Chapter 4
Outcomes for children and young people in out-of-home care
My name is Julia and I am 17 years old. I came into care at
the age of two. I have lived in 36 different homes. These homes included
residential care, foster care, kinship care and self placement. There was a
failed reunification when I was 12. I was then returned into care. I have been
to eight schools, two tertiary colleges and two behaviour management programs ...
This is only an overview of my time in care; it in no way
shows the hardships I endured in foster care or residential care, but it gives
you an outlook on what can happen to a kid in the system who is meant to be
protected. There are so many problems in the care system.[1]
Julia, Brisbane hearing,
17 April 2015
4.1
As Chapter 2 noted, the National Standards for out-of-home care
(National Standards) provide a framework for measuring and assessing the
outcomes for children and young people in out-of-home care. However, the
committee acknowledges that current data collection projects to report against
the National Standards are not yet sufficiently developed to provide an
assessment of outcomes for children and young people in care.
4.2
Drawing from evidence collected during the inquiry, this chapter assesses
the outcomes for children and young people in out-of-home care against the key
themes of the National Standards across the three main types of care (kinship
care, foster care and residential care), including:
-
safety and stability (standards 1 and 12);
-
participation in decision making (standards 2 and 3);
-
access to health and education (standards 4 to 7);
-
connection to family and community (standards 8 to 11); and
-
transition from care (standard 13).
4.3
Overwhelmingly, the committee found that outcomes for children and young
people in out-of-home care across these indicators remain poor.[2]
Based on a series of research projects undertaken by the Australian Institute
of Family Studies (AIFS),[3]
Dr Daryl Higgins told the committee:
...we know that the out-of-home care system as it currently
works is incredibly expensive...and we do not have good evidence for it having
good outcomes. If you look at the research evidence, there is very little
empirical data to say that children do well as a result of out-of-home care.[4]
4.4
This chapter examines why these outcomes remain poor across all types of
care and highlights best practice models to help improve outcomes for children
and young people.
4.5
Chapters 8 and 9 will examine specific outcomes for Aboriginal and
Torres Strait Islander children and young people and children with disability.
Safety and stability
Placement safety
4.6
Submitters and witnesses supported a child-first approach to child
protection that focusses on ensuring the safety and wellbeing of children. The
National Children's Commissioner, Ms Megan Mitchell, expressed concern that
current child protection frameworks do not focus on the needs of children:
I really do not think they [child protection authorities] put
children at the centre of their thinking, even though the system is actually
for them. I think that needs to be a cultural change.[5]
4.7
The committee considers that the safety and wellbeing of children and
young people must be the paramount consideration in all decision-making
processes for children placed in out-of-home care. Some of the most alarming
evidence the committee heard related to children being placed in unsafe
out-of-home care placements where their basic needs are not met. In some cases,
children continue to suffer physical, emotional and sexual abuse while in care.
Inappropriate placement decisions
4.8
As discussed in Chapter 2, across jurisdictions the demand for
out-of-home care services far outweighs the capacity of child protection
systems and service providers. Due to these demand pressures, evidence suggests
decisions about appropriate placements for children and young people are often
based on availability rather than need. Ms Michelle Waterford from Anglicare
Australia noted:
There is a lot of pressure, I think, from departments just to
get a young person into a placement. The services call them 'bums in beds'.[6]
4.9
A number of service providers highlighted that the necessity to place
'bums in beds' means that often children and young people are not placed with
carers best suited to their particular needs. Mr Julian Pocock from Berry
Street, a service provider in Victoria, told the committee that due to demand
pressures:
...we have children being inappropriately placed into
residential care when that is not the right option for them, or we have carers
asked to take on more and more kids when really that carer household is at its
capacity in terms of what it can do. We have siblings who cannot be placed
together, separated in the care system—with all the outcomes we know from the
royal commission and other places.[7]
4.10
Evidence suggests the prevalence of a 'bed availability driven' system
which forces providers to accept placements that may not be suitable for the
child or young person, particularly in residential care.[8]
Anglicare Victoria noted in its submission, residential care providers are:
...too often pressured into accepting placements that do not
take appropriate account of a given child or young person’s stage of
development, gender, mental health, behavioural tendencies and overall
potential to be a perpetrator and/or victim of harm in context of the mix of
other children and young people in the prospective residential care unit. Put
bluntly, the need to ensure that children’s safety, care and development needs are
met is often compromised for the sake of demand pressures.[9]
Allegations of abuse
4.11
As discussed in Chapter 3, the most common reasons children are placed
on care and protection orders and subsequently in out-of-home care is due to
abuse or neglect. A number of witnesses and submitters highlighted the effect
of this abuse on the development of children and young people in out-of-home
care.[10]
Mr Basil Hanna, Chairman of the Community Sector Roundtable for NGOs and
Government, told the committee that:
Child abuse begins with the destruction of that most basic
right that children have to be cared for and loved by those entrusted with
their care ... [they] are not in this position by choice, by accident or by some
horrible biological act of fate; they are in this position because they were
physical, sexually and/or emotionally abused by adults in whom they placed
their love and trust. That action, singular or repetitive, has changed their
lives. These children are voiceless and vulnerable.[11]
4.12
Most alarmingly, the committee heard in some cases children and young
people continue to experience abuse while they placed in out-of-home care. At
its Brisbane hearing, the committee heard from a range of young consultants
from the CREATE Foundation, the peak body representing the voices of all
children and young people in out-of-home care.[12]
One CREATE consultant told the committee of physical and emotional abuse she
suffered during her time in care from age two from foster parents, other
children in foster care and residential placements, and from her birth father
during a failed reunification. She was physically abused throughout a nine year
placement with a foster family before she was moved to a new foster family
after a failed reunification:
One afternoon we got into an argument. I cannot really
remember what it was about, but I ducked and they asked me why. I told them
that my previous foster carers would hit me. We had a very long and serious
talk about all the things that they did and that they would have to tell the
department about all the stuff because it was wrong. I then told them about the
abuse that my dad had inflicted on me during the failed reunification.[13]
4.13
The committee heard from two experienced foster carers who noted the high
incidence of sexual abuse among children in foster care:
Our own experience is that two of the three children we have
fostered experienced prolonged and severe sexual abuse from a range of family
members or 'friends of the family'. We know of at least twenty paedophiles who
routinely raped these children over many years of their childhood but were
never taken to court. These men are consequently at liberty to continue to prey
on vulnerable children...The lack of action increases the number of victims of
these paedophiles and it sends a clear message to the children that their
stories are not important, and that the social structures in which they live,
to some extent condone this abuse.[14]
4.14
Submitters suggested abuse and trauma are particularly prevalent in
residential care facilities. Mr Bernie Geary, the Victorian Commissioner for
Children and Young People told the committee of particular concerns about the
incidence of sexual abuse in residential care:
Sometimes they were [exploited] by organised people in the
community, sometimes they were just bad buggers in the community who were
assaulting our kids, but so often it was the kids on each other and that speaks
to that funnel where we are tipping kids and their dreadful issues on top of
each other.[15]
Addressing trauma
4.15
The committee heard that existing models of care, particularly
residential care, do not adequately address issues of ongoing trauma for
children and young people in care. Brooke, another CREATE young consultant,
told the committee her experience of residential care varied between 'good and
not so good', with the worst examples reflecting an institutional environment:
I was placed in placements where there was a 6 pm curfew and
no-one was allowed in or out. However, the youth workers would not finish their
shift until 10 pm. There were placements where they would not drive the young
people anywhere at all after school or to do any activities on the weekends.
They would not even pick the young people up. There are also placements out
there that have very limited food. One situation was so bad that my dad had to
go and buy groceries for the placement that I was in at the time. One placement
I was in made me feel like I was institutionalised due to the physical
appearance of the property. The bedroom doors were metal. All the doors had
locks on them and even the beds were bolted to the floor.[16]
4.16
Brooke told the committee that such institutional settings are not
appropriate to ensure the safety and stability of children and young people in
care:
All of these things should not happen if you are trying to
make a child feel safe, comfortable and nurtured. On one occasion when the department
could not find me a placement, they actually admitted me to hospital. I had
nothing physically wrong with me; there was just a shortage of placements. I
stayed there overnight and a placement was found for me the next day.[17]
4.17
A number of submissions were highly critical of existing models of
residential care that do not provide support services to address trauma.[18]
Mr Gregory Nicolau provided the committee with photographs of residential
facilities in Victoria that his organisation, Australian Childhood Trauma
Group, was reviewing on behalf of the relevant department. Mr Nicolau explained
to the committee:
[Y]ou can see a photo of a refrigerator with hardly anything
in it. Often the food is kept within the office and children have to ask
permission to get food and have the door unlocked. There are some organisations
that have only recently taken locks off doors and there are some that have put
locks back on doors. The office is locked. There are signs up. They do not
always say 'No clients past this point', but some will say that young people
may not come into the office space and so forth ... Some of these houses have a
window, like a nurses station, where they can look out into the main community
areas. It is prehistoric—or at least 1800s. It is no way to care for children
who have been harmed or have come out of really deprived circumstances and it
does not create a healing environment.[19]
4.18
These submissions suggested the lack of trauma treatment in existing
models of residential care facilitate particularly poor outcomes for children. Dr
Phil West, a former residential care worker, submitted the following example:
Recently, I worked in
a unit where two of the children (teenage boys) wet their beds, and in another,
where a fifteen-year-old boy defecates in his pants. They are not receiving any
counselling/trauma-healing programs related to these physiological
manifestations of their emotional pain. Instead, our care is that they are not
going to school, allowed to go to bed at any time, sleep in till 12 or 2 pm and
are smoking weed or taking ice three-four times per week! This is not care, it
is State-sanctioned neglect.[20]
Investigating out-of-home care
complaints
4.19
To assist children and young people in addressing safety concerns and
reporting allegations of abuse, the CREATE Foundation recommended that
independent children's commissioners or guardians be given powers to
investigate individual complaints from children and young people in care.[21]
4.20
As noted in Chapter 2, all jurisdictions have established independent
children's commissioners or guardians.[22]
The role and responsibility of these offices differs across jurisdictions based
on the relevant state and territory legislation. Ms Noelle Hudson from the
CREATE Foundation noted the inconsistencies across jurisdictions in
investigating individual complaints:
is a serious limitation. In jurisdictions where children and
young people are not able to have individual complaints acted upon, they are
left without an independent representative to hear their voice and stand up for
them when they are at their most vulnerable.[23]
4.21
Brooke, a CREATE young consultant, highlighted the importance of a
complaints mechanism for children in care that is independent from the
department:
When a young person raises an issue they have about a carer
or a youth worker with the department, normally a visit is arranged. When this
happens a carer or youth worker has time to clean up their mistakes whereas if
it is unannounced they cannot hide anything. When a child raises an issue of
alleged abuse, more investigation needs to be done. In my experience, both the
police and the department listen to and believe what the carer says rather than
what the child says and the case just gets brushed off. Maybe there needs to be
an investigation team set up separately from the department to look into such
issues. After all, it is about protecting the child and safety of the child,
and that should be the most important concern because it is all about the
children.[24]
4.22
In addition to investigative powers, the committee heard that the
ability of commissioners or guardians to visit children in care differs widely
across jurisdictions. In most jurisdictions with an 'official visitor' program,
the visitor is limited to supervising children in residential care facilities.
The committee heard the independent visitor model administered by the
Queensland Office of the Public Guardian is unique in that the visitor may
visit children in all forms of care, including foster care and relative/kinship
care. This provides children in these forms of care with an opportunity to
report any issues or concerns directly to a representative of the Office of the
Public Guardian for investigation (see Box 4.1).
Box 4.1 – Best practice – Queensland Community Visitor Program
The Queensland Office of the Public Guardian (OPG) administers a Community Visitor Program
for children in residential care and home-based care. Programs in other jurisdictions only visit
residential care facilities (NSW, Victoria, ACT).
In 2004, following a recommendation by the Queensland Crime and Misconduct Commission, the
then official visitor program was extended to all children in care.
In 2013, the Commission of Inquiry found a range of issues with the program, including that by
visiting all children in the out-of-home care system, much time, money and effort was necessarily
wasted in visiting children and young people who were relatively happy with their placements. The
Commission of Inquiry recommended regular visits be continued to those children considered the
most vulnerable.
OPG told the committee it now seeks to classify the degree of vulnerability of children and young
people to determine the frequency of visits. Each decision as to the vulnerability and frequency of
visiting is unique to the particular needs of the child or young person.
The key roles of the community visitor include:
- • develop a trusting and supportive relationship with the child as far as possible, which is
seen as critical in being able to perform the function of the community visitor;
- advocate on behalf of the child by listening to, giving voice to and facilitating resolution
of their concerns and grievances;
- seek information about and to facilitate that child or young person's access to support
services; and
- acquire and report on the adequacy of information given to the child about their rights.
The community visitor also acquires information and reports on the physical and emotional
wellbeing of the child and the appropriateness of the home or facility to ensure the child's needs are
being met.
Source: Ms Catherine
Moynihan, Office of the Public Guardian, Committee Hansard, Brisbane, 17 April
2015, pp 58 – 59.
4.23
The committee heard that the Queensland community visitor model provides
an important service to children in care. Adina, a CREATE young consultant,
noted that the community visitor were more effective in resolving issues than
the community service organisation (CSO) providing the care service:
I had a lot of CSOs and they were all different in the way
that they worked. They always said they were going to come out and they never
did. They were really dodgy. I felt like I could not rely on them. I never made
a strong relationship with them, whereas my CV [community visitor] came once a
month always when she said she would. She knew everything about the department
and she was able to always tell me what my rights were and what I was entitled
to. She was always there for support. She was so reliable. She was just lovely.[25]
4.24
The committee also heard support for the introduction of independent
visitor models in those jurisdictions that do not have them. Mr David Pugh from
Anglicare in the Northern Territory, which does not have an independent visitor
program, told the committee at its Darwin hearing:
When a child is placed in care in the Northern Territory, as
in most jurisdictions, the only people who can ever scrutinise the quality of
that care are the funding body—in this case the Department of Children and
Families—or the agency themselves. In the area of disability, we do not see
this. We see a strong independent visitor program, where others can come in and
provide a voice for the person in care, but not in out-of-home care. It just
shocks me that, in out-of-home care, the most vulnerable of citizens have no
independent arbitrator for them.[26]
Placement stability
4.25
While all jurisdictions acknowledge the importance of stability and
security for children in out-of-home care, the committee heard this is not
adequately addressed in practice across jurisdictions. The National Children's
Commissioner, Ms Megan Mitchell, told the committee:
I think our care and protection systems
have historically been somewhat remiss in looking at the long-term stability
and safety of the child. They generally respond to incidents, or they did in
the past. I do think the states and territories are trying to amend that and
enhance legislation and practice so that there is a focus on a permanent
pathway from the beginning. However, that is not as common as it should be.[27]
4.26
As noted in Table 2.5, AIHW's 2011–12 data on the number of placements
for children upon exiting out-of-home care indicates that the longer children
spend in care, the more likely they are to have multiple placements.[28]
According to AIHW, of the children exiting care in 2011-12, 63 per cent had one
to two placements, 22 per cent had three to four placements and 15
per cent had more than five placements.[29]
4.27
While AIHW's statistics only measure up to five placements, the
committee heard this number can be significantly higher for children in
long-term care. At its Brisbane hearing, one CREATE consultant noted during her
time in care between the ages of nine and seventeen, she went through 50
placements.[30]
At its Hobart hearing, Ms Jarcinta Short, who was in out-of-home care for 18
years, told the committee the numbers of placements she experienced were 'too
many to count'.[31]
4.28
CREATE's 2013 Report Card indicated a great variation in the number of
placements prior to exiting care across jurisdictions. Across Australia, CREATE
found 57 per cent of children and young people reported having one or two
placements. In NSW this proportion was as high as 70 per cent whereas in the
Northern Territory this proportion was significantly less, indicating children
generally experienced a greater number of placements.[32]
CREATE found that while 83 per cent of children and young people were 'quite'
or 'very happy' in their current placement, many were not as satisfied with
their placement history due mostly to instability and moving.[33]
4.29
The committee heard placement stability was one of the most important
aspects contributing to positive outcomes for children and young people in
care.[34]
Ms Patricia Murray, CEO of Wanslea Family Services told the committee:
If you get the placement right early and they are not
churning through the system, then the chances of getting it right later are
much higher. It does make a difference.[35]
4.30
Adina, a young consultant with CREATE, told the committee her positive
experience in care was due to the stability of her placement arrangement:
In my opinion, the biggest reason that I [thrived] in foster
care is simple: I had—and still have, even though I have turned 18—a stable,
loving family. I was not shifted from family to family, I never moved schools
and I have only just moved out of the town I grew up in.
My family and I forget that I am not their biological child.
This is what every foster child deserves. This is an issue for so many children
and young people in care. They do not ever get a chance to build up stable
relationships with the adults around them, there is no chance to make friends
and they cannot trust anyone.[36]
4.31
Ms Short, who experienced many placements breakdowns, told the committee
of the importance of a stable placement on providing long-term stability once
a young person ages out of the care system:
The only connection I ever made was with my last carers; I
was with them for six years. It took me a while to realise that they were not
going to give up on me, no matter how naughty I was. They were my family and
they will always be, and I even still see them to this day—and I am 21.[37]
4.32
A number of submitters were critical of the 'churn' many children and
young people experience through a large number of placements.[38]
Noting the difficulties faced by child protection authorities in finding
suitable placements for all children in care, Mr Basil Hanna, CEO of Parkerville
Children and Youth Care in Western Australia, referred to this 'churn' as
'system abuse':
It is very difficult for the child protection-family services
department to be able to place all of their children. It is extremely
difficult. Their mandate is to provide children with a safe home. However,
because that is their mandate, often children are placed in placements that are
not safe—not clinically safe—for those children. And what happens is that the
placements break down and children bounce around. One wonders, if we were
sitting here in 20 years time, if there would be a royal commission about
system abuse that is occurring today?[39]
4.33
Jurisdictional approaches to achieving placement stability are examined
in more detail in Chapter 7.
Participation in decision making and planning
4.34
As noted in Chapter 2, all states and territories have a charter of
rights for children and young people in care that establishes the rights of
children and young people to be involved in the decisions that affect them
while in care. However, the committee heard the role of children and young
people in this process was not adequately addressed.
4.35
The National Children's Commissioner, Ms Mitchell, told the committee
that all state and territory departments have policies and practices in place
to involve children and young people in the decision making process, but that:
It is really important to understand that children have
agency; they can understand a lot of things. I am so impressed by kids as I go
across the nation talking to them. Really young kids understand stuff if you
engage with them. I think for children in these circumstances it is really
critical. I am not saying that they are going to get what they want
necessarily; it is about having a dialogue.[40]
4.36
A number of submitters and witnesses highlighted the importance of
ensuring the voice of the child is heard in decision making processes that
affect them.[41]
In its submission, the CREATE Foundation asserted that 'listening and
responding to the views of children and young people in the care system should
be a cornerstone of best practice'.[42]
Ms Noelle Hudson from the CREATE Foundation told the committee that CREATE's
research supported the findings of the 2013 Queensland Child Protection
Commission of Inquiry:
...although the principle of children being able to have a say
about their decisions, about coming into care and about their lives is more
recognised in Australian policy and practice, in reality, children's voices are
often not heard in court and decisions are generally made for them without
their input.[43]
4.37
Evidence suggested that the benefits of including children and young in
decision making processes were far reaching. Ms Catherine Moynihan from the
Queensland OPG told the committee the expected benefits include:
-
more confidence in court that the child or young person has been
involved in decision making;
-
more stable placements as the child or young person is in a
position to take ownership of placement decisions and less likely to be
resentful or resistant;
-
resolving school issues for children and young people and
negotiating continued school attendance;
-
a greater stake for children and young people in their case plans
and contact decisions; and
-
reduced risk of mental health problems as they are less likely to
consider themselves powerless victims of the whims of adults.[44]
Placement decisions
4.38
A number of submitters noted the importance of involving children and
young people in decision making about placements. Mr Justin Cooper, program
manager for the Salvation Army's Therapeutic Youth Residential Service in
Tasmania, emphasised the impact of participation on achieving good outcomes:
The biggest concern is the voice of the child, what service
they want to enter—not being told, 'This is option A, and option B is the
streets; so you need option A.' It is about actually hearing the voice of the
child. That includes when they are going into a different model of care.
Whether it be therapeutic care, whether it be foster care or whether it be...college
care, the child actually has to be involved in the process, not just told,
'That's where you're going.' It is their life. They need to control some
portion of it, because control has been taken away; they are in chaos. So they
need to control that: 'Yes, I will give therapeutic resi a go.' Otherwise, it
makes the job 10 times harder, to try and support them and move them forward as
well.[45]
4.39
However, the committee heard young people are not often included in this
process. At the committee's hearing in Melbourne, representatives from the
Youth Movement Initiative in Bendigo highlighted the lack of involvement for
young people in case planning discussions:
We feel like zoo animals because we cannot – there are so
many workers in the room and we may, if we are lucky, know two or three of
them. Then they get to hear our life stories and make decisions on our lives
that we do not really get a say in a lot of the time.[46]
4.40
Likewise, Ms Jarcinta Short told the committee in Hobart she would have
appreciated having greater involvement in placement decisions during her time
in care:
I would like to have been thought of, instead of my case
worker just placing me in places they thought I should be. Was it necessary for
me to be removed? If it was not, then I should not have been removed. So my
solution would be to ask the child, to put them first and have them be involved
in the consideration and in the decision-making. With matching kids to care, I
think it is a really good idea for case workers to do a tick sheet with
children—the things that they like to do and what makes them them—and then pass
it on to a carer that they think would be suitable for that child.[47]
4.41
At its Brisbane hearing, the committee asked CREATE young consultants
for their views on how and at what age children should be involved in the
decision making process. Julia told the committee that children all ages should
be listened to in making decisions about placements and other issues:
...children should be listened to from three years old. I know
that sounds really young, but there are different ways you can engage with
children. You can have them draw a picture of what they want. You can have a
casual conversation with them. Obviously, what they are saying will not be
taken on as much, but everyone should be listened to no matter what. I think
that, as they get older, their opinion should weigh a lot more but when they
are younger they should still be listened to, even if it is not as much.[48]
4.42
Julia noted, based on her own experience:
I did not even know I had a CSO [child safety officer] until
I was 12, until I reunified, and I did not have a CV [community visitor]. If I
had either one of those I could have told them that I was being abused in the
foster home that I was in for nine years. Obviously, I would have been able to
tell them if I was getting hit. Without anyone there to listen to me and talk
to me about that, I could not tell anyone. So I think everyone should be
listened to, no matter what age. It is just a different level of engagement and
also a different level of how much information you take on from them.[49]
Case planning
4.43
One key opportunity to involve children and young people in the decision
making process is through development of their individual case plan. According
to AIHW, a case plan is an individualised, dynamic, written plan or support
agreement for children in care, outlining the goals of ongoing intervention and
the outcomes and actions required to achieve these goals. It usually includes
information on needs assessments, relative/kin contact arrangements and living
arrangements.[50]
4.44
As noted in Table 3.1, based on data from Queensland, Western Australia,
Tasmania and the ACT only, an estimated 90 per cent of children in care had a
current documented and approved case plan at 30 June 2012. Data for other
jurisdictions is not currently available.[51] In its submission, the Northern
Territory Department of Children and Families noted that at 31 March 2014, 76
per cent of children had a current care plan.[52] The
Productivity Commission reports similar proportions of children with current
documented case plans across jurisdictions. Excluding NT and SA, 82.1 per cent
of children nationally had case plans (80.5 per cent of Aboriginal and Torres
Strait Islander children, and 83.1 per cent of non-Indigenous children) at 30
June 2014.[53]
4.45
However, these statistics do not give any indication of the level of
engagement children and young have in the development of these case plans.
CREATE's 2013 Report Card found that less than one third of respondents knew
anything about their case plans and only one third of those who knew about a
plan knew something of its contents and had been involved in its preparation.
Similarly, only 25 per cent of children were aware of having an individual
education plan.[54]
CREATE recommended:
Involving children and young people in their case planning,
including the development of care plans, is necessary to improve the
participation of children and young people in the important decisions that
affect their lives.[55]
4.46
The committee heard concerns about the level of involvement children and
young people have in the case planning process. The National Children's Commissioner,
Ms Mitchell, noted:
Many pieces of legislation require that case planning and
reviews ensure that children's voices are heard, that they are engaged in the
process, but in practice it does not happen as much as I would like.[56]
4.47
The CREATE Foundation noted in practice, 'the participation of children
and young people in decision-making is mediated by caseworkers and carers' and
suggested participation of children and young people in decision making 'is
enhanced through well-developed relationships with both carers and
caseworkers'.[57]
CREATE noted in its 2013 Report Card that only 65 per cent of children and
young people reported being able to contact caseworkers when they wanted to.
CREATE also identified the high turnover of caseworkers as a barrier to
establishing and maintaining good relationships.[58]
4.48
The committee heard that approaches to case planning differ across
jurisdictions. In Western Australian, the WA Ombudsman is currently undertaking
a follow up report to test the recommendations from its 2011 own motion
investigation into case planning for children in care.[59]
The 2011 report found that while the Department of Child Protection had
developed a series of policies and procedures for care planning and that care
plans had been prepared for nearly all children, many plans had not been
reviewed and many children had not received appropriate health care and
education planning.[60]
4.49
The Commissioner for Children and Young People Western Australia noted in
its submission that despite improved collaboration between the relevant
government agencies, only 35 per cent of case plans reviewed by the Ombudsman
Western Australia in 2011 had the appropriate health assessment plan, and 22
per cent had the required education assessment.[61]
4.50
In Victoria, the Youth Movement Initiative provided the committee with
its 2014 report on 'best interest' case planning by the Department of Human
Services. The report, prepared by young people in care, expressed significant
concerns about the 'poor' experience of case planning, noting 'it negatively
impacts on how young people are supported in their education'. The report
recommended that the department engage more closely with young people in
developing case plans that focus on long-term stability, education and housing
outcomes.[62]
Documentation and identification
4.51
The committee heard that a significant challenge for children in care
was accessing identity documents. The committee notes that this issue was also
raised during the committee's 2014 inquiry Grandparents who take primary
responsibility for raising their grandchildren.[63]
The National Children's Commissioner, Ms Mitchell, advised that the committee at
both the state and federal level there are proof of identity and parental
consent requirements that are unable to be met in some cases for obtaining
identity documents, passports and Medicare cards. Ms Mitchell notes this may
mean:
...that a child is unable to receive timely treatment for
health conditions, they miss out on sporting and other opportunities, can have
difficulties enrolling at school, families are prevented from taking overseas
holidays together, or the child in care is left in Australia when they do.[64]
4.52
In additional documentation provided to the committee, Ms Mitchell
recommended:
-
the relaxation of proof of identity and parental consent
requirements for children in care;
-
the prioritisation and centralisation of passport and identity
document sourcing within child protection departments; and
-
identifying points of specialist contact within the Departments
of Health, Foreign Affairs and Trade, and Immigration and Border Protection
supported by an agreement to fast track the recognition of citizenship, issuing
of Medicare cards and issuing of passports for children in care.[65]
4.53
Similarly, Professor Fiona Arney, Chair of the Council for the Care of
Children in South Australia, advised the committee of issues in obtaining
Australian citizenship that 'potentially affects many vulnerable children and
young people, and in particular, children and young people in out of home care'.[66]
Professor Arney noted two cases from February 2015 of young Aboriginal people
in South Australia experiencing difficulties in gathering enough evidence to
apply for 'Proof of Citizenship' to obtain an Australian passport. The young
people were informed by the Department of Immigration and Border Protection
(DIBP) that 'Proof of Aboriginality' was insufficient evidence to apply for
'Proof of Citizenship'. Professor Arney noted these hurdles 'reflect a systemic
issue facing other children and young people in Australia who are vulnerable
through no fault of their own'.[67]
4.54
The committee heard that in addition to identity documents, carers had
difficulties in obtaining permission for children in care where the relevant
department is designated the child's guardian. At its Brisbane hearing, Xena
from the CREATE Foundation told the committee permissions and approvals for
children in care is 'too bureaucratic – the process takes too long and it means
kids miss out on opportunities'.[68] In one example Xena
shared with the committee, she was unable to attend a school trip to New
Zealand because she was unable to get signatures from both parents for the
passport application. In another example:
I had an opportunity to go on a special camp for kids in
care. It included horse-riding, team bonding and learning about who you are as
a person. Because some of the kids, including me, did not have permission from
the department, no-one could go horse-riding. We were only allowed to sit on
the horses...The department did not give permission because they said that the
activity was too high-risk and too dangerous. This experience was a big blow to
my confidence. I loved horses and the fact that I could not take part in the
activity just did not make sense to me and made me really angry at the time.[69]
4.55
Xena expressed the view that the current requirements for identification
documents for children in care:
...creates a situation
where children and young adults are unable to fully integrate or participate
and do things that other young people who are not in care can do.[70]
4.56
The committee notes that the issue of identification documents is
currently under active consideration by the Australian Children's Commissioners
and Guardians (ACCG) and the subject of dialogue with the Department of Social
Services in the context of the National Framework.[71]
Access to health and education
Education outcomes
4.57
The available evidence indicates that education outcomes for young
people in care are generally worse than for the general population across
jurisdictions. The Commission for Children and Young People Victoria noted in
its submission, based on data from the Victorian Child and Adolescent
Monitoring System, 'children in out of home care generally have lower levels of
educational achievement than the general student population'.[72]
4.58
While the committee notes that the integration of NAPLAN data with the
CP NMDS will assist to improve the available data on outcomes for school
aged children, the currently available data on these outcomes is limited. Anglicare
Victoria's 2014 Children in Care Report Card found children in care are
much less likely to attend preschool compared to their peers (18.8 per cent
compared with 2.1 per cent), and more likely to experience bullying (35.0 per
cent compared with 23.5 per cent).[73]
The CREATE 2013 Report Card also highlighted a number of negative education
outcomes for school aged children, particularly 'disrupted schooling due to
changing primary schools, with those in residential care reporting more changes'.[74]
Effect of stigma and low
expectations
4.59
The committee heard that young people in care were not supported to
achieve academically based on negative assumptions about their ability and
ambition by child protection authorities. Mr Paul McDonald, CEO of Anglicare
Victoria, noted that negative assumptions can in some cases lead to negative
outcomes:
Maybe that is our narrative about these kids—that we in fact
do not believe that they will get that far; we lack ambition.[75]
4.60
Ms India Spicer, a care leaver from the Youth Movement Initiative in
Victoria, told the committee that the stigma of being a 'foster kid' limits educational
opportunities for children in care:
There is such stigma attached to foster kids and to kids who
are in care or who have had a care experience. We are automatically seen as
people who come from a low socioeconomic status and that we are always going to
be in that status; we are not going to get out of it, we are not going to
achieve anything. So when we do, there is such surprise – and it is offensive.
I never had any doubt that I would go to university, and it is just horrifying
that everyone else does.[76]
4.61
Similarly, Ms Kate Finn, another care leaver, told the committee that
young people in care have to 'fight' negative assumptions to get resources to
access education:
I had to fight to finish year 12 because I was not supported.
I turned 18 before year 12 started. The department did not want to pay for my
books to go to school. I had to argue with them to get that for a start. Then
the agency – I was very lucky that they gave me supported accommodation for the
year, but I was on my own there. I had nobody there helping me get through that
last year and I very nearly failed. I see this as a repetitious process.[77]
4.62
Ms Finn suggested that the stigma attached to out-of-home care continues
to affect young people after leaving care and going into tertiary education:
...the fact that I managed to fight to get there and did
eventually get in was a shock, because it is so unheard of. And that would be
nationwide. The expectation is so low from a community standpoint, from the
departmental standpoint, from the agencies and the wider general public. It is
so low; there is no expectation that you would.[78]
4.63
Witnesses suggested there is 'a need for cultural change, particularly
around expectations and aspirations' for young people in care, to combat the
negative assumptions and stigma.[79]
Health outcomes
4.64
Evidence to the committee suggests that health outcomes for children in
care across a range of indicators are generally poor. The Commission for
Children and Young People Victoria, drawing from data collected by Anglicare's
Child in Care Report and CREATE, noted 'children in care experience poor health
compared to their peers in the general population'.[80]
4.65
CREATE's Report Card found that 80 per cent of children in care reported
having good or excellent health, with those in the 15-17 year old age group
reporting 'feeling less healthy than the younger age groups'. However, the
committee notes that this data should be interpreted with caution as it relies
on self-reporting.[81]
4.66
Particular health outcomes for Aboriginal and Torres Strait Islander
children will be examined in Chapter 8.
Chronic health issues
4.67
Children in care are more likely to experience chronic health issues. Anglicare
Victoria's 2014 Children in Care Report Card found that 63.2 per cent of
children and young people in care experienced a greater incidence of chronic
health problems or disabilities, compared to 37.0 per cent of their peers in
the general population. [82]
4.68
A number of submitters noted that the high incidence of chronic health
issues among children was due to a lack of access to healthcare services.[83]
The Victorian Commission for Children and Young People (CCYP) suggested in its
submission the Commonwealth consider measures to reduce the cost of health care
services for children in care that would 'give priority access for general and
specialist healthcare' services, such as:
...creating a specific out of home care medicare item number
that would enable priority access to treatment without costs.[84]
4.69
Another suggested measure to improve access to healthcare services was the
establishment of specific programs that target children in care. The committee
heard that as part of Victoria’s Vulnerable Children’s Out of Home Care Five
Year Plan, that the Victorian Government has developed the 'Pathways to
Good Health' program that aims to link up health and community services to
develop health management plans for children in care (see Box 4.2). The
Victorian CCYP suggested that this program may provide a model for other
jurisdictions to help improve access to healthcare services.[85]
Box 4.2 – Best practice – Pathways to Good Health
The Pathways to Good Health Project aims to provide a comprehensive healthcare approach that is based on the National Clinical Assessment Framework for Comprehensive Health Assessments for
Children and Young People in Out of Home Care. The project commenced in November 2012 as
an initiative led by the Department of Health (DoH) in partnership with the Department of Human
Services (DHS), based in the North and West metropolitan areas of Melbourne.
The program includes an initial health check by a general practitioner, referral as required for a
multi-disciplinary assessment (involving a paediatrician, mental health clinician and speech
pathologist) and the development of a health management plan. Brokerage funds are available to
purchase specialist services and equipment where public services cannot be accessed in a timely
way.
According to the Victorian CCYP, the April 2014 DHS Update of Progress indicates that of the
385 children eligible for the program, only 41 per cent (160) have had an initial health check, 32
per cent (1240) have attended a multi-disciplinary team clinic and only 30 per cent (115) have
health management plans that have been completed.
An evaluation of the project is being proposed.
Source: Commission for
Children and Young People (Victoria), Submission 45, pp 12–13; Victorian
Government, Submission 106, p. 8.
4.70
The Victorian CCYP submitted that the 'Pathways to Good Health' project
has been slow to demonstrate improved health outcomes and suggested instead the
development of a pilot program based on other established health care schemes,
such as the Australian defence personnel scheme, to improve access to
healthcare services.[86]
Mental health issues
4.71
Children in care are more likely to experience mental health issues, and
associated emotional and behavioural problems. A 2007 review by AIFS found that
children and young people in care experience relatively negative outcomes when
compared to the general population in regard to mental health. It also
highlighted a strong coincidence of early trauma and abuse and subsequent
placement instability for children and young people with high support needs.[87]
Anglicare's 2014 report found one of the most striking differences between
children and young people in care and their peers is their experience of
emotional and behavioural difficulties (53.4 per cent compared to 13.3 per
cent).[88]
4.72
As noted in Chapter 3, children in care are likely to come from
backgrounds of significant social disadvantage and experience multiple forms of
trauma, abuse and neglect. A number of submitters noted the significant link
between trauma and mental health issues.[89]
The Royal Australian and New Zealand Council of Psychiatrists emphasised that:
the importance of stable, attuned care-giving adults cannot
be overstated. Infants who experience extremes of abuse or neglect are at risk
of failure to thrive, reduced brain size, impaired development and even death;
even when their basic physical requirements are met. All this can lead to
ongoing mental health issues.[90]
4.73
As with chronic health issues, the committee heard that children in care
do not have access to the mental health services they need. Dr Sara McLean from
the Australian Centre for Child Protection told the committee that a South
Australian study into children who needed professional help for their mental
health concerns found 54 per cent of children in care were identified as
needing support, and only 26 per cent had obtained some support over the
last six months.[91]
4.74
Submitters and witnesses supported improving access to mental health
services for children in care.[92]
For example, the Victorian Government recommended the Commonwealth introduce a
specialised Medical Benefits Schedule item for children in out-of-home care to
address the inequity for children in care to access healthcare services.[93]
Connection with family
4.75
The committee heard connection with family, including parents, siblings
and extended family is integral to the development of positive outcomes for
children and young people, particularly in Aboriginal and Torres Strait
Islander communities.[94]
The importance of family connection for Aboriginal and Torres Strait Islander
communities will be examined in detail in Chapter 8.
4.76
Professor Cathy Humphreys from Melbourne University told the committee
that research indicates that maintaining positive connection with family is
important for ensuring positive outcomes for children:
The research is clear that good quality contact between
children in out-of-home care and their parents, and in the context of good
professional supports, promotes positive outcomes for children. Importantly,
research shows that continued contact between children in care and at least one
biological parent is positively correlated with children's current wellbeing
and that high levels of externalising behaviours are evident where there is no
contact.[95]
Kinship care
4.77
One of the key means of supporting connection with family for children
and young people in out-of-home care is placement in relative/kinship
arrangements. As noted in Chapter 1, across jurisdictions more children are
placed in relative/kinship placements than other forms of care.[96]
4.78
A number of submitters highlighted the benefits of relative/kinship care
for assisting children in care maintain connection with family. Professor Cathy
Humphreys and Ms Meredith Kiraly from the University of Melbourne noted in their
submission that research indicates:
Kinship care provides for greater stability of care,
maintains children’s wider family connections, and improves the chances of
brothers and sisters being kept together.[97]
4.79
However, evidence to the committee suggested children in
relative/kinship care arrangements do not have access to the same supports and
services as other forms of care, particularly for those children with complex
needs.[98]
Research commissioned by the Benevolent Society highlighted 'the need for a specific,
well-resourced practice framework to support kinship carers and their
families'.[99]
4.80
Current models of relative/kinship care and supports available to
children and carers are examined in Chapter 6.
Siblings
4.81
The committee heard that, despite efforts by jurisdictions to place
sibling groups together, many sibling groups are separated in care. The CREATE
Foundation noted 36 per cent of respondents reported being placed in split
arrangements, separated from siblings. CREATE urged 'that siblings in out-of-home
care, wherever possible, must be supported to stay together; and where
co-placement is not possible, they must be enabled to maintain regular contact
with each other while in care'.[100]
4.82
The committee heard directly from sibling groups who were separated in
care. At its Hobart hearing, sisters Jarcinta and Sarah Short told the
committee they were placed in care separately and had to rely on their foster
carers to arrange contact:
We did not get told the reasons why. So we lost contact for a
few years. Then Jarcinta's last foster carers reunited us, and we basically had
to get to know each other all over again.[101]
Maintaining connection with
families
4.83
The committee notes there is not currently sufficient data to measure
how many children in care maintain contact with birth families, or leave care
to return to birth families. In Victoria, Anglicare estimated that 50 per cent
of children who come into care return back to the family home within six
months.[102]
However, similar estimates are not available nationally.
4.84
Submissions emphasised the importance of incorporating the views of
children and young people in decisions about connection to family. CREATE noted
in its submission:
...connection with birth family is an emotive issue that is
complex, but it is very important to young people that caseworkers and carers
involve them in the decision-making and not assume that they know what’s best
for them. They have said they want to participate in decisions not only about
the frequency of contact but also how it is supervised and where contact occurs.[103]
4.85
However, witnesses noted that incorporating the views of children in
these decisions can be particularly challenging when placement with family may
not be in the child's best interest. Mr Basil Hanna, CEO of Parkerville
Children and Youth Care in Western Australia, told the committee:
My experience in dealing closely with kids who come into
care, no matter how much abuse that they have suffered, they all want to go
back to biological their mum or dad. That is a hard thing, because when you
say, 'Listen to the voice of the child,' and the child says, 'I don't want to
be here; I want to go home. I want to go back to mum and dad.' You know it is
not safe for that child to go home to mum and dad.[104]
4.86
At its Brisbane hearing, Adina from CREATE told the committee:
[W]hen I first went into foster care, which was when I was
age 11, I really wanted to go back to my parents, because I thought that was
what was normal and I was comfortable there. I was never allowed to. Now,
thinking back, I am just glad that I never did. So it just shows that it is a hard
thing. I think you should sometimes listen to the kids, but sometimes it is not
always in their best interests.[105]
4.87
In his submission, Rev Graham Guy, who was removed from his family and
placed in foster care as a child, noted the need for alternative options for
children and the importance of considering the views of the child, saying that he
did not want to be 'forcibly removed', and would have preferred to have been
placed with extended family rather than placed in foster care.[106]
4.88
Noting these challenges, the committee heard that there is scope to
improve the ways children are consulted on connection with families. Mr Hanna
noted:
As a sector, we are not always totally honest with the child.
We are also not timely with the child. When the child comes into care, do we
sit down with that child, age appropriate, and tell them why they are in care?
Sometimes we do, sometimes we don't. It is very difficult to talk about the
voice of the child when every child says, 'I don't want to be in care.' The
fact is that they need to be in care, and it is a difficult conversation to
have. As a sector, I do not think we do it well enough.[107]
4.89
Support for families to maintain contact with children in care is
examined in Chapter 5.
Transition from care
4.90
The committee heard that one of the most significant gaps in current
service provision for young people is the transition from care at age 18. A
review by AIFS into transition from care found young people leaving care are
'one of the most vulnerable and disadvantaged social groups,' with the vast
majority of care-leavers suffering from, or at a great risk of suffering,
negative outcomes in their social and psychological functioning, financial
status, and educational and vocational pursuits.[108]
4.91
These risks are particularly acute for young people with disability
transitioning from care. The needs of young people with disability are examined
in Chapter 9.
Data on transition
4.92
There is a significant dearth of data on the numbers of children
transitioning from care, and outcomes for them once they leave the child
protection system.[109]
According to AIHW, in 2012-13, 9 360 children were discharged from
out-of-home care, of which 34 per cent were aged 15-17 years. This includes
children and young people returning to families or other placements and does
not distinguish young people transitioning to independence.[110]
Data collected by the committee from states and territories indicates that most
jurisdictions do not collect data on the numbers of children transitioning to
independence.[111]
4.93
The committee heard there is no national data collected on outcomes for
children once they leave care. The committee notes AIFS is undertaking a study
into transition from care, Beyond 18, funded by the Victorian Department
of Health and Human Services which will explore the experiences of young people
in out-of-home care and their experiences transitioning from care in Victoria.[112]
Dr Daryl Higgins told the committee that while the study is still in its early
stages, it aims to provide 'better
information about what it was that can predict those better outcomes and what
it was that can predict some poorer outcomes that will help inform service
system improvements'.[113]
4.94
The limited available data suggests that outcomes for children
transitioning from care are particularly poor. The CREATE Foundation's 2013
Report Card found that of the respondents who had left care:
-
35 per cent were homeless in the first year after leaving care;
-
35 per cent completed Year 12;
-
29 per cent were unemployed (compared to the national average at
the time of 9.7 per cent); and
-
70 per cent were dependent on Centrelink for some form of income
support.[114]
4.95
Few jurisdictions monitor the outcomes of children transitioning from
care. The Western Australian Department for Child Protection and Family Support
noted its Out-of-Home Care Reform Plan will be implemented from January 2016
and includes established indicators for the measurement of outcomes for
children leaving care.[115]
4.96
Associate Professor Philip Mendes from Monash University, whose research
focuses on the needs of care leavers, told the committee:
[W]e do not have any informed data in Australia at all on
what happens to young people beyond 18...We do not have that information here; we
desperately need it.[116]
4.97
The committee acknowledges that data on children and young people once
they leave care is not addressed by current data collection projects under the
National Framework. Associate Professor Mendes brought the committee's
attention to a model used by the Department of Education in the United Kingdom,
and recommended a similar model be adopted in Australia:
It traces all care leavers in England, segregated by each
local government until they are 21; shows how they are going with employment,
housing, education, higher ed access ... and involvement; if it is happening with
youth justice and so on. Policy makers can make an informed judgment about what
is being done well, and equally what needs to be done better...getting a national
database up like that would greatly inform knowledge of policy and practice and
where we need to go [117]
Transition planning
4.98
The committee heard that across jurisdictions, young people begin
preparation for transition from care at 15 years old. All states and
territories require young people to have a 'leaving care' or 'transition from
care' plan. The New South Wales Department of Families and Communities (FACS)
advised the committee a leaving care plan:
...addresses accommodation, employment and income, education
and training, knowledge of personal history including cultural background,
contact with family members, legal issues, and independent living skills
including financial management and health and lifestyle issues. Plans also
detail which services and supports will be provided by who. Both the age and
capacity of the young person are considered and it is acknowledged in the FACS
guidelines that younger care leavers are likely to need more support than 18
year olds.[118]
4.99
The committee heard that as part of the National Framework, states and
territories have developed the Transitioning from out-of-home care to
Independence: A Nationally Consistent Approach to Planning.[119] The
resource aims to provide a nationally consistent approach to planning for young
people transitioning from out-of-home care.[120]
4.100
Where planning occurs early, and adequate support is provided by case
workers, the committee heard that transition from care can be a positive
experience. Ms Sarah Short told the committee in Hobart:
My transition from care was pretty breezy actually. It was
really good. I had the support of my case worker and my foster carers. My case
worker went through everything that I needed to go through when moving out and
where I could get extra support, just getting everything lined up, so that,
when I did turn 18, it was easier to move in and I had everything planned out.
So mine was quite easy.[121]
4.101
In many cases, young people do not have a transition from care plan. As
Table 3.1 shows, the available data indicates across three jurisdictions, an
estimated 77 per cent of young people had a transition from care plan at 30
June 2012. Similarly, CREATE's 2013 Report Card indicates 64 per cent of young
people surveyed did not have a leaving care plan.[122]
4.102
In some case, transition planning does not occur until just prior to
leaving care. Ms Short's sister, Jacinta, noted her transition was more
difficult as she was not transitioned into the 'Moving on Program' until two
weeks before her eighteenth birthday. As a result, she told the committee '[t]he
first few months were hard because I was not used to all of it'.[123]
4.103
Similarly, Ms Brooke Gregson, another care leaver in Tasmania, told the
committee that her transition was not planned far enough in advance: 'I think
it was too late...it was only a couple of months before we turned 18 that the
subject really came up.' She further noted: 'I actually missed quite a number
of months of school due to that fact—that it was so stressful trying to find
somewhere to live'.[124]
Ms Angela Adams from UnitingCare Burnside emphasised the importance of
beginning transition planning as early as possible:
...we need to be thinking about it earlier. Past practice has
been that young people have had hurried leaving-care plans prepared at the 17
or 17 ½ that are not suitable.[125]
4.104
Where planning does occur, the committee heard in some case young people
are not supported by child protection authorities to identify suitable options.
Ms Brooke Gregson told the committee of her experience leaving care:
I found the transition quite difficult. The man from the
department who was supposed to help me did not help as much as I think he
should have. He made numerous appointments, but every time he called up with
another excuse to say he could not come. At the end of it, he basically gave me
the choice of going to the Moving On program or being homeless ... That put a lot
of pressure on me and my carers at the time because I was running out of time
and needed somewhere to live. After a couple of months, we finally found a place
to live, but it was a lot more difficult than I think it should have been and I
hope that other children have a much easier experience with it.[126]
4.105
Without this support, leaving care can be a significant shock. Mr Bryan
Seymour, who was placed in out-of-home care in NSW for 18 years noted in his
submission of the 'shock' and 'severe emotions that followed' leaving care:
The main challenge was fear. Suddenly the safety net was gone
– after having to file an invoice for every expense in my life there was suddenly
no security – financial, psychological, practical support was instantly all
gone.[127]
4.106
The committee heard even the terminology of 'leaving care' can be
daunting for young people planning for their transition from care. Ms Angela
Adams from UnitingCare Burnside told the committee that feedback from young
people is that:
...even the terminology 'leaving care' is scary. For some of
them, they have only just started to settle into a permanent placement, if they
have been lucky, with a carer and then we say, 'Right, let's talk about leaving
care.'[128]
4.107
Witnesses suggested that the term 'leaving care' should be replaced with
one that emphasises the need for ongoing support. Mr John Avent from the
Salvation Army's Westcare in Melbourne told the committee they use the term
'continuing care':
...because we continue to care for the young people after they
leave the service. The service intervention formally may stop, but engagement
with the young people continues, so we do not use the term 'leaving care'; we
use the term 'continuing care'. I think even the language you use can define
the way you think about an issue.[129]
Transition support
4.108
Most jurisdictions provide formal programs for young people
transitioning from care (such as the 'Moving on Program' in Tasmania).[130]
Some service providers, such as UnitingCare Children, Young People and
Families, noted they are also 'currently developing a good practice trauma
informed framework for leaving care planning. This includes a focus on training
for caseworkers and carers to better support young people leaving care'.[131]
4.109
The committee heard that the Victorian Government has also trialled more
intensive support for care leavers. The Springboard Program aims to link care
leavers to community organisations to assist in engaging in education and
employment (see Box 4.3).
Box 4.3 – Best practice – Springboard Program
The Springboard program, established by the Victorian Government in 2012, provides intensive
support for young people transitioning from residential out-of-home care who are not engaged in
education, training or employment.
Springboard is part of the existing suite of transition and post-care services funded by the
Victorian Government. The program is delivered by community-based organisations with
specialist skills supporting young people with education, training and/or employment, including:
- individually tailored and responsive assessment, planning and services;
- flexible outreach case work to engage, or re-engage, in education, training and/or
employment to prepare them for long-term sustainable employment;
- strong links with the department, residential out-of-home care providers, post-care
support information and other relevant services; and
- a culturally competent service responsive to the needs of Aboriginal young people and
those from diverse cultural backgrounds.
The Victorian Government noted a recent evaluation found that the program is achieving
outcomes for young people in line with the expected trajectory of education and employment
outcomes including:
- all participants had recorded addressing one or more barriers that inhibit their
engagement in education and employment; and
- 40 per cent of participants had achieved sustained participation in education or
employment.
Source: Victorian Government,
answer to question on notice, 30 April 2015 (received 22 May 2015).
4.110
The Stand By Me Program, also trialled in Victoria, aims to provide more
general support for young people leaving care, and has indicated initial
positive results (see Box 4.4).
Box 4.4 – Best practice – Stand By Me program
In 2012, Berry Street developed the Stand By Me pilot program to provide an intensive generalist case work support service that targets young people leaving the care system to better support a
successful transition to independent adult living. The program is based on broad elements of the
UK Personal Adviser Model. As at July 2014, there were twelve young people participating in the
pilot program in Victoria.
The program builds a relationship with the young person before they leave the care system,
extending into the period post care, and the service follows the young person and is able to offer
medium to long term support in the post care period through an assertive outreach model that
matches resources to the young person’s identified need at the time.
An initial evaluation by Monash University suggests the program 'is developing effective ways of
working with young care leavers and other program stakeholders'. The evaluation found the program offers potential benefits in:
- reducing the likelihood of homelessness;
- addressing trauma and improving access to mental health support;
- accessing specialist leaving care, employment, education and training supports;
- re-establishing family contact;
- enhancing stability of placements while in care; and
- maintaining links with out-of-home care supports.
Source: Berry Street,
Submission 92, p. 15; Sue Meade and Philip Mendes, Interim Evaluation Report
for the Berry Street Pilot Program – Stand By Me, Social Inclusion and Social
Policy Research Unit, Monash University, July 2014, pp 5–6.
4.111
However, the committee notes these pilot programs are only available to
a limited number of young people on a voluntary basis. For the majority of
young people who are not eligible for these programs, support is limited. Mr
Justin Cooper from the Salvation Army in Tasmania told the committee that
limited supports were available for young people outside of the formal
transition programs:
We are extremely limited in what we can access for them, to
the point that we have had to go out and create our own independent living
program—at a cost to our therapeutic residential program because we have had to
manipulate our limited resources and budgets. That is because we have found
that there is basically nothing for our kids to transition into if they do not
meet the requirements of the MOP [Moving on Program] or another program. They
do not have options here, so we see them go back to couch-surfing, we see them
to go back to family situations that are high risk, we see them regress back
into crime because they find safety in being incarcerated...[132]
4.112
Submitters highlighted the significant disparity between funding for
after-care services and out-of-home care services.[133]
Once young people leave care, there is limited capacity to provide specialised
after-care supports. Mr Cooper noted that the existing resources of service
providers to provide after-care support are already stretched:
We have a part-time role, but it is only part-time, and he
has to cover ten clients. That makes it very difficult when he is trying to
link them into Centrelink, do their financial budget for them, get the Hydro
bill paid, get their groceries in. Usually we find they are running out of
options, and the placement breaks down, they are evicted and they are back on
the street. It has really made life difficult.[134]
Housing and homelessness
4.113
The transition and lack of after-care support means a large proportion
of young people leaving care experience homelessness. A recent survey of
homeless young people in Victoria, Western Australia, New South Wales, the
Australian Capital Territory, South Australia and Queensland, The Cost of
Youth Homelessness in Australia Study, found nearly two-thirds of homeless
youth surveyed (63 per cent) had been placed in some form of out-of-home care
by the time they turned 18 years old. Of the young people who were placed in
out-of-home care, 63 per cent had been placed in residential care, 45 per cent
in kinship care and 33 per cent in foster care.[135]
4.114
However, evidence suggests there is a significant lack of data on the
number of care leavers experiencing homelessness. Ms Jessica Fielding, from
Yfoundations, a peak body representing young people at risk of experiencing
homeless, estimated that '50 per cent of young people leaving care will
experience homelessness at some point in their lives'.[136]
Ms Fielding noted some of the challenges in calculating the number of young
people from care experiencing homelessness:
...because so many young people are couch surfing and are
hidden, essentially, we actually do not know the real figure of how many young
people are experiencing it. We do know that a lot of young people are coming
from the out-of-home care system, though.[137]
4.115
The committee heard the Commonwealth provides support through the Transition
to Independent Living Allowance (TILA) payment of up to $1 500 for young people
between 15 and 25 years old leaving out-of-home care to meet the costs of
moving to independent living. As part of the National Framework, the TILA was
increased from $1 000 to $1 500. DSS noted that from 1 January 2015 to 1 September 2015,
211 young people had received a TILA.[138]
4.116
Witnesses suggested that while the payment was useful, it does not
adequately support young people exiting care. Associate Professor Mendes told
the committee:
[T]he general view in the field would be that, yes, that payment
is helpful. But what you find with young people leaving care, a lot our
research would show between 18 and 21, they are likely to move four, five or
even 10 times. There are stories, yes, they might be able to buy the furniture,
the fridge, the bed, although emphasising that money does not actually go
directly to the young person anyway; it goes to an agency which is registered
in the particular state or territory to buy the goods for them. Regardless,
even if they do get a lot of really necessary furniture with that payment, it
is unlikely to meet their needs in an ongoing way.[139]
4.117
The CREATE Foundation further noted the availability of the TILA
differed across jurisdictions and suggested 'the administrative arrangements of
the state and territory child protection agencies must ensure TILA is uniformly
available to eligible young people'.[140]
4.118
A number of submitters supported increased financial and practical
support in providing safe and secure housing for all young people leaving care,
structured around the experience of leaving care as an ongoing process.[141]
Associate Professor Mendes noted that leaving care is not a 'one-off' event:
...mostly we are talking about this construction of leaving
care as being this one-off event: you have turned 18 and, like a racehorse that
turns two— all the racehorses at the same time—you are suddenly an adult,
suddenly independent and you are ready to live on your own. It just does not
work out that way. I think the Commonwealth government, in looking at that
money, should be thinking about what the real situation is, as opposed to what
they are providing.[142]
4.119
The committee heard a number of organisations are working on developing community-based
programs to assist young people leaving care into safe and secure housing. At
its Melbourne hearing, Ms India Spicer, a recent care leaver, told the
committee she is part of a group that has set up a peer support program for
young people leaving care to provide support:
Once you leave care, you do not really have anyone to turn
to. There is no-one who you can go to for the little things...We are trying to
provide support and just make the system better because we have all had a
really crappy, hard time of it.[143]
4.120
In its submission, YFoundations recommended supporting the reform of
state and territory children and youth service systems to an integrated
community of schools and services approach 'which recognises the diverse
support, needs of young people will ensure young people are adequately
supported and can transition into adulthood'.[144]
YFoundations noted a whole-of-community approach to supporting young people
transitioning from care had recently been trialled in Geelong (see Box 4.5)
and could be taken as a model for implementation.
Box 4.5 – Best practice – The Geelong Project
The Geelong Project (TGP) began in 2012 to test the effectiveness of a proactive 'whole of
community' approach to early intervention over a period of three years.
TGP is supported by Commonwealth and Victorian Governments and led by Time for Youth in
partnership with Swinburne University, Barwon Youth and Geelong Region Local Learning and
Employment Network. TGP is grounded in community collaboration and is 'a world-first
innovation that can identify early youth at-risk of homelessness, school drop-out and other complex
inter-related issues'.
TGP links schools and community services to identify young people who are at risk of becoming
homeless. TGP reports that during the pilot phase, it proactively identified and intervened with 95
young people and 43 family members, where homelessness and school disengagement were
identified at high risk. As a result of TGP's intervention:
- 100 per cent of the young people have remained engaged in school, increased engagement
or returned to school; and
- 100 per of the young people supported have retained or obtained safe sustainable
accommodation, including:
- 86.2 per cent remained in or returned home (after leaving or regularly couchsurfing)
- 13.8 per cent supported into alternative accommodation when home was not
appropriate.
Source: YFoundations,
Submission 85, pp 12–13; The Geelong Project, http://www.thegeelongproject.com.au/
(accessed 26 June 2015).
Higher education and training
opportunities
4.121
The committee heard one of the most significant barriers for care
leavers was accessing higher education and training opportunities. A recent
report by LaTrobe University, Out of care, into university: Raising higher
education access and achievement of care leavers, found care leavers
'rarely transition to higher education'.[145]
Ms Spicer told the committee at its Melbourne hearing the her school assumed
she would not go to university based on her experience in care:
They just decided that because I was a foster kid it meant
that I must want to not be at school, that I did not want to go to university.[146]
4.122
The Out of care into university report aimed to provide the basis
for a national agenda for improving education outcomes for care leavers by
'highlighting the nature and extent of the problem, and suggesting practical
solutions within both the education and community service sectors'. The report
recommended three key reforms to improve the access and achievement of care
leavers in higher education (also outlined in a submission to the inquiry by Dr
Andrew Harvey, Director of the Access and Achievement Research Unit, La Trobe
University):
-
collection of nationally consistent data on higher education
access and outcomes;
-
revising the 1990 national equity framework to recognise the
out-of-home care cohort in as a disadvantaged cohort; and
-
extending legislative support for young people in out-of-home
care beyond 18 years old.[147]
4.123
Dr Harvey noted the lack of data on education outcomes for young people
in care once they turn 18 years old had a significant effect on assessing how
to improve education outcomes for young people in care:
...we do not know how many people from out-of-home care are in
higher education—no universities collect data on it, the Department of
Education does not collect data on it—and consequently there is no pressure
from that source for universities to act specifically around this category.[148]
4.124
The committee heard that the United Kingdom has undertaken a range of
reforms to increase the proportion of care leavers entering higher education
that may be applicable to Australia (see Box 4.6). Dr Harvey told the committee
this initiative was based on an extensive research report that 'created a
policy initiative that has led to massive change and massive increase in
populations within higher education'.[149]
Box 4.6 – Best practice – UK Education Support
In 2000, the Frank Buttle Trust sponsored the first major report into the experiences of care leavers
in higher education in the UK, By Degrees: Going from Care to University, which aimed to
increase the university participation rates and achievement levels of care leavers.
Following this report, the UK has initiated a number of policy and legislative changes:
- care leavers recognised as an under-represented group in higher education and
participation monitored;
- 'Quality Mark' awards introduced to recognise higher education providers that demonstrate a commitment to young people in care;
- care leavers recognised as a distinct university target group;
- institutional level provision of bursaries, accommodation, personalised support, outreach,
admissions policies, and the employment of dedicated staff for the care leaver group;
- statutory requirement for local authorities to support young people aged 16 to 24 in
education (Children (Leaving Care Act 2000);
- statutory £2 000 local authority bursary for young care leavers (Children and Young
Persons Act 2008); and
- regulations to strengthen transition planning, extend the right to have a personal advisor
to the age of 25 and recognise the central role that further education and training
personnel should take in planning ongoing educational transitions for young people
beyond compulsory schooling.
As a result of these changes, the proportion of 19 year old care leavers in higher education has
increased from one per cent in 2003 to six per cent by 2013.
Source: Dr Andrew Harvey,
Committee Hansard, 20 March 2015, p. 25; Harvey et al, Out of care, into
university: Raising higher education access and achievement of care leavers, pp
13–14.
Extending leaving care age to 21
4.125
A number of submissions suggested that transitioning from care at 18
year old was inappropriate for most young people, particularly those who had
experienced trauma, abuse and neglect. Recent care leaver Ms Jarcinta Short
told the committee: 'I think 18 is a bit too early to be chucked out into the
world.'[150]
Similarly Mr Basil Hanna told the committee that there is a double standard for
children in care, compared to children who live with families:
Times have changed and most people who have teenaged children
do not exit them at the age of 18. But we do. It is a hard world to be exited
into at the age of 18 without proper supports. Do we give proper supports to
children who exit care at the age of 18? Absolutely, categorically not, but we
expect them to survive. These are children who have come from a vulnerable
childhood. My kids, when they got to 18, fortunately came from a stable home
and they stayed long after 18. A lot of these kids have had multiple placements
and we still abandon them after 18. We do not adequately arm them to take on
the world.[151]
4.126
To improve outcomes for housing, education and healthcare, the committee
heard significant support for extending the statutory age for support to 21
years old.[152]
Based on his extensive research, Associate Professor Mendes strongly
recommended providing support to young people leaving care until at least 21
years old:
...we have got to move from discretionally to mandatory support
beyond 18 to at least 21. At the moment, every state and territory, I think
that is correct, has some legislation, or at least policy, talking about
support until 21 or even 25 in a number of states, but unfortunately the
resources allocated to this group of young people is minimal. It does not meet
the needs. It is well below where it needs to be.[153]
4.127
The committee notes that following recommendations by the 2013 Queensland
Child Protection Commission of Inquiry, the Queensland Government has already
agreed to provide a coordinated program of post-care support for young people
until at least the age of 21, and to fund non-government services to provide 'a
continuum of transition to independence services, including transition planning
and post-care management and support'.[154]
Committee view
4.128
As discussed in Chapter 2, while the committee notes there is a lack of
national data on the outcomes for children and young people in care, evidence
collected during this inquiry suggests current out-of-home care frameworks
facilitate poor outcomes across a range of indicators. The committee is
concerned that despite the establishment of the National Framework and a number
of state and territory inquiries, outcomes for children and young people in
out-of-home care remain poor.
4.129
The committee acknowledges the importance of listening to the voice of
children and young people in discussions about placements and care planning.
The committee also recognises the importance of providing independent
mechanisms for investigation of complaints by children and young people while
in care. The committee suggests nationally consistent powers for independent
child guardians and commissioners could provide an effective mechanism for
these complaints to be heard.
4.130
The committee acknowledges that demand pressures for all types of care
across jurisdictions means children and young may not enter placements that are
best suited to their particular needs. The demand to put 'bums in beds'
compromises the safety and stability of placements and affects the ability for
children and young people to achieve positive outcomes while in care.
4.131
The committee acknowledges the difficulties faced by children and young
people in care in obtaining parental consent for identity documents at the
Commonwealth, state and territory level. The committee supports the
recommendations by the National Children's Commissioner and Professor Fiona
Arney for the Commonwealth to address how to streamline these processes for
children and young people in care.
4.132
The committee recognises the importance of family connection for
children and young people in out-of-home care. Strategies for improving the
connection between children and their families are examined in Chapter 5.
4.133
The committee particularly recognises the need to improve education and
health outcomes for children and young people in out-of-home care. The
committee recognises the effect of stigma on 'foster kids' and the need to
improve the level of community and institutional expectation for these
children.
4.134
One of the most significant gaps identified by the committee is the
support available to young people transitioning from out-of-home care. The
committee recognises the terminology of 'leaving care' incorrectly implies that
young people no longer require care once they turn 18 years old. The committee
supports the terminology 'continuing care' to highlight the need to provide
ongoing support to young people through the transition period and afterward.
4.135
The committee notes while there is a significant lack of national data
on the outcomes for young people once they leave care, evidence collected
during this inquiry indicates young people are more likely to experience
homelessness and be exposed to drug and alcohol misuse and physical and sexual
abuse. The committee is strongly concerned by the lack of support available to
young people transitioning from care and supports lifting the age young people
can receive support to 21 years of age. The committee also supports the
development of strategies to assist young people transitioning from care access
education and employment opportunities.
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