Communities of practice (CoP) and communities of interest (CoI) are ways of sharing, connecting and informing for people living with disability. This paper covers all aspects of CoPs and CoIs.
People living with learning or intellectual disability, their families and other interested people are welcome to attend.
Julia Farr Youth is looking for a self-starting, values-driven Executive Officer for a range of executive, secretariat, organisational and project support.
Invitation to tender for an independent evaluation of Purple Orange's Inclusive School Communities Project
December 6th will be the first of what will become an annual conference and celebration for and by people living with disability in South Australia. If you live with disability, we would love you to join us.
How accessible should all new homes be? There is an important discussion happening right now in Australia about this issue. Get involved and help shape a more accessible future!
There is an information kit for NIDS stakeholders about the new Commonwealth government agency called the NDIS Quality and Safeguards Commission (NDIS Commission).
Storytelling has the power to build community, inspire action, and change the way we view the world. That's why we're dedicated to sharing stories of the people our organisation exists for.
We are thrilled to be assisting Our Voice SA, a self-advocacy organisation for people living with intellectual disability, on an important project about engaging with the NDIS and connecting with community.
In 2018 the YWCA Adelaide are launching Y Connect that seeks to empower young women living with disability to identify and progress their goals for employment or career development.
The hardest part about having severe Juvenile Arthritis is that people don’t realise how seriously damaged my joints are or how sick I can become because of my compromised immune system. For more than 10 years I have been regularly pumped full of the latest drugs every month via an intravenous infusion. They make me feel quite sick but they also help to control the joint swelling and pain. It has been a bit of a logistical nightmare to be chained to a drip for several hours every month and then feel quite unwell for a bit, especially when my daughter was a baby. And it is often hard for people to understand that I need such intense drug therapy for a condition that sounds so common. But just recently I had my last infusion (hopefully forever) because there is a new drug available that I can take as a tablet every day instead. This will be so much easier, I am so lucky!