Mrs Bonanno is among an estimated 9 per cent of Australian women of childbearing age who have a disability, but little is known about their health during pregnancy, birth and the first year of motherhood. Researchers from La Trobe University and the Royal Women’s want to change that by improving the way disabilities are identified at maternity hospitals.
This guide has been created to help you put in place some safeguards to ensure the person with disability you care for is properly provided for, if something were to happen to you. It outlines actions carers can take now to ensure safeguards are in place, should the time come when they are no longer able to care for the person with disability.
The CYP guide is based on the conditions outlined in the National Disability Insurance Scheme (Restrictive Practices and Behaviour Support) Rules 2018 and has been developed “to acknowledge that children and young people with disability require special consideration and safeguarding in order to protect them from harm whilst actively promoting their development and upholding their legal and human rights.”
This podcast series features casual conversations with families of children with disability and/or developmental delay and the professionals they work alongside. The aim is to support and build families’ knowledge, skills and confidence when navigating the early childhood intervention (ECI) landscape. It is also an opportunity for parents to share their individual stories of everyday life in family with a child diagnosed with a disability and/or developmental delay.
How much funding a family receives depends on how well the family can advocate for themselves, how much supporting paperwork they have been able to collect from medical professionals, the level of understanding the random case worker assigned to the family has and how well they communicate the families needs to the funding body the NDIA.
Sue Grier has always worried about what might happen to her autistic son when she dies, but her concerns have grown due to proposed changes to the National Disability Insurance Scheme (NDIS).
Disability, domestic violence a ‘catch 22’ as Indigenous children removed from mothers, royal commission hears
Babies are being removed at birth from First Nations mothers living with disabilities, the disability royal commission has heard. Giving evidence in Brisbane, Ms Schwartz said she had witnessed the removal of Indigenous babies first hand. “I would call it a heinous practice,” she said.
“We are among the most seriously disadvantaged members of the Australian community, and are also experts on the impact of policies on us,” says First Peoples Disability Network Chief Executive Officer Damian Griffis. “This week, a number of First Nations people with disability will give evidence about the different racist and ableist systems that harm our children.”
Kimberly’s sunny, athletic and inquisitive about everything. But for years she harboured terrible secrets about what happened to her. Janine Fitzpatrick investigates why her school failed to heed credible warnings that she was in danger.
This broad suite of NDIS related content has been designed to support parents and carers of children with disability to navigate the NDIS. It has been developed in collaboration with subject matter experts.
New data released has revealed the significant impact the National Disability Insurance Scheme (NDIS) is having on young Australians with disability and their families.
With good quality relationships, children and young adults with cognitive disability feel “valued, respected and cared about” in their daily lives and, in turn, give carers more job satisfaction and self-respect, international researchers say in a new paper published in the international Disability & Society journal.
More than isolated: the experience of children and young people with disability and their families during the COVID-19 pandemic
The main message of this report is that urgent action is needed to attend to the many inequities that people with disability and their families and carers face on a daily basis. Without movement on these issues, any future widespread emergencies will again produce substantial destabilisation for these households, with similarly detrimental impacts. This report sets out the key findings of the survey, devised by Children and Young People with Disability Australia (CYDA), that captures the impact of COVID-19 on children and young people and their families and identifies unmet needs for resources and information as well as identifying areas requiring responses and future research priorities.
The Mission Australia Youth Survey has taken a disability lens to its data for the first time Young people with disability are more likely to report poor mental health and are twice as likely to have been bullied in the past year than young people without disability, according to data analysis from Mission Australia.
The Disability Support Toolkit has resources for front line workers supporting people with disability who have been impacted by violence and abuse. The Toolkit is a result of the Disability Pathways Project, which aimed to improve responses for people with disability who have been impacted by sexual assault, domestic and family violence.