833:17:10 — Preparing for effective meetings and collaboration 453611:04:09 — The role of advocates and communication tips 535277:44:32 — Addressing systemic challenges and future outlook Guest Links🌐 Empowered to Thrive Consulting 📧 empoweredtothriveconsulting@gmail.com 📞 785-513-9735 specialedrising.com Ray's Respite Care: https://www.gofundme.com/f/join-rays-respite-care-mission

  6. Sep 1

    Vaccines, Autism & Politics: Where’s the Evidence?

    In this episode of Special Ed Rising: No Parent Left Behind, Mark Ingrassia examines recent claims from President Trump and HHS Secretary Robert F. Kennedy Jr. suggesting a connection between vaccines and autism. Mark asks a simple question: Where’s the evidence? The episode looks at decades of research involving hundreds of thousands of children, including large studies, meta-analyses, and systematic reviews examining the MMR vaccine, thimerosal, and vaccination more broadly. The research has consistently found no evidence that vaccines cause autism. Mark also discusses why rising autism diagnoses do not automatically establish a cause, the retraction of the original 1998 vaccine-autism study, and the importance of distinguishing legitimate scientific questions from conclusions made before the evidence is available. Most importantly, this conversation is about families. Parents need accurate information, qualified professionals, meaningful services, and support—not fear, confusion, or unnecessary guilt. We should continue researching autism. We should ask difficult questions. But we also have to be willing to follow the evidence. IN THIS EPISODETrump and RFK Jr.'s claims about vaccines and autismWhat decades of research actually showThe MMR vaccine and autismThimerosal and vaccine safetyWhy autism prevalence alone doesn't establish causationThe impact of misinformation on familiesWhat policymakers should be focusing on instead Don't follow the person. Follow the evidence. RESOURCES & SOURCESHviid et al. (2019), Annals of Internal Medicine — Nationwide study of MMR vaccination and autism involving more than 650,000 children. MMR Vaccination and Autism: Nationwide Cohort StudyMadsen et al. (2002), New England Journal of Medicine — Population-based study examining MMR vaccination and autism in more than 500,000 children. Population-Based Study of MMR Vaccination and AutismTaylor, Swerdfeger & Eslick (2014), Vaccine — Meta-analysis of cohort and case-control studies examining vaccines and autism. Vaccines Are Not Associated With Autism: Meta-AnalysisDeStefano & Shimabukuro (2019), Annual Review of Virology — Review of the evidence surrounding the MMR vaccine and autism. The MMR Vaccine and AutismPrice et al. (2010), Pediatrics — Study examining prenatal and infant exposure to thimerosal and autism risk. Prenatal and Infant Exposure to Thimerosal and AutismWorld Health Organization (2025) — Global expert review reaffirming that available evidence does not show a causal relationship between vaccines and autism. WHO: Vaccines and Autism Evidence ReviewAutism Science Foundation — Evidence-based information and research on vaccines and autism. Autism Science Foundation: Autism and VaccinesDisability Scoop (August 12, 2026) — Michelle Diament, “Doctors, Advocates Call Out Trump For Claims About Autism.” Disability Scoop: Doctors, Advocates Call Out Trump For Claims About Autism Visit specialedrising.com for more resources and information. Question everything. Demand evidence. Listen to autistic people. No Parent Left Behind.

  7. Aug 24

    Travel Without Limits: Accessible Travel with Matthew Alexander

    In this episode, Matthew Alexander shares his inspiring journey of founding a travel agency dedicated to supporting families with children who have special needs, including autism. He discusses the importance of accessible travel, how to plan inclusive vacations, and the transformative benefits of travel for individuals with disabilities. keywordsaccessible travel, autism, special needs, family vacations, travel planning, inclusive travel, disability accommodations, travel tips, autism travel, travel with special needs key topics The origin of Matthew Alexander's travel agency supporting families with special needsThe importance of understanding autism from a first-hand perspectiveHow travel can positively impact individuals with disabilitiesKey questions families should ask for accessible accommodationsThe role of partnerships and relationships in providing accessible travel optionsInnovative solutions for accessible travel including hotels, airlines, and cruisesThe significance of planning and communication in accessible travelResources and programs that support travelers with hidden disabilities Sound Bites "Travel can be transformative for people with disabilities.""Understanding autism from a first-hand perspective helps create better travel experiences.""Accessible travel is about more than just wheelchairs; it includes medications, sensory needs, and emotional support." Website https:Professional Accessible Travel Hub https://specialedrising.com/ Ray's Respite Care: https://www.gofundme.com/f/join-rays-respite-care-mission

4.5
out of 5
11 Ratings

About

This former Special Ed classroom teacher is on his own with a microphone, to share some of the magic he's learned in his 36+ years in the field. Stories, strategies, and a true grasp for what life can be like for parents and caregivers of Disabled children are waiting here! Witnessing, first hand, your challenges in the home has invigorated my desire to share what I know and to be a cheerleader for your lives and the lives of your child using mindfulness as a fulcrum to success. You are not alone and your life matters. Join me as we let go and grow together!

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