Podcasts about autism diagnosis

Motherhood has a way of rewriting the plans we were so sure we had figured out.For Susanna Peace Lovell, that meant becoming a mother to her daughter, Arizona, who is neurodivergent and has autism, ADHD, anxiety, and significant allergies. For Jacqueline, it meant infertility, loss, a 24-week premature birth, a four-month NICU stay, and eventually learning that her oldest son has autism and ADHD, and her younger son also has ADHD and sensory processing disorder.In this deeply personal conversation, Jacqueline and Susanna talk about what happens when motherhood looks nothing like the version you imagined—and how you learn to find yourself within it.They open up about receiving a child's diagnosis, the instinct to immediately jump into "fix it" mode, the fear of what the world will think of your child, and the invisible mental load of raising a child with additional needs. They also talk about something caregivers don't hear nearly enough: you are allowed to have needs, joy, interests, dreams, and an identity outside of caring for everyone else.Susanna shares the importance of compassion—for our children, for other mothers, and especially for ourselves—and why finding people who simply get it can change everything.In this episode:When motherhood doesn't look the way you imaginedProcessing an autism or ADHD diagnosisThe invisible work of parenting a neurodivergent childWhy gratitude and overwhelm can exist at the same timeLetting go of the pressure to "fix" everythingWhat other people don't understand about raising a child with additional needsBuilding a village when you can't do it aloneRediscovering joy and identity outside of caregivingWhat Susanna would tell a mom who just received her child's diagnosisWhy your child is still the exact same child they were before the labelSusanna also shares her work with We Are Brave Together, a community supporting the mental health and wellness of caregiving moms, and the anthology Suddenly Brave Together, featuring letters from experienced caregiving mothers to moms who are just beginning this journey.If you've ever wondered where you went while taking care of everyone else—or you're navigating a motherhood story you never saw coming—this conversation is for you.Connect with Susanna:SusannaPeaceLovell.comInstagram: @mamapeaceLearn more about We Are Brave Together:WeAreBraveTogether.orgSupport the show__________________________________________________________________________________Her Village is more than a podcast—it's a space for real connection, honest conversations, and meaningful friendships in the places we live.If you want to go deeper and stay connected beyond the podcast, you can join us here: joinhervillage.co

In Illinois, there are two categories of experts that can diagnose autism: psychologists and developmental physicians. But because openings with these experts are few and far between, families can be put on a waitlist that could last anywhere from months to years.That is, until now. Gov. JB Pritzker signed the Illinois Speech-Language Pathology and Audiology Practice Act early July and it allows speech-language pathologists trained in autism diagnosis evaluation to diagnose the condition in children under age three enrolled in the state's Early Intervention program.In the Loop sits down with the lead researcher of the study and hears from two mothers of children with autism about navigating the process of getting a diagnosis. A GUESTS: Megan Roberts, professor, Roxelyn and Richard Pepper Department of Communication Sciences and Disorders at Northwestern UniversityKiana Spears, parent of a child who was diagnosed as part of the Reduce the Wait studyDebra Vines, CEO and founder, The Answer Inc.For a full archive of In the Loop interviews, head over to wbez.org/intheloop. 

Send us Fan MailWhat if laughter could become one of your most powerful tools for getting through the hard moments of autism parenting?In this episode of the Mother's Guide Through Autism Podcast, Brigitte sits down with author, speaker, and fellow autism mom Andrea Moriarty for an honest, hopeful, and often very funny conversation about raising her son Reid, now 32.Andrea shares what those early years after Reid's autism diagnosis were really like, from the overwhelm and uncertainty to learning that she didn't have to figure everything out alone. They talk about the importance of building a support system, leaning into their children's strengths, and finding creative solutions when the traditional path simply doesn't fit.They also dive into Andrea's newest book, Daffy, a tell-all comedy for moms about using laughter as life support. Andrea explains how a getaway with other autism moms helped her realize just how much humor had been keeping them afloat—and inspired what she now calls the “Laughter Alliance.”You'll also hear some of Andrea's favorite practical life hacks for making everyday life a little easier, including batch cooking, smoothie pops for selective eaters, “Tasting Tuesday,” and even simplifying your wardrobe to save precious mental energy.Most importantly, Andrea reminds us of something so many autism moms need to hear:You're not doing it wrong. This is hard. You don't have to do it alone.In this episode, they talk about:• Andrea's journey raising her autistic son Reid• Music therapy and discovering Reid's strengths• How laughter can help us process difficult experiences• Andrea's “Laughter Alliance” for autism moms• Simple life hacks that reduce stress and mental overloadABOUT ANDREA MORIARTYAndrea Moriarty is an author, speaker, workshop leader, and autism mom. She is the author of One Track Mind, Radical Inclusion, and Daffy. Her work offers a refreshing and hopeful perspective on both the challenges and triumphs of parenting a son with autism, blending honesty, affection, humor, and hope.Andrea also cofounded Banding Together, a music therapy nonprofit, and has served on the boards of Young Life Capernaum, New Village Arts, and Able Arts Work.

An autism diagnosis changed everything for Harry and Gus Psaros—but not in the way they expected. Together, this father and son share an honest conversation about fear, hope, parenting, and what happens when you stop focusing on limitations and start looking for possibility. ABOUT GUESTS Harry Psaros is the author of “From Struggle to Strength”, a memoir about raising his son Gus after he was diagnosed with autism at age 3 (https://www.harrypsaros.com/). Gus Psaros is a recent Kent State University graduate pursuing a career in physical therapy. CHAPTERS (0:00) Introduction (0:41) Diagnosis Drive Home (3:21) Early Signs and Denial (5:06) Gus on Being Different (6:49) Kindness as Superpower (7:55) Setbacks (9:24) Brain Balance Breakthrough (11:07) Finding Balance and Burnout (11:58) Senior Year and College Leap (14:38) Gus' Vision Board and Big Goals (15:24) Calling on Dads to Step Up (18:27) Conclusion

What if your hardest parenting season is also part of God's greater purpose? Raising a child with special needs can feel lonely, exhausting, and uncertain. In this heartfelt episode, Cynthia Barkley shares her family's journey through a premature birth, an autism diagnosis, and years of advocacy, therapy, and unwavering faith. Her story is a powerful reminder that even in life's most difficult moments, God is present, working through every challenge. Cynthia opens up about receiving her son Josiah's autism diagnosis, processing grief, and learning to trust God's plan while navigating the complexities of autism, ADHD, sensory processing disorder, and other developmental challenges. She also shares practical advice for finding resources, building a support system, advocating for your child, and maintaining hope through every season—from early intervention to adulthood. Whether you're a parent, caregiver, educator, or someone supporting a family with special needs, this conversation offers encouragement, practical wisdom, and the reassurance that you are never alone. In This Episode Cynthia's journey through a premature birth and autism diagnosis Processing grief while holding onto faith Finding resources and building a strong support network Advocating for therapies, services, and educational needs Navigating multiple diagnoses, including ADHD and sensory processing disorder Homeschooling and supporting lifelong learning Helping siblings navigate life with a special needs family member Transitioning into adulthood after high school Why it's never too late for growth, independence, and new opportunities The role of prayer, community, and perseverance in everyday life Encouragement for parents who feel overwhelmed or isolated Key Takeaways You don't have to walk this journey alone. Advocacy is a marathon, not a sprint. Give yourself grace during difficult seasons. Community and friendship make a tremendous difference. Faith provides strength when answers are hard to find. Every child has unique gifts and God-given purpose. Progress may look different than expected, but every milestone matters. Enjoyed This Episode? If this conversation encouraged you, please subscribe, leave a review, and share it with another parent or caregiver who could use a reminder that hope is always possible—even on the hardest days.   Sponsor The Rising Above with Becky Davidson Podcast, Make A Difference. https://forms.gle/Zi2SWGwP29arNDAm9    

My guest this episode is Julie Day, an autistic author and advocate from London who writes children's books featuring autistic characters finding confidence — the kind of books she never had growing up undiagnosed. Her path to indie publishing began with a recurring dream she had to write down, and it carried her through a late Asperger's diagnosis and a life-threatening heart illness she turned into a book to help others. Find more author advice, tips, and tools at our Self-publishing Author Advice Center, with a huge archive of 2,000+ blog posts, and a handy search box to find key info on the topic you need. We invite you to join our organization and become a self-publishing ally. About the Host Howard Lovy is an author, developmental editor, and writing coach with a long career in journalism and publishing. He works with writers at many stages of their careers, with a focus on helping them develop their ideas and strengthen their work while preserving their unique voices. He lives in Northern Michigan. About the Guest Julie Day is an autistic author and advocate who mainly writes children's books featuring autistic characters finding confidence, as well as articles about autism, and creates videos about autism and being autistic. She also writes memoir-style guides about a heart condition and autism, and adult mysteries featuring a character with a heart condition. You can find her on her website, Instagram, and YouTube.

Why are so many autistic women missed in childhood? And what happens when a parent's journey to understand their child leads to a life-changing discovery about themselves?In this episode of The Child Psych Podcast, we welcome Julie M. Green, author of Motherness: A Memoir of Generational Autism, Parenthood, and Radical Acceptance. Julie shares her powerful story of parenting an autistic child, navigating a late autism diagnosis, and finally making sense of a lifetime of experiences that had never quite fit together.For many women, autism goes undiagnosed for decades. Traits are often misunderstood, hidden through masking, or mistaken for anxiety, perfectionism, sensitivity, or social difficulties. Julie's journey sheds light on the unique presentation of autism in women and girls, while offering hope for those seeking answers later in life.In this conversation, we explore:▪️ Autism in women and why so many girls are missed▪️ Late autism diagnosis and its emotional impact▪️ Parenting an autistic child▪️ Masking and autistic burnout▪️ Neurodiversity and self-acceptance▪️ Autism in families and generational autism▪️ Supporting autistic children and autistic parents▪️ Identity, belonging, and mental health▪️ What radical acceptance looks like after diagnosisWhether you're a parent of an autistic child, an educator, clinician, or someone wondering if you may be autistic yourself, this episode provides valuable insight into autism spectrum disorder, neurodivergence, parenting, and self-discovery.Julie's story is a powerful reminder that understanding ourselves can happen at any age—and that sometimes the people we love most help us find our way there. Hosted on Acast. See acast.com/privacy for more information.

Ron Funches has built a career turning the things that once made him feel different into his greatest strengths. Once bullied in school for his soft and higher pitched voice, it's now his trademark in standup, and helped launch his voice acting career. Ahead of a performance at Just for Laughs Montreal, Ron reflects on how fatherhood, his son's autism diagnosis, and his own recent autism diagnosis after appearing on The Traitors, have changed his understanding of himself and the unique gifts that shape his comedy.

Sarah Crawford, CEO of TLC, joins Shannon to talk about some of the challenges facing today's families, including burnout, barriers to healthcare and much more.  Today's jargon term is Respite!  00:00 Intro & Today's Guest Preview 00:35 Welcome to Autism Live & Community Mission 03:19 How to Participate, Podcasts & Viewer Support 06:20 Autism Care Today Gala & Family Grants 08:54 Jargon of the Day: What Is Respite Care? 11:53 Why Caregivers Need Respite Support 14:49 Finding Safe, Trusted Respite Providers 18:47 The Oxygen Mask Principle for Parents 19:50 Meet Sarah Crawford, CEO of TLC 22:22 The TLC Story: From Three Families to Thousands Served 26:01 Parent Burnout, Caregiver Stress & Finding Support 32:31 How Disability Impacts the Entire Family 37:15 First Steps After an Autism Diagnosis 44:04 Medicaid, Waitlists & Fixing Broken Systems 50:37 Hope, Advocacy & Building Better Support Networks

Dr. Mary Barbera reflects on nearly three decades in the autism world as both a mom and professional. She shares how denial, long waitlists and limited early support can delay progress for children with autism or developmental delays. She emphasizes the importance of assessment, early action, parent-led intervention and individualized plans, while introducing the free Barbera Early Childhood Assessment (BECA) as a starting point for families seeking clarity and next steps.

Send us Fan MailIf you are navigating an autism diagnosis with your child, you already know how heavy and isolating the journey can feel. But there is a side to this story we don't hear often enough: the father's perspective.In this episode, host Brigitte Shipman sits down with Harry Psaros—an autism father, advocate, board member for the Autism Caring Center, and best-selling author of “From Struggle to Strength: A Father's Journey with Autism and the Power of Hope and Positivity.” When a child is diagnosed, mothers and fathers often process their grief in completely different ways. Harry shares his mission to break down that barrier, open up the conversation for dads who are struggling to accept a diagnosis, and give families the tools to stay on the same team instead of growing apart. If you are feeling exhausted, overwhelmed, or looking for a reason to find hope in the middle of a hard day, this down-to-earth conversation will remind you that you are not alone in the wilderness.In This Episode, You Will Learn:- Why fathers often react differently to an autism diagnosis and how to bridge the communication gap.- Practical advice on keeping your marriage and relationship strong through caregiving stress.- How to shift from survival mode to finding genuine hope, positivity, and resilience.- The inspiration behind Harry's book, From Struggle to Strength, and his advocacy work for families.

Julie M. Green's son was diagnosed autistic at three. She wasn't diagnosed until 44 — almost a decade of advocating fiercely for her child's needs while missing her own. In this episode, we talk about why that gap is so common, and what finally closed it for her.For Julie, recognition didn't arrive in a single lightning-bolt moment. It came slowly, over years of small things adding up — until meeting another late-diagnosed autistic woman gave her a model she'd never had for what autism could actually look like. We talk about masking and why it's not a conscious choice, the survival strategy of becoming the "quiet girl" who stays small to avoid getting anything wrong, and the way that same people-pleasing can quietly open a person up to harm.We also cover the things that often go unspoken: alexithymia, the difficulty of naming your own emotions even when you feel them intensely; face blindness and the social minefield it creates; and the particular weight of maternal guilt when you don't yet know why parenting feels so much harder for you than it seems to for everyone else. Julie shares how she's reframed burnout, why she now believes modelling rest matters more than martyring herself for her son, and what radical acceptance really looks like, including on the days it still feels out of reach.If you'd like to know more about Julie M. Green's work, check out:Her memoir, Motherness: A Memoir of Generational Autism, Parenthood, and Radical AcceptanceHer weekly Substack newsletter, The Autistic MomHer article in The Globe and Mail, "Receiving an Autism Diagnosis as an Adult Is Not 'Trendy'"Julie M. Green on InstagramJulie M. Green's websiteTheme music: "Everything Feels New" by Evgeny Bardyuzha. All episodes written and produced by Kristen Hovet.Send in your questions to otherautism@gmail.com Buy me a coffee!Book a life-coaching session with me!The views, opinions, and experiences shared by guests on this podcast are their own and do not necessarily reflect those of the host or production team. The content is intended for informational purposes only and should not be taken as medical or professional advice. Please consult with a qualified healthcare provider before making any decisions related to your health, fitness, or wellness. 

In this week's rebroadcast, Anneke Flinn and Robyn Stephen, Director and Principal Clinician at Melbourne Child Development, and Speech Pathology consultant at Melbourne Paediatric Specialists, discuss the speech pathologist's role in Autism diagnosis. SPA and the presenters of this podcast acknowledge that this episode was originally recorded in 2024. As terminology and perspectives evolve over time, the original episode title and some of the language used may no longer reflect current preferred terminology. To support respectful and contemporary practice, the title of this episode has been updated. We recognise and respect that terminology preferences vary among neurodivergent people and communities, and we value approaches that honour diverse perspectives and individual preferences. Robyn has provided her own reflection on neuro-affirming care and the language we use when working with Autistic people. She also wanted to highlight that if you decide to delay a diagnostic decision for a few months whilst you monitor the child in a new setting such as kindergarten that this is not a watch and wait period as far as support is concerned. Intervention including parent and educator coaching should commence during this time as soon as possible using the child's strengths to enhance their function. Rebroadcast reflection provided by Courtney Reddacliff, speech pathologist and member of the Podcast Reference Group. Speech Pathology Australia acknowledges the Traditional Custodians of lands, seas and waters throughout Australia, and offers our respect to Elders, across all times and places. The Speak Up podcast recognises the central role of yarning and oral storytelling in Aboriginal and Torres Strait Islander culture, how this translates to knowledge translation, and that colonisation has interrupted these practices of Language and knowledge sharing. The Speak Up podcast acknowledges the need for truth-telling and deep listening, the central role that Language plays in connecting Aboriginal and Torres Strait Islander People with Culture, Country, and Community, and the interwoven nature of health, and social and emotional wellbeing. We recognise that the Traditional Owners of the Lands across Australia have been here since time immemorial, and that their sovereignty over this land, was never ceded. Free access to transcripts and a full list of resources and references for this podcast, is available via the SPA Learning Hub (https://learninghub.speechpathologyaustralia.org.au/). You will need to sign in or create an account. For more information, please see our Bio, or for further enquiries, email speakuppodcast@speechpathologyaustralia.org.au Disclaimer: © (2026) The Speech Pathology Association of Australia Limited. All rights reserved. Important Notice, Please read: The views expressed in this presentation and reproduced in these materials are not necessarily the views of, or endorsed by, The Speech Pathology Association of Australia Limited (“the Association”). The Association makes no warranty or representation in relation to the content, currency or accuracy of any of the materials comprised in this recording. The Association expressly disclaims any and all liability (including liability for negligence) in respect of use of these materials and the information contained within them. The Association recommends you seek independent professional advice prior to making any decision involving matters outlined in this recording including in any of the materials referred to or otherwise incorporated into this recording. Except as otherwise stated, copyright and all other intellectual property rights comprised in the presentation and these materials, remain the exclusive property of the Association. Except with the Association's prior written approval you must not, in whole or part, reproduce, modify, adapt, distribute, publish or electronically communicate (including by online means) this recording or any of these materials.

In this deeply moving episode of Autism for Badass Moms, Rashidah welcomes Kecia Johnson, a 42-year-old mother, 5-year colorectal cancer survivor, autism advocate, and an eight-time author from Denver, Colorado. She shares a journey that is almost impossible to imagine. Kecia shares the unimaginable journey that began in early 2020 when severe rectal pain was repeatedly dismissed during the height of the COVID-19 pandemic—until an emergency biopsy revealed colorectal cancer.What followed was months of chemotherapy, radiation, severe treatment complications, second-degree burns, isolation, and a fight to survive.But surviving cancer was only the beginning.Kecia opens up about the lasting effects of treatment, including radiation toxicity, nerve damage, brittle bones, early menopause, chronic pain, and mobility challenges. As she struggled to rebuild her own health, she also began recognizing developmental and sensory differences in her daughter, Journei. Kecia pursued evaluations that ultimately led to an autism diagnosis. About Our GuestKecia Johnson is the creator of the Cancer Could NEVA healing movement. Her journey is rooted in resilience, faith, and transformation. She uses her voice to break stigmas around trauma, chronic illness, and neurodiversity; creating safe spaces where women can heal, be seen, and rise boldly in their truth.Kecia also founded Kolourful MUVA to empower mothers of children with autism and special needs. Providing emotional support, resources, and income tools, she helps women move from survival to purpose. Through international speaking, podcasting, and community work, Kecia demonstrates how to rebuild and thrive with impact, even in the hardest seasons.Kecia resides in Colorado with her family.Connect with Kecia:Instagram: www.instagram.com/iamkeciajFacebook: iamkeciajTik Tok: iamkeciajIn this episode we discuss:00:00 Badass Moms Welcome00:57 Global Community Thanks01:57 Meet Keisha Johnson05:49 Early Symptoms Dismissed08:29 Cancer Diagnosis Shock11:14 Chemo and Radiation 15:50 Isolation 20:48 Natural Remedies Turning Point30:11 New Setbacks35:24 Advocacy and Sensory Clues40:06 Back To California41:51 Autism Diagnosis 44:45 Moving to Colorado45:58 Mom Support System48:27 Cancer Recovery Reality49:45 Advocacy Awakening53:00 Judgment and Stigma01:01:07 School Readiness Plan01:02:38 Ignorance01:06:39 Kolourful MUVA Mission01:08:59 Launching and Resources01:13:54 Badass AdviceIf this episode resonated with you:-Follow the Autism for Badass Moms Podcast-Leave a review to help other autism moms find this community-Share this episode with a parent who may feel unseen or misunderstoodInstagram: www.instagram.com/theabmpodcastFacebook: www.facebook.com/theabmpodcastJoin us every Tuesday for more inspiring stories and insightful discussions that empower and uplift.

A late autism diagnosis can reframe everything you thought you knew about why your work, your relationships, and even your own field have felt harder than they should. For Marina Livis, that reframe arrived after years of being told she was too literal, too this, too that, with no one stopping to ask why.In this episode of The Traveling Therapist Podcast, I sit down with Marina to talk about what came after she was finally diagnosed, the licensing hurdles she refused to let stop her, and how all of it shaped the niche she serves now. We also get into the insurance mess so many traveling therapists are sorting through right now, and why she is rethinking how she wants to run her practice.In This Episode, We Explore…The long-distance relationship that quietly kicked off her traveling therapist journey.What being called "too literal" actually looked like on the job.The evaluation that was supposed to help her and ended up doing the opposite.Signs of autism in women that often slip right under the radar.Why she is stepping back from insurance platforms and panels.Connect with Marina Livis:Website: https://www.marinawellness.comBook a consultation button on her site (routes through her EHR)Kym's Resources:Bill Like a Boss: https://kymtolson.kartra.com/page/Bill-Like-A-Boss100 Side Hustles for Therapists: https://kymtolson.kartra.com/page/opt-in-100-side-hustlesThera AI Hub: https://kymtolson.kartra.com/page/AI-Tools-for-TherapistsCoaching with Kym: https://calendly.com/kymtolson/30minThe Traveling Therapist Facebook Group: https://www.facebook.com/groups/onlineandtravelingAre you ready to take the plunge and become a Traveling Therapist? Whether you want to be a full-time digital nomad or just want the flexibility to bring your practice with you while you travel a couple of times a year, the Portable Practice Method will give you the framework to be protected! ➡️ JOIN NOW: www.portablepracticemethod.com/Connect with me:www.instagram.com/thetravelingtherapist_kymwww.facebook.com/groups/onlineandtraveling/www.thetravelingtherapist.comThe Traveling Therapist Podcast is Sponsored by:Berries: Say goodbye to the burden of mental health notes with automated note and treatment plan creation! www.heyberries.com/therapistsAlma: Alma is on a mission to simplify access to mental health care by focusing first and foremost on supporting clinicians www.helloalma.com/kym

How does a father change his attitude about his son's autism diagnosis? In this clip, Jamiel Owens talks about what it was like to learn about his son's autism and how he shifted his perspective from grief to acceptance. Jamiel Owens is the host and creator of The Ausome Show, a co-host of The Ben & Jay Show, and a self-described all-around public server. As the father of a young adolescent boy with autism, Jamiel encourages other fathers to open up about their feelings regarding their child's diagnosis.  Welcome to Autism Tips & Tools, where we highlight the best practical guidance from previous episodes of Autism Knows No Borders. Whether you're a self-advocate, a family member, or a service provider, there's something here for you! This conversation with Jamiel Owens was originally released on August 27, 2020. Would you like to know what Jamiel would have done differently in the early years of his son's diagnosis? Click the link below for the full conversation and be sure to subscribe to hear more from people connected to autism inspiring change and building community.    A Father's Path to Autism Acceptance, with Jamiel Owens Let's work together to transform how the world relates to autism. ----more---- We appreciate your time. If you enjoy this podcast and you'd like to support our mission, please take just a few seconds to share it with one person who you think will find value in it too. Follow us on Instagram: @autismpodcast Join our community on Mighty Networks: Global Autism Community Subscribe to our YouTube channel: Global Autism Project We would love to hear your feedback about the show. Please fill out this short survey to let us know your thoughts: Listener Survey

Send us Fan MailIn this episode of A Mother's Guide Through Autism, host Brigitte Shipman sits down with Maureen Brice and Dr. Nicole Dolan to explore a deeply profound side of caregiving: the parent's own nervous system, trauma history, and energetic frequency.When your neurodivergent child has a meltdown, does your own anxiety or anger immediately skyrocket? You are not alone. Maureen Brice and Dr. Nicole Dolan dive into why our children act as powerful mirrors, triggering unhealed parts of our own childhood conditioning. They share how shifting out of survival mode and consciously clearing your internal blocks can completely change the emotional climate of your home. If you are a mother feeling burnt out, exhausted, and stuck in a loop of reactive parenting, this conversation offers the roadmap, permission, and actionable energetic tools you need to heal your family from the inside out.In This Episode, You Will Learn:- How our children's behaviors unconsciously trigger past ancestral and childhood conditioning.- The science and energy of co-regulation—why your child feeds off your nervous system's internal state.- Practical strategies to recognize parental burnout and halt chronic fight-or-flight loops.- The power of releasing judgment to build a sustainable, compassionate home life.

In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Nyck Walsh, writer, therapist, and advocate, who shares their journey to identifying as Autistic and ADHD later in life.Nyck reflects on growing up feeling fundamentally different — navigating school, relationships, and work without the language to understand why things felt harder than they seemed for others. Like many late-identified adults, they developed ways to cope, adapt, and push through, often at the expense of their own well-being.It wasn't until adulthood, through a combination of burnout, reflection, and exposure to neurodivergent experiences, that Nyck began to recognise themselves, leading to a deeper understanding of their needs, identity, and way of being.This is a conversation about unlearning, self-acceptance, and choosing a different way forward.

In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Dale Pickles — host of Sendcast and Managing Director of B Squared — for a wide-ranging conversation on late diagnosis, education systems, and what it really means to support neurodivergent people.Dale shares how he grew up surrounded by special education — yet still missed his own Autism and ADHD. It wasn't until 2023, prompted by supporting his daughter through her diagnosis journey, that everything finally clicked.This is a conversation about understanding yourself, supporting the next generation, and rethinking systems that weren't built for neurodivergent minds.

Hour 2 of the Chris Hand Show | Aired Thursday 05-28-26See omnystudio.com/listener for privacy information.

In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Jason Killian, an engineer, hiking instructor, and long time member of the club, who shares his journey to understanding himself as Autistic in his 40s.Growing up in a neurodivergent household, Jason was unknowingly accommodated in early childhood. Despite strong academic performance, Jason struggled with social integration, bullying, and later workplace dynamics, experiences that only made sense years later through the lens of Autism.This is a conversation about understanding your needs, building a life that fits, and what changes when you finally have the right framework.

Award-winning author Danielle McLaughlin tells PJ how her neurodivergence shapes her storytelling and why "rituals" became the anchor for her newest novel. Hosted on Acast. See acast.com/privacy for more information.

Warning: This episode includes discussion of terminal cancer, sudden bereavement, grief, burnout, and mental health struggles. Please listen with care.In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Scott Simpson, a late-identified Autistic and ADHD creator, former broadcast journalist, and widowed father who has been raising his son solo since 2016.After decades working in radio, Scott's life began to unravel through grief, burnout, and the collapse of the structures that had quietly supported him for years. What followed was a search to understand executive functioning, ADHD, and eventually Autism.Together, Angela and Scott explore hidden support needs, burnout after loss, Autistic shutdown, identity through memoirs and community, and why many late-identified adults only recognise their needs once life's scaffolding disappears.This is a conversation about grief, structure, survival, and finally understanding yourself.

In this Tough Girl Podcast EXTRA episode, we catch up with Paula "Must Try Harder" McGuire — author, speaker, triathlete, wing-walker, double TEDx speaker, mental health ambassador… and proudly, a trier. Based just outside Glasgow, Paula has been adventuring since 2015 and has built a reputation for trying something new every day — including completing 366 new experiences in 2020. But the years since we last spoke have brought extraordinary challenges. Paula shares openly about being diagnosed as autistic at 44, having a stroke at the end of 2021 and developing epilepsy, going through a divorce after 15 years of marriage, losing her home to a flood, and navigating post-stroke fatigue — all while spending six months in enforced van life. We talk about how adventure supported her through the hardest moments, how her neurodivergent brain fuels her love of planning and trying, and why you don't need to be the best at something to enjoy giving it a go. Paula also reflects on writing her book Adventures for Bored Adults (commissioned by Penguin), rediscovering her love of swimming, and learning acceptance in the face of uncertainty. Honest, funny and deeply human, this conversation is about resilience, identity, and continuing to say yes — even when life doesn't go to plan. ***  New episodes of the Tough Girl Podcast drop every Tuesday at 7 AM (UK time)! Make sure to subscribe so you never miss the inspiring journeys and incredible stories of tough women pushing boundaries.  Do you want to support the Tough Girl Mission to increase the amount of female role models in the media in the world of adventure and physical challenges? Support via Patreon! Join me in making a difference by signing up here: www.patreon.com/toughgirlpodcast.  Your support makes a difference.  Thank you x *** Show notes Who is Paula Being based just outside of Glasgow Being adventuring since 2015 TGP Episode  Working as an electronic note taker and captioner for deaf people TGP Extra Episode  6 years since we last spoke  How things have changed over the past few years in quite negative ways before eventually turning to a positive thing  In 2020 trying something new every day 366 new things (leap year!) Starting off the year really positively  How it became an adventure in creativity Feeling exhausted after the year was over  What that the last few years have taught her  Figuring out her place in the world of adventure  Being ready to relax  Social media not coming naturally to her  Struggling with the negativity of social media  Paula has tried hard enough - Paula is done. Being diagnosed with Autism at 44 6 months of enforced van life (November 24 - May 25) At the end of 2021 having a stroke and developing epilepsy  Her husband leaving her after 15 years and going through a divorce  Losing her house after a flood  One thing after another  Feeling that the universe had turned against her Feeling very lucky Brain tumour?? Start to prepare for Paula last Christmas  Moving on with a stroke and the potential for more strokes in the future  How the adventures from before really supported her Reminding herself of things she achieved, things that she'd failed at and survived Adventure and acceptance  Continuing to do fun things    A to Z of Adventure Post stroke fatigue  Not sticking to things - buying all the gear Getting the most mental stimulation in the trying  Wanting to be the person who tries it all  Her love for swimming and going back to it again and again Her neurodivergent brain - the planning, the execution, the reflecting  Being butterfly minded  Why you don't need to be the best at everything to enjoy having ago Coping with how your brain works  How her entire life has become clear after her diagnosis Advent(ure)  Writing a book commissioned by Penguin Book: Adventures for Bored Adults: Games. Challenges. Activities. Treats. How to connect with Paula on social media Supporting people with mental health Advice for women going through lots of challenges    Social Media Website: www.paulamusttryharder.co.uk Instagram: @pmusttryharder Facebook: @pmusttryharder

A mother shares her journey to her child's ASD diagnosis, what she noticed, how she found answers, and what came next. We then shift the focus to her, how she manages stress, builds support, and stays grounded for her child. Because parent self regulation isn't optional, it's essential.

Executive Director at the RSPB, Emma Marsh, joins Ben for a conversation that connects leadership, late autism diagnosis, and the often-overlooked role of nature in how we regulate and function.Diagnosed autistic in 2023, Emma reflects on what it means to navigate senior leadership as an autistic woman, the decision to disclose at work after years of masking, and how that moment reshaped both her identity and the way she leads.Ben and Emma dive into the power of nature and how fundamental it is for neurodivergent brains. From birdsong and the dawn chorus to simple ways of reconnecting with the natural world, Emma explains why nature can feel like a reset for the nervous system in ways modern environments often can't.They also explore why so many workplaces still unintentionally exclude neurodivergent people - and what it looks like to move beyond awareness into systems that actually support people and their brains.Join us at hidden20.org/donate.________Host: Ben BransonProduction Manager: Phoebe De LeiburnéVideo Editor: James ScrivenSocial Media Manager: Charlie YoungMusic: Jackson GreenbergHead of Marketing: Kristen FullerThe Hidden 20% is a charity founded by AuDHD entrepreneur, Ben Branson.Our mission is simple: To change how the world sees neurodivergence.No more stigma. No more shame. No more silence.1 in 5 people are neurodivergent. That's 1.6 billion of us - yet too many are still excluded, misunderstood, or left without support.To break the cycle, we amplify voices, challenge myths, and keep showing up. Spotlighting stories, stats and hard truths. Smashing stereotypes through honest voices, creative campaigns and research that can't be ignored.Every month, over 50,000 people turn to The Hidden 20% to feel safe, seen and to learn about brilliant brains.With your support, we can reach further, grow louder, and keep fighting for the 1 in 5 who deserve more.Join us at hidden20.org/donate.Become a monthly donor.Be part of our community where great minds think differently.Brought to you by charity The Hidden 20% #1203348______________Follow & subscribe…Website: www.hidden20.orgInstagram / TikTok / Youtube / X: @Hidden20charityBen Branson @seedlip_benEmma Marsh RSPB LinkedInhttp://www.rspb.org.uk/If you'd like to support The Hidden 20%, you can buy a "green dot" badge at https://www.hidden20.org/thegreendot/p/badge. All proceeds go to the charity. Hosted on Acast. See acast.com/privacy for more information.

Beyond the Sessions is answering YOUR parenting questions! In this episode, Dr. Rebecca Hershberg and I talk about...   Why many parents worry that using the word "autism" might make their child feel different or labeled, and how to think about that fear. What research and clinical experience suggest about telling your child sooner rather than later. How giving a diagnosis a name can actually feel empowering and help your child make sense of their experiences. What it looks like to take a neuroaffirming, strengths-based approach when talking about autism. How to explain autism to a young child in developmentally appropriate, non-pathologizing language.Why this doesn't have to be one big, serious conversation and how to follow your child's lead over time. The value of being the one who defines what autism means for your child, before the world does. Simple ways to normalize and support your child through representation, stories, and everyday conversations.   This episode will help you understand how to talk about neurodiversity in a way that feels simple, affirming, and age-appropriate, so your child can better understand their brain, their strengths, and the ways they experience the world.     REFERENCES AND RELATED RESOURCES:  

the importance of early autism screening tools, pediatric evaluations, and timely intervention. They also address common autism myths and misconceptions, including the belief that autism spectrum disorder (ASD) cannot improve. Dr. Lyons discusses how early intervention programs can significantly improve outcomes. Evidence-based therapies such as ABA therapy (Applied Behavior Analysis) and PRT (Pivotal Response Treatment) are explored as powerful tools to enhance communication skills, social development, and adaptive behavior. The conversation also highlights underlying health factors like gut health, sleep disorders, and nutritional deficiencies that may impact autism symptoms. Dr. Theresa Lyons and Dr. Foojan explore the complexity of autism spectrum disorder, emphasizing that autism is not a one-size-fits-all condition. They discuss co-occurring conditions such as ADHD, anxiety disorders, and dyslexia, and how overlapping symptoms can complicate diagnosis and treatment. Topics like high-functioning autism, masking behaviors, and emotional meltdowns at home are also examined, encouraging parents to trust their instincts regardless of their child's external presentation. The episode sheds light on the intense stress parents face during autism meltdowns, including emotional exhaustion and physical strain. Dr. Lyons shares research indicating that parents of children with autism may have a 20–30% higher risk of PTSD due to chronic stress. She offers practical emotional regulation strategies for parents and explains how maintaining calm during meltdowns can help de-escalate challenging situations. The discussion also explores the emotional toll of raising a child with autism, including feelings of guilt, isolation, and overwhelm—especially in public settings. They talk about coping strategies, social withdrawal, and the impact on siblings, who may also experience increased stress or trauma. A groundbreaking clinical trial using EMDR therapy (Eye Movement Desensitization and Reprocessing) is discussed, showing promising results in reducing PTSD symptoms in parents while improving emotional regulation in children. Finally, the episode focuses on empowering autism families through therapy, communication strategies, and strong emotional support systems. Dr. Lyons emphasizes teaching independence, fostering autonomy, and supporting both parents and siblings. The role of siblings in long-term caregiving, challenges faced by non-speaking individuals with autism, and the importance of building self-esteem are all addressed. Dr. Foojan highlights the need for parents to release guilt and make confident, informed decisions while accessing the right autism resources and support networks.

Autism rates are soaring around the world. It's a trend that troubles Dame Uta Frith who has been studying the disorder for more than six decades. She says the idea of autism on a spectrum has expanded so much it's starting to lose any meaning at all. More and more, the diagnosis is being used to describe people with all kinds of social challenges or sensory issues. She worries that some people are self-identifying as autistic, even glamourizing it, fueled by social media instead of a specific clinical diagnosis. Dame Frith is an Emeritus Professor at University College London and says questions need to be asked to ensure autism research is robust and support is given appropriately.

The word "mum" was Karina McHardy's first official red flag that something was going on with her toddler son. He was saying it - and then one day it was gone. 

#ThisMorning | Why #Parents are Begging for an #Autism #Diagnosis | Lawrence Diller, MD, Behavioral Therapist & Pediatrician | #Tunein: broadcastretirementnetwork.com #Aging, #Finance, #Lifestyle, #Privacy, #Retirement, #wellness

Send us Fan MailThis episode was originally released on Your Trauma Talks and is being shared here with permission so our audience can hear this meaningful conversation. In this interview, host Rahul K. Maharaj speaks with Brigitte Shipman and Joseph Shipman about faith, advocacy, acceptance, autism, and neurodiversity from both the mother's and autistic adult's perspective. The conversation explores grief, hope, stigma, self-compassion, and the power of understanding autism more deeply.Episode highlights Brigitte's journey through diagnosis, grief, advocacy, and self-compassion Joseph's perspective on growing up autistic and navigating stigma and missed social cues Advocacy without losing yourself Why being different is powerful What every parent needs to understand about neurodiversityListen to the original episode here: https://www.buzzsprout.com/2359531/episodes/18741535

How can technology help us diagnose autism earlier and get kids the support they need sooner?In this episode, I sit down with Dr. Cheryl Tierney to talk about an exciting advancement in autism diagnostics and how technology is helping clinicians and families access answers faster. With long waitlists and limited specialists in many areas, getting an autism diagnosis can sometimes take months or even years. Dr. Tierney shares how new technology is helping change that.We dive into the EarliPoint system, an FDA-cleared diagnostic aid that uses eye-tracking technology to analyze a child's viewing behavior while watching short social videos. The system collects an incredible 120 data points per second, giving clinicians objective data to support diagnostic decision-making. Even more exciting, the assessment takes only about 12 minutes and can be used with children as young as 16 months.Beyond diagnosis, we also talk about how this technology can support clinicians like speech therapists, BCBAs, and occupational therapists by providing data on social engagement, receptive language indicators, and problem-solving skills. That means we can track progress over time and better understand whether interventions are truly moving the needle.I also loved our conversation about interdisciplinary collaboration and the importance of having someone “quarterback” a child's care so families receive consistent guidance. This episode highlights how innovation, research, and teamwork can make earlier diagnosis and better support possible for so many families.#autism #speechtherapyWhat's Inside:Why skipping foundational ABA texts worries me for the future of the fieldThe ethical responsibility professionals have to collaborate across disciplinesWhy refusing services based on another therapy provider can harm learnersMentioned In This Episode:EarliPoint HealthEarn CEUs with a community of peers. Join the ABA Speech ConnectionABA Speech: Home

In this episode we explore the complex world of autism spectrum disorder (ASD) in children, featuring practical guidance from Dr. Teresa Lyons, an autism expert, scientist, and parent of a child with autism.    Dr. Theresa Lyons is an international autism educator, Ivy League-trained scientist, and autism parent. Dr. Lyons holds a Ph.D. from Yale and is the founder and CEO of Navigating AWEtism, a platform designed to turn complex autism science into clear, practical guidance for families.   Dr. Lyons' perspective is so powerful. She brings both rigorous scientific training and lived experience as the parent of a child with autism. She's worked with families in more than 21 countries, helping parents move from fear and confusion to confidence and clarity. Key Topics Discussed: What autism is and how it is diagnosed through observation on a spectrum The influence of changing diagnostic criteria and rising awareness Early signs and red flags for autism in infants and toddlers The importance of differentiating misinformation from evidence-based practices How families can prioritize support strategies tailored to their child's strengths The role of collaboration between parents, professionals, and educators Myths about autism, including misconceptions about listening and cognition The connection between vaccines and autism, and how to approach medical decisions Supporting parental mental health and managing emotional regulation Scientific advances in identifying biomarkers and personalized interventions Practical at-home steps for fostering communication and emotional stability   Resources:  Dr. Thersea Lyons' LinkedIn Navigating AWEtism's Website  Navigating AWEtism's YouTube Page Psychology Today  Autism Speaks    Connect With Us: Stay tuned for the next new episode of “It Happened To Me”! In the meantime, you can listen to our previous episodes on Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “It Happened To Me”.    “It Happened To Me” is created and hosted by Cathy Gildenhorn and Beth Glassman. DNA Today's Kira Dineen is our executive producer and marketing lead. Amanda Andreoli is our associate producer. Ashlyn Enokian is our graphic designer.   See what else we are up to on Twitter, Instagram, Facebook, YouTube and our website, ItHappenedToMePod.com. Questions/inquiries can be sent to ItHappenedToMePod@gmail.com. 

is an autism diagnosis actually helpful for your child — or could it hurt them?many parents hesitate to pursue an evaluation because they worry about labels, stigma, or putting their child “in a box.” but avoiding the diagnosis doesn't change whether your child is autistic. what it changes is how clearly you understand your child and how effectively you can support them.in this episode of EVOLVE with Dr. Tay, we break down both the logistical and emotional realities of autism diagnosis. Dr. Tay explains why a diagnosis can unlock support, provide language for self-understanding, and help families move toward greater acceptance and advocacy while also acknowledging the grief and stigma that can arise along the way.this episode is especially helpful if you're in the pre-diagnosis stage or if your child was recently diagnosed and you're still processing what that means for your family.in this episode, you'll hear:why an autism diagnosis doesn't change your child and instead gives clarity on how to support themthe logistical benefits of diagnosis, including access to services and support systemshow evaluations create a roadmap for understanding your child's strengths and support needsthe emotional side of diagnosis, including grief and adjustment for parents and childrenwhy many autistic adults wish they had known their diagnosis earlierhow giving your child language to understand their brain can support self-acceptancehow stigma and ableism influence how families think about diagnosiswhy avoiding the label can unintentionally reinforce shame or confusionhow parents can help shape a neurodiversity-affirming narrative about autismtimestamps00:00 understanding autism diagnosis: a parent's dilemma06:54 logistical benefits of an autism diagnosis13:36 emotional aspects of autism diagnosis19:06 navigating stigma and self-advocacyresources⚡️ learn more about autism evaluations through Dr. Tay Concierge Clinical Carehttps://drtaylorday.com⚡️ if your child already has a diagnosis and you're wondering how to talk with them about it, check out the masterclass inside EVOLVE the membershiphttps://drtaylorday.com/membership⚡️ continue learning from me >>Instagram @the.dr.tayTikTok @the.dr.tay

In this conversation, author, screenwriter and teacher Claire McGowan shares what it's been like to receive an autism diagnosis at 43 — and how that discovery is reshaping her understanding of her life, identity, and creative work.In this episode, we discuss:Claire's late autism diagnosis and the path that led to itThe mix of grief, anger, relief, and curiosity that followedGrowing up in Northern Ireland in the 80s and why autism wasn't on the radarSensory overwhelm — from public transport to event spacesHyperfocus, productivity, and writing 28 books in 14 yearsWhat Claire hopes will change in how society supports autistic adultsClaire also shares about the importance of talking about neurodiversity.Claire McGowan website https://www.clairemcgowan.co.uk/Claire's book The Other Couple  https://www.clairemcgowan.co.uk/booksClaire on Instagram https://www.instagram.com/clairemcgowanwriterSupport the showRATED IN THE TOP 0.5% GLOBALLY with more than 1,000,000 downloads! If you are an autistic person who has written a book about autism or if you have a guest suggestion email me at info@theautisticwoman.com. InstagramKo-fi, PayPal, PatreonLinktreeEmail: info@theautisticwoman.comWebsite June 24-28, 2026 In Rewilding Together

Dr. Hoffman continues his conversation with Theresa Lyons, PhD, a Yale-trained scientist and medical strategist who became an autism expert after her daughter's diagnosis and now runs AWEtism.net.

Autism, Functional Medicine, and Personalized Interventions: A Conversation with Theresa Lyons, PhD, a Yale-trained scientist and medical strategist who became an autism expert after her daughter's diagnosis and now runs AWEtism.net. Lyons describes dissatisfaction with conventional guidance that offers limited drugs for irritability and primarily ABA (Applied Behavioral Analysis), which is insurance-covered, often recommended at 40 hours/week, uses extrinsic rewards, and may help some skill-learning but has controversies and limitations for social development; she contrasts newer approaches such as RDI (Relationship Development Intervention) and PRT (Pivotal Response), which aim to build intrinsic motivation but are typically not covered by insurance. The discussion covers autism heterogeneity, changes in diagnostic categories (e.g., Asperger's folded into autism), and research including a Boston Children's Hospital study reporting 37% of children in a cohort lost their autism diagnosis over time (diagnosis based on observation). Lyons addresses debates about rising autism prevalence, noting multiple potential contributors and rejecting single-cause explanations, while citing risk-factor examples such as family autoimmune history and air pollution exposure. She outlines a functional medicine “why” approach using constipation as an example (root causes vs. symptomatic treatment), and emphasizes basic, low-risk steps such as evaluating diet, inflammation, hydration/electrolytes, and blood work for nutrients. Specific topics include gluten-free approaches (mechanisms involving gut permeability, immune burden, and CNS effects), dairy/inflammation, vitamin D deficiency and monitoring, melatonin as a well-studied short-term aid in autism (considered safe for a couple of years in studies) while still seeking underlying causes, and omega-3 fatty acids for focus and inflammation. Lyons explains leucovorin (folinic acid, prescription vitamin B9) as a targeted approach for children with folate receptor antibodies (reported in ~70% of autistic children), discusses the value and cost (~$300) of specialized testing from one U.S. lab, and notes reports of major speech and behavior improvements in responders, with dosing nuances. The episode also reviews evidence and cautions around the microbiome, including fecal microbiota transplant (FDA-approved for C. difficile; discussed as having an ~80% response rate in autism-related studies when gut issues are a key driver, but with major donor/compatibility considerations) and probiotics (some small trials and high costs). Other themes include “clean eating,” organic foods and toxin-load considerations tied to genetic detoxification vulnerabilities, discussion of acetaminophen/Tylenol in pregnancy in the context of glutathione pathways and personalized risk, and using genetics to guide interventions. Lyons warns that analysis of top autism TikTok videos found ~70% were inaccurate or overdramatized, recommending social media only for ideas, not decision-making. She also highlights parent stress, citing emerging research on increased PTSD risk among autism parents, and emphasizes support and community. Lyons advises parents to understand their child's specific health drivers and match them to appropriately specialized clinicians, noting her curated doctor listings in The Lyons Report.

There's a long-held idea that autism is more prevalent in boys than girls—the CDC says it's three times as common. But a growing body of research suggests the reality is more complicated. In a new study, researchers tracked autism diagnoses in millions of Swedish people born from 1985 to 2022. They found that the prevalence of autism is actually pretty even across the sexes, but people with “female” stamped on their birth certificate are often diagnosed later in life.  Host Flora Lichtman speaks with epidemiologist Caroline Fyfe about what this study teaches us about the prevalence of autism. Then, psychology researcher Rachel Moseley, an autistic woman herself, shares how late and missed diagnoses can affect autistic people. Guests: Dr. Caroline Fyfe is an epidemiologist at the University of Edinburgh who studied sex differences in autism diagnoses.  Dr. Rachel Moseley is a researcher in psychology at Bournemouth University in the UK, studying the experiences of autistic adults.Transcripts for each episode are available within 1-3 days at sciencefriday.com. Subscribe to this podcast. Plus, to stay updated on all things science, sign up for Science Friday's newsletters.

In this episode of 'Autism for Badass Moms,' host Rashidah welcomes Kanisha, a 40-year-old registered nurse in Houston and mom to five-year-old Zoë (diagnosed at 2.5, verbal with limited communication), shares her journey from early concerns and self-referral for evaluation to an ADOS-based diagnosis and the therapies that followed. She opens up about balancing full-time work, navigating limited support, starting full-day ABA, and witnessing Zoë's significant progress.At the heart of the conversation is disclosure. Kanisha explains why she told only a small circle at first, choosing privacy over overwhelm and commentary. She reflects on finding community online and encourages moms to move at their own pace, trust their discernment, and protect their peace.In this episode, we talk about:00:00 Welcome to Autism for Badass Moms (Show Intro)00:46 Today's Topic: Who Do You Tell First After an Autism Diagnosis?02:18 Meet Kisha & Zoe: A Diagnosis That Changed Everything04:42 Early Red Flags: 12–18 Months, Speech Concerns & Being Dismissed07:58 Two-Year Turning Point: Sensory Signs & Suspecting Autism11:22 The Daycare Wake-Up Call: Social Struggles & “Final Piece” Moment13:52 Taking Control: ECI, Child Find & Getting Evaluated Without Waiting16:45 Diagnosis & Insurance Hurdles: Fighting for Speech/OT Services20:03 School vs. Daycare Reality: When Half-Day Support Isn't Enough21:44 Choosing ABA: Fear, First Days, and Finally Seeing Progress24:26 Breakthroughs & Reframing the Future: From Level 3 to New Milestones26:16 The Grief After Diagnosis: Mourning Dreams, Milestones, and the Unknown32:27 Who We Told (and Who We Didn't): Processing the Diagnosis35:34 Grief, “What Ifs,” and Preparing for Every Outcome36:53 Protecting Your Child: Privacy, Boundaries, and Unwanted Advice38:56 Finding Your Tribe: Podcasts, Threads, and Support Groups That Get It44:14 Real-Life Logistics: Summer Break, Programs, and Working Full-Time47:36 Advice to New Autism Moms: Tell People at Your Own Pace51:48 What Makes Her Badass + Closing Reflections and How to Connect56:58 Final Takeaway: Discernment, Peace Over Pressure, and Guest Call-OutConnect with Kanisha:Instagram: www.instagram.com/mamanish20Resource shared:YouTube: confessionsofanautismmomIf this episode resonated with you:• Follow the Autism for Badass Moms Podcast on your favorite platform• Leave a review to help other autism moms find this community• Share this episode with a parent who may feel unseen or misunderstoodInstagram: www.instagram.com/theabmpodcastFacebook: www.facebook.com/theabmpodcastYouTube: autismforbadassmoms

*Learn more about The Brief Collective's Scaling Summit happening May 3rd-May 6th, 2026 and reserve your spot!---In this episode, I chat with Jennifer, VP of Strategy & Innovation at creative agency Marks. She shares her journey from traditional advertising to becoming a leader in brand strategy, and how her autism diagnosis helped many of her ways of thinking finally make sense. We talk about the power of emotional detachment and truth-telling in creative work, plus why adaptability and future-focused thinking matter more than ever—especially for small agencies and independent designers.Guest Name: Jennifer MurtellGuest Linkedin: Connect with her.Episode Mentioned:S12E4: Six Sneaky Places Design Businesses Leak Time & Money with Shannon MatternLinks:The Design Minimind - My 1:1 coaching program for designersDownload my FREE Creative Direction Figma Template (includes 4 audio trainings as well)Get 30% off of your HoneyBook subscription - The CRM I use in my studio.*Enjoy 1 month of Showit FREE with my code “HelloJune” when you sign up.*Earn $100 after you run your first payroll with Gusto, my payroll and compliance software.*Get 50% off your first year of Flodesk, my email marketing software.**Some are affiliate links which means I may earn a commission.Connect With Us:Our Free Facebook CommunityOur WebsitePodcast InstagramHello June Creative InstagramThe Design MinimindJoin The Creative Diaries (my email list)Tags:designer, design, brand design, brand identity design, design studio, design business, graphic design, brand designer, better podcast, brand designer podcast, logo design

Are parents of children on the autism spectrum raising kids with mental telepathy powers — or is that just a fascinating myth? And can you really self-diagnose autism in today's world of digital information overload?In this powerful episode, Chuck Tuck sits down with Dr. Theresa Lyons to unpack the truth behind autism, offering parents clarity, compassion, and hope. Together, they explore how neurodiversity, parenting, mental health, diet, and communication shape life on the spectrum. You'll learn why some children may lose their autism diagnosis over time, how diet and nutrition can ease symptoms, and why understanding the difference between meltdowns and tantrums is key to calmer homes.Dr. Lyons also dives into the challenges of self-diagnosis and the ongoing debate around communication tools for non-verbal individuals, grounding every insight in years of research and personal experience. Most importantly, this episode reminds every parent that autism isn't a verdict—it's a journey of understanding, patience, and connection.If you're curious, a parent feeling overwhelmed, or seeking trusted guidance, you're not alone. Join this heartfelt conversation, share it with someone who needs support, and help spread awareness and hope across the neurodiversity community.

I sit down with Leland Vittert to talk about his childhood diagnosis of autism and the extraordinary role his father played in shaping his resilience. We explore why removing adversity from children often backfires, and how discipline, honesty, and responsibility can become acts of love. This conversation isn't about romanticizing struggle, it's about learning how to do hard things and refusing to be defined by limitations.SHOW HIGHLIGHTS00:00 - Introduction02:10 - Autism Diagnosis and Early Childhood05:40 - A Father's Radical Commitment08:05 - Growing Up Without Friends10:55 - Self-Esteem Outside School and Sports13:20 - Why Adversity Was Never Removed17:30 - Learning You Can't Be Broken20:05 - Living With Autism as an Adult23:45 - Discipline Versus Accommodation27:00 - Teaching Social Skills Deliberately30:40 - Protection, Trust, and Character34:50 - Letting Kids Become More39:35 - Discipline as Strength45:10 - Parenting Without Expectations48:10 - Final Reflections and Where to Find Leland***Tired of feeling like you're never enough? Build your self-worth with help from this free guide: https://training.mantalks.com/self-worthPick up my book, Men's Work: A Practical Guide To Face Your Darkness, End Self-Sabotage, And Find Freedom: https://mantalks.com/mens-work-book/Heard about attachment but don't know where to start? Try the FREE Ultimate Guide To AttachmentCheck out some other free resources: How To Quit Porn | Anger Meditation | How To Lead In Your RelationshipBuild brotherhood with a powerful group of like-minded men from around the world. Check out The Alliance. Enjoy the podcast? Leave a review on Apple Podcasts, Stitcher, or Podchaser. It helps us get into the ears of new listeners, expand the ManTalks Community, and help others find the tools and training they're looking for. And don't forget to subscribe on Apple Podcasts | Google Podcasts | SpotifyFor more, visit us at ManTalks.com | Facebook | Instagram

Are you a late-diagnosed autistic, or are you considering getting an evaluation? Autistic Self-Advocate and podcast host Sara Bradford talks about why she decided to seek an autism diagnosis as one of her new year's goals. The following clip is from a roundtable discussion with our Global Autism Community where community members shared their personal and professional goals for the new year. Welcome to Autism Tips & Tools, where we highlight the best practical guidance from previous episodes of Autism Knows No Borders. Whether you're a self-advocate, a family member, or a service provider, there's something here for you! This conversation with our Global Autism Community was originally released on February 11, 2022. Would you like to learn new strategies to stay motivated and meet your milestones? Click the link below for the full conversation and be sure to subscribe to hear more from people connected to autism inspiring change and building community.  Setting Goals, with the Global Autism Community Let's work together to transform how the world relates to autism. ----more---- We appreciate your time. If you enjoy this podcast and you'd like to support our mission, please take just a few seconds to share it with one person who you think will find value in it too. Follow us on Instagram: @autismpodcast Join our community on Mighty Networks: Global Autism Community Subscribe to our YouTube channel: Global Autism Project We would love to hear your feedback about the show. Please fill out this short survey to let us know your thoughts: Listener Survey

Welcome back to Dial Emma and a very happy new year to you all!Each week, I'll be answering your dilemmas with honesty, empathy, and a few therapeutic truth bombs to help you make sense of life's stickiest moments. If you've ever wished you had a therapist in your back pocket, Dial Emma is here to help.This week, I'm joined by Dr. Emma Offord, a clinical psychologist, neurodivergence specialist and founder of Divergent Life. We're unpacking a dilemma from a listener who has been diagnosed with autism at 38. The diagnosis initially brought her relief, but now the dust has settled, she has been left with a sense of being unmoored from everything she once knew.How does this listener find her authentic self again, after a life spent blurring her true identity by people-pleasing and masking?In this episode, we discuss the challenges of receiving a neurodivergent diagnosis later in life, the complexities of identity, the societal expectations that contribute to masking, and the importance of self-acceptance and understanding our own sensory needs. Dr. Emma Offord also emphasises the need for a supportive community during the process of unmasking and embracing who we truly are.If you have a dilemma for Emma, please fill out this form. ---Dial Emma is hosted by Emma Reed Turrell, produced by Lauren Brook.---Social media:Emma Reed Turrell @emmareedturrellDial Emma @dialemmapodcastEmail: contact@dial-emma.uk

Once primarily limited to severely disabled people, autism began to be viewed as a spectrum that included children and adults far less impaired. Along the way, the disorder also became an identity, embraced by college graduates and even by some of the world's most successful people, like Elon Musk and Bill Gates.Health Secretary Robert F. Kennedy Jr. has called the steep rise in autism cases “an epidemic.” He blames theories of causality that mainstream scientists reject — like vaccines and, more recently, Tylenol — and has instructed the C.D.C. to abandon its longstanding position that vaccines do not cause autism.Today, Azeen Ghorayshi explains what's really driving the increase in diagnoses.Guest: Azeen Ghorayshi, a science reporter for The New York Times.Background reading: Should the autism spectrum be split apart?There are no easy answers for parents of children with autism.Photo: Eric Gay/Associated PressFor more information on today's episode, visit nytimes.com/thedaily. Transcripts of each episode will be made available by the next workday.  Subscribe today at nytimes.com/podcasts or on Apple Podcasts and Spotify. You can also subscribe via your favorite podcast app here https://www.nytimes.com/activate-access/audio?source=podcatcher. For more podcasts and narrated articles, download The New York Times app at nytimes.com/app.

Elyse Myers, (writer/creator) stopped by to talk to JVN all about her new book That's A Great Question, I'd Love To Tell You, living with ADHD, and navigating parenthood after being diagnosed with Autism as an adult. From masking and people-pleasing to boundaries and self-acceptance, Elyse shares the before/after of getting language following her diagnosis. Plus! We also dig into how she writes and why the Midwest is low-key the best.   Elyse Myers is a writer and comedian who achieved mainstream recognition as a digital content creator. Deemed "The Internet's Best Friend," Myers continues to serve her audience of more than 10M+ with relatable stories, twisted Q&A's over coffee, and acts as an advocate for countless topics such as ADHD, imposter syndrome, body image and more by allowing herself to be seen, unfiltered in a genuine and hilarious way. Full Getting Better Video Episodes now available on YouTube.  Follow Elyse Myers on Instagram @elyse_myers and Tiktok @elysemyers Follow Getting Better on Instagram @gettingbetterwithjvn  Follow Jonathan on Instagram @jvn Check out the JVN Patreon for exclusive BTS content, extra interviews, and much much more - check it out here: www.patreon.com/jvn  Senior Producer, Chris McClure Producer, Editor & Engineer is Nathanael McClure Production support: Chad Hall Our theme music is also composed by Nathanael McClure. Curious about bringing your brand to life on the show? Email podcastadsales@sonymusic.com. Learn more about your ad choices. Visit podcastchoices.com/adchoices

Calm your mind. Change your life. Try Calm by heading to https://calm.yt.link/2lLJh1b. ———————— This week, Shan sits down with Grammy-winning artist Chrisette Michele opens up about being diagnosed with autism as an adult and the way that revelation helped her understand her rhythm, her relationships and what safety really means for her. She shares how music became one of the few places that always made sense, how her mom stood by her through the unknown, and how she finally began to remove the mask and meet herself. Later, we bring in expert Maria Davis-Pierre, LMHC, founder of Autism in Black, Inc., to guide a deeper conversation around autism, neurodivergence, intimacy, and how we show up for those we love. Whether you're neurodivergent, in a relationship with someone who is, or simply want to deepen your understanding, this episode invites you to explore how love, safety, and authenticity coexist. Follow Chrisette Michele: Instagram: https://www.instagram.com/chrisettemichele/ Website:chrisettemichele.com Follow Maria Davis-Pierre & Autism in Black: Instagram:https://www.instagram.com/autisminblack/ Website: https://www.autisminblack.org/ Sign up for the 5th Annual Autism In Black Conference Virtual or In-Person Attendance: https://funnel.autisminblack.org/2025-autism-in-black-registration-page?aff=Christina-Schmidt Want more Lover? Shan's AI trained to give you her advice → http://loversbyshan.com Get a free weekly Love Letter → http://loversbyshan.com/newsletter Join the Lovers Community → https://www.loversbyshan.com/community Explore free quizzes + worksheets → http://loversbyshan.com/quizzes

Elyse Myers, one of the internet's biggest comfort creators, joins Vic for a conversation that feels like a warm hug. With over 12 million followers across social media, Elyse is known for her comedic storytelling, relatability, and the way she helps people feel seen in their messiest, most human moments. In this episode, Elyse opens up about her new book, That's a Great Question, I'd Love to Tell You, a stunning mix of poems and stories she describes as “a modern art museum,” and the life lessons behind it. From how to stop overanalyzing yourself and make peace with anxiety, to why she embraces body neutrality over toxic positivity, to what her break from the internet taught her about simplicity, boundaries, and joy, this conversation is honest, healing, and full of heart. Tune in to laugh, reflect, and remember that peace doesn't come from having all the answers, it comes from simply being here.Get her new book, That's a great question, I'd love to tell youInstagram: @elyse_myers// SPONSORS // LMNT: LMNT is offering a free sample pack with any purchase, that's 8 single serving packets FREE with any LMNT order. This is a great way to try all 8 flavors or share LMNT with a friend. Get yours at DrinkLMNT.com/realpod.CozyEarth: Go to cozyearth.com and use code REALPOD for 40% off best selling temperature-regulating sheets, apparel, and more.Nature's Sunshine: Go to natures sunshine.com and use the code REALPOD at checkout for 20% off your first order plus free shipping. Winx: Head to hellowinx.com/realpod for 50% Winx @ Walgreens. Please note that this episode may contain paid endorsements and advertisements for products and services. Individuals on the show may have a direct or indirect financial interest in products or services referred to in this episode.Produced by Dear Media.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.