Podcasts about Special needs

In Episode 215 of The Homeschool Show, Amanda talks with Nikki Cooper (specialneeds@nche.com)  about homeschooling children with special needs, offering practical encouragement for families who are just getting started or are looking for additional support. Their conversation covers common questions about IEPs, choosing curriculum, finding community, and giving yourself permission to adjust your approach as your child's needs change. Nikki also shares how families can connect with NCHE's special needs support resources.Melanie also talks with Katherine Marker from the North Carolina Educational Assistance Authority to explain the ESA Plus Scholarship for students with disabilities. They discuss who may qualify, how eligibility is determined through the public school evaluation process, what the application timeline looks like, and how homeschool families can prepare before applying.Helpful Links:  ECAC Parent CenterESA+ OverviewDocumentation Requirements

Tegan is a former Canadian resident and full-time engineer who now calls Pittsburgh home, where she's a full-time mom of three, always chasing sunshine and finding adventure in everyday family life. Known in the Rare and Mighty (RAM) community for her honest, "no sugarcoating" approach and her thoughtful exploration of special needs theology, Tegan shares the life-changing journey that began when her middle daughter, Eloise, was diagnosed with the rare genetic condition FOXG1 syndrome at just ten months old. In this deeply moving conversation, Tegan opens up about navigating the heartbreak of a late miscarriage, the shock of an unexpected diagnosis, and the difficult questions that challenged her faith. She reflects on how prayer, community, and God's unwavering presence reshaped her understanding of suffering, goodness, and unconditional love. Together, we explore the difference between grieving the future you imagined and finding joy in the life you have, the daily invitation to sacrificial love through caregiving, and how raising a child with special needs has transformed Tegan's relationship with God. She also shares the beautiful story behind naming her youngest son, Boaz, and what redemption has looked like for her family. Whether you're walking through hardship, caring for a loved one with disabilities, or wrestling with faith in difficult seasons, Tegan's honesty, wisdom, and hope will encourage you to discover God's love in unexpected places.

Send us Fan MailWhat if the reason you still don't feel well isn't just your body... but the place you spend the most time?In this episode of Never Been Sicker, Michael Rubino sits down with functional medicine physician Kurt N. Woeller, DO, FMAPS to discuss why environmental exposures, especially mold and mycotoxins, are so often overlooked in medicine. Together, they explore why many patients continue searching for answers while an important piece of the puzzle is never investigated.Dr. Woeller explains why symptoms like fatigue, brain fog, headaches, poor sleep, digestive issues, allergies, and chronic inflammation can persist when environmental exposure isn't addressed. He also shares why testing both the home and the body creates a much clearer picture than either one alone.The conversation covers real patient stories, common mistakes people make when they suspect mold, and why removing ongoing exposure is often one of the most important steps toward recovery.Whether you're struggling with chronic illness, supporting a loved one, or simply want to understand how your environment impacts your health, this episode offers practical insight into a topic more physicians are beginning to recognize.-----------------------------------------------------------------------------------------------CHAPTERS:00:00 Introduction00:19 Meet Dr. Kurt Woeller01:08 Why mold is missed in medicine03:19 Biggest mistakes people make after mold exposure05:08 Can hidden mold make you sick?06:43 Why environmental medicine matters08:18 Why you can't heal while ongoing exposure continues09:29 Why testing the body alone isn't enough12:07 Why testing the home alone isn't enough14:06 How combining both tests changes treatment16:14 Why comprehensive testing matters18:17 One camera angle isn't enough20:41 Test, don't guess22:52 How targeted testing can save time and money28:58 Why data still needs clinical guidance29:28 Real patient success story36:01 Why people normalize feeling sick39:08 Common symptoms of mold exposure45:48 Rapid-fire questions48:23 Where to find Dr. Kurt Woeller50:07 Closing thoughts-----------------------------------------------------------------------------------------------

Send us Fan MailSend us Fan MailIn this heartfelt episode of Living the Dream with Curveball, we have an inspiring conversation with Wendy Ernzen, a dedicated mother, advocate, and host of the podcast *Let's Plant Houses*. Wendy shares her personal journey as a parent of a daughter with autism, shedding light on the unique challenges families face when navigating support systems that often fall short.Wendy opens up about her daughter's diagnosis and the profound impact it had on her life and career. She discusses the importance of advocacy and the need for parents to connect with one another to share resources and experiences. Throughout the episode, listeners will gain insight into the realities of parenting a child with intellectual and developmental disabilities, including the hurdles of securing appropriate educational and therapeutic support.The conversation delves into the significance of storytelling and lived experiences in fostering empathy and understanding within communities. Wendy emphasizes the need for honest discussions about the challenges faced by families and how these narratives can drive change in support systems.As Wendy reflects on her podcast, she shares her vision for cultivating a community where families feel seen, heard, and supported. This episode is a must-listen for anyone interested in advocacy, parenting, and the power of shared experiences.What You'll Learn in This Episode:- The journey of parenting a child with autism and the impact on family dynamics- Strategies for navigating educational and support systems- The importance of community and connection among parents- How storytelling can foster empathy and drive change- Insights into future trends in support systems for individuals with disabilitiesFor more information on Wendy Ernzen and her podcast, visit letsplanthouses.com and connect with her on LinkedIn.Support the show

✨ "I believe that in our ancestry we were equestrians, and that's why it's connected so hard with my family." – Louis HookFor 35 years, the Compton Cowboys mission has run a self-development program in Compton, California, that leverages horses to help kids grow into upstanding young men and women — serving roughly 30 kids a year. Founding member Louis Hook and HeartMath practitioner Kansas Carradine, who has worked alongside the organization for years, join Rupert Isaacson to talk about the mission's history and how it works today.What started when Louis's sister Maisha Akbar moved to Compton's Richland Farms neighborhood in 1988 has grown into a four-track program covering horsemanship, equine science, farming, and self-development. Kansas brings the science side of the conversation, explaining how heart rate variability and heart coherence research from the HeartMath Institute is being used to help kids and horses regulate together.The conversation ranges from the history of West African cavalry culture and Mansa Musa to the concept of epigenetic and intergenerational trauma, and what Louis calls "Shadow PTSD" in kids growing up in high-violence neighborhoods. It's a wide-ranging discussion about ancestry, the funding challenges facing Black equestrian nonprofits, and why reconnecting to the history of Black horsemanship matters for healing.If you want to support the show, you can do so at Patreon: https://www.patreon.com/LongRideHome

3 Days of Emuna - Maintaining Emuna with My Profoundly Special Needs Son - Rabbi Jablon by Shapell's Rabbeim

In this episode of A Tale of Two Hygienists, Jessica and Dave welcome Candi Kidd, RDH, BSDH, MEd, to discuss the unique challenges patients with special healthcare needs face when accessing oral healthcare. From medically complex and tube-fed patients to collaborating with caregivers and healthcare teams, Candi shares practical strategies for creating more inclusive, compassionate, and effective dental experiences. This conversation challenges clinicians to rethink accessibility, advocacy, and the future of patient-centered care.   In this episode, we discuss:   Common barriers to oral healthcare for patients with special healthcare needs   Oral health considerations for medically complex and tube-fed patients   Collaborating with caregivers and interdisciplinary healthcare teams   Adapting preventive, therapeutic, and educational approaches   Creating more inclusive and compassionate dental experiences   The role of advocacy in improving access to care   Practical strategies clinicians can implement immediately   Where dental education and healthcare systems can continue to improve   Connect with Candi Kidd:   Email: candicea31@gmail.com Instagram: @the.sunnysister   Connect with the Hosts:   Jessica Atkinson: jatkinson@endeavorb2b.com Dave Torres: dtorres@endeavorb2b.com

LETS PLAY TWO On this new episode of LIVE FROM MY OFFICE it's the rare doubleheader of guests.First up is Josh Soloman from The Empty Pockets band.They are GREAT and we talk about their new album recorded at the legendary Abbey Road studios in London.We also hit the big benefit concert for WILLS PLACE an amazing, inspiring, diner employing Special Needs adults.Then part two features Jared Burton and his dad, Keith.They're back to talk about addiction, recovery, and sober living.They have good news about what NARCAN can do on this special episode. Thanks for listening. SHOW NOTEScochranshow.comtheemptypockets.comSerenity HouseGet the book "Shadows of Sobriety" by Keith Burton on AMAZON Thanks to our sponsor, ABT Electronics. Get $25 off your next purchase of $150 or more by using the promo code COCHRAN2025 online or in person!Watch This Episode on our Live From My Office YouTube ChannelCheck out what I'm doing with my friends at Real American MediaFollow me on Substack.With each new episode, the first three listeners thatemail me“SURVIVE 2025!” will be eligible to win a $25 ABT Giftcard as long as you include your mailing address and that phrase!Don't forget to subscribe to listen to “Live From My Office” wherever you get your podcasts, and e-mail the show with any questions, comments, or plugs for your favorite charity!

In this episode of A Tale of Two Hygienists, Jessica and Dave welcome Candi Kidd, RDH, BSDH, MEd, to discuss the unique challenges patients with special healthcare needs face when accessing oral healthcare. From medically complex and tube-fed patients to collaborating with caregivers and healthcare teams, Candi shares practical strategies for creating more inclusive, compassionate, and effective dental experiences. This conversation challenges clinicians to rethink accessibility, advocacy, and the future of patient-centered care.   In this episode, we discuss:   Common barriers to oral healthcare for patients with special healthcare needs   Oral health considerations for medically complex and tube-fed patients   Collaborating with caregivers and interdisciplinary healthcare teams   Adapting preventive, therapeutic, and educational approaches   Creating more inclusive and compassionate dental experiences   The role of advocacy in improving access to care   Practical strategies clinicians can implement immediately   Where dental education and healthcare systems can continue to improve   Connect with Candi Kidd:   Email: candicea31@gmail.com Instagram: @the.sunnysister   Connect with the Hosts:   Jessica Atkinson: jatkinson@endeavorb2b.com Dave Torres: dtorres@endeavorb2b.com

In this episode of The Best Dam Podcast, Jill sits down with the Magon and Shawn Peuker, the strategic masterminds behind The Rae of Hope Foundation. Together, unpack the world of nonprofit advocacy and explore how a basic plan of infrastructure and personal persistence can transform a chaotic, high-stress environment into a highly manageable roadmap for bringing next-generation support and community to special needs families.The discussion dives deep into the high-stakes world of modern nonprofit operations—from turning a personal 10-year passion project inspired by their resilient daughter Raelynn into a fully realized foundation to adapting to massive operational changes like expanding from a single recipient model to serving multiple beneficiaries across Southern Nevada. Magon and Shawn also break down the eye-opening results of their unique community-building methods, sharing how they balance customized care packages and personal vetting with helping beloved local families thrive right here in Boulder City and beyond.DISCUSSIONThe Evolution from a Personal Dream to a Growing Network: Magon explains how a deep passion born out of navigating their daughter's seven strokes quickly scaled from a 10-year vision into a fully realized, multi-beneficiary network built to safely meet the region's growing support demands.The Core Philosophy of Structural Inclusion: Rather than allowing rigid age limits or condition criteria to disrupt a family's access to help, the foundation operates on a strict blueprint of open qualifications, allowing families dealing with any physical or mental needs to establish a foundational sense of stability.The Funding and Seed Money Advantage: Drawing on their extensive background managing family resources, Magon and Shawn bring a deep understanding of financial commitment to their daily operations, and establish the foundation before community events dramatically scale their capabilities.The Vetted Family Reality Check: Shawn highlights how connecting with a client's real-world environment dictates successful care package distribution and long-term interaction.Integrating Custom Care Packages and Commerce: To break down financial barriers, Shawn shareas how their digital store allows donors to purchase merchandise or actively sponsor a child's customized monthly supplies to improve efficiency.The Structured Lifelong Connection Routine: The foundation facilitates a strict cyclical routine of keeping beneficiaries connected to all future social gatherings and community events.The Mentorship Power of the Parent Network: Magon points out a heartwarming shift in company dynamics where experienced special needs parents naturally step in to teach, share trusted medical resources, and resolve complex care issues for new families in a real-world environment.High-Stress Rehabilitation via Healthcare Guidance: For overwhelmed families who cannot safely access clear guidance or handle complex insurance systems immediately after a diagnosis, Shawn and Magon implement specialized peer advocacy to effectively redirect parental energy into productive, stabilizing focus.The Light-Hearted Sense of Humor Standard: To ensure every family dynamic remains healthy and completely resilient, the household conducts an unfiltered routine of inside jokes and shared laughter, figuring out that embracing funny moments establishes a positive path toward overall family health.Collaborative Main Street Alliances: Emphasizing that there is no true competition when supporting local development, Magon highlights her seamless, on-the-ground collaborations with neighboring businesses like Celeste from Lady Lux Cleaning to orchestrate large-scale regional initiatives.The Unbeatable Value of Community Trust: Jill, Magon, and Shawn highlight how vital earning and maintaining the trust of devoted subscribers and local donors is to the community, reinforcing that when individual local organizations adapt and support one another, the entire town elevates together.LEARN MOREThe Rae of Hope Foundation: Explore their full lineup of customized care packages, beneficiary sign-up forms, and online merchandise donation options. https://raeofhopefoundation.org/Boulder City Chamber of Commerce: Head over to the Chamber website or stop by the office to discover how joining the local network can help jumpstart your business marketing and connect you with trusted industry experts. https://www.bouldercitychamber.com/RAE OF HOPE FUNDRAISING EVENTSBoulder City Community Garage Sale, July 17-19Southwest Diner Fundraiser for The Rae of Hope Foundation, July 25 at the Southwest DinerCraisy Daisy Fall Market, September 11-12, 10am-6pmFirst Annual Rae of Hope Benefit Dinner at the Boulder Creek Golf Club Pavilion, October 9, 2026https://raeofhopefoundation.org/upcoming-eventsKEYWORDSMagon Peuker, Shawn Peuker, The Rae of Hope Foundation, Special Needs Advocacy, Nonprofit Operations, Community Care Packages, Family Support Networks, Boulder City Chamber of Commerce, The Best Dam Podcast, Podcast Interview#MagonPeuker #ShawnPeuker #RaeOfHopeFoundation #SpecialNeedsSupport #NonprofitAdvocacy #BoulderCityCommunity #SmallBusinessAlliances #TheBestDamPodcast #PodcastInterview

Fabian Picardo was in Parliament today giving what will be his final budget address as Chief Minister. We discussed some of the highlights from the morning session as he outlined the government's spending plans against the backdrop of the UK/EU treaty, which will be signed next Tuesday in Brussels.Disability Pride month is celebrated in July, Donovan Galia and Jenny Victory of the Special Needs and Disability Office will tell us about the work being done to promote inclusion and equity on the RockAnd members of the Youth Service have been honing their skills both behind and in front of the camera, the Youth Service has been providing media production training and experience, we'll find out how that's been going. Hosted on Acast. See acast.com/privacy for more information.

A tragic accident has raised questions after a 10-year-old boy attending a special needs school in Komatsu City went missing during class and was later found dead in a nearby waterfall. According to the school, the boy had a relatively mild disability and had no difficulty communicating. However, three years ago he had left the school building through the main entrance on his own. Since then, the school said it had strengthened supervision of students and ensured that doors remained locked. Episode notes: ‘Boy, 10, dies after disappearing from Ishikawa special needs school': https://barrierfreejapan.com/2026/07/04/boy-10-dies-after-disappearing-from-ishikawa-special-needs-school/

Hey friend,  Have you ever felt a wave of sadness or loss about your parenting experience that you couldn't explain — and then immediately felt guilty for feeling it? Do you love your kid completely and still sometimes grieve the summer, the milestones, or the parenting experience you thought you'd have? Has scrolling through other families' photos ever left you with a feeling you couldn't quite name? I'm Ashley — a mom living with chronic illness in a neurodivergent family. If you're dealing with constant fatigue, brain fog, inflammation, and broken sleep while trying to keep up with your kids, you're not alone. Chronic Illness Moms is a podcast for moms with chronic illness or chronic symptoms who want stress relief, better sleep, and simple, realistic habits that actually work inside a full, demanding life. In this episode, I'm naming the grief that doesn't get a funeral — the loss of the parenting experience you imagined before any diagnosis was part of the picture. This is the heaviest episode of June and one I think a lot of us have been waiting for someone to say out loud. Grief and gratitude can exist at the same time, and this episode gives you permission to feel both.   Part 3: Resources and Links Mentioned 1:1 chronic health coaching: https://ashleybraden.com/coaching Join the free Chronic Health Moms Facebook community: https://www.facebook.com/groups/chronichealthmoms Hearthwell Naturals magnesium cream (mentioned for bedtime wind-down): https://payhip.com/hearthwellnaturals   Related Episodes: 222. Survival Mode Was Never Meant to Be Permanent: The Truth About Chronic Stress and Burnout No One Tells Exhausted Moms 219. Feeling Overwhelmed by Your Child's Emotions? This is Why   Connect with Me: Contact → hello@ashleybraden.com Facebook Page → https://www.facebook.com/chronicillnessmoms Facebook Group → https://www.facebook.com/groups/chronichealthmoms Instagram → https://www.instagram.com/chronicillnessmoms YouTube → https://bit.ly/chronicillnessyoutube

Are you a caregiver running on absolute empty, or a parent walking through a season of loss that feels completely colorless? Join Nancy Sabato as she sits down with author Paula Romang (Thriving in a Barren Place) for a raw, honest look at the trials of raising a child with severe disabilities and surviving deep grief. Paula opens up about the spiritual struggle of wondering if your trials are a punishment, the exhaustion of constant medical schedules, and how she found a solid bedrock beneath her feet when her world collapsed. Don't give up in the dark—tune in to find a friend who truly understands the long, hard road. www.paularomang.com"He heals the brokenhearted and binds up their wounds." — Psalm 147:3www.thecallwithnancysabato.com

In this episode of This is Yoga Therapy, host Michele Lawrence sits down with Renata Sumar Gaertner, C-IAYT, the director and lead teacher of Yoga for All Abilities, carrying forward her mother's legendary Sonia Sumar Method.Renata began her yoga journey at just three years old and completed her first Hatha training at twelve. Raised alongside her sister, Roberta, who was born with Down Syndrome, Renata witnessed firsthand the profound developmental power of an individualized practice. Bridging her lifelong lineage roots with a degree in Speech Therapy and a postgraduate specialization in Language Disorders, Renata has dedicated her life to making yoga accessible and empowering for individuals with disabilities, neurodiversity, and additional needs.In this conversation, we explore:The Myth of the Standard Template: Shifting away from a "one-size-fits-all" approach to physical alignment and defining what personal alignment truly means for a student's physiological safety and growth.The Neurobiology of Development: The reality of what happens when individuals navigating Down Syndrome, cerebral palsy, or autism practice a structured, individualized yoga protocol.Establishing Nervous System Safety: How practitioners and parents can use breath, vocal resonance, and deep attention to build baseline safety for children with severe sensory processing challenges or communication barriers.Moving from Fear to Service: Shifting our mindset out of intimidation when working with complex additional needs and stepping into heart-centered, professional care.ResourcesLearn more about Renata's work & global trainings: Visit SpecialYoga.com to explore Part 1 and Part 2 certification pathways, continuing education modules, and private mentoring support.Support the showConnect with Inner Peace Yoga TherapyEmail us: info@innerpeaceyogatherapy.comWebsiteInstagramFacebook

Guest: Marina Giblin, Senior Portfolio Manager

ITP 150 - Christian's story highlights both the opportunity and the complexity of international teaching. Now based in Singapore, he reflects on a career that began in North Carolina and expanded into leading international schools in Shanghai, Hong Kong, and Singapore. What starts as a conversation about getting into international education quickly becomes a thoughtful look at why teaching abroad remains a hidden pathway for so many educators, even as the world of international schools continues to grow.A major focus of the conversation is learning support in international schools and the uneven reality of inclusive education abroad. Christian shares what it looks like to work in special education overseas, explaining how schools differ in their ability to support students with ADHD, autism, and other neurodiverse learning needs. The discussion also unpacks the important distinction between learning support and language support, while exploring how more schools are being pushed to adapt as student needs become more visible and more widely understood.The episode becomes especially powerful as Christian speaks about life as a single father overseas raising a son with autism. He describes adopting his son in Hong Kong, recognizing early developmental differences, and facing the difficult reality that many international schools still cannot support children with moderate to severe special needs. His work creating a resource list for families searching for more inclusive schools adds a practical and hopeful dimension to the conversation, especially for international teachers with children who may feel their options are limited.-more information-The International Teacher Podcast is a bi-weekly discussion with experts in international education. New Teachers, burned out local teachers, local School Leaders, International school Leadership, current Overseas Teachers, and everyone interested in international schools can benefit from hearing stories and advice about living and teaching overseas.Additional Gems Related to Our Show:Greg's Favorite Video From Living Overseas - ⁠https://www.youtube.com/watch?v=UQWKBwzF-hw⁠Signup to be our guest  ⁠https://calendly.com/itpexpat/itp-interview?month=2025-01⁠Our Website⁠ -  ⁠https://www.itpexpat.com/⁠Our FaceBook Group - ⁠https://www.facebook.com/groups/itpexpat⁠⁠JPMint Consulting Website  - ⁠https://www.jpmintconsulting.com/⁠Hannah's Personal IG - https://www.instagram.com/thatexpatfamily?utm_source=ig_web_button_share_sheet&igsh=ZDNlZDc0MzIxNw=Greg's Personal YouTube Channel: ⁠https://www.youtube.com/playlist?list=PLs1B3Wc0wm6DR_99OS5SyzvuzENc-bBdO⁠Books (on Amazon) By Gregory Lemoine:Stay for the Show (2026) | Greg's first Childrens Picture Book⁠International Teacher Guide: Finding the "Right Fit" 2nd Edition (2025)⁠ | by Gregory Lemoine M.Ed.⁠⁠"International Teaching: The Best-kept Secret in Education"⁠⁠ | by Gregory Lemoine M.Ed.Apps by Greg:https://apps.apple.com/app/6755244840  1. Who's That? Name & Face Trainer  Nov 21, 2025https://apps.apple.com/app/6756509803   2. Facetag | Memory Trainer   Dec 16, 2025

Novelist, Ian Rankin talks to Brendan about the story of his life through the prism of five songs that have a special meaning for him. He talks about his son who lives with Angelman's Syndrome, why he's glad he wasn't an overnight success story and the complex life of a writer being so absorbed in another fictional world.

Race Week in Frankfurt – und Jan Stratmann ist zurück im Triathlon-Chat. Nach zwei Infekten, abgesagtem Kraichgau-Start und einer alles andere als ruhigen Vorbereitung spricht Jan mit Nick und Nils über seine letzten Wochen vor dem Ironman Frankfurt, den Formaufbau nach der Krankheit und warum der unfreiwillige Break vielleicht sogar genau richtig kam. Im Fokus steht natürlich die erwartete Hitzeschlacht: 37 Grad, heißer Asphalt, warmes Wasser und die Frage, wie man bei solchen Bedingungen überhaupt noch klug raced. Es geht um Kühlstrategien, Verpflegung, Stirnband vs. Cap, Special Needs, Hitzeanpassung in der Race Week – und warum Körpergefühl am Ende wichtiger sein kann als jede Pace-Vorgabe. Außerdem diskutieren die drei das starke Profi-Feld in Frankfurt, Kona-Slots, Renntaktik und Jans klare Haltung: Nicht einfach safe qualifizieren, sondern vorne mitracen. Dazu gibt's Stratis Schwimmphilosophie mit viel „stumpf ist Trumpf“, lange Serien, ehrliches Training und natürlich ein bisschen Race-Week-Chaos inklusive Kettenwachs-Odyssee. Werbung: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠PUSHING LIMITS CLUB⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Deine All-in-One Trainingsapp für Triathlon, Radfahren und mehr! Alles, was du für dein Training brauchst – immer griffbereit.

There’s a question that lives in the back of the mind of nearly every parent raising a child with special needs. It doesn’t announce itself — it just sits there, quiet and heavy. What happens to my child when I am no longer here? For a long time, that question had no good answer. Families navigated a maze of government benefits, legal documents, and financial systems — often alone, guided by well-meaning professionals who didn’t have the depth of specialization this work demands. In 2005, a financial planner from Charlotte decided that wasn’t good enough. Ryan F. Platt founded A Special Needs Plan with one mission: to serve families living with that fear and replace it with clarity, structure, and a road map forward. Today, the firm is an elite, nationally recognized practice serving families across the country. Ryan holds credentials most financial advisors have never heard of — including the Chartered Special Needs Consultant designation — because he believes this community deserves a true specialist. He’s a former president of The Arc of North Carolina, a speaker at national conferences, a published author, and a champion for families who have spent too long facing the impossible alone. Ryan, welcome to The BrandBuilders Podcast.

Russell Craig is a celebrated visual artist now based between Philadelphia, New York, and Wellington, Florida, who grew up in the foster care system from age five and spent a total of twelve years in the Pennsylvania prison system before building an art career that has taken him from a mural on the African American Museum in Philadelphia to the White House, the Democratic National Convention, and museum collections around the country.What makes Russell's story so striking is how directly his lived experience speaks to the populations equine-assisted practitioners are trying to serve — kids in foster care, people coming out of incarceration, and anyone navigating systems that were never built with their wellbeing in mind. He found his way through art, using it inside prison as both an escape and, eventually, as a plan for life after release.In this conversation, Russell and Rupert dig into what a horse-based program for foster kids and formerly incarcerated people would actually need to work — structure, mentorship, hands-on care, transportation, funding, and a real sense of separation from old environments — as well as the deeper parallels Russell sees between horses and his own experience of captivity and freedom.If you want to support the show, you can do so at Patreon: https://www.patreon.com/LongRideHome✨ "When it's built on good structure, it will stand." – Russell Craig

Emily Loftiss thought she knew what motherhood would look like... until her son Dalton was diagnosed with autism at 2.5 years old. In this deeply honest conversation, Emily shares the emotional journey of raising a nonverbal autistic child, the hardest moments after his diagnosis, how she and her husband have navigated the unknown together, and why she refuses to give up hope. She also opens up about finding joy in the middle of heartbreak, celebrating every small victory, and the advice every parent, whether raising a neurotypical or neurodivergent child, needs to hear. Thank you for supporting our sponsors!BabyGang is presented by Better Help. Sign up and get 10% off at https://BetterHelp.com/BABYGANGSkylight Frames: Go to https://MySkylight.com/BABYGANG for $30 off your 15-inch Calendar.HERS: Ready to reach your goals? Visit https://forhers.com/babygang to get personalized, affordable care that gets you.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Send us Fan MailSend us Fan MailIn this inspiring episode of Living the Dream with Curveball, we welcome Samantha Taylor, a passionate speech language pathologist, entrepreneur, and founder of Olive Speech Therapy. Samantha's journey took an unexpected turn at the age of 20 when she faced the heartbreaking loss of her son. This profound experience ignited her mission to advocate for children with communication challenges and empower families navigating complex systems.Samantha shares her personal story of transformation, detailing how the struggles of being a young mother to a profoundly deaf child propelled her into the field of speech language pathology. She discusses the importance of knowledge, advocacy, and the need for parents to trust their instincts when it comes to their children's health and education. Samantha emphasizes the significance of community support and how her experiences have shaped her approach to helping others.Listeners will gain valuable insights into the challenges parents face in advocating for their children, the founding of Olive Speech Therapy, and the creation of the Empowered Parent Network—a resource designed to provide confidence and support for parents of children with unique needs. Samantha's dedication to her work and her son shines through, reminding us all that every challenge can lead to unexpected opportunities for growth and connection.What You'll Learn in This Episode:- The impact of Samantha's personal experiences on her professional journey- Strategies for parents to advocate effectively for their children- The importance of community and shared experiences in parenting- Insights into the Empowered Parent Network and its mission- Tips for navigating the education and healthcare systems with confidenceFor more information on Samantha Taylor and her work, follow her on Instagram at @ParenthoodUnscripted and @OliveSpeechTherapy, and check out her new podcast, *Parenthood Unscripted*, for more empowering conversations.Support the show

On this episode of The Federalist Radio Hour, Ryan Bomberger, co-founder of The Radiance Foundation and Emmy Award-winning creative professional, joins Federalist Senior Elections Correspondent Matt Kittle to share his story as a son spared from abortion and saved by adoption. Bomberger also analyzes how abortion ideology and the death culture that promotes it have infiltrated American institutions. You can find Bomberger's memoir Should Have Been Aborted here. The Federalist Foundation is a nonprofit, and we depend entirely on our listeners and readers — not corporations. If you value fearless, independent journalism, please consider a tax-deductible gift today at TheFederalist.com/donate. Your support keeps us going.

Chalee and Chelsea are back to discuss current events from the beginning of summer.  We also discuss a couple of controversial cultural trends: boys are arguing less with their parents and young dads are dressing up as women for their daughters.  Please join us. 

In this episode of the TMA Connection, Tim sits down with Laura Weinstein, Chief Development Officer of the Harford Center, to highlight an incredible local nonprofit that has been championing abilities and enriching lives right here in Harford County since 1961. Shifting from her early career intentions in therapy to spending the last two decades dedicated to supporting individuals with developmental and intellectual disabilities, Laura shares the immense power of moving past clinical paperwork to build genuine, human-to-human connections. The conversation breaks down the critical realities adults face when aging out of the school system, the mechanics of managing highly individualized day habilitation and job-skill programs, and the massive financial hurdle placed on families when their child turns 21. Subscribe to The TMA Connection on your favorite podcast platform or watch the full episode on YouTube by searching "The TMA Connection." Don't forget to like, comment, and share — your support keeps the conversation growing!

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Attorney Whitney Knox Lee. Explains practical estate‑planning strategies—wills, trusts, powers of attorney—and how entrepreneurs, families, and especially parents of disabled children can protect assets, avoid costly probate, and maintain eligibility for critical benefits. The conversation also touches on integrating insurance with estate planning, small‑business contingency planning, and Lee’s personal mission and background in civil rights work. Purpose of the Interview Educate listeners on estate planning as a wealth‑preservation strategy (not just documents)—to reduce court costs, taxes, and confusion for families. Clarify the differences and roles of wills, trusts, and powers of attorney, including when each is appropriate and how they work together.] Highlight special considerations for entrepreneurs and families with disabled children or aging relatives, including insurance, operating agreements, and special‑needs planning. Share Lee’s values and practice approach, including culturally responsive service and sustainable advocacy rooted in prior civil‑rights work. Key Takeaways 1) Wills vs. Trusts vs. Powers of Attorney A will is not the plan—it’s just one piece and still goes through probate, which can be slow and expensive; think of a will as a “letter to the judge.] Revocable living trusts can help families bypass probate, reduce delays, and retain more control over how assets are managed after death. Powers of attorney (financial and health) are essential for incapacity scenarios; even 18‑year‑olds heading to college should have them so parents can access information if needed. 2) Why Insurance Belongs in the Plan Life insurance can protect the family’s ability to keep the home by paying off a remaining mortgage or covering living expenses—turning an asset into a sustainable legacy rather than a burden. For entrepreneurs, key‑person insurance can replace income when the owner can’t work, keeping the business afloat. 3) Minimizing Probate Costs and Taxes Probate involves court filings and legal fees; in some states fees scale with estate size (example discussed: percentage‑based fees in other jurisdictions), which can significantly erode wealth passed to heirs. Proper planning reduces those leakages. 4) Special‑Needs and Elder Planning Parents of children on need‑based benefits (e.g., Medicaid) must avoid transfers that jeopardize eligibility; the right trust structures preserve benefits while providing support. Elder law planning anticipates long‑term care costs (nursing home, assisted living, in‑home care) so families don’t have to deplete assets later. 5) Business Continuity for Owners Establish operating agreements and buy‑sell agreements that spell out who runs the business if the principal is incapacitated; pair with business powers of attorney. 6) Values, Audience, and Access Lee intentionally centers Black and Brown women and their families, grounding services in community uplift and transparent referrals to trusted financial pros (no paid referral arrangements). Contact approach: 15‑minute intake, then a four‑meeting process (legacy planning → design → review → signing). Notable Quotes (for pull‑quotes & captions) “Think of a will as a letter to the judge… a will still has to go through probate court. “A trust allows families to bypass probate altogether so they aren’t paying legal fees or leaving things to people who want to challenge the will. “Life insurance is a huge tool—it can help the family pay off the mortgage so they can keep the home and the equity.” “Estate planning is a strategy—not just documents.” “Even 18‑year‑olds should have powers of attorney—parents can’t just call doctors once kids are legal adults.” “I stay in my lane—I’m an attorney. I work closely with trusted financial professionals and make non‑compensated referrals.” “For special‑needs planning, don’t jeopardize need‑based benefits—use the right trust so support continues. “I want to build a sustainable practice that lets me serve my community and rest well, aligned with my family and values.” Quick Action Items (for listeners inspired by the episode) Draft or update POAs (financial and health) for every adult in the household, including college‑age children. Evaluate whether a revocable living trust makes sense to avoid probate and retain post‑death control. For business owners: review operating agreement / buy‑sell, add key‑person insurance, and create a business POA. Families with special‑needs dependents: consult on special‑needs trusts to protect benefits. #SHMS #STRAW #BESTSee omnystudio.com/listener for privacy information.

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Attorney Whitney Knox Lee. Explains practical estate‑planning strategies—wills, trusts, powers of attorney—and how entrepreneurs, families, and especially parents of disabled children can protect assets, avoid costly probate, and maintain eligibility for critical benefits. The conversation also touches on integrating insurance with estate planning, small‑business contingency planning, and Lee’s personal mission and background in civil rights work. Purpose of the Interview Educate listeners on estate planning as a wealth‑preservation strategy (not just documents)—to reduce court costs, taxes, and confusion for families. Clarify the differences and roles of wills, trusts, and powers of attorney, including when each is appropriate and how they work together.] Highlight special considerations for entrepreneurs and families with disabled children or aging relatives, including insurance, operating agreements, and special‑needs planning. Share Lee’s values and practice approach, including culturally responsive service and sustainable advocacy rooted in prior civil‑rights work. Key Takeaways 1) Wills vs. Trusts vs. Powers of Attorney A will is not the plan—it’s just one piece and still goes through probate, which can be slow and expensive; think of a will as a “letter to the judge.] Revocable living trusts can help families bypass probate, reduce delays, and retain more control over how assets are managed after death. Powers of attorney (financial and health) are essential for incapacity scenarios; even 18‑year‑olds heading to college should have them so parents can access information if needed. 2) Why Insurance Belongs in the Plan Life insurance can protect the family’s ability to keep the home by paying off a remaining mortgage or covering living expenses—turning an asset into a sustainable legacy rather than a burden. For entrepreneurs, key‑person insurance can replace income when the owner can’t work, keeping the business afloat. 3) Minimizing Probate Costs and Taxes Probate involves court filings and legal fees; in some states fees scale with estate size (example discussed: percentage‑based fees in other jurisdictions), which can significantly erode wealth passed to heirs. Proper planning reduces those leakages. 4) Special‑Needs and Elder Planning Parents of children on need‑based benefits (e.g., Medicaid) must avoid transfers that jeopardize eligibility; the right trust structures preserve benefits while providing support. Elder law planning anticipates long‑term care costs (nursing home, assisted living, in‑home care) so families don’t have to deplete assets later. 5) Business Continuity for Owners Establish operating agreements and buy‑sell agreements that spell out who runs the business if the principal is incapacitated; pair with business powers of attorney. 6) Values, Audience, and Access Lee intentionally centers Black and Brown women and their families, grounding services in community uplift and transparent referrals to trusted financial pros (no paid referral arrangements). Contact approach: 15‑minute intake, then a four‑meeting process (legacy planning → design → review → signing). Notable Quotes (for pull‑quotes & captions) “Think of a will as a letter to the judge… a will still has to go through probate court. “A trust allows families to bypass probate altogether so they aren’t paying legal fees or leaving things to people who want to challenge the will. “Life insurance is a huge tool—it can help the family pay off the mortgage so they can keep the home and the equity.” “Estate planning is a strategy—not just documents.” “Even 18‑year‑olds should have powers of attorney—parents can’t just call doctors once kids are legal adults.” “I stay in my lane—I’m an attorney. I work closely with trusted financial professionals and make non‑compensated referrals.” “For special‑needs planning, don’t jeopardize need‑based benefits—use the right trust so support continues. “I want to build a sustainable practice that lets me serve my community and rest well, aligned with my family and values.” Quick Action Items (for listeners inspired by the episode) Draft or update POAs (financial and health) for every adult in the household, including college‑age children. Evaluate whether a revocable living trust makes sense to avoid probate and retain post‑death control. For business owners: review operating agreement / buy‑sell, add key‑person insurance, and create a business POA. Families with special‑needs dependents: consult on special‑needs trusts to protect benefits. #SHMS #STRAW #BESTSteve Harvey Morning Show Online: http://www.steveharveyfm.com/See omnystudio.com/listener for privacy information.

✨ "They come in with a cane and feeling disabled, and then they say, 'Here, take the cane, honey. I'm gonna walk this horse.' We've seen this so many times we can't even number it." – Nancy Schier AnzelmoDescription Paula Hertel and Nancy Schier Anzelmo are the co-founders of Connected Horse, a California-based program that brings equine-assisted experiences to older adults living with dementia or memory loss — alongside their care partners. Backed by research conducted with Stanford University and UC Davis, Connected Horse is one of the first programs in the country to specifically serve this population in this way. Kansas Carradine, HeartMath-certified trainer and returning EAW guest, joins to explore the science of heart coherence, entrainment, and why horses may be uniquely suited to reach people that other approaches cannot.Connected Horse's work challenges the assumption that equine-assisted services are only for children or younger adults. Their Stanford and UC Davis pilot studies recorded statistically significant reductions in depression, anxiety, and caregiver burden — with 100% participant return rates at a six-month booster session. Participants regularly go from fearful and withdrawn to walking horses, speaking in full sentences, and feeling activated to change their lives. The program is designed to be failure-free: for the person with the diagnosis, for the care partner, and for the horses.In this episode, Rupert, Paula, Nancy, and Kansas explore the physiology behind what happens when a person leans their heart against a horse's neck, why dementia and autism require similar practitioner responses around pacing and unconditional presence, what ritual and ceremony have to do with cortisol regulation, and how social prescribing may bring programs like Connected Horse into mainstream healthcare. If you want to support the show, you can do so at Patreon: https://www.patreon.com/LongRideHomeIf you want to support the show, you can do so at Patreon: https://www.patreon.com/LongRideHome

Lisa Richer is a certified Neurodiversity Consultant and founder of Journey 2 Bloom. As a former elite athlete and mom of two neurodivergent boys, she brings a rare combination of lived experience and professional expertise to the families she works with. Lisa helps parents and educators stop trying to fit their kids into systems that weren't built for them — and start building environments where neurodivergent athletes can actually thrive. Her work centers on three things: understanding how each child is wired, building on their strengths, and giving them the clarity and confidence to find their own path. In this episode, Lisa shares her personal journey, practical strategies for supporting neurodivergent young athletes, and what parents can do right now to stop feeling stuck and start showing up differently for their kids. Connect with Lisa Richer  Journey2Bloom: journey2bloom.com & @journey2bloom LinkedIn Lisa Richer If today's conversation resonated, I will send one idea every Friday for sports parents.  Subscribe at hernanchousa.com

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Attorney Whitney Knox Lee. Explains practical estate‑planning strategies—wills, trusts, powers of attorney—and how entrepreneurs, families, and especially parents of disabled children can protect assets, avoid costly probate, and maintain eligibility for critical benefits. The conversation also touches on integrating insurance with estate planning, small‑business contingency planning, and Lee’s personal mission and background in civil rights work. Purpose of the Interview Educate listeners on estate planning as a wealth‑preservation strategy (not just documents)—to reduce court costs, taxes, and confusion for families. Clarify the differences and roles of wills, trusts, and powers of attorney, including when each is appropriate and how they work together.] Highlight special considerations for entrepreneurs and families with disabled children or aging relatives, including insurance, operating agreements, and special‑needs planning. Share Lee’s values and practice approach, including culturally responsive service and sustainable advocacy rooted in prior civil‑rights work. Key Takeaways 1) Wills vs. Trusts vs. Powers of Attorney A will is not the plan—it’s just one piece and still goes through probate, which can be slow and expensive; think of a will as a “letter to the judge.] Revocable living trusts can help families bypass probate, reduce delays, and retain more control over how assets are managed after death. Powers of attorney (financial and health) are essential for incapacity scenarios; even 18‑year‑olds heading to college should have them so parents can access information if needed. 2) Why Insurance Belongs in the Plan Life insurance can protect the family’s ability to keep the home by paying off a remaining mortgage or covering living expenses—turning an asset into a sustainable legacy rather than a burden. For entrepreneurs, key‑person insurance can replace income when the owner can’t work, keeping the business afloat. 3) Minimizing Probate Costs and Taxes Probate involves court filings and legal fees; in some states fees scale with estate size (example discussed: percentage‑based fees in other jurisdictions), which can significantly erode wealth passed to heirs. Proper planning reduces those leakages. 4) Special‑Needs and Elder Planning Parents of children on need‑based benefits (e.g., Medicaid) must avoid transfers that jeopardize eligibility; the right trust structures preserve benefits while providing support. Elder law planning anticipates long‑term care costs (nursing home, assisted living, in‑home care) so families don’t have to deplete assets later. 5) Business Continuity for Owners Establish operating agreements and buy‑sell agreements that spell out who runs the business if the principal is incapacitated; pair with business powers of attorney. 6) Values, Audience, and Access Lee intentionally centers Black and Brown women and their families, grounding services in community uplift and transparent referrals to trusted financial pros (no paid referral arrangements). Contact approach: 15‑minute intake, then a four‑meeting process (legacy planning → design → review → signing). Notable Quotes (for pull‑quotes & captions) “Think of a will as a letter to the judge… a will still has to go through probate court. “A trust allows families to bypass probate altogether so they aren’t paying legal fees or leaving things to people who want to challenge the will. “Life insurance is a huge tool—it can help the family pay off the mortgage so they can keep the home and the equity.” “Estate planning is a strategy—not just documents.” “Even 18‑year‑olds should have powers of attorney—parents can’t just call doctors once kids are legal adults.” “I stay in my lane—I’m an attorney. I work closely with trusted financial professionals and make non‑compensated referrals.” “For special‑needs planning, don’t jeopardize need‑based benefits—use the right trust so support continues. “I want to build a sustainable practice that lets me serve my community and rest well, aligned with my family and values.” Quick Action Items (for listeners inspired by the episode) Draft or update POAs (financial and health) for every adult in the household, including college‑age children. Evaluate whether a revocable living trust makes sense to avoid probate and retain post‑death control. For business owners: review operating agreement / buy‑sell, add key‑person insurance, and create a business POA. Families with special‑needs dependents: consult on special‑needs trusts to protect benefits. #SHMS #STRAW #BESTSupport the show: https://www.steveharveyfm.com/See omnystudio.com/listener for privacy information.

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Attorney Whitney Knox Lee. Explains practical estate‑planning strategies—wills, trusts, powers of attorney—and how entrepreneurs, families, and especially parents of disabled children can protect assets, avoid costly probate, and maintain eligibility for critical benefits. The conversation also touches on integrating insurance with estate planning, small‑business contingency planning, and Lee’s personal mission and background in civil rights work. Purpose of the Interview Educate listeners on estate planning as a wealth‑preservation strategy (not just documents)—to reduce court costs, taxes, and confusion for families. Clarify the differences and roles of wills, trusts, and powers of attorney, including when each is appropriate and how they work together.] Highlight special considerations for entrepreneurs and families with disabled children or aging relatives, including insurance, operating agreements, and special‑needs planning. Share Lee’s values and practice approach, including culturally responsive service and sustainable advocacy rooted in prior civil‑rights work. Key Takeaways 1) Wills vs. Trusts vs. Powers of Attorney A will is not the plan—it’s just one piece and still goes through probate, which can be slow and expensive; think of a will as a “letter to the judge.] Revocable living trusts can help families bypass probate, reduce delays, and retain more control over how assets are managed after death. Powers of attorney (financial and health) are essential for incapacity scenarios; even 18‑year‑olds heading to college should have them so parents can access information if needed. 2) Why Insurance Belongs in the Plan Life insurance can protect the family’s ability to keep the home by paying off a remaining mortgage or covering living expenses—turning an asset into a sustainable legacy rather than a burden. For entrepreneurs, key‑person insurance can replace income when the owner can’t work, keeping the business afloat. 3) Minimizing Probate Costs and Taxes Probate involves court filings and legal fees; in some states fees scale with estate size (example discussed: percentage‑based fees in other jurisdictions), which can significantly erode wealth passed to heirs. Proper planning reduces those leakages. 4) Special‑Needs and Elder Planning Parents of children on need‑based benefits (e.g., Medicaid) must avoid transfers that jeopardize eligibility; the right trust structures preserve benefits while providing support. Elder law planning anticipates long‑term care costs (nursing home, assisted living, in‑home care) so families don’t have to deplete assets later. 5) Business Continuity for Owners Establish operating agreements and buy‑sell agreements that spell out who runs the business if the principal is incapacitated; pair with business powers of attorney. 6) Values, Audience, and Access Lee intentionally centers Black and Brown women and their families, grounding services in community uplift and transparent referrals to trusted financial pros (no paid referral arrangements). Contact approach: 15‑minute intake, then a four‑meeting process (legacy planning → design → review → signing). Notable Quotes (for pull‑quotes & captions) “Think of a will as a letter to the judge… a will still has to go through probate court. “A trust allows families to bypass probate altogether so they aren’t paying legal fees or leaving things to people who want to challenge the will. “Life insurance is a huge tool—it can help the family pay off the mortgage so they can keep the home and the equity.” “Estate planning is a strategy—not just documents.” “Even 18‑year‑olds should have powers of attorney—parents can’t just call doctors once kids are legal adults.” “I stay in my lane—I’m an attorney. I work closely with trusted financial professionals and make non‑compensated referrals.” “For special‑needs planning, don’t jeopardize need‑based benefits—use the right trust so support continues. “I want to build a sustainable practice that lets me serve my community and rest well, aligned with my family and values.” Quick Action Items (for listeners inspired by the episode) Draft or update POAs (financial and health) for every adult in the household, including college‑age children. Evaluate whether a revocable living trust makes sense to avoid probate and retain post‑death control. For business owners: review operating agreement / buy‑sell, add key‑person insurance, and create a business POA. Families with special‑needs dependents: consult on special‑needs trusts to protect benefits. #SHMS #STRAW #BESTSee omnystudio.com/listener for privacy information.

In this heartfelt episode, Becky Davidson talks with a father about the realities of raising children with special needs while balancing faith, family, and ministry. He shares his family's journey following his daughter's rare genetic diagnosis and the challenges and blessings that came with caring for a family member with severe autism. Through these experiences, he reflects on how their lives, priorities, and faith were deeply transformed. The conversation explores the emotional impact of a diagnosis, the importance of community and church support, and the lessons learned through patience, perseverance, and trusting God during difficult seasons. Listeners will also hear practical encouragement for maintaining a strong marriage, seeking counseling, and building supportive relationships with other parents and caregivers. Filled with honesty and hope, this episode offers encouragement to fathers and families navigating the special needs journey, reminding them they are not alone and that faith and community can provide strength in even the hardest moments.

Incoming AAPD CEO Dr. Jessica Y. Lee joins host Dr. Joel Berg for an engaging discussion of her goals and vision for the Academy's future. She shares her journey through pediatric dentistry, delving into what excites her most as she shifts from academia to leader of the AAPD. In this heartfelt and genuine conversation, Dr. Lee compares taking on the CEO role to “coming home” and hopes to bring that sense of belonging to the newest generations of pediatric dentists as she takes the helm. Guest Bio: Dr. Jessica Y. Lee is Chief Executive Officer of the American Academy of Pediatric Dentist. Prior to taking on this role in June 2026, she was the Demeritt Distinguished Professor of Pediatric Dentistry and Senior Associate Dean for Faculty Affairs and Leadership Development at the University of North Carolina, as well as a professor in the Department of Health Policy and Management in the UNC Gillings School of Global Public Health. Dr Lee received her MPH and DDS degrees from Columbia University and her Certificate in Pediatric Dentistry and PhD in Health Policy and Management from the University of North Carolina at Chapel Hill where she was also a NIDCR National Research Service Award recipient. She is a board-certified pediatric dentist and an active member of the medical staff at UNC Hospitals and practices in the Dental Faculty Practice in the School of Dentistry. She has authored over 150 peer-reviewed manuscripts and is a renowned expert in health literacy and health disparities. She is dedicated to bridging the gap between medical knowledge and patient understanding and reducing health disparities. She has led projects funded by the NIH and HRSA. Dr Lee is involved in teaching, clinical practice, and research. In addition to her academic pursuits, Dr. Lee is actively involved in leadership, community outreach and education initiatives. She collaborates with healthcare providers, government agencies, and non-profit organizations. She served as the President for the American Academy of Pediatric Dentistry (AAPD) from 2020-2021. She is the recipient of numerous teaching and research awards including the 2008 AAPD Jerome Miller “For the Kids” Award. In 2010, she received the Presidential Early Career Award for Scientist and Engineers from President Barack Obama. In 2011, Dr Lee was named the ‘Pediatric Dentist of the Year” by the American Academy of Pediatric Dentistry and in 2021 she received the AAPD Merle C Hunter Leadership Award. See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

She Tried EVERYTHING for Autism Meltdowns… Then This HappenedFor years, holidays felt impossible for this family.She feared the holiday season just as much as you (probably) are?Vacations were WORSE. Packing bags triggered meltdowns.Car rides ended in chaos.Aggression, overwhelm, screaming, tears, survival mode.No rest.Then everything changed.In this deeply emotional interview with Ninka-Bernadette Mauritson from Barefoot Autism Warriors, she shares: how she experienced their FIRST meltdown-free holidays the moment she unticked “special educational needs” on her son's forms, how nervous system healing changed their family dynamic, why therapies  weren't enough, how her marriage, motherhood, and faith transformed, how she finally took a SPA DAY while her husband and boys swam peacefullyOne of the most powerful moments in this episode is when she says:“ special needs? That's not my son anymore.”This episode is for ambitious, crunchy, exhausted autism moms who feel trapped in holiday survival mode and wonder if peace is actually possible. It still is. Nothing is impossible for God.Premiering:"THE MELTDOWN LIBERATION INTENSIVE."If you want to learn what triggers holiday meltdowns in your child, and the strategy that leads to more peace for your child specifically, I'm launching a brand new "7 DAY MELT DOWN LIBERATION  INTENSIVE " on June 15. Details and info to grab your spot before doors close HERE. Disclaimer: ©BAREFOOT AUTISM WARRIORS | NINKA-BERNADETTE MAURITSON.Individual results may vary, testimonials are not claimed to represent typical results. All testimonials are from real clients, and may not reflect the typical patient's experience, and are not intended to represent or guarantee that anyone will achieve the same or similar results. Every person has unique level of commitment, experiences, exercise habits, eating habits, and applies the information in a different way. Thus, the experiences that we share from other people may not reflect the typical users' experience. However, these results are meant as a showcase of what these patients have achieved. You should not begin our program if you have medical condition that precludes the turnaround process or changes to nutritional or lifestyle habits. Barefoot Autism Warriors is an online coaching program that provide guidance and coaching. Our programmes are not a substitute for medical advice from a physician, and we do not diagnose medical conditions. Please consult a physician before beginning any exercise or diet program.2 ways to work with me Autism symptoms are not always (but sometimes)  spiritual. My son lost the symptoms that gave him the diagnosis, and lives a neurotypical life (independently) I have coached moms for 20 years. 1️⃣ Free consultationSend me a list of symptoms and what you've tried so far. I'll audit your child's issues and tell you what triggers your child's symptoms, and plan next steps to address them to get less stimming, tantrums, eloping, sensory issues, sleeplessness, and aggression without tests, protocols, or battling with your child. Write "audit" in the subj line to book a call with me. We can also connect via Telegram if you hate Zoom. 2️⃣ The Christian Autism Liberation Program (30 spots left for 2026/2027)Reduce symptoms noticeably.  Without the hamster wheel of holistic healing, tests, or extreme diets.InstagramPodcast/free guides and blogYoutube

✨ "What is HeartMath doing? They're measuring your care." – Kansas CarradineDescription Kansas Carradine is a HeartMath-certified trainer, acrobatic stunt rider, and equine guided educator based in the Sierra Nevada mountains of California. She spent years performing with the international touring show Cavalia — working alongside 70+ head of horses, many of them stallions — before dedicating her work to heart-based horsemanship and emotional regulation.What makes Kansas's approach distinctive is the bridge she builds between rigorous science and lived horsemanship. HeartMath is not just a breathing technique; it is a research-backed body of work measuring the electromagnetic output of the heart, heart rate variability coherence, and the demonstrable effect of human emotional states on the beings — horse and human alike — around us. For equine-assisted practitioners, that has profound implications.In this conversation, Rupert and Kansas explore how heart coherence can be layered into any equine-assisted modality, why horses are uniquely able to detect incoherent emotional fields, the science behind the toric field and biophoton emission, and how Kansas's own path — from a difficult childhood at a California trick-riding ranch, through Cavalia's global stages, to HeartMath certification — shaped her understanding of regulation, resilience, and the horse as healer. She and Rupert also announce a planned 2027 collaboration. If you want to support the show, you can do so at Patreon: https://www.patreon.com/LongRideHomeIf you want to support the show, you can do so at Patreon: https://www.patreon.com/LongRideHome

Washington Wednesday on Ken Paxton's landslide, World Tour on Colombia's presidential election, and a classical school for students with special needs. Plus, Daniel Suhr on Pope Leo XIV's call for moral guardrails, England's annual cheese-rolling race, and the Wednesday morning newsSupport The World and Everything in It today at wng.org/donateAdditional support comes from WatersEdge. Today's investment, tomorrow's thriving churches. 3.25% APY on demand. WatersEdge.com/invest WatersEdge securities are subject to certain risk factors as described in our Offering Circular and are not FDIC or SIPC insured. This is not an offer to sell or solicit securities. WatersEdge offers and sells securities only where authorized; this offering is made solely by our Offering Circular.From Pensacola Theological Seminary... Preparing students to preach God's Word. go.pcci.edu/startseminaryAnd from St. Dunstan's, inviting young men into the building arts and the adventure of holiness on a Blue Ridge Mountains farm... stdunstansacademy.org

We welcome back Chelsea Jacobs from Yellow House Story Shop to discuss the realities and rewards of homeschooling a child with special needs. Chelsea honestly shares her family's journey, including the adoption of her son Gabe from Rwanda, his cerebral palsy diagnosis, and the everyday joys and challenges of homeschooling alongside complex medical needs and other neurotypical children. With 14 years of homeschooling under Chelsea's belt, we hope this episode is a great encouragement to all who are walking the same path!RESOURCES+Buy some of our favorite books here! 10 Of Those + $1 shipping!+Build Your Family's Library: Grab our FREE book list here+Get our FREE ebook: 5 Essential Parts of a Great Education.+Attend one of our upcoming seminars this year!+Click HERE for more information about consulting with Carole Joy Seid!CONNECTHomeschool Made Simple | Website | Seminars | Instagram | Facebook | PinterestEPISODE LINKSLearn More about CTCMathMentioned in this episode:Pick up the book, Family Worship, wherever books are sold, or visit this link to learn how to get 30 percent off with a free Crossway Plus account.Family Worship

Today we're talking about something many families know they need to think about—but often don't know where to begin: financial planning for children with disabilities. My guest is Mary McDirmid, a Chartered Special Needs Consultant and the co-founder and COO of All Needs Planning, a nationwide firm built by caregivers, for caregivers. In our conversation, Mary walks us through why proactive planning matters so much and what it can actually look like in practice. We talk about creating comprehensive care plans, protecting essential benefits, and building a long-term vision that supports not just financial security, but overall well-being. This is an empowering, practical conversation designed to help families feel more prepared, more informed, and more confident about the future. About Dr. Devon Price  Mary McDirmid, ChSNC, is the COO and co-founder of All Needs Planning — a nationwide financial planning firm built by caregivers, for caregivers. A Chartered Special Needs Consultant, Mary brings both professional expertise and lived experience as a parent navigating the special needs journey. She specializes in helping families create comprehensive plans that address the financial, legal, and care needs of loved ones with disabilities — from diagnosis through adulthood and beyond. Mary is co-author of the upcoming book Care, Protect, Grow: A Guide to Building Lasting Security for Your Loved One with Special Needs (Wiley, May 2026), which provides a compassionate, step-by-step roadmap for families facing the question of “what happens when I'm no longer here?” Things you'll learn from this episode   Why early, ongoing planning is essential for families raising children with special needs How the Care, Protect, and Grow framework supports a comprehensive, long-term vision for care How creating and regularly updating care plans ensures continuity and security for loved ones Why involving siblings and considering long-term roles is an important part of the planning process How active advocacy and participation shape more effective, personalized support systems When and how to begin these conversations so families feel prepared rather than overwhelmed Resources mentioned Mary McDirmid's website Care, Protect, Grow: A Guide to Building Lasting Security for Your Loved One with Special Needs by Mary McDirmid Book a free meeting with Mary Care, Protect, Grow (on Mary's website) All Needs Planning Learning Lab ABLE National Resource Center Learn more about your ad choices. Visit podcastchoices.com/adchoices

Bodie & Marissa Connolly share their family's story as well as share different resources and programs for families of children with special needs that have helped them as they walk through life living every day to the fullest. We hope this episode is encouraging and provides hope in knowing that you are not alone!

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Attorney Whitney Knox Lee Explains practical estate‑planning strategies—wills, trusts, powers of attorney—and how entrepreneurs, families, and especially parents of disabled children can protect assets, avoid costly probate, and maintain eligibility for critical benefits. The conversation also touches on integrating insurance with estate planning, small‑business contingency planning, and Lee’s personal mission and background in civil rights work. Purpose of the Interview Educate listeners on estate planning as a wealth‑preservation strategy (not just documents)—to reduce court costs, taxes, and confusion for families. Clarify the differences and roles of wills, trusts, and powers of attorney, including when each is appropriate and how they work together.] Highlight special considerations for entrepreneurs and families with disabled children or aging relatives, including insurance, operating agreements, and special‑needs planning. Share Lee’s values and practice approach, including culturally responsive service and sustainable advocacy rooted in prior civil‑rights work. Key Takeaways 1) Wills vs. Trusts vs. Powers of Attorney A will is not the plan—it’s just one piece and still goes through probate, which can be slow and expensive; think of a will as a “letter to the judge.] Revocable living trusts can help families bypass probate, reduce delays, and retain more control over how assets are managed after death. Powers of attorney (financial and health) are essential for incapacity scenarios; even 18‑year‑olds heading to college should have them so parents can access information if needed. 2) Why Insurance Belongs in the Plan Life insurance can protect the family’s ability to keep the home by paying off a remaining mortgage or covering living expenses—turning an asset into a sustainable legacy rather than a burden. For entrepreneurs, key‑person insurance can replace income when the owner can’t work, keeping the business afloat. 3) Minimizing Probate Costs and Taxes Probate involves court filings and legal fees; in some states fees scale with estate size (example discussed: percentage‑based fees in other jurisdictions), which can significantly erode wealth passed to heirs. Proper planning reduces those leakages. 4) Special‑Needs and Elder Planning Parents of children on need‑based benefits (e.g., Medicaid) must avoid transfers that jeopardize eligibility; the right trust structures preserve benefits while providing support. Elder law planning anticipates long‑term care costs (nursing home, assisted living, in‑home care) so families don’t have to deplete assets later. 5) Business Continuity for Owners Establish operating agreements and buy‑sell agreements that spell out who runs the business if the principal is incapacitated; pair with business powers of attorney. 6) Values, Audience, and Access Lee intentionally centers Black and Brown women and their families, grounding services in community uplift and transparent referrals to trusted financial pros (no paid referral arrangements). Contact approach: 15‑minute intake, then a four‑meeting process (legacy planning → design → review → signing). Notable Quotes (for pull‑quotes & captions) “Think of a will as a letter to the judge… a will still has to go through probate court. “A trust allows families to bypass probate altogether so they aren’t paying legal fees or leaving things to people who want to challenge the will. “Life insurance is a huge tool—it can help the family pay off the mortgage so they can keep the home and the equity.” “Estate planning is a strategy—not just documents.” “Even 18‑year‑olds should have powers of attorney—parents can’t just call doctors once kids are legal adults.” “I stay in my lane—I’m an attorney. I work closely with trusted financial professionals and make non‑compensated referrals.” “For special‑needs planning, don’t jeopardize need‑based benefits—use the right trust so support continues. “I want to build a sustainable practice that lets me serve my community and rest well, aligned with my family and values.” Quick Action Items (for listeners inspired by the episode) Draft or update POAs (financial and health) for every adult in the household, including college‑age children. Evaluate whether a revocable living trust makes sense to avoid probate and retain post‑death control. For business owners: review operating agreement / buy‑sell, add key‑person insurance, and create a business POA. Families with special‑needs dependents: consult on special‑needs trusts to protect benefits. #SHMS #STRAW #BESTSteve Harvey Morning Show Online: http://www.steveharveyfm.com/See omnystudio.com/listener for privacy information.

Walter Sterling takes the Midnight Misfits through a wide-ranging overnight show covering new UFO disclosures, NSA files, alleged alien-human hybrid programs, military abductions, crashed craft, alien body types, and Ross Coulthart's reporting on possible government contact with non-human intelligence. Walter also digs into major conspiracy questions surrounding Princess Diana's death, the Obama chef mystery, 9/11, ancient Sumerian creation theories, and chilling alien messages. Plus, he reflects on free-form radio, special needs education, IEPs, apraxia, dyslexia, and why parents must stay on top of schools, while Florida Stories brings meth busts, fentanyl on the highway, drag racing, bizarre rescues, tragic accidents, and the wild crime stories that define late-night radio. Learn more about your ad choices. Visit megaphone.fm/adchoices

There is a dangerous partnership between Big Government, Big Pharma, Big Psychiatry, and Big Education to label children with diagnoses, drug them, and profit from it all, explains Autistic Freedom Network Founder Sven Scharpen, who experienced it firsthand. In this explosive interview on Conversations That Matter with The New American magazine Senior Editor Alex Newman, Scharpen details ... The post Exposing the Pharma-Psychiatry-Education-Special Needs-Industrial Complex appeared first on The New American.

If you've ever wondered what your husband might be feeling—but not saying—this episode is for you. Since so many of our listeners are special needs moms carrying the emotional and practical load of daily life, Becky Davidson invited Steve Chatman to help shed some light on what's often going on in the minds and hearts of special needs dads. Together, they explore the emotions many dads struggle to express: feeling overwhelmed, disconnected, lonely, inadequate, or even unsure of how to communicate what they need. Steve shares honest insight into why dads sometimes pull back emotionally and offers practical ways moms can better understand and support their husbands without adding more pressure to an already full plate. This conversation is real, encouraging, and filled with relatable moments that will make you laugh, think, and maybe even spark some meaningful conversations at home. If you've ever felt like you and your spouse are missing each other in the middle of the special needs journey, this episode offers a compassionate look into how to reconnect, strengthen your marriage, and remember you're on the same team.

Our guest this week is Nathan Simpson of Colorado Springs, CO an aircraft mission planner for the U.S. Air Force and father of nine children including one with tuberous sclerosis.  Nathan and his wife, Stefanie, have been married for 19 years and are the proud parents of nine children ranging in age from 3 months to 17 years, including six year old Tevia, who has tuberous sclerosis.  The family lives outside of Colorado Springs on a working farm, with all types of animals and Stefanie home schools the children.  Nathan has also been a member of the SFN Matermind Group in Colorado.  It's an enlightening, uplifting and inspiring story about a young couple, with a large family and a demonstrated spiritual dimension to their lives, all on this episode of the SFN Dad to Dad Podcast.Order your copy of the new 21CD book: Dads Raising Chidlren With Special Needs & Disabilities: A Guide For 21st Century Dads on Amazon: https://amzn.to/4tdvjcvJoin 21CD on the SFN U.S. Tour, a 30 day, 50 state, 60+ stop tour taking place from May 21 to June 21, 2026: to strengthen and grow the Special Fathers Network as well as give away 2,000 copies of our new book.  Click here to see the full tour schedul and register for the venuw closest to you: https://21stcenturydads.org/us-tour-venue-details/ Show Notes - Email – simpson.nathan@pm.meTSA website - https://tuberous-sclerosis.org/information-and-support/what-is-tsc/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.Join the SFN U.S. Tour in one of 60+ locations all across the U.S. from May 21st to June 21st.  Go to www.21stCenturyDads.org for additional informaiton. Please conisder hosting, co-hosting or simoly joining the tour near your home.  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/  

This past week was FULL of special needs mom life.Appointments, Make-A-Wish, Special Olympics, end-of-year school celebrations and field trips, caregiver trainings, paperwork, and so much more.All in the same week.And that emotional whiplash can take you out if you don't know how to process it.In this episode, I'm sharing what it looks like to use coaching tools in the middle of actual real life as a special needs mom.I'm giving you a peek inside how I coached myself through the challenges, and how it impacted not just my life but the lives of those around me. >>>Book a Consult Call

Most of us know someone who's raising a child who has special needs. Danny brings up some of the common challenges he's seen parents face in that situation. You'll then hear Sandra Peoples and Jim Daly address what churches can do to help a parent who's raising a child with special needs. At the end, John and Danny will give you ideas for assisting parents who need help. Find us online at focusonthefamily.com/parentingpodcast. Or call 1-800-A-FAMILY. Receive the book Unexpected Blessings for your donation of any amount! Take the 7 Traits of Effective Parenting Assessment Experiencing God's Grace in a Special Needs Family Counseling Consultation and Referrals Overcoming Guilt in The Face of Special Needs Support This Show! If you enjoyed listening to the Focus on Parenting Podcast, please give us your feedback.

Legendary songwriter, performer, and actor Steve Earle joins Andy Frasco on the show this week for an interview that spans his entire career. This deep dive touches on him running away from home as a kid, doing drugs at a young age, being a recovering addict, and his role as a parent to a son with special needs. Steve Earle is one of the great orators of our time, and that is on display during this world-saving interview. He also talks about opening for Bob Dylan and his friendship with his hero, Townes Van Zandt. They even get into his love of New York Yankees baseball and Premier League Soccer.

Almost 100 episodes later, and this one still knocks me to my knees. In this MVP replay, I'm sharing one of my most powerful episodes in honor of Mother's Day. In this episode, I share a poem by an unknown author that I came across that made such an impact on me, called “I am the Child.” Link to read the poem: http://www.oafccd.com/lanark/poems/child1.html

In this episode, Dr. K explores the "burden of potential" and why being labeled a gifted child often leads to a cycle of burnout, perfectionism, and deep-seated shame. He argues that gifted children are actually "special needs" because their developmental requirements are fundamentally different from the average child, yet they are often forced into school systems that prioritize raw results over the vital study habits needed for long-term success. What to expect in this episode: The Trap of Raw Intellect: Why gifted kids often fail later in life because they "skip levels" of habit-building in early school years, leaving them without the skills to handle a "wall" where intelligence alone isn't enough. Mansion vs. Shack: A deep dive into why achieving high potential actually requires more work, not less, and how society's expectation that things should be "easier" for smart people sets them up for failure. The Shame Gap: Understanding how shame lives in the discrepancy between your lofty internal expectations and your actual accomplishments, leading to chronic avoidance and the "smart kid" ego. The "Scenic Route" in Life: Dr. K shares his personal journey from a 2.5 GPA in college to becoming Harvard faculty, illustrating how letting go of ego and comparison is essential for true progress. The "Surprise Me" Practice: A practical Nyani Yoga exercise for retraining your brain to embrace acceptance and let go of paralyzing expectations in everyday life. Matching the Pace of the Child: Why gifted kids are naturally drawn to video games, which perfectly match their challenge level, while traditional school often moves at a "snail's pace". Advice for Parents and Mentors: Why slowing down for a struggling gifted child is a mistake and why they often need more challenge, not less, to rediscover their motivation. Dr. K's NEW Guide to Love, Sex, & Relationships is coming May 2026! Pre-order now: https://bit.ly/4dO3x0VHG Coaching : https://bit.ly/46bIkdo Dr. K's Guide to Mental Health: https://bit.ly/44z3SztHG Memberships : https://bit.ly/3TNoMVf Products & Services : https://bit.ly/44kz7x0 HealthyGamer.GG: https://bit.ly/3ZOopgQ Learn more about your ad choices. Visit megaphone.fm/adchoices