Our Voice SA members Libby Crawford and Gavin Burner talk about what self-advocacy and speaking up means to them and how it's helped them in their lives.
Equality Lawyers is now offering a free 30-minute consultation via Zoom conference or phone until 31 July 2020. The first consultation is a great way for people with disability and their families to better understand their legal rights and what the next steps could be.
Are you living with disability and working in retail or aged or disability care? We are looking for people to share their employment stories for our next podcast.
COVID-19 has had a big impact on the way we live our lives, especially when it comes to social interactions. As more of us stay home to control the spread of the virus, we must use different ways to stay connected with friends and family. This article shares 5 ways you can stay connected with others during COVID-19.
When Maria Cantanzariti, who lives with complex disability, needed to get a Covid-19 test, it was a horrible experience. But, there's a solution.
We want to keep you updated during this period while we are working at home during COVID-19. This page provides information on the current projects we are working on at JFA Purple Orange, and how they will help people living with disability.
It’s important to stay well and take care of yourself and others during this period. This coping calendar by Action For Happiness has 30 great self care ideas on how you can look after your physical and mental wellbeing.
To support the wellbeing of our staff, we have closed our office building and all staff will be working from alternative locations. The phone numbers remain the same if you need to contact us during business hours.
Stay informed about Covid-19. We will continue to update this page with relevant news and information. Easy English resources included here.
We’ve all heard that dogs are man’s best friend. But for Mark, and many people all over the world, they are so much more. They are independence, support and safety. Producer April Dwyer, brings us the story of a man who rebuilds his life after an acquired brain injury with the help of two unlikely friends.
Purple Orange is seeking expressions of interest from people living with disability and family members in SA who would like to be a member of our new Co-design Council (CDC).
Everyone needs to feel connected, but a lot of men - disability or not - just aren’t connected enough. But how can men who are feeling disconnected, build connection? I sat down with three men, at different stages and ages of life to discuss their experiences of creating connection.
Christine Priest knew she wanted to experience sex, but didn't think she ever would. She had to reach her own breaking point, before breaking through the stigma and assumptions that prevented her from seeing herself as a sexual being. Now she's sharing her story, with that hope that others will feel empowered to discuss their needs. Check out our latest podcast episode where Christine urges us to talk about sex.
Do you live with disability or have a family member living with disability? Do you want to take part in a 90 minute focus group, for which you would receive a $60 gift card as a thank you?
Click here for answers to all your questions about the Disability Royal Commission.
We carried out an online survey to explore the views and experiences of public transport for South Australians living with disability.
Click here to find out what the Disability Royal Commission wants to know about your experiences with education and learning.
There is an empty champagne bottle, proudly displayed as a trophy, in the office of Reinforce, an advocacy group for adults living with intellectual disability.
This policy submission was made to the Joint Standing Committee on the National Disability Insurance Scheme about NDIS Planning in September 2019.
School is an important time in all of our lives. It’s when we explore what we like to do, learn social skills and begin to develop our identity. But school isn’t all self-discovery and excitement; students face pressure academically and socially. These things are challenging for everyone, but if a school doesn’t support its students to be fully included, it’s even harder.
When Ellen Fraser-Barbour was 19, she decided to travel on her own to India. Everyone told her it was a bad idea. "You are crazy," they said. "You are deaf. You are blind! You can't travel on your own!" But Ellen decided that was their anxiety. It wasn't her anxiety. So she persevered with her plan.
At Purple Orange, our aim is to create a world where all people who live with disability get a fair go in life. That won’t happen unless Aboriginal and Torres Strait Islander People are listened to, respected, included and given choice and control over how they live their lives, as their community also includes people who live with disability.
Headshot Day was organised by Belle Owen and Lisa Gascoigne of Y Connect. Belle explained about the work they do, and why they organised Headshot day.
We know something needs to be done about plastic waste, which is why campaigns to ban the straw are gaining momentum. But could banning the straw create another problem with dire consequences for many?
The consultation period for the South Australian Government’s first Disability Inclusion Plan has now opened.
When Ellen Fraser-Barbour was 19, she decided to travel on her own to India. Everyone told her it was a bad idea.
"You are crazy," they said. "You are deaf. You are blind! You can't travel on your own!" But Ellen decided that was their anxiety. It wasn't her anxiety. So she persevered with her plan.
Listen to the newest Purple Orange podcast episode on the link above.
Read the story and see photos of Ellen's trip to India here.
I was 19 years old when I had a rare non-blood related stroke caused by an abscess on my brainstem pons (think of the brainstem as an apple and the seeds are the abscess). I was in a coma for 3 weeks, I wasn’t supposed to wake up! I survived, but with a condition called Locked-in Syndrome, I could not communicate verbally or move.
I came to Julia Farr Centre (now called Highgate Park) in 1993, 13 March. My nana’s birthday. For the first 5 to 6 years, I didn’t go out in public. My reason for this was that my face was severely affected, and if I couldn’t cope with the way I looked, then how could the public! I was also in deep denial and depression for 19 years! All I had was mum, nurses and TV. Even when technology improved I refused to learn how to use a PC.
When I did start going out, I would only go out with mum. It wasn’t until my birthday in June, 2008, when my nana rang me and I heard her voice. There was something in her voice that told me that I had to go see her now, but she lived in Perth. How was I to get to Perth when I had a disability? I mentioned to Ross, my carer, about wanting to go to Perth. Unknown to me, he had done it all before, and soon enough I was on a plane with mum and Ross to Perth.
We want to see a world where everyone is included, respected and gets a fair go in life. We can't get there without acknowledging that our office sits on the land of the Kaurna people. Like people living with disability, we recognise that Aboriginal and Torres Straight Islander people continue to experience inequality and division. We want them to know we are their allies. We believe their culture, history, diversity and deep connection to the land deserves our highest respect.