On the bustling Cake Tin concourse in Wellington, a young DJ was warming up the crowd ahead of the sold-out 2026 Super Rugby Pacific Grand Final, with handpicked mixes of popular songs for the fans. For many 14-year-olds, performing at a major sporting event would be a daunting prospect. But for Waikanae's Harper Ahern, aka DJ Harpz, it was just another gig, and the latest milestone in a growing musical career. He wasn't even nervous. “It doesn’t really matter where I play, a

For Auckland father Craig McKinlay, the flexibility of Individualised Funding (IF) and the responsiveness of Manawanui have made a significant difference to his family. Craig is the agent for his two sons, Jacob, 15, and Connor, 14, who both have autism and ADHD. Jacob has moderate to severe autism and was diagnosed at around three or four years old. Connor was diagnosed last year with Level 1 autism. While their diagnoses are similar, their support needs are different, so ea

Debbie has spent years dreaming about creating a business that combines her creativity, love of animals, and desire to build something of her own. With support from Manawanui's Fund for Good, that dream took a big step forward when she received an xTool laser engraving machine.

Jessica creates handmade covers for medical devices that help people feel more comfortable, confident, and like themselves. With support from Fund for Good, she upgraded her sewing equipment and workspace, making it easier to work independently and create custom pieces for her clients. The new setup is already making a meaningful difference, enabling Jessica to continue supporting others while building a future that works for her.

The DSS Bill has sparked significant debate across Aotearoa New Zealand’s disability community. While the Government says the Bill will provide “clarity and stability to the system which supports thousands of disabled New Zealanders”, many, including Manawanui, are concerned the Bill will negatively impact how disability support is delivered, particularly Individualised Funding. A key concern is that the Bill shifts a large portion of the substantive detail out of the pri

Emma's recent therapy intensive in New York marked another important milestone in her journey. Born with a complex brain disorder, she continues to make remarkable progress through determination, consistency and specialised therapy. Alongside hard work in the clinic, Emma and her family created lasting memories together, returning home with something far more valuable than souvenirs - progress. Every step forward is worth celebrating.