The most recent COVID outbreaks have raised familiar concerns about one of the most complex mainstream interfaces: health and NDIS. And more specifically, what NDIS supports can a person access when they are in hospital?
The first doses of vaccine arrived on Australia’s shores on February 15 and most of the highest priority people were to have received at least a first dose by April. The strategy was sound – but you need more than words on a page to make strategy become reality.
Just over a quarter of Australians in the National Disability Insurance Scheme (NDIS) are fully vaccinated – behind the national average – with hundreds of thousands of people yet to have a jab despite being in the federal government’s highest priority groups.
Frustrated disability groups say the Australian government has failed to protect the nation’s most clinically vulnerable people during the pandemic. Now, they have put forward an 11-point plan to urgently improve the vaccine rollout for the disability community.
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.
These resources have been produced to help people with disability and low English literacy understand more about coronavirus vaccinations. The resources include a social script, visual schedule, Easy English document and Key Word Sign video.
The report analyses and summarises the evidence presented during public hearing 6. It suggests that psychotropic medication, which are drugs that affect a person’s mind, emotions or behaviour, is being over-prescribed to people with cognitive disability to deal with what are commonly described as ‘behaviours of concern’. Medical evidence along with observations from family and carers indicate people with cognitive disability often experience serious negative consequences from using psychotropic medication And there is not much evidence to support the effectiveness of psychotropic medication as a way to address behaviours of concern
Disability representative organisation People with Disability Australia has found people with disability are struggling to work out if they are eligible for COVID-19 vaccines and are getting extremely inconsistent access to vaccination appointments.
David Littleproud defends stalled COVID-19 vaccine rollout to people in disability care accommodation
But just 999 have received a shot, which is less than 4 per cent of the people living in the facilities. Mr Littleproud, when asked if that figure was “good enough”, said “yes, because it’s part of the scheduled rollout”.
And while the positive impacts are widespread across specific patient groups, it has been particularly beneficial for vulnerable populations, such as those accessing the National Disability Insurance Scheme (NDIS).
I spoke not in my capacity as President of People with Disability Australia, nor as a board member on any of the other boards that I sit on. I spoke as a disabled woman and a carer who, like many of us, has spent a lifetime battling disability and mainstream services and systems.
The federal government’s given up putting a date on when all Australians will get their COVID-19 vaccination, as one of the nation’s largest disability service providers says not one of their residents has received a jab;
Hospital admissions for NDIS Participants can mean a challenging game of ‘who is doing what’ when considering the Support Coordination role, the Participant, the State- or Territory-funded health supports, and inpatient clinical teams.
This report finds that Victoria’s mental health system operates in crisis mode, has “catastrophically failed to live up to expectations” and must be rebuilt. Demand has now overtaken the capacity of the system. Among the final report’s 65 recommendations, outlined in a mammoth five-volume report, are the phasing out of seclusion and restraints treatments over the next decade, and making compulsory treatments an option of last resort.
Jo Abi fears what will happen to her two autistic teenage sons when she is no longer around to communicate when they need health care, she told the Disability Royal Commission on Tuesday.