Raised in institutions, Sir Robert Martin advocated for the rights of persons living with disability. He became one of the world's most influential leaders. Knighted in 2020, this is his story.

Mitch has global development syndrome and found fame in TVNZ's Four to Flatting. In this next chapter with Mitch, he has once again left the family home to live independently with new flatmates.

Sophie-Maude lives with OCD, Autism, ADHD, and Tourette's, and uses music to express her world. A chart-topping single at 17, five years ago - she now has 11 songs on Spotify, and a bright future.

A blind skier, Thomas Coysh, has a sense of freedom on the slopes. He's working towards qualifications to compete at the 2030 Winter Paralympics. At speeds of 100km per hour, it comes with risk.

Every day at dawn, Todd heads to work. Todd's a concreter. He has overcome challenges associated with being autistic and having verbal dyspraxia. Focused and thorough, he is an invaluable employee.

In this second episode of CP and Me, we focus on more lived experiences, taking an informative and entertaining approach where viewers learn about Cerebral Palsy firsthand. Revealingly honest.

Luka Willems is a man of many talents. At 22, Luka, who lives with Down syndrome, is setting the bar high within the community, showing that people with Down syndrome can explore many opportunities.

A right arm amputation after an aggressive bone cancer hasn't halted Rylee's love for para-swimming. One year post-chemo, 15-year-old Rylee aims to compete at the 2028 LA paralympics.

CP and Me is full of great New Zealanders. World Cerebral Palsy Day is 6 October, and in episode one, we learn about CP from firsthand experiences. It's raw, emotional, funny, and insightful.

17-year-old Charli Gardiner-Hall dreams of competing at the Paralympics. Charli has Sturge-Weber syndrome, a rare neurological disorder. Struggling through childhood, Para sport saved her life.

During childbirth, Lydia suffered a brain injury. This is an intimate profile of Lydia, her devoted husband, Christian, and how to balance life's challenges while parenting their five-year-old son.

Ollie and Ethan King have a chronic and rare condition, Duchenne Muscular Dystrophy. With limited options, the boys' parents have put their faith in a drug trial that could be life-changing.

Zak Nielsen is a tenacious teenager with Pit Hopkins syndrome. His father, Craig, has worked hard all his life to provide a world of growth and development for Zak in Taranaki.

Name almost any sport and Craig Harrington's probably given it a crack. But now the below-knee amputee is facing one of his biggest challenges – taking on the adaptive CrossFit World Games.

Four-year-old Willow lives with Mucolipidosis, a life-limiting condition. The whānau live by the mantra; ‘Don't count the days, make the days count' which encompasses their positive thinking.

Over 14,000 Kiwis are affected yearly by an acquired brain injury. In part three of My Fragile Brain, when Hayden and Nikita return home, they adjust everyday activities.

The impact of head injury is explored in this three-part series. In one of NZ's leading rehab centres, we follow the recovery of Hayden, struck down by a car.

Over 14,000 Kiwis are affected yearly by an acquired brain injury, the impacts are largely unseen. Over three parts, My Fragile Brain explores what brain injury looks like through patients.

A natural go-getter, 12-year-old Jack hasn't let his sight impairment slow him down. Jack's ambitious nature has led him to surf lifesaving and gymnastics, exceeding everyone's expectations.

Ollie Schimanski lives with a debilitating rare condition, similar to childhood dementia, Sanfilippo syndrome. His family shares their positive approach dealing with one of life's hardest challenges.

Tom Little was just five when he was diagnosed with ADHD. He struggled with social cues and felt isolated and frustrated. But his world changed when he met a teacher who welcomed his differences.

It's fierce competition for our NZ teams at the Deaf Basketball 3x3 World Cup. Staying at Gallaudet University, USA, the world's first deaf campus, players discover the potential of an inclusive world

A two-part Deaf special following NZ 3X3 Deaf Basketball teams' trip to Gallaudet University in the USA. We learn firsthand the challenges players overcome as they prepare for the trip of a lifetime.

A Matariki special of culture and inclusion. We join an Idea Services group from Masterton at Te Anga Paua ō Aotearoa National Kapa Haka Festival and see how culture positively impacts wellbeing.

Casey Brady is constantly on the move and determined to walk again. When Casey sets her mind to achieve, she does. Motherhood is her next target, we explore this new world with her.

Finn Murphy's life-defining moment was caught on camera. Just 500m from home, he collided with an oncoming vehicle. Determined to push limits, Finn has high hopes of representing NZ on the water.

Tamara is autistic, a mother, a CEO, and an advocate, raising awareness for others. This insightful episode draws viewers into her world & shows the importance of inclusive communities.

Brad's life changed in an instant after a pro-wakeboarding trick went terribly wrong. Attitude Pictures launches a new season with this revealing and personal story of the courage it takes to adapt.