Chapter 4 - Young people in residential aged care facilities
These young people can't
use a buzzer, can't shout out for attention and yes, we know that nursing homes
are understaffed and aren't really set up for high maintenance care for these
ABI patients but does that really explain the missed PEG feeds, the discarded
dressings on the floor, the lack of cleanliness in the room or the horrendous
bed sores that sometimes never heal. This is the cry for help of some of the
most marginalised in our society today.[311]
Introduction
4.1
In May 1990, this Committee reported on its inquiry
into accommodation for people with disabilities.[312] The Committee found that it was not
appropriate for young people to share accommodation, such as nursing homes,
with older people and cited the recommendation of the 1986 Nursing Homes and
Hostels Review:
More appropriate care services should be found as a matter of
priority for younger people with disabilities in general purpose nursing homes
predominantly for aged persons.[313]
4.2
Despite these recommendations, young people with
disabilities are still accommodated in residential aged care facilities and the
number has been increasing over the last decade. At the present time there are
over 6000 young people (those aged under 65 years) in residential aged care
facilities with the Committee hearing that in Victoria
a nine year old is accommodated in an aged care facility.[314] Many submissions noted that with
improved medical outcomes for severe spinal and head injuries and other
illnesses, more young people will be in need of care in the future. Very young
people, even with severe disabilities, may have normal life expectancy and
require support for 40 to 50 years. Some people with degenerative conditions,
such as Huntington's Disease, may require complex medical care for ten or more
years.
4.3
Another group of disabled people who will require care
in the future are young people with disabilities being supported at home by
ageing parents. In many instances these young people will require residential
care, often when their parents become frail and/or infirm or when the level of
home services available can no longer adequately meet their changing needs.[315]
4.4
While witnesses stated that aged care facilities were
not appropriate for young people, they access this form of accommodation
because there are no reliable alternative options. The Young People in Aged
Care Alliance (YPACA) stated:
In fact, nursing homes are perceived as 'dumping grounds' for
people that the system has given up on and, while these options remain, all
people with existing disabilities or newly acquired disabilities are
potentially at risk.[316]
4.5
Aged care providers were also concerned that young
people are placed in their facilities as the needs of the frail aged and young
disabled 'couldn't be more diverse and both groups suffer to a greater or
lesser extent'.[317] The parent of a 24
year old currently residing in an aged care facility stated:
Staffing levels in the Aged Care Facility may be consistent with
care for people in the end stages of life, but they are nowhere near to being
adequate for the different and more intense needs of young people with complex
care needs.[318]
4.6
The Office of the Public Advocate Victoria
also noted that:
The younger cohort is likely to have a significant
representation of high level care needs. This group includes young people
physically incapacitated through road and other trauma. There are a proportion
of people with an Acquired Brain Injury (ABI) as a consequence of alcohol
misuse and trauma. There are also people experiencing the degenerative effects
of specific medical conditions such as Multiple Sclerosis (MS) and Huntington's
disease. The group is therefore likely to represent a broader and at times more
complex range of care issues than older people who are more likely to have
similar disabilities such as dementia and age related frailty. As a consequence
this group of people represents particular challenges in devising accommodation
options that can meet both their physical care and psycho-social needs.[319]
4.7
This chapter looks at the issues surrounding the
accommodation of young disabled people in aged care facilities as well as the
provision of services for those living in the community.
The number of young people in aged care facilities
4.8
Young people enter aged care facilities because of
disabilities arising from a variety of reasons including Acquired Brain Injury
(ABI), Motor Neurone Disease (MND), Multiple Sclerosis (MS), malignant brain
tumour or Cerebral Palsy. Data provided by the Department of Family and
Community Services (FaCS) indicate that the number of young people aged under
50 in residential aged care in May 2005 is less than in July 2002, decreasing
from 1075 to 1007 (this latter figure does not include a small number in the
ACT). During this time, the number aged under 65 years increased from 5994 to 6398.[320] The National Alliance of Young
People in Nursing Homes (NAYPINH) stated that in early 2004 there was a 'spike'
in numbers entering nursing homes with an additional 73 young people
accommodated in aged care facilities between January and March 2004.[321]
Table 4.1: Number of persons aged under 65 years in residential aged
care facilities as at May 2005
State |
0-49 yrs |
50-59 yrs |
60-64 yrs |
Total |
NSW |
399 |
955 |
955 |
2 309 |
VIC |
214 |
655 |
663 |
1 532 |
QLD |
228 |
591 |
528 |
1 347 |
SA |
71 |
188 |
208 |
467 |
WA |
60 |
197 |
216 |
473 |
TAS |
21 |
71 |
67 |
159 |
NT |
14 |
31 |
21 |
66 |
ACT |
X |
17 |
28 |
45 |
AUSTRALIA |
1 007* |
2 705 |
2 686 |
6 398* |
Note: The small number of residents in the ACT
makes them potentially identifiable. These figures have been suppressed to
protect the privacy of the individuals concerned.
* Totals do not
include the small number of residents in the ACT.
Source: DoHA, Submission
168, Additional Information 20.6.05 (FaCS).
4.9
A more detailed analysis of young people in aged care
facilities is difficult to obtain. NAYPINH stated that 'it is very difficult to
know what type of disability young people already in aged care facility have
because the Department of Health and Ageing does not collect data according to
disability type, just according to location and age ranges'.[322] However, some indicative information
was provided to the Committee. NAYPNH cited the following breakdown of young
people in aged care facilities:
- Acquired Brain Injury (ABI) 30%
- Physical Disability 27%
- Neurological 23%
- Intellectual/psychiatric 20%[323]
4.10
Individual organisations also provided information. The
Multiple Sclerosis (MS) Society of NSW stated that there were 100 people under
the age of 60 years with MS in aged care facilities in NSW.[324]
4.11
There are 6.5 cases of Huntington's Disease (HD) per
100 000 of population. In NSW there are around 400 people at any one time
with HD. The Australian Huntington's Disease Association NSW stated that in
2002 there were 75 people under 65 years with HD in residential care. Of these,
31 aged under 50 years were in residential care with 23 in nursing home, and 8
in hostels; 33 aged between 50 and 60 years were in residential care with 27 in
nursing homes, 3 in hostels and one in a psychiatric hospital and 2 others
in care but the level not known.[325]
4.12
The number of young people who are either in acute care
hospital beds or in the community who are viewed as 'at risk' of entering aged
care facilities is unknown. However, the MS Society of NSW indicated that there
were approximately 300 people in New South Wales
who MS Society outreach workers have identified as being at immediate risk of
being admitted to aged care facilities if there is even a slight change to
their current support systems.[326]
4.13
NAYPINH predicted that there will be 10 000 young
people in nursing homes by 2007 if the current trends continue and stated that
'the current rate of entry for young people at the moment is a young person
entering an aged care facility somewhere in Australia every day of the week'.[327]
Younger people with disabilities in the community
4.14
As well as evidence about young people already living
in aged care facilities, much evidence was received by the Committee concerning
people with disabilities living in the community who face the prospect of
becoming residents in aged care facilities because no other suitable
accommodation is available. As noted above, it is not known how many people may
fall into this category but a number of groups at risk were identified
including those people who are cared for by ageing parents and those whose
medical needs cannot be supported by community based services.
Ageing carers
4.15
Many ageing carers have provided care for family
members for years, if not decades. This length of caring takes its toll on
ageing carers: physically, financially, socially and emotionally. At a time
when others have enjoyed a long retirement, carers face the anxiety of what
will happen to their children once they require aged care. For many people with
a disability, and indeed their carers, one of their biggest fears is that if
community services are unavailable, there will be no option but to enter a
nursing home. One parent told the Committee:
Probably the most important thing that I would like to mention
today is our fear for the future. While we love looking after Paul
at home, we will not always be here to do this. I am terrified about what will
happen to Paul after we have gone. I would never
expect my other children to take over this responsibility. They deserve a life
of their own. There has to be somewhere in the future for our young people to
be accommodated for either respite or long-term care. This problem affects us
all: it is our kids that we are talking about, and it could happen to anybody’s
family. I really hope and pray that things will change for the better in the
future.[328]
Case study – UnitingCare
network
This week the parents of a young man of 48
approached our network. This man, who has an intellectual impairment, was
admitted to hospital. He now requires constant attention for feeding and
toileting which his parents, 70 and 75, cannot do, being themselves too frail
to get him out of bed and too tired after years of supporting him to motivate
him into doing even the simplest things – like sitting up – for himself. The
hospital wanted him to go home. No supported accommodation was available – the
only option for this young man was a residential aged care facility.
Submission 57, p.8 (UnitingCare).
4.16
In November 2004, the Minister for Family and Community
Services announced that State and Territory Community and Disability Services
Ministers had accepted a plan to help ageing carers of disabled children. A
working party of officials is to provide advice as to the steps governments
will take to:
- consult with older carers of people with disabilities
to understand the present unmet needs for support and future needs for care of
their sons and daughters;
- provide more transparent planning for future
service provision and allocation of resources;
- provide greater confidence amongst older carers
that, with cooperation between the Australian, and State and Territory Governments,
the needs of their sons and daughters will be better met; and
- enable increased personal/family provision for
future care.
4.17
The Ministers also agreed to negotiate with the Commonwealth
on mutually acceptable arrangements to meet the respite needs of carers over 70
years of age. The Commonwealth has allocated $72.5 million over four years for
respite for older parents caring for children with a disability, subject to it
being matched by State and Territory Governments.[329]
Living in the community with
disabilities
4.18
There are many people with severe disabilities who live
at home. They do so with the help of family members and government and
community funded support services. The Committee was provided with many cases
where families have gone to extraordinary lengths to support their family
members at home.
4.19
The burden on carers can be extremely high and carers
may also have the additional responsibilities of raising the family as well as
being the bread winner. Some children take on the role of carer for their
affected single parent or when the healthy parent is working. In the case of
inherited diseases the Committee heard that it is not uncommon to see some
carers who care for more than one family member or may be at risk themselves. A
practitioner stated that one person reported caring for family members for 30
years: affected spouse and several affected adult children all under the age of
65 years.[330]
4.20
The impact of chronic illness and the stress of care on
families are considerable. Support groups noted that marriage breakdowns were
not uncommon and this further exacerbated the care and accommodation needs of
disabled people. The Cerebral Palsy League of Queensland indicated that family
breakdown sometimes resulted in children being placed in aged care facilities:
...the reason sometimes children with disabilities end up living
in nursing homes is that there is a family breakdown because of the high
support needs around the child. They just cannot cope. They cannot get enough
support when the child is younger and then as the child gets beyond adolescence
they grow heavy to lift and some of those sorts of things occur. They do not
have enough support and there is a lot of stress put on the family unit.[331]
Crying out for help
I am a 46 year old mother. He is 21 years old
now. He was 17 when he got severe hypoxic brain injury while he was depressed.
I am really tired. My husband and I are both worn out over this past 3½ years.
My son is only 21. He needs the stimulation of young people. He loves older
people but he is not old.
He had to be assessed by ACAT (Aged Care
Assessment Team) because there was no one else to assess him. I just had to
hand back 63 days of respite care (Federally funded) because there was no
suitable place in Geelong for him to go. We are crying out for Home First hours (State funded)
to be topped up so we can have active night duty because he has severe sleep
apnoea. But the Federal and State Governments do not have their acts together.
It broke my heart going through the nursing
home process with my 21 year old son. We were shown a mixed room – a man in his
90s in one corner, an elderly lady with dementia in another, and my son was to
be put in the other corner.
I went home with my son and cried my eyes out
and never went back. So we have never had respite yet.
Submission 47, p.2 (Karingal)
4.21
The failure of services to respond to changes in needs
was seen as a further problem. The Hunter Brain Injury Service commented that
the lack of long-term case management for young people with traumatic and
acquired brain injury is a significant issue. There is inadequate ongoing
oversight of the changing needs of clients, particularly in relation to
reassessment and/or coordination of services, and crisis intervention that can
occur in a timely manner. The Service stated that 'our experience indicates
that this contributes significantly to the breakdown of support services at a
community and family level, as well as increasing the burden of care for
(primarily) family'.[332]
4.22
The MND Association stated:
The thing with motor neuron disease is its rapid progression,
requiring rapidly changing services to meet rapidly changing needs. One of
those needs is supported accommodation. At the moment, many people access aged
care services for that support and, as we have outlined in our submission, that
is inappropriate. We, like Young People in Nursing Homes, are arguing strongly
for much more flexible models of funding to allow people to purchase support that
will assist them to live in their own homes for longer, allow their carers to
continue to contribute to their care and support and enable them to live
fulfilling lives while still being part of their own community – and not,
because of lack of capacity in their own homes, be forced into an aged care
setting...[333]
4.23
In some cases the complex care needs of the disabled
person become so high that it is no longer possible for families to care for
them. Evidence from those supporting people with degenerative diseases and
brain tumours indicated that care needs can progress to a very high level which
requires specialist support. Care needs for different conditions also progress
over different periods of time. For example, with Huntington's Disease, the
duration of the illness is approximately 20 years although with better
care, some patients live for 25 years. Patients spend approximately
10 years in the community and 10 years in residential care.[334] For people with motor neurone
disease, progression is rapid and requires ever changing services to meet
rapidly changing needs.[335]
4.24
Southern Health commented that services were often
directed to work with people who are at the lower end of care rather than for
people at the higher end of care.[336]
While ParaQuad stated:
A lot of our clients are in nursing homes merely because there
are not enough services in the home to accommodate them. After people with
these types of disabilities have had their disability for more than 20 years
they start getting more and more functional, medical and psychosocial problems
– this is not necessarily related to their chronological age – and, as the
in-home services do not increase and there is no other service for them, they
are therefore forced into nursing homes.[337]
4.25
The Gippsland Carers Association observed that 'family
carers are facing an ever increasing pressure to care at all costs, against an
ever-dwindling supply of care support services due to demand outstripping
supply'.[338]
4.26
Supported accommodation was often seen as the preferred
option for accommodating disabled people in the community. However, in some
cases a person's health needs or behaviour may be such that services in
supported accommodation are inadequate. Supported accommodation is also not
always available and there are long waiting lists for places in most, if not
all, facilities.
Mark's
story – A Huntington's Disease case history
The following is an example of a typical case
the HD Social Workers have experienced.
Mark is 36 years old, single and has never
worked.
He lived alone in private rental in Sydney but was evicted for inability to look after his
flat and erratic rent payment. He is now living with a sibling in a provincial
town and is on a Disability Support Pension. He was originally on Newstart.
Sibling brought him to the HDS [Huntington's
Disease Service] at Westmead
Hospital where he was diagnosed clinically and on
MRI.
Mark has dementia and psychotic thinking; he has
been seen by a psychiatrist and prescribed an anti-psychotic drug which he will
not take. He requires prompting and supervision with washing, dressing, meal
preparation, cleaning and money management and his siblings believe he needs
residential care.
He was admitted to Lottie Stewart Hospital for respite/assessment but he absconded
after two days as Mark does not believe he has HD. He often goes
missing for days, travelling by train to Central Railway Station and not coming
home until the early hours of the morning or he may go missing for days.
Action
The Mental Health Team initially would not
get involved as HD is not a mental illness 'within the meaning of the Act'.
They visited once after a call from the HD psychiatrist. ACAT refused to take
referral for...low level hostel assessment because of his age (36) but have
accepted referral for Boarding House assessment. He is on a waiting list for
this but there are no licensed boarding houses close to his siblings.
He is on a waiting list for Co-options to
assist his sibling.
He is on a waiting list for a local case
manager.
He is on a waiting list for public housing.
His siblings are adamant that he is not
capable of living alone. His reverse day/night sleep pattern and habit of
roaming for days will mean he will not be able to be contained at home for
services to come but [an assessment] cannot be approved unless services have
been tried.
Mark was referred to the NSW HD Service after his
eviction and he was already well into his illness.
Submission 63, p.6 (Australian Huntington's Disease
Association (NSW)).
4.27
The Gippsland Carers Association pointed to the
experience in Victoria
where, as at 31 December 2003,
there were more than 4000 people aged under 65 years on the supported
accommodation needs register. Of these, 83 per cent were for people with an
intellectual disability. The average length of time that those with an urgent
application for shared supported accommodation was approximately
140 weeks. It should be noted that many individuals received a range of
support services to meet their immediate support needs while awaiting entry to
supported accommodation.[339]
4.28
It was reported that the lack of suitable supported
accommodation for people with ABI, resulted in young people being accommodated
inappropriately in state accommodation, private rental, caravan parks or at
home with a carer. In such circumstances, young people often are unable to
obtain adequate services, particularly high need services and to ensure that
these are maintained at an adequate level. Often the cost of community services
puts them out of reach for those in need. In addition, it was stated that the
services are often withdrawn due to the cognitive and behavioural issues
associated with some clients because of occupational health and safety risks to
workers.[340]
4.29
The issues surrounding the delivery of disability
services is discussed in more detail later in this chapter.
Young people living in an aged care facility
4.30
Many witnesses spoke of the extreme difficulty of
reaching a decision to move a young person to an aged care facility and of
their frustration that there are few other options. They spoke of the social
isolation, the lack of rehabilitation services for those with ABI, and the lack
of specialist equipment and palliative care for those with degenerative
diseases and other disabilities in facilities that are there to care for the
frail elderly. There was also concern that once that difficult decision had been
made, barriers exist to young people accessing those facilities and, if
circumstances change, for young people to move out.
No other options
4.31
Young people are placed in aged care facilities as
there is no other option to meeting their particular needs. Young people move
from the community when their requirements can no longer be met by community
based services or they may move directly from an acute hospital setting
following, for example, a traumatic injury. The Victorian Brain Injury Recovery
Association stated:
You are fine one day, but something occurs. You could spend a
few days in intensive care and within a fortnight find yourself in a nursing
home bed because the acute care hospital needs your bed. If you are lucky you
might be medically stable by then. I come across a couple of patients a year
who, within two to three weeks of their injury, are already in a nursing home
bed.[341]
4.32
The Younger People in Aged Care Alliance (YPACA) also
commented that some young people have been placed in aged care facilities when
foster placements failed:
Some young people have gone into the care of the state
department. When the department has not been able to find an adequate foster
family or the foster placement has broken down, a child in care can end up in a
nursing home because there is no other option. They can also end up in
hospital.[342]
4.33
Witnesses also commented that the lack of palliative
care resulted in young people being placed in aged care facilities. The
Neuro-Oncology Group of NSW stated that there is no long term palliative care:
Our palliative care service is an acute service, as are a lot of
palliative care services around the state. That means they will take only
people with acute short-term problems and people who look like they will die in
the next couple of weeks. If somebody is going to be there for three or four
months they will find a nursing home for them if they can.[343]
The Group added that families are often asked to sign a
nursing home form prior to entering a palliative care unit.
4.34
Other evidence indicated that families had chosen a
nursing home to keep the young person close to them. For example, Liverpool
BIRU stated that:
I have known families that will accept a less attractive nursing
home because the daughter can visit on the way home from school. That, to them,
is more important than a really superb unit.[344]
4.35
Even when accommodation is being sought in an aged care
facility, it can be difficult to get an assessment for a place or to find a
place.[345] The reluctance to undertake
aged care assessments for those under 65 years was raised a number of times in
evidence. Under the Aged Care Act 1997
younger people with disabilities will be accepted into residential aged care
only 'where there is no alternative'. The Department of Health and Ageing noted
supported accommodation for younger people with disabilities 'appears to fall
short of demand for these services' and that residential aged care becomes an
'option of last resort on compassionate grounds'.[346]
4.36
The guidelines for Aged Care Assessment Teams (ACAT)
indicate that younger people with disabilities may be assessed and approved as
eligible for residential aged care if they need the intensity, type and model
of care provided in such facilities and no other more appropriate services are
available. The Committee received evidence that in some areas ACATs are
refusing to assess anyone who is under the age of 65. ParaQuad Victoria
noted that this 'means these people are at home and at risk because there are
not enough services'. The only alternative is to admit them to the acute
sector.[347]
4.37
There was also evidence that ACATs will not assess
people until they have trialled other services. In some cases, trialling other
services may be difficult or inappropriate. The NSW Huntington's Disease Association
has found that people with HD are often not referred to the NSW Huntington
Disease Service until they are well into their illness and it is then too late
to trial them at home with these other services.[348]
4.38
After younger people have been assessed for aged care
accommodation, they often encounter long waiting lists. Evidence was received
which indicated a reluctance or even refusal by some aged care facilities to
provide accommodation.[349] Palliative
Care Victoria
stated that a survey of the placement of MND patients in 2001-2003 showed that for
those over 65 years the average time waiting for placement in a nursing home
was 81 days. For those under 65 years there was an average wait of 190 days.
Of those still waiting to be placed, or who had died before placement, the
average wait was 568 days.[350]
4.39
The parents of one young person with ABI commented:
Nursing Homes do not readily accept Young People as they find
them too difficult to manage and handle. To get Rod into a Nursing Home in
itself was a difficult process and to transfer him to a more conveniently
located Nursing Home that is of a satisfactory standard is almost impossible. To
get him into this current nursing home we had to convince them by offering to
take him out on day trips, bathe him and generally be around to take the
pressure off them.
We as parents live some distance away which makes it difficult
and expensive to visit regularly, which of course we do! John
has a 170km return trip and Karen 110km return trip,
and Karen actually lives next door to Coledale
Hospital which specializes in
nursing and rehabilitation care but cannot take Rod as he is already placed. The
catch 22 of the nursing home world.[351]
4.40
The NSW Huntington's Disease Association also pointed to
the refusal of nursing homes to take people with HD because:
- their difficult behaviour and they are
disruptive to older, frail patients;
- their physical symptoms;
- they require extra food, butter, cream, Sustagen,
etc;
- they require extra time for feeding;
- they often require special beds or chairs such
as the fallout bed which costs approximately $2000;
- lack of funding for people with HD because the
cognitive impairment does not rate high on the Resident Classification Scale;
and
- nursing staff are distressed by having to care
for such young patients.[352]
Funding issues are discussed later in this chapter.
Lack of independence
4.41
Many submissions spoke of the lack of independence of
young people in aged care facilities.[353]
Young residents must comply with the rules of the facility where staff levels
and routines are aimed at assisting the very frail and to ensure that all
requirements are met within a limited time period. HOPES pointed out that tasks
which residents may be able to carry out with time and support are performed by
staff on a communal basis. HOPES commented that 'in every aspect of life the
resident becomes the receiver of care, never a productive member of the
community'.[354]
4.42
One parent reported:
Amber also has no choice about
aspects of her daily life that the rest of us take for granted. She is given
dinner at about 5pm and then put to
bed at approximately 6pm when the
elderly residents are in bed. This represents a complete loss of the dignity
and independence every young Australian has a right to expect. Amber
wants to be able to choose what she would like to eat or drink or what time she
goes to bed and also what she wants to wear.[355]
4.43
Liverpool BIRU noted that the routines of aged care
facilities also disconnects residents from normal routines such as shopping and
preparing meals which provide opportunities to exercise and stimulate
rehabilitation therapy as well as allowing participation in, and add a purpose
to, life.[356]
4.44
Excessive time in bed, typical of the routine for
elderly in nursing care, was an often cited frustration for young residents.
The space available for personal belongings is also small: there is no room for
mementos, posters or other personal possessions. The young person may have to
relocate rooms as the needs of other residents take priority. This means that
they must adjust to new surroundings and may have to 'renegotiate' their
relationships with new room partners. Residents receive regular intrusions from
other residents who may wander into their room, creating difficulties in
protecting their few possessions from loss and maintaining privacy.
Melissa's
story – Living among the frail elderly
Melissa is now 31 and is still in her SRS. She was
one of 43 people aged between 30-39 in 2004 living in an aged residential
facility in Victoria. (Dept. Health and Ageing, 2004) Mislead to
believe it catered for people like my sister; she resides in a 'nursing home'.
After Melissa was placed I was able to get back on my feet
and have been trying to get an appropriate placement for her ever since. Melissa sits among the aged. Her 'spark' for life
has gone – she has no friends there and no one able to communicate effectively
with her. The facility is catered for the aged, she does not go on 'outings',
there are no activities. Her personal appearance is neglected due to the number
of beds and shortage of staff. A small thing to you or I, but Melissa loves a bath. For the latter reason she
cannot have this simple luxury. Being an aged care facility, there are no
appropriate disposal units to cater for her Menstrual Cycle. A simple plastic
bag in her room is used.
To cater for the amount of 'residents' tea
and coffee are pre made in a large jug with the milk already added. A sight you
or I would balk at – A daily standard Melissa has had to live with. Melissa is isolated and feels 'abandoned'. She
recently surprised me with her understanding by saying "I need to get out
– everyone is old – no one talks to me". My heart breaks over and over
when I go to see her. I know where she will be – sitting on her own.
The figures say there are 6000 others like
Melissa living an undignifying and 'abandoned' life.(ypinh website) I say
undignifying because these are young people – young people who deserve to live
in surroundings that suit their age. They are entitled to have appropriate care
to match their age. The disabled are the vulnerable of our community yet we
cannot provide appropriate accommodation to suit their needs. They are left
sitting amongst those who are, to be blunt...waiting to die.
Submission 236, pp.3-4 (Ms Amy Seadon)
Lack of social and emotional
support
4.45
The Committee heard evidence that many young people in
aged care facilities suffer from depression. Young people may be separated from
their partners and/or children and social networks. The partner of one young
person in a nursing home stated:
He has set times for meals and you have to try and work around
that. It costs about $11 by taxi. As you can imagine, in any partnership the
dynamics change. So it is different.[357]
4.46
Those with children find it particularly difficult as
there are often no facilities to make visits enjoyable for children. Having
parents living with large numbers of very elderly frail residents when they are
already trying to cope with separation can be very distressing. Many people
reported that their children stopped visiting as they found it too upsetting.
4.47
Many submissions commented that depression was
exacerbated by living with the very elderly or demented and witnessing the
deaths of older people in their homes.[358]
Many facilities do not have single rooms available so young people must share
rooms with people who are elderly and sometimes have dementia. Such living
conditions lead to depression, loneliness, frustration and boredom. This
compounds problems for those young people already experiencing mood swings and
behaviour and impulse control difficulties as a result of their illness or
disability such as acquired brain injury. The Liverpool BIRU observed:
More commonly, the person with an ABI in a high level
residential aged care facility has cognitive and communication problems and is
not able to clearly articulate their views. For some, their distress or
frustration with their circumstances becomes manifested in challenging
behaviours such as screaming, swearing, throwing objects and hitting out. The
person becomes labelled 'difficult' and can become feared by other residents,
visitors and sometimes the staff.[359]
4.48
The MS Society of NSW commented that this situation leads
to depression and 'it is not unusual for people to "give up and lose
hope" and as a result deteriorate very rapidly on admission'.[360]
4.49
Young people in aged care facilities want to be able to
maintain and develop community interests and activities and to participate in
the community and have a social life. However, all too often they become
isolated. Friends are discouraged by the sounds and smells of aged care
facilities. The wife of one young person commented:
Friends are reluctant to visit an establishment where all the
other elderly residents are wandering around in various stages of dementia or
all lined up in the sitting room staring into space.[361]
4.50
As a result, young people in aged care facilities receive
fewer and fewer visitors as time passes and they lose the opportunity to grow
socially with their peers. As one witness commented, 'a nursing home has a very
different feel and message to a home in the community'.[362]
4.51
Witnesses also commented that young people in residential
aged care are further isolated because in many jurisdictions they are excluded
from participating in a range of community based recreation programs provided for
people with disabilities as they target people living in the community.[363] The Victorian Brain Injury Recovery
Association stated:
Once you are in your aged care bed, you cannot access any of the
state services: you cannot get a case manager unless you were already on a
funded scheme when you went in and you cannot get access to any day programs.
You cannot get access to any of the resources that are going to allow you to
get out.[364]
4.52
Aged care facilities may also lack appropriate
transport and the extra staff needed to enable a disabled person to access
community programs. However, Liverpool BIRU noted that 'being able to access
such programmes could offer an opportunity to socialise with peers and
participate in everyday community life'.[365]
4.53
Entertainment and activities within facilities are
aimed at the aged. One parent noted that entertainment and stimulus in his
son's aged care facility are sing-a-longs of songs from the early 1900s, bingos
etc.[366] This situation is exacerbated
as the majority of aged residents are female and the majority of young
residents with ABI are male.[367]
4.54
Another submitter commented on a young girl in an aged
care facility:
Providing her with the ongoing stimulation and interaction that
she so badly needs to feel part of society has proved extremely difficult. The
aged care facility is somewhat out of the way, but is the only facility
available. Fiona has no interaction that I have
observed with other residents, noting that her own behaviours have been
reported at times as being challenging (I have not personally observed any
particularly challenging behaviours from her). Nevertheless, I believe that
many of the behavioural problems she has experienced are a direct result of the
inappropriate treatment and isolation she has experienced within an aged care
facility. For example, despite repeated requests and Fiona's
known wishes, she was repeatedly showered by male staff.[368]
Lack of support for specific needs
We have seen a deterioration in Fiona
in the last 12 months. I have to say her level of emotional and psychological
trauma over her four years in an aged care facility is more severe than the
psychological and emotional trauma she has experienced as a consequence of a
severe brain injury. That is the quality of the environment we have been
dealing with.[369]
4.55
One common problem facing young disabled people in aged
care facilities is the lack of time and skills of staff to address their
specific needs. For example, the MND Association of NSW noted that people with
motor neurone disease may have severe communication difficulties which are
often mistaken for intellectual impairment. If staff do not take the time to
understand the person, this can be very isolating and frustrating especially
for younger people with MND.[370]
4.56
The Victorian Brain Injury Recovery Association
provided this example of the difficulties of providing adequate services in
some aged care facilities:
...the therapist was coming into the nursing home, but the nursing
home staff resented therapists coming in and they resented the physio coming in
and showing them how to settle this man so he could be comfortable in bed. They
assessed that he had no pain, whereas we were going in and saying: 'This man's
stuck up in his bed like this. This man is clearly distressed.' The physio
would show them how to have him as relaxed as can be and how he could
communicate. The nursing home did not want anything to do with that. They said
their nurses knew how to do it and they did not want the therapists there. So
his wife has taken this man home.[371]
4.57
It was also noted that severe ABI residents may exhibit
behavioural problems such as shouting, inhibition, wandering, 'hitting out' arm
and leg movements. This is seen as disruptive and unacceptable behaviour. In
the case of one person supported by Liverpool BIRU, assistance was offered with
designing and implementing a behaviour management plan oversighted by staff
from the BIRU. The program was not able to be instituted because, even with
education, the facility could not provide sufficient and consistent staffing to
implement the program. The facility then sought the person's admission to a
psychiatric hospital. This was refused as the person's problems stemmed from
their brain injury and not mental illness. As a result, 'pressure was
inappropriately placed on the family to take the young man home'.[372]
4.58
The Physical Disability Council of Australia also
commented that residential aged care facilities were not obliged to respond to
the changing needs of younger people with disability, either via monitoring and
reassessment or development of an Individual Service Plan as required of
disability services in some States, such as NSW.[373] The Neuro-Oncology Group of NSW supported
this view and provided the following example of a women who had died of a brain
tumour in a nursing home:
Her swallowing needs, her need for speech pathology, changed in
a matter of days. The relative came in to find her mum with a mouthful of food.
We do not know how long she had been there like that, because yesterday she
could swallow and the next day she could not. That is the sort of fluctuation
that can happen with people with brain tumours. They did not have that regular
review of equipment needs, swallowing needs, physiotherapy needs. So the allied
health element is fantastic and a really important part of things.[374]
4.59
The Darwin Community Legal Aid Service highlighted the
problems of young Indigenous people in aged care facilities. It noted that most
were from remote Northern Territory
communities, placed in the facilities under Adult Guardianship Orders. They had
little contact with family members who cannot afford to travel to visit them in
urban centres. Their first language is usually an Aboriginal language. The
Service stated that young people are disproportionately represented in
physically aggressive incidents at facilities with allegations of sexual and
physical assault against frail elderly residents.[375]
4.60
The Australian Huntington's Disease Association (NSW)
concluded:
Young people with disabilities living in nursing homes do not
experience the same rights and standards recognised in the Disability Services Act 1987. This is because funding for the frail
aged is provided by the Commonwealth Government and the responsibility for the
provision of care for young people with disability, including those with
Huntington Disease lies with the various State Governments.[376]
Lack of appropriate rehabilitation
and other services
4.61
Submissions commented that aged care facilities were
often ill equipped to provide appropriate rehabilitation and allied health
services including occupational therapy, physical therapy, speech
therapy/pathology and high level medical care.[377]
Rehabilitation
4.62
The Committee heard that for people with brain injury,
slow improvements can be made over a lengthy period of time either
spontaneously or with appropriate rehabilitation. Others may make few gains but
have the potential to maintain their abilities. There were many examples given
in evidence of the importance of rehabilitation. There were cases where young
people who had been aged care facilities for some years had, with appropriate
rehabilitation, been able to progress to the point where they were able to move
into the community. For example, the Victorian program ABI: Slow to Recover
provided cases studies of its work which emphasised rehabilitation.
4.63
While programs like ABI: Slow to Recover may be
delivered in aged care facilities, it is the exception rather than the norm.
The Liverpool BIRU noted that when older people moved to an aged care facility,
provision of care increases as their health deteriorates and abilities are
lost. It stated 'that continuum from a rehabilitation-enabling focus to helping
someone to move on with their life is lost when people go to nursing homes,
because they are different structures'.[378]
Liverpool BIRU concluded that 'this means that we have young people attempting
to continue their rehabilitation and live a life with meaning in a milieu that
is oriented to assisting older people maintain their abilities, manage their
deteriorating heath and end their life with dignity'.[379]
4.64
The Liverpool BIRU went on to note that it is very
difficult to provide individual rehabilitation in aged care facilities. For
example, people with memory problems may need visual prompts to help them
remember to undertake certain tasks: leaving a person's toothbrush and
toothpaste near the hand basin may prompt them to remember to clean their
teeth. Rehabilitation is also time consuming and there are limited
opportunities for one-on-one rehabilitation activities in high level aged care
facilities. NAYPINH commented that therapy services paid for out of bed
subsidies are severely rationed across all residents and 'are nowhere near
enough to meet the needs of a younger person'.[380] One submitter observed:
The Facility has neither the time, resources or staff to
undertake rehabilitation. They do not see that they are funded to do so,
either. In fact from their own management perspective, I suspect [the young
person] is much easier to deal with, being currently unable to walk, then she
would be with further rehabilitation although I believe she has the physical
capacity to recover many critical skills, such as walking.[381]
4.65
The impact of the lack of rehabilitation on individuals
can be significant. Headway Victoria
provided this case study:
A young man entered a nursing home following a traumatic brain
injury. At the point of entering the facility he was able to manage his own
transfers from bed to wheelchair and wheelchair to toilet with assistance.
However, staff found this to be too intensive and were concerned about back
injuries. They insisted on the use of a hoist even though the man was in an
active rehabilitation mode and being able to do his own transfers was a
requirement of him being able to move out of the facility. Over time, through
lack of regular reinforcement, his ability to manage his transfers declined.
The lack of priority given to the rehabilitation goals of the
individual is the key issue here. Nursing staff can often consider therapeutic
input as the role of therapists however the rehabilitation potential of the
individual is best supported by a coordinated approach across the disciplines.[382]
4.66
The importance of rehabilitation is not limited to
those with acquired brain injury. Those suffering from degenerative diseases
also require therapy.
4.67
Witnesses commented that younger people residing in
nursing homes are precluded from funding that could provide further
rehabilitation or access to community social and recreational programs and
other disability services. It was viewed that once a person moved into aged
care accommodation, funding for these services were not provided by State
authorities.[383] Many witnesses
commented that once a person moves from a community based support package to
Commonwealth aged residential facilities, they cannot access disability
services under Commonwealth State
and Territory Disability Agreement (CSTDA) even though they are part of the
CSTDA target group.[384] The Agreement
is discussed further in this chapter.
Provision of specialised equipment
4.68
The Committee also heard of the lack of appropriate
equipment required by some residents. In evidence it was stated that in some
jurisdictions, for example Victoria and NSW,
specialised equipment is not available through State programs. As a
consequence, electric wheelchairs to facilitate access to the community,
electric riser chairs to facilitate comfortable seating for communal
activities, appropriate pressure care devises electric adjustable beds and
other equipment is not provided.[385]
The MND Association of Victoria noted that residential aged care facilities are
required to make available a range of disability equipment but generally only
provide minimum equipment or equipment at a basic standard. The Association
stated:
Can I say that it is very embarrassing, when we have a person
living at home with an electric high-rise bed that bends in the middle and
vibrates, that they cannot take that with them when they go into a nursing
home, because the electric bed has been provided by the state – and, of course,
the Commonwealth does not fund equipment to that level. They also cannot take
their electric recliner chair, which improves their comfort during the day.
They have difficulty accessing appropriate levels of posture support, particularly
mattresses to prevent pressure. They are often left in situations where their
inability to communicate means that harried and hurried staff do not deliver
the services that they need. Quite often, it is only because of interventions
from outside the aged care service that their needs are actually met.[386]
4.69
The Committee also heard evidence that some providers
did not encourage residents to use specialised equipment. HOPES Inc for
example, stated that facilities may discourage younger residents from purchasing
their own equipment such as electric wheelchairs in case they run into elderly
residents or damage doorways. Should younger residents choose to
purchase their own specialised equipment they are responsible for all costs
involved. HOPES indicated that this situation leads to increased dependence and
reducd physical ability for the younger resident.[387]
4.70
NSW Health responded to the evidence of lack of
equipment in aged care facilities. It stated under its Program of Appliance for
Disabled People (PADP) people in the community were entitled to equipment. People
in nursing homes are entitled to PADP if it is for a piece of customised
equipment but, if it is a piece of equipment that can be used by other
residents in the residential aged care facility, then NSW stated that is the
responsibility of the residential aged care facility to provide. That is within
the funding arrangements. Further:
There is a degree of overlap and confusion about that policy. I
understand that. We are trying to resolve it. It has been a longstanding issue
between the Commonwealth and the state. But PADP is one of the programs that is
absolutely critical to supporting people with disability in the community. I
know that New South Wales Health has increased its investment in dollar terms
by 70 per cent over the last five years, and it is still not enough to be fair.[388]
4.71
ACROD argued that the schemes providing equipment for
the disabled are fragmented and that all levels of government should develop a
coordinated approach to the provision of aids and appliances and gave the
example of the Continence Aids Assistance Scheme where funding is provided by
the Commonwealth for those under 65 and those over 65 who work for eight or
more hours per week. Those over 65 years and not working must access a State
funded scheme.[389]
Mary's
story- no medical devises from government's cost shifting
Mary
is aged 54 and is a resident in a residential aged care facility.
Mary requires a pressure management device on her
bed to prevent the occurrence of bed sores, to address chronic hypersensitivity
and discomfort, to optimise comfort levels, and to enhance quality of life.
The residential facility is required to
provide pressure management devices, and supplies a "ripple foam
mattress" which is inappropriate for people with MND, and who require a
variable air pressure ripple mattress. The air pressure mattress provides
alternating and variable pressure support which optimises comfort, reduces
pressure areas and which significantly reduces the requirement for turning of
the person and repositioning
The residential aged care facility will not
purchase the appropriate pressure care device and the state [Victoria] Aids and Equipment program will not fund
people living in residential aged care which is funded by the Commonwealth
Submission 77, p.5 MND Association of Victoria
Risks of living in aged care facilities
4.72
Witnesses also argued that there were risks of mixing
severely disabled people with people with dementia. For example, the MND
Association of Victoria stated that people with MND living in residential aged
care facilities increasingly face the risk of assault or disruption to life
support equipment by other residents. Some people with MND require ventilatory
support, while many have PEG feeding tubes. This,
combined with severe physical disability, can place them at risk of assault or
interference with their medical equipment by people who are physically able but
suffering from dementia. The Association stated that in one reported instance,
a person with dementia had to be restrained from disconnecting ventilation
equipment from a person with MND who was unable to protect or defend themselves
due to their disability. Other reports had been received of people with
dementia abusing and attacking people with MND in their beds. The Association
concluded that 'these events highlight the existing risks of having people with
severe physical disability but mentally able living in an environment where
other residents are physically able but suffering from dementia'.[390]
Impact on staff
4.73
The Australian Nursing Federation commented that it was
important to recognise that aged care nursing is a specialised area of nursing.
Younger people with disabilities have quite different needs:
Because nursing of older people is a specialised area, nurses
who work in aged care – particularly in residential facilities but across the
whole community and other settings too – will have those specialised skills for
looking after older people. Therefore, it is putting an extra demand on them to
also have specialised knowledge of younger people with disabilities which could
require quite different care from looking after older people.[391]
4.74
Evidence was received that staff suffered as they battled
'with delivering quality care to both groups within a budget designed (for
better or worse) for one group'.[392]
The following examples of problems for aged care staff providing care for young
people were provided to the Committee:
-
There is a lack of appropriate training in
working with people with high support needs especially those with Motor Neurone
Disease, multiple sclerosis or other similar conditions. ABI Behaviour
Consultancy noted that often aged care facilities cannot afford comprehensive
training for staff, which typically exceed $1000 per day for inservice workshops
and backfill costs.[393]
- Nursing young people is physically demanding on
staff if the person is in a wheelchair and is unable to weight bare. There are
often no lifting machines and the staff have to lift the person manually.
- Staff are not trained in counselling clients and
often worry when confronted with a younger client who is depressed and just
looking for someone to listen to them.[394]
-
Nursing home staff lack the capacity to invest
time in communications issues with those who either have lost their capacity to
communicate in the usual manner or who never had that capacity.[395]
-
The high turnover of staff and use of temporary
or agency staff often means that staff on duty are not aware of the specific
needs of some people in the facility. The MND Association of Victoria gave the
example of a person with MND, with no use of their arms or ability to speak,
being delivered meals, but because they cannot feed themselves. The meals are
taken away uneaten, and the person is unable to communicate that they need to be
fed. The information regarding feeding and communication is available in the
patient file.[396]
-
Many facilities face chronic staff shortages and
there is little or no time to provide the necessary attention for high needs
patients, for example, people with MND require PEG feeding and/or ventilation.[397] In addition staff are not trained to
deal with people who exhibit behavioural problems:
As a result of his brain injury, Rod exhibits antisocial and
abnormal behaviour. Nursing Home Staff are usually intimidated by his behaviour
and either spend minimal time with him or avoid him all together. Staff have
complained to Management about his behaviour. (What more evidence could one
need of a complete lack of training for such patients.) They do not know how to
deal with him so they choose to ignore him as much as possible. There is little
or no empathy.[398]
4.75
The ANF Victorian Branch noted that there is currently
no ability for homes with residents with severe behavioural problems to access
funding for additional resources to manage such clients, either in the short or
long term. In the past, this has led to some facilities attempting to evict a resident
in order to protect other residents and staff or trying to get such people back
into a public hospital.[399]
Moving young people out of aged care facilities
...we need to move beyond the scoping, the data gathering, the
researching and the counting to actually piloting some of these initiatives
across the country to a greater extent than has been done already, as well as
putting in place measures to prevent more younger people from entering nursing
homes.[400]
I have gone on reference groups, I have watched studies being
done and, at the bottom line, we are still in the same position as we were at St
Vincent's eight years ago. There is no where for Chris
to go.[401]
4.76
Witnesses called on government to institute programs to
move young people out of inappropriate aged care facilities. NAYPINH
recommended the establishment of a National Exit Program with a target of
moving 700 young people per year out of aged care facilities. NAYPINH estimated
that it would cost on average $49 million per year to achieve this target. NAYPINH
argued that a range of accommodation options and support options for young
people in aged care facilities is achievable, necessary and cost effective.[402] It noted that there were examples
where young people had been successfully moved out of aged care facilities. In Western
Australia, for example, 95 young people resident in
aged care facilities had been moved back into the community over a period of
approximately four years.[403]
4.77
YPACA argued that the Commonwealth needs to take a
leadership role by linking outcomes, that is the number of people no longer in
aged care facilities who are leading quality lives in accommodation of choice,
to state funding levels. This would ensure that funds were quarantined for this
purpose.[404]
Models of accommodation services
Most people want to stay at home, but not everybody. The best
care is flexible care that allows people to have some options. You cannot get
one package that fits everybody.[405]
The critical factor should not be the age of the person but
rather the need for high level nursing care.[406]
4.78
As part of its inquiry, the Committee visited four
facilities providing care for younger people with disabilities. In Victoria,
Carnegie House provides accommodation for three people with MS; in Western
Australia the Committee saw models of care that were
Huntington's Disease specific, MS specific and brain injury specific. In
evidence, the Committee received a range of views on they type of accommodation
required for young people in residential aged care facilities and those at risk
of moving into aged care. Some groups supported the development of innovative
models of cluster or congregate housing, some conceded that certain individuals
may require a more intensive medical care setting while others argued that all
care should be provided individually in the community.
4.79
The concept of cluster or congregate housing drew a
range of comments from witnesses. Some concerns were raised about
institutionalisation, lack of privacy and choice and past poor experience.
YPACA stated that it did not support cluster accommodation, 'where eight people
are congregated together because they may have similar needs and because there
is a building there for it'.[407]
4.80
YPACA also commented that special purpose nursing
homes, cluster homes and other forms of enforced congregation were not a
solution.[408] They represented a form
of institution and are a service provision that is imposed on people with
disabilities. YPACA proposed a person-centred approach and pointed to examples
of people with quite significant needs associated with their disability who
live in the community in their own homes:
There are many models out there of people with very high support
needs living in the community. We are proposing to start from where the person
is and what supports the person needs, not from an eight-bed facility or
whatever...the health needs can be met through domiciliary nursing services that
come in through regular health systems et cetera. Personal carers are very well
trained [409]
4.81
The Cerebral Palsy League of Queensland is proposing to
utilise a model which involves a number of houses within a suburb where two or
three people may live. Carers are able to provide services to people who live
nearby but there is not a 'cluster' and residents can be part of the community.[410]
4.82
NCOSS stated that congregate care was not supported in New
South Wales. Instead, 'the disability sector in New
South Wales will be pushing very much for as small as possible and as
integrated as possible'. NCOSS saw some dangers in congregate care:
There are some dangers in creating congregate care that
restricts opportunity and restricts involvement. It can also restrict
involvement of the family, and we would need that to be monitored. In New
South Wales there has been a problem with disability
services in that they have not received any deliberate or structural monitoring
for over four years. We are very concerned that should processes be set up
without that monitoring and quality at the front end services would again be
relaxed and we would get into institutionalisation.[411]
4.83
The Office of the Public Advocate Queensland
also argued that, for some, congregate care raises concerns. There are examples
where congregate care has led to segregation of people and where the values
that are brought to bear by the people who are working there are less than
optimal. The Office of Public Advocate stated:
What I am aware of without any doubt is that in Queensland
we have quite a few mini-institutions which look like ordinary suburban houses.
They are mini-institutions because of the institutional mindset brought to them
by some of the people that work in them. Some of the other group homes are
completely different from those. I have been to group homes that look and feel
like homes. It varies greatly, depending upon the ingredients and the mix.[412]
4.84
The Office of the Public Advocate went on to comment
that congregate care models probably work where people will clearly benefit
from being together and choose to do so. If people do not have a say in where
they live and with whom they live, difficulties may arise: where congregate
arrangements are 'meaningful and related to the individual needs and
aspirations of the people they can work'.[413]
4.85
NAYPINH reported that in Victoria,
'the Government's ideological stance will not countenance the development of
shared supported accommodation settings because "congregate" care is
seen to be outdated and irrelevant'. However, they stated:
It remains a fact that the states have stopped developing
congregate living situations. The fact that social interaction and community
are vital for young people fails to impact this entrenched and fashionable
view, a detail which demonstrates that if responses are left to the dictates of
policy alone, they will inevitably fail.[414]
4.86
Witnesses also provided evidence of where an individual
package had been developed to meet particular needs. In Hervey
Bay in Queensland,
former residents of the Bush Children's Service are now supported by a
community based service which is administered by a registered nurse. The Office
of the Public Advocate commented:
The notion of an almost mobile medical service seems to be a
critical part of arrangements that work well for this cohort...These are very
individualised arrangements. Two or three people might live together but it certainly
has an individual focus...We are talking about very fragile people who get that
level of support within their own home in the community.[415]
4.87
The MND Association of Victoria also supported
individual programs aimed at keeping people in their own homes and stated 'the
minute you start talking about facilities you immediately stop thinking...If you
are going to bury money and infrastructure in a building, for example, it is
locked up for ever. The minute you get three people in there with long-term
disabilities that facility is effectively taken out of the available options
for other people'. The MND Association supported keeping people in their homes:
One of the best ways to keep people at home is to invest in case
coordination and case management that can help look at the services that are
available within a community. Self-care packages can be developed with friends,
relatives and neighbours within the local community to help that person remain
at home for longer...That means there are no facility costs. They are with
their carer. With small amounts of brokerage, we can bring in enough services
to help them remain at home and to help the carer keep on caring better for
longer.[416]
4.88
While aged care accommodation was generally not
supported, there was evidence that this may remain a viable choice for some
people. The Committee was provided with examples where there were benefits from
proximity to family and networks.[417] In
some cases, the complex needs of a person may only be met in a nursing home
setting and it was mooted that groups of people could be accommodated in a
cluster or specially set aside area or wing in an aged care facility. The
Queensland Government commented that individual circumstances and issues needed
to be examined in order to assess the appropriateness of aged care
accommodation.
It is important to acknowledge accommodation of some younger
people with a disability in such facilities may not be inappropriate and may be
the most practicable option. It is desirable to provide age appropriate care
and age appropriate facilities/circumstances...
Younger people with a disability due to degenerative diseases
such as muscular dystrophy, multiple sclerosis or motor neurone disease may
enter an aged care facility towards the end stage of life when high levels of
care may be required.
It is also evident that some people with a disability access
aged care facilities due to an early onset ageing condition. In these instances
the need for aged care nursing may outweigh the need for disability support. For
example, people with certain disabilities such as Downs Syndrome are more prone
to early onset dementia conditions. As these ageing conditions progress, the
individual may reach a point where their need for aged care and monitoring
outweighs their need for disability support.[418]
4.89
The AMA pointed to the particular difficulties of
providing facilities for young people in rural and regional areas. As there may
not be enough young people with disabilities to justify a stand alone facility
in each town, the AMA commented that it may be necessary to redefine the roles
of some residential facilities. This would enable them to improve the scope of
the services that they provide to better meet the needs of all residents. The
AMA concluded:
In this way, a new type of residential home would emerge in
regional and rural areas, providing services for people of all ages with
complex, chronic conditions and disabilities, with staff trained in and
sensitive to the needs of younger people with disabilities.[419]
4.90
NAYPINH also commented on the provision of services in
rural areas:
Young people in remote or rural areas may choose, because the
numbers are not as high or the services do not exist, to remain in a nursing
home because it keeps them near their family and friends. If that were the
case, then the states would be responsible for providing the funding to take
the services into the nursing home that these young people do not currently get
– services around equipment, physio, rehab, higher staffing ratios and so on.[420]
4.91
Liverpool BIRU supported some accommodation in aged
care facilities but as a cluster attached to the facility:
Some people will be managed really well in a nursing home
because it has the infrastructure that is required by that person and the
location is close to their family. If there were clusters then there would be
expertise, and that would resolve some of the issues that we found in looking
at the problems of people living in nursing homes.
This arrangement was
described as resourcing a small group in a different way than the rest of
residential population.[421]
4.92
The Australian Huntington's Disease Association of NSW
commented that accommodation solutions come back to the actual disability:
Because of the progressive nature of Huntington's Disease there
are going to be people under the age of 65 who require a nursing home standard
of care. But they need those extra bits, such as being perhaps in a cluster or
group. Similar to the way you might have a dementia specific unit in a nursing
home, you might have a Huntington's
specific unit which young people would be in together. They would not be
sharing rooms. They would get extra things, such as being taken out, as well as
the extra food they need, the extra time they need for feeding and all those
sorts of things.[422]
4.93
The MS Society of Victoria
provided the example of Cyril Jewell
House at Keilor. This is a facility for 15
people attached by a passageway to a 30-bed nursing home. Core funding is
provided by the Department of Health and Ageing and top up disability funding
from the Victorian Department of Human Services. The Society commented that
this funding works well in providing additional care resources and a community
access service that assists residents to get out into the community.[423]
4.94
Carnegie House in Victoria
and Fern River
in Western Australia provide
examples of shared supported accommodation. Carnegie is a
three bed house for people with MS. It is funded by both the Commonwealth and
the State:
...for the Carnegie house and also for a second innovative pool
pilot we have at a shared supported accommodation service that we also run, the
Commonwealth funding is used for nursing and therapy and the state funding is
used to provide personal-care attendance and community access. It is almost
broken up down the lines of clinical services and non-clinical services – personal-care
attendants and trained staff. The Victorian government, as well as other
governments, has a significant problem with accepting that nursing services are
an essential part of a disability service.[424]
4.95
Fern River
provides six supported units with three people in each unit. There are 24-hour
on-site carers. Funding is provided by both the Commonwealth and the State as
the Young People in Nursing Homes Project.[425]
Amber's
story – Changes to lifestyle after moving out of a nursing home
Amber is 30 years old and has Cerebral Palsy and
an intellectual disability. After six years of living in a nursing home she has
moved into supported accommodation. After six days in the supported
accommodation, her mother wrote:
Amber has settled into the home extremely well and
already there is a difference in her personality. She is laughing, which is
something she has not done for a long time. She is also interacting with the
other clients very well and the carers at the home are surprised with how well
she has adjusted to the move in such a shore period of time.
Amber now has a choice of what she would like to
do, what time she wants to get to bed and what she wants to eat and even what
clothes she would like to wear for the day. She had none of these choices at
the nursing home. She Doesn't have to go to bed at 5.30 pm anymore and her food is home cooked, not
pureed hospital food.
Amber can now access physiotherapists,
occupational therapists and speech therapists. She was never able to do this in
the nursing home. Amber lost her ability to use sign language, to chew her food
properly, as it was pureed; she also lost a lot of muscle tone because of the
lack of exercise and her weight dropped down to 39 kilos.
She does not have to endure the indignity of
having to take laxatives and given suppositories for her bowels anymore. With
nutritional food and exercise her bowels should work normally again.
Amber's personality is really shining through
since she has left the nursing home. At long last she has a life worth living.
Submission 217, p.2 (Ms G Foyle).
An individual approach
4.96
Witnesses were wary of supporting the development of one
proposal or one model of accommodation because of the nature and the range of
disabilities.[426] It was acknowledged
that there is a finite range of service models available but it was argued that
the States and the Commonwealth should develop a range of options for support
and accommodation.[427]
4.97
While there was debate about the type of accommodation
model, there was general support for an individualised approach, namely that
the needs and wants of the individual should be paramount. The MND Association
of Victoria, for example, stated:
Where younger people with disabilities and people living with
MND require "nursing home" levels of support, services should be made
available in an environment that delivers services based on the needs created
by their disability, not their age, and not services based on an age group
needs other than theirs. Services must be focussed on addressing the needs
created by the disability, not on the delivery of a generic service model. Services
need to be individualised and focussed, with packages of support being used to
optimise outcomes.[428]
4.98
The MS Society of Victoria
provided details of individual care plans which move away from systems and
pre-determined programs and concentrate planning around an individual and his
or her needs.[429]
4.99
The Office of the Public Advocate Qld commented while
there are pockets of good practice these need to be extended across the
country:
The impression I get – and we have not surveyed nationally to
any degree – is that there is a generalised situation of people under the age
of 65 in nursing homes and then there are spots of good practice. Beverley
has identified the one in Hervey Bay.
We are aware of Western Australia
with a cohort with multiple sclerosis that were moved out. You will probably
find in each jurisdiction that, hopefully, there would be some good practice,
but it has not been addressed systemically to bring that good practice to bear
on a fairly major cohort of people.[430]
4.100
In order for an individualised approach to be
successful, a number of options need to be available. NAYPINH supported
extending the range of options to enable young people and their families to
have a choice about where they live and how they are supported. NAYPINH noted
that for the 95 young people moved back into the community in Western
Australia, 20 new supported accommodation options
developed. These included moving home with supports to live with family, moving
into dedicated facilities designed to support individuals with Huntington's
Disease, group homes and moving to nursing homes in country towns to be closer
to family and friends.[431] The Alliance
concluded:
Whatever supported accommodation 'option on the spectrum' a
young person chooses, it needs to function as a real home: a home to leave from
and a home to return to.[432]
4.101
Witnesses argued that the main barriers to ensuring
that a range of options and model services were available include funding difficulties;
fragmentation of services both across and within jurisdictions; and lack of
leadership. NAYPINH commented the Western Australian project succeeded because:
it had an excellent process in place from the outset; and the
money, energy and desire to achieve the changes it wanted. It shows that with
the political will and desire to do something and a dedicated funding stream to
do it, success is possible.[433]
Current funding arrangements
It appears that because Todd has
been classified as being eligible for nursing home placement, he is doomed to
spend the rest of his life there. I believe that State and Federal government
policies are part of this problem. Why would the state funded DADHC want to
take on the costs of Todd's care, when he is
being 'looked after' by the federally funded nursing home. Because you are in
one, excludes you from the other.[434]
Aged Care Act
4.102
As noted above, young people may be accommodated in
aged care facilities if there is no other option. For Commonwealth funded
accommodation, an Aged Care Assessment Team (ACAT) assesses the person's needs
and they receive a Resident Classification Scale (RCS) level. The majority of
younger residents receive RCS level 1-3 subsidies (high care levels). Those
young people in nursing homes who receive the disability support pension are
classed as concessional residents, entitling the provider to the concessional
resident supplement.[435] The basic
subsidy amount is supplemented by other payments including oxygen supplement
and enteral feeding supplement.[436]
4.103
Many witnesses pointed out that the ACAT's assessment
is designed to measure the multiple pathologies of elderly people, which were
described as 'lots of little problems associated with ageing, where you can
claim in every question as part of the RCS'.[437]
However, many younger people in aged care facilities have complex medical
needs, for example, ventilator support and gastrostomy meals and also require a
high level of physical assistance. It was argued that the RCS does not capture
the care needs of younger people who have major deficits in particular areas,
nor does it take into account the person's psychosocial needs which mostly stem
from the particular age group they are in.[438]
The Physical Disability Council of Australia also commented that the ACAT's
assessment may underestimate or discount cognitive, behavioural, support,
cultural and personal issues.[439] In
addition, ACROD stated 'funding formulae have failed to keep pace with the real
costs of assisting people who have complex medical support needs'.[440]
4.104
NSW Health commented that the RCS assumes a model
whereby funding levels decrease as independence increases. In the case of a
younger person who has an acquired brain injury, for example, therapy needs may
intensify as rehabilitation progresses, resulting in the need for greater
funding levels, or at least maintenance of funding to meet therapy costs.[441]
Residential aged care subsidies
4.105
Many witnesses argued that residential aged care
subsidies were insufficient to meet the needs of those younger people with high
needs in aged care facilities.[442] For
example, the Carrington Centennial Trust, an aged care facility which provides
care for a number of young people, submitted that younger persons require
higher numbers of staff hours to meet their nursing and exercise needs than
aged residents. In a case provided by the Trust, a young person required a
total 8.9 hours of care per day, excluding diversional therapy, compared with
5.1 hours of nursing care provided to a Category 1 frail aged resident. The
young person with ABI was assessed as a Resident Classification Scale Category
2 attracting funding of $94.76 per day. The frail elderly resident was assessed
as Category 1 and received $105.57 per day. The Trust noted that 'despite the
younger person requiring more intensive type of care and therapies, the RCS
fails to recognise this state of affairs'.[443]
4.106
The CEO of the Trust stated that it had been approached
to take other young people but stated that it could not 'fund $98 000 or
$100 000...to care for a younger disabled person, when I can get someone who
is 75 or 78 coming into a nursing home and the level of funding is commensurate
with the level of care I am giving'.[444]
4.107
In comparing the funding levels in residential aged
care facilities and disability services, it was noted that the maximum subsidy
received in residential aged care is around $43 000.[445] NAYPINH stated that funding levels
for young people in the community may range from $75 000 to $90 000
per annum in the non-government sector and that in some States the cost per
head for a disability service may be as much as $107 000.[446] NAYPINH provided this more detailed
analysis of comparative funding:
Table 4.2: Comparative funding for a young person through disability
services and for a young person in residential aged care
Indicative person with a
disability with full service
|
|
YPINH
with high needs
|
CRU Accommodation
|
$57 000
|
|
Category 1 bed fee
|
$43 000
|
Day Activity program
|
$22 000
|
|
Supplements
|
$1 000
|
Transport
(mobility allowance)
|
$1 500
|
|
Day Activity
|
unmet
|
Case Management
|
$2 500
|
|
Equipment
|
unmet
|
Transport
|
own cost
|
|
Therapy
|
unmet
|
Total
|
$82 500
|
|
|
$44 000
|
Source: Submission 160, p.23 (NAYPINH)
4.108
The MS Society Australia
commented:
We see perverse situations where someone will be sitting in a
state disability bed worth somewhere between $60,000 and $80,000 a year and
then, because they need a higher level of support, they get moved on to a
service that is worth $45,000 a year just because there is a registered nurse
on the premises.[447]
4.109
The NAYPINH concluded that:
While it is difficult to draw exact comparisons across funding
jurisdictions and individuals, it is clear that the aged care subsidy model
with its various care levels is not designed for younger people with
disabilities...The current subsidy arrangements cannot meet their needs without
substantial cost subsidisation of care resources from other residents in the
same facility.[448]
4.110
The NAYPINH went on to argue that it was the
Commonwealth's responsibility to provide adequate care for young people in aged
care facilities even those that are there 'due to the failure of the CSTDA
jurisdictions and other systems...failure to give due recognition to genuine need
will not suppress its existence'. The NAYPINH believed that younger people will
continue to reside in residential aged care facilities because of 'demand
issues in State Disability Services, pressure on acute care beds, geographical
considerations and the sheer force of timing demands between the competing
interests of health and disability'. As such, it argued that the Commonwealth
should provide increased services levels and targeted standards through the
Aged Care Act for young people in nursing homes.[449]
4.111
This argument was echoed by VBIRA which stated that:
VBIRA realises that persons with severe ABI have been admitted
to government supported nursing homes for many years, not because they fit the
requirements of being frail and aged but under emergency or compassion
provisions of the federal and state agreements, where the state has no other
option available. By persisting with this practice CSTDA after CSTDA...the
federal government has by default accepted responsibility for funding the
accommodation and care of persons who need special care and rehabilitation.
Actions speak louder than words.[450]
Innovative Pool
4.112
Under the Aged Care Innovative Pool, the Commonwealth has
offered flexible aged care places to the States and Territories and other aged
care providers for time limited pilots for the provision of aged care services
in new ways and for new models of partnership and collaboration. In 2002-03 two
specific categories of people with a disability were targeted. The first were
people with disabilities who are ageing and the second were younger people with
disabilities in residential aged care who would be more appropriately placed in
disability-funded accommodation.
4.113
DoHA stated
that while nine projects were approved in 2002-04 for people ageing with a disability,
no applications were received in 2002-03 for projects for younger people in
nursing homes. In 2003-04, one pilot project was approved for the MS Society of
Victoria
to assist the transition of younger people with disabilities from aged care
homes to more appropriate accommodation. Carnegie House provides three places
funded by the Commonwealth over two years. No other States have taken up
funding under the Innovative Pool to assist moving young people out of
residential aged care although early discussions have taken place around
proposals in the ACT, South Australia
and Victoria.[451]
4.114
The Department concluded:
While the Department of Health and Ageing is seeking to address
the issue of younger people with disabilities inappropriately placed in residential
aged care in a limited way through the Aged Care Innovative Pool, the main
structural vehicle for change is the CSTDA. Since the CSTDA is managed by the
Department of Family and Community Services, officers from the Department of
Health and Ageing are working with their colleagues in the Department of Family
Services via the Aged Care – Disability Joint Policy Forum, which aims to
improve the co-ordination of policy issues around the aged care – disability
interface, on this important issue.[452]
4.115
The Victorian Government stated it was seeking to
progress small scale jointly funded initiatives through the Pool and that the
result can inform future development of jointly funded options. However, the
Government went on to state that 'the lack of flexibility and sustainability in
the CIP Program is limiting opportunities to develop long-term care
alternatives.[453]
4.116
NSW Health argued that the Innovative Pool presented a
possible mechanism to develop alternative models for supporting younger people
in aged care facilities but stated 'the current timing and funding restrictions
applied to these places by the Commonwealth would first need to be
reconsidered'.[454] Other witnesses
also noted that the Innovative Pool is not designed to provide on-going or
longer term services with Melbourne Citymission stating that it had concerns
'about raising expectations of accommodation and service options that have no
long term funding base because sources are non-recurrent'.[455]
4.117
The MS Society of Australia,
which obtained funding for Carnegie House in Melbourne,
saw problems in the design of the Innovative Pool which hampered groups from
doing likewise:
The other reason why we cannot replicate it in every state is
the design of the innovative pool. That again is part of the reason why it took
two to three years to get that house going. I think you have heard evidence
from other people who have put in innovative pool proposals to their state
government and they have not actually made it across the border to Canberra.
The innovative pool is a good concept that has been absolutely tortured by the
bureaucrats into a scheme that is almost unworkable because it needs to get
through the state sausage machine before the Commonwealth can adjudicate on it.
If you fail at that step, the Commonwealth does not even see the good idea.[456]
4.118
The MS Society Victoria
provided more evidence on the problems with accessing the Pool for the Carnegie
House project and pointed to prescriptiveness of the Aged Care Act and the
policy and funding imperatives of state disability services. It stated that:
Some States reportedly refused to take part out in the Pool due
to the rigidity of the guidelines, and the lack of incentive. But with some
states expressing an unwillingness to participate, providers in those states
saw no future in putting resources into service development given the projects
would not be supported.
This closed off any opportunity for young people to benefit from
the program.[457]
4.119
Another barrier for the States is the lack of access to
ongoing funding: a facility may be established but the States may not be able
to sustain in the long term.
4.120
The Society also noted that the time constraints on the
Pool made the State Governments reluctant to participate. It stated that if the
Pool were restructured so that there was joint funding, 'you could have 10 or
12 [new facilities] in every state very quickly. The technology, the models and
the skills of assessment and service delivery are there.'[458]
Commonwealth
State Territory
Disability Agreement (CSTDA)
4.121
The Commonwealth State Territory Disability Agreement
(CSTDA) provides the national framework for the provision of government support
to specialist services for people with severe and profound disabilities. The
Commonwealth is responsible for planning, policy setting and management of
specialised employment assistance. The State and Territory Governments have
similar responsibilities for accommodation support, community support,
community access programs such as day programs and respite. Support for
advocacy, information and print disability is a shared responsibility.
4.122
Bilateral agreements between the Commonwealth and each
jurisdiction covering agreed areas of mutual concern have been established. In
all States and Territories, except the Northern Territory,
younger people in residential aged care has been identified as an area to be
addressed. Work plans developed under the agreements aim to address both
accommodation options and access to services for younger people with a
disability living in residential aged care.[459]
The Department of Family and Community Services (FaCS) stated:
One of the key projects of national disability administrators is
to specifically look at the care needs of those younger people who are in
nursing homes. Our intention, as part of that process, is to encourage the
states and territories to provide care for those people within their own
environments in accommodation support services and, most importantly, to try
and minimise the need for younger people with disabilities to go into aged care
nursing homes in the future.[460]
FaCS indicated that it was 'taking a lead role and is
currently working cooperatively with relevant State and Territory departments
through the multilateral and bilateral agreements under the CSTDA to explore
alternative support models for younger people in residential aged care
facilities'.[461]
4.123
However, ACROD argued that 'while the bilateral
agreements linked to the CSTDA do intend to progress the issue
of younger people inappropriately housed in residential aged care, they give it
no urgency: unless given a higher priority, it is unlikely to be resolved by
the conclusion of the Agreement'.[462]
4.124
The Victorian Brain Injury Recovery Association also
stated:
...in the first CSTDA there was a timetable that had to be
followed by the States to meet the federal requirements. That has never been
followed, and the Commonwealth has continued to accept [that] year after year –
we are now into the 15th year. And so the nursing homes are clogging up with
people who have been accepted compassionately by the Commonwealth. We are not
criticising the Commonwealth for doing it, except to say that, if the
Commonwealth is going to continue and persist in allowing, please provide the
funds to allow providers to give the care that is necessary.[463]
4.125
The MS Society of Victoria similarly stated 'government's
support the aspirations of people with a disability, and have endorsed
community living and choice as core principles of disability services, however
in the case of young people in nursing homes, practical delivery of this rhetoric
through the CSTDA has been miserable'.[464]
4.126
ACROD stated that the incidence of young people
inappropriately housed in nursing homes is an example of 'the suspicion about
cost shifting which so inhibits development of sensible policies in these
areas' and that:
There are some good statements of intention within
cross-government agreements. The Commonwealth State Territory Disability
Agreement includes some statements of intention around improving the linkages
across government, and there are some commitments to improve the interface
between aged care and disability services, but in the formation of that
agreement the federal Department of Health and Ageing is hardly involved and
has no sense of ownership over the outcomes of that agreement.[465]
4.127
The Gippsland Carers Association also commented on cost
and stated:
The overwhelming cost of the 5/6 bed group home option ($100,000
per bed in Victoria)
compared to the cost of aged care residential services is a further
disincentive for states and territories to hold up their end of the CSTDA
bargain.[466]
4.128
NAYPINH stated that the State systems are largely
fulfilling their obligations under the CSTDA for those with intellectual and
other congenital disabilities. However, the State disability systems 'struggle
with the reality of developing and sustaining services to people with acquired
disabilities who have additional rehabilitation or nursing needs'. This group
includes people with ABI, and neurological conditions such as MS. The NAYPINH
commented that 70 per cent of people accessing services through the CSTDA have
an intellectual disability, while over 80 per cent of young people in aged care
facilities have an acquired disability. NAYPINH concluded that 'this shows the
lack of capacity of the CSTDA sector to plan and provide for people with an
acquired disability' and pointed to the under representation of acquired
neurological conditions in the disability accommodation sector that is
dominated by intellectual disability and congenital conditions. It argued that
congenital disabilities have more predictable outcomes that makes the planning
and resources of supports and services simpler than for acquired disabilities.[467]
4.129
The NAYPINH recommended that young people in aged care
facilities be made a priority under the CSTDA and that disability funds can
follow young people with complex needs into aged care nursing homes and provide
for their different support needs while they live there.[468]
4.130
NAYPINH went on to note that under the CSTDA, it is
agreed that the provision of 'services with a specialist clinical focus' are
excluded from the agreement (Section 5(4)(b)). While noting that the term is
not defined, 'it is assumed that at the time of agreement, it was most probably
meant to refer to acute, sub acute health services and rehabilitation'.
However, NAYPINH commented that:
...in practice, it has given effective permission for the States
to avoid responsibility for young people needing what they call 'nursing home
level of care'. Every State jurisdiction is trying to resist providing accommodation
services with a nursing component, which is the nub of the problem for the
YPINH group.[469]
4.131
NAYPINH concluded that the States thus have the backing
of the CSTDA itself to take up their position, saying it is a Commonwealth
responsibility to provide services to this complex needs group, while the
Commonwealth tries to use the same agreement to press the responsibility back
to the States:
The practical effect of this clause serves to both neutralise
the current Commonwealth argument; and to underline the need for a discrete
approach to deal with the YPINH problem...The various bilateral agreements about
YPINH are simply not strong enough to overcome this inherent flaw in the CSTDA
framework. The States are simply not accountable to deliver the solution
through the CSTDA.[470]
The NAYPINH called for the urgent redrafting of clause 5 of
the CSTDA with appropriate financial agreements and accountabilities.
4.132
The MS Society of Victoria
also commented on this aspect of the CSTDA:
The almost total lack of availability of nursing care in
disability services is something that must be addressed by the CSTDA
administrators...If nursing could be included in the CSTDA suite, it would serve
to significantly reduce the transfer of people from CSTDA to aged care.[471]
4.133
Another matter highlighted by NAYPINH was the lack of
involvement of the Commonwealth Department of Health and Ageing. It noted that DoHA
is the largest funder of disability services for young people in aged care
facilities at the Commonwealth level and as such 'needs to have a direct role
in the negotiation and monitoring of the CSTDA agreements going forward.
NAYPINH recognised that DoHA is
involved indirectly through interdepartmental liaison groups, 'this is
inadequate and cannot replace direct input and accountability'.
4.134
The Disability Services Commission Western Australia
stated that there is a lack of information on the needs and profile of young
people in aged care facilities and noted that it is important to recognise that
'not all young people in nursing homes fall within the CSTDA target group. Some
of these people may be chronically ill, recovering from an illness or accident,
require palliative care, or have aged care needs due to premature ageing.'[472]
4.135
NSW Health stated:
The Bilateral Agreement is a significant and essential step to
finding long lasting and effective solutions. However, the work required will
take some time and will not result in immediate changes for individuals. It is,
therefore, essential that younger people living in nursing homes are not disadvantaged
in the interim. As an intermediate step, ways to improve access to additional
support services for younger people living in nursing homes are being
investigated by DADHC, including access to a range of services from mixed
funding sources. This will require cooperation across both the disability and
aged care sectors.[473]
4.136
NSW Health pointed to the enormous problem of
supporting disabled people in the community:
My understanding is that that would be happening. The problem is
– and this is a very real problem – is around whether it is sustainable. I am
not here to speak for DADHC. But there are increasing numbers of individuals
being cared for in the community by DADHC where in some cases the annual cost
of care is up to $900,000. There are very many individuals whose annual cost of
care is over $500,000...Per person per year. Because they require 24-hour
personal care by individuals it is an enormously significant impost. As I say,
the question is, despite the desirability of the best model of care – the
ethical considerations and all those things – as there are increasing numbers
of people with profound levels of disability surviving, there is a very real
question as to whether the model is sustainable.[474]
4.137
Concerns were also raised about future needs. Witnesses
stated that demand for services will continue to increase as people, many with
very high needs, may now survive a catastrophic event through advances in
medicine. Medical advances and improved health care systems also mean that
people with degenerative neurological conditions are surviving longer and
enjoying a better quality of life. The NAYPINH concluded that:
The result is that the number of people with acquired
disabilities in Australia
is growing and existing disability systems – established to deal with the
comparative predictability of congenital disabilities – are ill-prepared to
deal with the complexity and more intensive needs of young people with acquired
disabilities.[475]
4.138
The MS Society of NSW also voiced concern and stated:
The thing that strikes me about the whole sector is that there
is no recognition of unmet need. There is no planning forward in terms of the
next wave of people with disabilities. As I alluded to in my opening address,
we have identified some 300 people with MS that will need further care if there
is a change in their current support networks. That is going to happen. There
is no recognition of that; there is no forward planning in those areas and
there is no understanding of unmet need.[476]
4.139
Demand will also increase with the rise in disability
that accompanies an ageing population. NAYPINH submitted that in NSW, where
there is significant unmet need, some non-government organisations have
estimated that there are over 7000 people with disability in NSW in need of
supported accommodation and around 4000 ageing carers of young people with
disability who require, or will soon require, support. However, NAYPINH went on
to state that this is seen as an underestimate with over 10 000 currently
on the Victorian and NSW waiting lists.[477]
4.140
In relation to the CSTDA, FaCS stated that:
Whether it is a CSTDA accommodation support service or an aged
care place that is provided outside the CSTDA, I think it is fair to say that
the assumption in both cases is that the service is meeting the needs of the
person...if a person is receiving an accommodation support service or a nursing
home service, those service providers are meeting that person's need.[478]
FaCS commented that there is no barrier in the CSTDA to
anyone in a range of housing options from accessing a component of support out
of CSTDA:
It is up to the States and Territory how it manages the
expenditure of those funds on people with disabilities...They know they are
responsible for the planning and policy setting. It is possible that the States
are making decisions about what they see as relative priorities...As long as they
spend the money they have committed to spend on people who are in the target
group of the CSTDA, which are essentially people with disabilities, it is up to
them what they spend that money on.[479]
4.141
FaCS also commented on the provision of specialist
clinical services. It noted that the intention of the clause is primarily aimed
at separating what would be regarded as health interventions, such as mental
health services, acute health treatment etc from the CSTDA as the CSTDA's purpose
is to provide continuing day-to-day life needs. This provision arose as a
result of the clarification of responsibilities in the first CSTDA agreement in
1991. FaCS stated:
...[people with disabilities] may need physiotherapy for their
physical disability. They may need speech therapy for their communications
needs. Beyond a very minor level, those therapy services and acute treatment
type services are not considered to be part of the CSTDA...the purpose of the clause
was very much around trying to draw a line between the purpose and scope of the
CSTDA and the provision of health and allied health services that would
generally be available to anyone in the community.[480]
4.142
FaCS concluded:
People with disabilities...are perfectly entitled to access the
allied health services. The provision of those services is the responsibility
of the State government along with the provision of accommodation support. Both
are matters of State government funding and management. All we are trying to do
in the CSTDA, by agreement, is make it clear that what is being funded. As the
minister said, that does not stop a State putting together a package of
services for a person which includes whatever physiotherapy and allied health
services they need. It is simply a State decision and a State responsibility.[481]
Changes to funding arrangements
4.143
Witnesses argued that the current funding arrangements
entrenched problems in access to services for those living in the community and
hindered attempts to move young people out of aged care facilities. ACROD
submitted that younger people would be better served if they were housed in the
community but:
The principal barrier to this occurring is the disagreement
between the Commonwealth and State governments about who has funding
responsibility (and associated suspicion about cost shifting). The way forward
requires a funding model that combines ongoing and indexed Commonwealth Health
and Aged Care Funding and State Disability Services funding.
The younger people who reside in nursing homes often have
high-level physical support needs or complex medical needs (requiring
ventilator support and gastrostomy meals, for example). But the funding
available to aged care services or to disability services is alone insufficient
to support these younger people to live in the community. Funding formulae have
failed to keep pace with the real costs of assisting people who have complex
medical support needs.[482]
4.144
ACROD advanced the view that in relation to those young
people moving out of aged care facilities, the Commonwealth should allow the
aged care funding that it provides for the aged care place to follow the person
into the community. The funding would need to be indexed so it would increase
in line with the cost of living and for the States to provide the difference
between the Commonwealth funding and the amount required for the person to live
in the community.[483] NCOSS also
supported this approach and stated that 'this change would align service
provision to these younger people with disabilities towards the current
Commonwealth and State legislation which prefers people with disabilities to be
offered the same life chances eg accommodation, opportunities etc as people
without disability of the same age'.[484]
4.145
YPACA supported individual funding so that the funding
remained with the person. YPACA went on to note that individualised funding is
seen by people with disabilities as being a step towards independence.[485] Australian Home Care Services stated
that individual funding means that 'we do not have the notion that we put
people in a place and they stay there forever. Rather, it means that we have a
continual planning process, that we open the system up and that we can step
people up and down and move them to where they will receive the support they
need'.[486]
4.146
NCOSS recommended that younger people in aged care
facilities could be transferred to an Extended Aged Care at Home (EACH) or
Community Aged Care Package (CACP) whereby the funding is used to support the
person either at home or in a small group situation. Community care programs
are discussed later in this report.
4.147
The Victorian Government noted that although younger
people with disabilities are able to access services through the residential
aged care program, 'there are funding and policy issues that affect service
provision for this group'. The Victorian Government stated that it is engaged
with the Commonwealth to progress these issues and indicated that 'the
Victorian Government has consistently argued that while it accepts its
responsibilities under the Commonwealth States and Territories Disability
Agreement (CSTDA) people with disabilities who require residential aged care
services are not readily provided for under the Agreement'. The Government
concluded that it strongly favoured the joint development of sustainable and
long-term solutions with the Commonwealth.[487]
4.148
Evidence to the Committee pointed to significant
barriers in establishing accommodation options due to fragmentation of the
system. While there have been successes where the accommodation model is
appropriate, where the funding has been put in place and where adequate
services have been available, the very small number is tangible evidence of the
barriers in place. In NSW for example, evidence from the Liverpool BIRU
indicated that the Department of Housing modified houses and that people like
the Lions Club were very interested in getting a property and then being able
to renovate it but 'those discussions can only go so far when you cannot
actually guarantee that the person that is moving into the house will have the
support'.[488]
4.149
There was continued emphasis during the Committee's hearings
on the successes in Western Australia
and Victoria of the independent
living housing projects as being a result of a coordinated approach:
The success in Western Australia
is probably attributable to the fact that there was a project. They got all of
the stakeholders together – the Commonwealth, the Disability Services
Commission, Housing and perhaps Health. They dedicated money and gave a mandate
to this project to complete the job. They were the key success factors.[489]
4.150
Cyrill Jewell House in Victoria
is another example where all stakeholders came together. The MS Society of Victoria
stated that 'it is a model that shows that a cross jurisdictional funding
arrangement can work without threatening the integrity of each sector and
actually working in the interests of young residents'. The Society concluded:
It is a promising development, and is the only effective way
forward to resolve the issue, since the YPINH group have dual eligibility for
both disability and aged care, so both jurisdictions must work to design the
solution.[490]
4.151
Another matter raised in evidence was the level of
nursing care a person may require. The MS Society of Victoria
stated that this was the 'defining issue' as disability services seem to be
unwilling or unable to consider the provision of nursing as part of disability services.[491] The parents of one young person in
an aged care facility also commented that they had been told that there was no
other option for their son as 'there is no nursing care for his needs in the
disability system'.[492]
4.152
Melbourne Citymission concluded:
Within an existing fragmented service system, there is a need
for cross-sector partnerships to develop a co-ordinated approach across the
acute sector, sub-acute rehabilitation services, disability services and aged
care. As a result, co-operation is needed across all levels of government. Inflexibility
or inadequate funds in one area frequently leads to cost-shifting into another
area. In such an environment, the needs of the individual can become a
secondary consideration.
Cross government collaboration is required to assist with the
development of an integrated, cross sector policy response to assessment and
placement of people requiring high levels of care. Such a policy might include,
'a short term role for nursing homes in emergencies, assessment, slow stream
rehabilitation and transition to other accommodation settings (Fyffe et al,
2003:60) rather than being seen as 'the end of the line' where no future
alternatives exist. In addition to preventing long term placements in the first
place, it is also important to work to develop pathways out of such placements
for those currently in inappropriate aged care facilities.[493]
4.153
The NAPYINH argued that there was a need for a systemic
change if sustainable solutions are to be developed and called for all levels
of government to take on the responsibility to do so. It stated that the
expectation that the States will solve the young people in aged care facilities
problem on their own is unrealistic:
In many ways, it is also undesirable as neither the CSTDA nor
other programs, including the Innovative Pool, contain satisfactory
accountability mechanisms to ensure targets are set and met; money is dedicated
and delivered to YPINH; or that joint responsibility is defined. These three
preconditions must be met before we can confidently move forward and the
problem of accountability that, for YPINH remains a very real one, is dealt
with.[494]
4.154
NAYPINH went on to argue that the existing policy
frameworks and jurisdictional boundaries cannot lend themselves to resolving
the problem quickly because 'there is no incentive or rationale to do so'. The
Commonwealth needs to take on a leadership role and be financially committed to
developing and maintaining supported accommodation options for young people in
aged care. NAYPINH concluded:
A major step towards the solution is a multi jurisdictional
targeting of the YPINH issue through a national taskforce linked to the CSTDA.[495]
4.155
Such a taskforce would involve all jurisdictions to
oversight and implement the supported accommodation options young people need
and include:
-
funding provided by the Commonwealth and States
and Territories for each young person transferring from residential aged care
to supported accommodation elsewhere. The funding arrangement would be
recurrent and be maintained for the individual's lifespan;
- where young people choose to remain in
residential aged care the State or Territory concerned would fund the delivery of
all support services and the Commonwealth would continue to fund the bed costs;
- the States and Territories would provide capital
and funds for any costs associated with adapting or modifying existing accommodation
options;
- the States and Territories would provide a
seeding grant for each young person living in residential aged care or in
community based supported accommodation to assist with equipment needs and any
modifications needed to buildings;
- the Commonwealth and States and Territories to provide funding for transitional programs;
- in the first instance, funding should be
provided to allow 700 young people to be offered supported accommodation
options each year over a five year period; and
- funding to follow the individual.
Council of Australian Governments
4.156
The Council of Australian Governments (COAG) meeting on
3 June 2005 agree that there
was room for governments to discuss areas of improvement in the Australian
health system. The COAG Communiqu stated that 'governments recognised that
many Australians, including the elderly and people with disabilities, face
problems at the interfaces of different parts of the health system. Further,
governments recognised that the health system can be improved by clarifying
roles and responsibilities, and by reducing duplication and gaps in services'. Included
in the ways in which the health system could be improved were:
-
simplifying access to care services for the
elderly, people with disabilities and people leaving hospital; and
- helping younger people with disabilities in
nursing homes.[496]
4.157
COAG agreed that Senior Officials would consider these
ways to improve Australia's
health system and report back to it in December 2005 on a plan of action to
progress these reforms. It was also agreed that where responsibilities between
levels of government need to change, funding arrangements would be adjusted so
that funds would follow function.
Conclusion
Our concern, quite frankly, is that we will run out of puff
unless there is something that happens at a higher decision-making level than
we can marshal...We are trying to be solutions based, not problem identifiers. There
are problems out there – we know it and you know it. We are saying that there
is a range of ways in which we can solve this. Our challenge is not to see it
for the one-offs. Let us take the higher calling here and the high moral ground
and, across all of our areas of politics and government, say, 'This needs to be
solved.' We do have some solutions – let us solve it. We can identify the
solutions, but again it needs to be taken at a much higher level of
decision-making. That is why we believe today is critical. This is a watershed
for us.[497]
4.158
One of the most difficult aspects of this inquiry has
been the issue of young people in aged care facilities. The Committee is
strongly of the view that the accommodation of young people in aged care
facilities is unacceptable in most instances. Young people should not be in
aged care facilities as these facilities and services are designed for, and
respond to, the needs of the frail elderly. Elderly residents have care needs,
health needs and social needs which are quite different from young people.
4.159
Aged care facilities are not places which readily
enable a young person to socialise with family and friends. They are not places
where young people can listen to their music or have their own space. They are
generally inward-looking places with little interaction with the greater
community as would benefit, and is needed by, a young person.
4.160
Evidence suggests that the environment of an aged care
facility significantly reduces the ability of an individual to work towards a
future, redevelop life skills and re-establish social and inclusive networks.
This is particularly the case for young people with acquired brain injury. For
those young people with, for example, degenerative disease, aged care
facilities may not provide the specific complex health support or palliative
care required.
4.161
The Committee therefore considers that there is an urgent
need to provide alternative services for young people in aged care facilities
particularly those aged less than 50 years. The Committee considers that
programs must also be in place to ensure that more young people are not placed
in aged care facilities inappropriately. The Committee is of the view that the
way forward is for all jurisdictions, the Commonwealth and the State and
Territory Governments, to work cooperatively to identify viable solutions.
4.162
Having coming to the conclusion that aged care facilities
are not appropriate for young people, the Committee was mindful of the fact
that in certain circumstances there may be no alternative accommodation
options. This is particularly the case in rural and regional areas where there
are fewer services to support young people in the family or the community. In
such cases, families may choose aged care accommodation, even with a lesser
level of services, to keep their young person close to them and their community
of origin.
4.163
In order to achieve the aim of moving young people out
of aged care facilities, the fundamental requirement is for the provision of
appropriate services in the community that meet the needs of each person. The
Committee has visited successful models of supported accommodation and has noted
the outcome of the Young People in Nursing Homes project in Western
Australia. The Western Australian project resulted in
95 people accessing a variety of accommodation arrangements to meet their
needs.
4.164
The Committee does not consider that it is of benefit
to be prescriptive about models of accommodation and service delivery. The
situation of each person is different: type and level of disability; family
circumstance; and geographical location. What is evident to the Committee is
that there must be a range of accommodation options for young people who are
moving out of aged care facilities with matching provision of services.
Accommodation options may range from the family home to specialised group
cluster housing. Which ever it is, appropriate services with adequate funding
are the basis of success as is the willingness of all stakeholders to work
together to provide innovative solutions.
4.165
The success of projects under the Innovative Pool and
in Western Australia underscores
the need for a co-ordinated and collaborative approach. Unfortunately, it
appears that the main push for change to the provision of services by
government has been left up to individual interest groups. A solution to moving
young people out of aged care facilities needs whole of government commitment
and coordination of government and non-government funds and expertise.
4.166
The Committee has noted that helping young people with
disabilities in nursing homes is now to be considered by Senior Officials for
the Council of Australian Governments. The Officials are to report to COAG in
December 2005. The Committee considers that this will be an important step in
improving access by young people in aged care facilities to other support
services. However, the Committee considers that solutions already exist and
that the Senior Officials should concentrate their efforts in extending those
models which have already proven to be viable.
Recommendation 22
4.167 The Committee is
strongly of the view that the accommodation of young people in aged care
facilities is unacceptable in most instances. The Committee therefore
recommends that all jurisdications work cooperatively to:
-
assess the
suitablity of the location of each young person currently living in aged care
facilities;
- provide alternative
accommodation for young people who are currently accommodated in aged care
facilities; and
- ensure that no
further young people are moved into aged care facilities in the future because
of the lack of accommodation options.
Recommendation 23
4.168 The Committee
notes that the Council of Australian Governments has agreed that Senior
Officals are to consider ways to improve Australia's health care system,
including helping young people with disabilities in nursing homes, and to
report back to COAG in December 2005 on a plan of action to progress these
reforms. The Committee recommends that the Senior Officials clarify the roles
and responsibilites of all jursidictions in relation to young people in aged
care facilities so as to ensure that:
-
age-appropriate
accommodation options are made available; and
- funding is
available for the provision of adequate services to those transferring out of
aged care facilities.
The Committee supports every endeavour to reach a positive
outcome.
Recommendation 24
4.169 That the Senior
Officials' report to the Council of Australian Governments include:
-
support for a range of
accommodation options based on individual need;
- ways in which the
successful accommodation and care solutions already in place can be extended to
other jurisdictions;
- identification of
barriers to the successful establishment of accommodation options and provision
of adequate support services by all levels of government; and
- identify a
timeframe for the establishment of alternative accommodation options and the
tr
ansfer of young people out of aged care facilities.
Recommendation 25
4.170 That the Commonwealth and State and Territory
Governments work cooperatively to ensure that any barriers to accessing funds available
under the Innovative Pool are removed so that the desired objective of this
initiative in providing alternative accommodation options for young people in
aged care facilities is met.
4.171 The Committee recognises that, in rare instances, young
people may choose to remain in an aged care facility. In such cases, the
Committee considers that it is necessary to ensure that there are adequate
services that address not only accommodation needs, but also specialist health
needs, allied health support, equipment and psychosocial needs. Particular
attention is required to ensure that young people are encouraged to maintain
social links and to feel part of the wider community.
4.172 The Committee considers that in order to achieve the
level of services required by young people in aged care facilities, cooperation
by the Commonwealth and State and Territory Governments is required. The
Committee considers that governments will need to examine the assessment tool
used to evaluate the complex care needs of young people in aged care
facilities. Cooperation and collaboration will also be necessary to establish
mechanisms to provide rehabilitation and other disability-specific health and
support services and ways to ensure that those caring for young people in aged
care facilities have the appropriate skills to meet complex care needs.
Recommendation 26
4.173 The Committee recognises that in rare instances, a
young person may choose to remain in an aged care facility. In such
circumstances, the Committee recommends that the Commonwealth and the States
and Territories work cooperatively to reach agreement on:
-
an assessment tool to address the complex care
needs of young people in aged care facilities;
- mechanisms, including a funding formula, to
provide rehabilitation and other disability-specific health and support
services, including specialised equipment; and
- ways to ensure
that the workforce in aged care facilities caring for young people has adequate
training to meet their complex care needs.
Recommendation 27
4.174 That the Department of
Health and Ageing collect data on young people in aged care facilities by
disability type.
4.175 The Committee has also noted the growing number of
older carers of disabled young people. While a working party of officials has
been established to provide advice on assisting ageing carers and the
Commonwealth has provided funding to be matched by State and Territory
Governments for respite care, the needs of carers are becoming acute. The
Committee considers that the investigations being undertaken by the working
party must be expedited in order to identify ways for the needs of the family
members of older carers to be better met.
Recommendation 28
4.176 That the Commonwealth and State and Territory Governments
give priority to the efforts of the Working Party established in November 2004
to examine succession planning for ageing carers of children with disabilities
and appropriate support for respite for carers.
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