Introduction
Referral of inquiry and terms of reference
1.1
The Joint Standing Committee on the National Disability Insurance Scheme
(NDIS) was established on 1 September 2016. The committee is composed of five
Members and five Senators.
1.2
The committee is tasked with inquiring into:
- the implementation, performance and
governance of the NDIS
- the administration and expenditure
of the NDIS; and
- such other matters in relation to
the NDIS as may be referred to it by either House of the Parliament;
1.3
After 30 June each year, the committee presents an annual report to the
Parliament on the activities of the committee during the year, in addition to
other reports on any other matters it considers relevant.
1.4
The committee is also able to inquire into specific aspects of the
Scheme. The committee agreed to undertake an inquiry into the provision of
hearing services under the NDIS on 30 November 2016.
1.5
The terms of reference for the inquiry are as follows:
- That
the joint committee inquire into and report on the provision of hearing
services under the National Disability Insurance Scheme (NDIS), with particular
reference to:
-
the eligibility criteria for determining access to, and service needs
of, deaf and hearing impaired people under the NDIS;
-
delays in receiving services, with particular emphasis on early
intervention services;
-
the adequacy of funding for hearing services under the NDIS;
- the accessibility of hearing services, including in rural and remote
areas;
-
the principle of choice of hearing service provider;
-
the liaison with key stakeholders in the design of NDIS hearing
services, particularly in the development of reference packages;
- investment in research and innovation in hearing services; and
-
any other related matters.
Reporting by the committee
1.6
Initially, the committee delayed the completion of its report because it
was expecting the release by the NDIA of key operational guidelines relating to
a) the access criteria to the Scheme for deaf and hard of hearing people and b)
to the development of early intervention reference packages. The NDIA indicated
that they would release these guidelines for by the end of April 2017.[1]
1.7
On 1 September 2017, the NDIA publically released the access criteria to
the NDIS. The NDIA is yet to release the early intervention reference packages.[2]
1.8
As a result, the committee has decided to release this interim report,
which focuses on these two critical issues: the access criteria to the NDIS for
deaf and hard of hearing people and early intervention services.
1.9
The committee intends to release its final report once the early
intervention reference packages have become public. The final report will
discuss the reference packages and will address the other terms of reference
not covered by this interim report as well as additional issues raised by
participants.
Structure of interim report
1.10
This interim report is comprised of three chapters, as follows:
-
this chapter (chapter one) outlines the administration of the
inquiry and provides an overview of hearing services and the transition to the
NDIS;
-
chapter two discusses the eligibility criteria and the recently
released NDIA guidelines for determining access to the NDIS; and
-
chapter three focuses exclusively on early interventions issues
and the development of the early intervention reference packages.
Conduct of the inquiry
1.11
The committee received 55 submissions to the inquiry from individuals
and organisations. These submissions are listed in Appendix 1.
1.12
The committee also conducted two public hearings on 20 February 2017 and
24 March 2017.
1.13
Transcripts from these hearings, together with submissions and answers
to questions on notice are available on the committee's website.[3]
Acknowledgements
1.14
The committee would like to thank the individuals and organisations that
made written submissions to the inquiry, as well as those who gave evidence at
the two public hearings. We are grateful for their time and expertise.
Note on terminology and references
1.15
References to submissions in this report are to individual submissions
received by the committee and published on the committee's website. References
to Committee Hansard are to official transcripts.
1.16
The committee intends to use the term deaf and hard of hearing to encompass
the diverse community that has some form of hearing impairment, including
people who identify as deaf, hard of hearing, or deafblind.
1.17
The diversity of the deaf or hard of hearing community was best
described by Ms Philippa Angley, Executive Officer to the Chief Executive
Officer, National Disability Services:
NDIS participants
with hearing impairment are diverse. There are those who acquire a hearing
impairment as they age, which is well after they have developed language;
children who are born deaf or who may become deaf as a young child; children
who may receive a cochlear implant, children born to parents who decide that
their child will be part of the deaf community and not receive a cochlear
implant or may receive hearing aids; there are people who are born or become
deafblind, and I think they are a particularly marginalised group within the
disability population; there are Indigenous Australians with hearing loss;
there are those living in rural and remote areas, where access to services is much
more limited; and, of course, there are people from culturally diverse
backgrounds.[4]
1.18
Ms Angley noted that as a consequence of this diversity, attention
should be focussed on the need to design and implement an NDIS that supports
all eligible people with hearing impairment and their varied needs: 'There is
no single solution that will meet the needs or preferences of all'.[5]
Overview of hearing services
1.19
One in six Australians is affected by hearing loss. Prevalence rates for
hearing loss are associated with increasing age, rising from less than one per
cent for people aged younger than 15 years to three in every four people aged
over 70 years.[6]
1.20
In Australia, between 9 and 12 children per 10 000 live births will be
born with a moderate or greater hearing loss in both ears. Around another 23
children per 10 000 will acquire a hearing impairment that requires hearing
aids by the age of 17 through accident, illness or other causes.[7]
1.21
All babies born in Australia are screened for hearing loss at birth
under the Australian Government’s Universal Newborn Hearing Screening program.
Those who receive a 'refer' result from their screening (or are detected later)
will go on to a diagnostic service and then, if a hearing loss is diagnosed,
attend Australian Hearing and/or a Cochlear Implant service for further
assessment and assistance.[8]
1.22
The majority of hearing services are provided by the Hearing Services
Program (the Program), which provides services to a range of people with mild
to profound hearing loss, including children and young adults, some Indigenous
Australians and aged and disability pensioners. The Program is delivered
through Australian Hearing and through other accredited private sector
providers.
1.23
Therapies, including education and communications programs are mostly
delivered by a range of private providers, including charitable organisations.
Access and referral pathways to these services vary depending on jurisdictions.
Hearing Services Program (the Program)
1.24
The Office of Hearing Services (OHS) was established in 1997 to
administer the Hearing Services Program (the Program). The Program provides
access to subsidised hearing services and devices for eligible people, and
supports research that assists with reducing the incidence and consequences of
hearing loss in the community.[9]
1.25
The Program has two streams for the delivery of hearing services: the
Voucher Scheme and the Community Service Obligations (CSO). Additionally, it
supports and funds program-relevant research, including through the National
Acoustic Laboratories (NAL).
1.26
Hearing services are provided under the Voucher Scheme by a national
network of private hearing services and Australian Hearing.
1.27
Australian Hearing is the sole provider of hearing services for the CSO
stream.[10]
The organisation was originally established by the Australian Government in
1947 to provide hearing services to children and veterans who suffered hearing
damages during World War II. Australian Hearing is a statutory authority
constituted under the Australian Hearing Services Act 1991, reporting to
the Minister for Human Services.
The Voucher Scheme
1.28
The Voucher Scheme enables eligible clients to obtain hearing services
and devices from a national network of private hearing services providers and
Australian Hearing. In 2015–16,
around 690 000 clients received a service under the Scheme, with approximately
1.2 million services being delivered. The average age of eligible clients was
77, with 89 per cent of program clients aged over 65.[11]
1.29
The Scheme gives participants access to a wide range of fully or
partially subsidised hearing devices, maintenance, and ongoing support. These
services are provided by approximately 300 private providers, offering services
out of approximately 3700 sites, accredited with the program, including
Australian Hearing.[12]
1.30
The majority of people who receive a voucher from the program are over
65 years of age and are ineligible for the NDIS. Voucher clients who are not
eligible for the NDIS will continue to receive services through the Program.
Community Service Obligations (CSO)
1.31
The Community Service Obligations (CSO) provides specialist services to
young Australians aged 0–26
years, including young NDIS participants, Voucher eligible adults with complex
hearing needs, Indigenous groups, or participants in the Remote Jobs and
Communities Program or the Community Development Employment Projects Program.[13]
1.32
In 2015–16, DHS
provided $65.3 million to Australian Hearing for CSO services.[14]
Australian Hearing reports that under the CSO in 2015–16:
-
29 850 children or young adults under 21 received 67 864
services;
-
3628 young adults aged between 21–26
received 7736 services;
-
23 344 adults with specialised needs received 53 771 services;
-
4300 Indigenous people received 8256 services; and
-
578 cochlear implant speech processors were funding through the
speech processor upgrade program.[15]
1.33
Australian Hearing services include assessing hearing, fitting hearing
devices and providing counselling and rehabilitative programs to enable
eligible customers to manage their hearing impairment.[16]
1.34
Australian Hearing works closely with newborn hearing screening programs
and early intervention agencies to streamline service access. Newly diagnosed
children are offered an appointment within two weeks of the referral receipt.[17]
1.35
The system has been described as world class, especially in the field of
early intervention services and programs for newborns and young children:
The system that we have achieved for early identification of
hearing loss and effective engagement with intervention services beyond that
identification is, without doubt, at the forefront of services internationally,
arguably matched only by services in Denmark...[18]
Transition of services to the NIDS
1.36
Commonwealth, state and territory programs providing services and supports
to people who are deaf and hard of hearing are transitioning in full or in part
to the NDIS.
1.37
There are four Commonwealth programs transitioning in full or in part to
the NDIS. They are:
-
Hearing Services Program (the Program) funded by the Department
of Health transitioning part of its services to eligible NDIS participants. It
is expected that by 2019–20,
when the NDIS reaches full national roll out, a portion of program clients
under 65 years of age will transition to the NDIS;[19]
-
National Auslan Interpreter Booking and Payment Service (NABS)
funded by the Department of Social Services. Funds for clients under 65 years
will be transitioned to the NDIS;[20]
-
Remote Hearing and Vision Services for Children up to 18 years of
age in outer and remote locations across Australia funded by the Department of
Social Services. It is a small program currently providing services to fewer than
60 children[21]
via remote service delivery methods. The Royal Institute for Deaf and Blind
children is the sole provider of this program. It is expected most participants
will be eligible for the NDIS. The program is transitioning in full to the NDIS;[22]
-
Better Start for Children with Disability, which assists eligible
children with developmental disabilities to access funding for early treatment,
diagnostic and management services. Under the program, children under the age
of six with an eligible diagnosis can access early intervention funding up to
$12 000 (a maximum of $6 000 per financial year). There are currently more than
5900 children receiving services under the program of which more than 1500 have
a primary disability of hearing impairment or deaf blindness.[23]
It is expected that most children will be eligible to the NDIS. The program is
transitioning in full to the NDIS.[24]
1.38
State and territory support programs for deaf and hard of hearing
people, including early intervention programs are also transitioning to the
NDIS. These programs were mostly delivered by the non-government sector, which
received block funding to provide a range of services.
The NDIS Transition Plan
1.39
The NDIA anticipates that approximately 16 000–20 000 participants with
hearing impairment will enter the NDIS by 2019–2020.[25]
1.40
The National Disability Insurance Agency (NDIA) advised that as of 31 March
2017 there are 1966 NDIS participants with hearing impairment. This represents
approximately three per cent of current NDIS participants.[26]
1.41
In February 2016, the Department of Health released the Hearing Services
Program NDIS Transition Plan. This transition plan describes the 'activities,
dependencies and timeframes', that need to take place to effectively support
the transition of eligible Hearing Services’ clients to the NDIS.[27]
1.42
The transition plan identifies the key objectives and the proposed
strategies to ensure a smooth transition. The plan also identifies the roles
and responsibilities between Department of Health (Health), Department of
Social Services (DSS) and the National Disability Insurance Agency (NDIA).
1.43
The scope of the transition plan includes identifying and implementing
the activities that will enable program clients who will be eligible to move
across to the NDIS to receive services. It will also identify program clients
who will not be eligible to move to the NDIS and how the Program will continue
to support those clients e.g. clients over 65 years of age, and clarify
responsibilities of stakeholder agencies for ensuring a successful transition.
1.44
In its submission to this inquiry, the NDIA advised that it was
undertaking a range of activities to ensure support under the NDIS for people
with hearing impairment is appropriate, evidence based and consistent with the National
Disability Insurance Scheme Act 2013 (the NDIS Act). These activities
include, but are not limited to:
-
developing guidance material for use by NDIA National Access
Team, planners and Local Area Coordination (LAC) partners on levels of hearing
loss likely to require NDIS supports;
-
developing reference packages to guide planners and LAC partners
in building participant plans, including guidance on reasonable and necessary
funded supports;
-
supporting arrangements for transition of people from former
Commonwealth Programs;
-
designing referral pathways with a particular focus on early
childhood/early intervention (ECEI) to ensure appropriate supports are received
as early and efficiently as possible;
-
working with service providers to assist their transition to the
NDIS environment; and
-
working with key stakeholders and deafness/hearing loss
communities to build their understanding and engagement in NDIS processes.[28]
1.45
The NDIA advised the committee it was 'developing evidence based
guidelines to support consistency in decision about accessing the NDIS and
reasonable and necessary supports for people with hearing impairment'.[29]
1.46
In its submission, the NDIA also provided information about the
development of the reference packages both for early interventions and for
evidence based reference packages across the lifespan.[30]
1.47
During the course of the inquiry, the NDIA advised the committee it was
anticipating releasing the early intervention reference packages by the end of
April 2017.[31]
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