“Everyone with access needs – including disabled people, older people, Māori, migrants, people with English as a second language, and those with temporary injuries - must have an equal opportunity to live life without being hindered by barriers to participation.”
My name is John. I’m from Bluff. And I believe every word of this statement, so aptly expressed by the Access Alliance. People with access needs absolutely deserve an equal opportunity to live life without constantly having to try to overcome problems and difficulties on a daily basis.Read more
My name is Anamaria, I am the carer for my 17-year-old grandson Razeal, and we live in Wanganui. Razeal suffers from a brain injury; we have spent the last 15 years battling ACC and the last five years in court trying to get Razeal the proper care he needs. In the process, we have been confronted with systemic barriers that have made it extremely difficult for Razeal to gain funding for services that are essential to his learning and long-term growth.Read more
Using a wheelchair hasn’t stopped Merle Bradley going snorkelling or getting out into the rugged West Coast bush.
[Story originally published at Mental Health Awareness Week 21-27 September 2020]Read more
Masks are a big part of the fight against Covid-19 in New Zealand, but for a large part of the Kiwi community, they are also an added complication when it comes to being understood.Read more
I had a taste of accessibility – and I want it for keeps!Read more
Differently Abled tells the story of Graeme Axford.
Born with severe dyslexia and misunderstood throughout much of his childhood, Graeme rose above stigma and systemic exclusion to become a social worker. But after being overlooked for a job at CYF (now Oranga Tamariki) Graeme smelled a rat and decided to challenge the decision. What ensued was a long arduous, time-consuming battle.Read more
During the COVID-19 lockdown, I joined the Virtual Teddy Bear’s Picnic hosted by Marama Davidson from the Green Party. It was pitched as a children’s event but was attended solely by parents of voting age who wished to express some of their concerns in lockdown.Read more
Finding out about the COVID-19 lockdown scared me terribly because I knew I’d have to deal with it by myself. With my Asperger's I'm more capable and independent than a lot of others but I think everyone with any kind of special needs should have access to community support whenever they need it. Especially during a national state of emergency.Read more
I have special needs and medical complexities including epilepsy. I love school so much. My Mummy spent a lot of time researching schools with good inclusion and low roll numbers to accommodate my immune-deficiency. I had only been at school full-time for a few months when we first heard about Coronavirus, and then I stopped school.Read more