Autism Dadcast

Gaz and Andrew

An unfiltered, unflinching, and occasionally inappropriate deep dive into the world of autism parenting-from a dad's perspective.

  1. 23H AGO

    "No One Has Ever Failed"

    Steven has no autistic children. No family connection. No commercial interest. He just watched a movie and couldn't look away. In January, he was driving his van on the M1, listening to a documentary called The Spellers. It's about non-verbal autistic children who learned to communicate by pointing to letters on a board. 48 minutes in, he pulled over and cried. The children in the film all said the same thing: "I'm in here." Since then, he's read over 120 books written by non-speaking autistics and their parents. He's watched every video he could find. He wakes at 4am to research for three hours before his day starts. He's joined 20+ autism groups. He's created a free resource site called Presume Competence. And he has one message for parents: the method has a 100% success rate. No one has ever failed. In this conversation, Steven explains what he's learned — not from professionals, but from the people who've lived it. He talks about optical dyspraxia and why your child might not be able to catch a ball. He explains why screens flicker in ways neurotypical eyes don't notice. He describes the six sensory buckets that overflow into meltdowns. He shares why swimming pools regulate, why routines matter more than we realize, and why time perception might explain everything. He sat with Paddy Curran, a non-speaker from Birmingham, and had a full conversation through a letterboard. Letter by letter. And he nearly cries just talking about it. The spelling board is the world's cheapest education device. The entire internet is built from 26 letters. Your child already knows them. They just need a way to show you. Steven's goal: a spelling practitioner in every town in the UK. Free resources. No cost to learn. Because if your child can point to a letter, they can say anything. This is what presumed competence looks like.

    37 min
  2. 2D AGO

    We Had to Hand Our Son Over

    Luke has four children. Three of them are autistic. His youngest, Oscar, is non-verbal with PICA — he'll eat anything, including sand and his own faeces. For years, Luke and his wife managed. He gave up his job as an HGV driver because the phone calls from home couldn't wait two hours for him to get back from Hereford. His parents were their only support network — his dad had worked with disabled children his whole life. Then his dad died unexpectedly. And his mum said the words no one wants to hear: "I can't do it on my own anymore." Support workers came on weekends. Some were good. Others turned up 45 minutes late, by which point Oscar had stripped naked and was too dis-regulated to leave. One time, staff at a soft play centre had to tell the support workers that Oscar was naked — because they hadn't noticed. Eventually, Luke and his wife had to say the hardest thing a parent can say: we can't meet his needs anymore. They explored residential care. The council's response? They wanted to explore foster care first — because it was cheaper. No support systems. No respite for the foster family. Just school. Luke asked them directly: "Why do you think complete strangers are going to do a better job than we did for eight years?" They won. Oscar is now in a specialist residential setting with speech and language therapy, 24-hour support, and a chance at communication. Luke still has full parental responsibility. They see him every fortnight. They can bring him home whenever they want. But it doesn't sit right. It never will. Luke also shares the fight for his middle son's EHCP — tribunal, legal battles, a previous school that sent nothing but a date of birth when asked for evidence. That education costs £120,000 a year. Half a million pounds by the time he finishes secondary school. And he says something most parents won't say out loud: "I hate autism." Not everyone's autism. His autism. The one that means his family can't go to Christmas gatherings. The one that meant handing his son over. The one that doesn't fit the "superpower" narrative. This is what the system doesn't want you to see.

    31 min
  3. 4D AGO

    I Diagnosed Myself at 10

    At 10 years old, during lockdown, Charlotte watched a BBC series about autism. She saw herself in it. So she did what most adults wouldn't — she researched it, gathered the evidence, and presented it to her parents.They didn't believe her at first. She didn't fit the stereotype. She wasn't a boy obsessed with trains.She was put on the pathway. She waited 3 years. She went through half of secondary school undiagnosed, unsupported, and struggling.When the diagnosis finally came, it wasn't a surprise. She already knew. It was just clarity — recognition from the outside.But the years without support took their toll. Charlotte developed functional neurological disorder. She had seizures. She ended up in hospital. She left secondary education with no GCSEs.And that's when she started her Instagram account.From a hospital bed, she began sharing her story. She found community. She found purpose. She started speaking out — first online, then at youth parliament, then at Westminster.When Gaz and Andy met her at a rally outside Parliament, she was 16. It was her first ever public speech. She'd never even put her hand up in class before.Now she attends youth parliament every week, sits with councillors and decision-makers, and advocates for the changes she never had.Her mom watches from the sidelines, proud of the daughter who diagnosed herself and fought her own corner when no one else would.This is what's possible when someone finally listens.

    14 min
  4. NOV 9

    Autism Dadcast: Episode 22 — “Strong Dads, Scary Thoughts & Small Wins”

    Gaz and Andy sit down for one of the most open chats they’ve ever had. It’s been a long few weeks, and with Christmas creeping up, the lads talk about the heavy stuff that comes when things finally go quiet — the late-night fears about the future, the weight of responsibility, and that nagging thought every SEND parent has but never says out loud: what happens when we’re gone? They dive into what it really means to be “strong” as an autism dad — not in the gym sense (though that comes up), but mentally and emotionally. How patience has replaced pride, how autism strips away ego, and how much you change when your world revolves around a child who needs you in ways you can’t explain to anyone else. There’s reflection on how far their kids have come, what progress actually looks like, and why the little moments — eye contact, a word, a shared laugh — feel bigger than any milestone the world measures. They also talk about physical health, mental fatigue, and the quiet importance of keeping your body strong enough to handle what’s ahead. Because being a SEND parent isn’t a sprint — it’s a marathon you didn’t sign up for, and you can’t afford to sit it out. Heavy, hopeful, and funny in all the right places. Exactly what Dadcast does best. #AutismDadcast #AutismAwareness #SENDParenting #AutismParents #AutismDads #Neurodiversity #AutismAcceptance #SpecialNeedsParenting #AutismCommunity #AutismJourney #MentalHealth #FuturePlanning #Resilience #DadLife #ParentingPodcast

    1h 32m

Ratings & Reviews

5
out of 5
5 Ratings

About

An unfiltered, unflinching, and occasionally inappropriate deep dive into the world of autism parenting-from a dad's perspective.

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