Whose choice? Exploring multiple perspectives on music therapy access under the National Disability Insurance Scheme.
Lee, Juyoung ; Teggelove, Kate ; Tamplin, Jeanette 等
Whose choice? Exploring multiple perspectives on music therapy access under the National Disability Insurance Scheme.
Introduction
Prior to 2012, approximately 410,000 Australian people had been
supported through "traditional block-funded service
approaches" (Dowse, Wiese, Dew, Smith, Collings, & Didi, 2016,
p. 81), where large organisations or institutions received a block
funding to manage a large number of people with a range of different
needs. In this previous welfare system, some stakeholders argued that
understanding and supporting each individual's unique needs was
difficult, and a major reform of disability funding mechanisms was
considered necessary by what was then Rudd's Labour Party
(Buckmaster, 2012). After an extensive investigation, the Productivity
Commission (2011) concluded that the previous disability support system
was "underfunded, unfair, fragmented, and inefficient, and gives
people with a disability little choice and no certainty of access to
appropriate supports" (p. 2). The Commission further emphasised the
fundamental changes that the new National Funding system should provide
to the people such as:
* entitlements to individually tailored supports based on the same
assessment process,
* certainty of funding based on need,
* genuine choice over how needs are met (including choice of
provider), and
* local area coordinators and disability support organisations to
provide grass roots support and a long-term approach to care with a
strong incentive to fund cost effective early interventions
(Productivity Commission, 2011, p. 2).
Consequently, the government announced a funding plan called the
National Disability Insurance Scheme (NDIS). Commonwealth, state and
territory governments, who used to manage the disability funding system,
were reestablished as a single agency called the National Disability
Insurance Agency (NDIA) in 2012 (Buckmaster, 2012). In July 2013, the
NDIA launched trials across a number of regional sites nationwide
including the Barwon region in Victoria and the Australian Capital
Territory, and since July 2016, the service has been instigated across
Australia.
The NDIS places a strong emphasis on increased choice for people
with disabilities, tailoring support packages to the individual needs
identified by participants and allowing participants to prioritise the
services they wish to access and to select their own providers. However,
in the first two years of NDIS trials at various sites, some
participants reported their choices to access certain services, such as
music therapy, had been denied by authorities in the NDIA (McFerran,
2016; McFerran, Tamplin, Thompson, Lee, Murphy, & Teggelove, 2016).
For example, several service users' requests to include music
therapy in their NDIS plans were rejected in the trial region of New
South Wales, and participants were advised to seek a speech therapist
who is musical or told that music therapy is just like instrumental
lessons (McFerran, 2016). Paradoxically, some music teachers who
specialise in providing services for people with disabilities have been
told that only music therapy services can be funded. To understand this
phenomenon a group of researchers from the National Music Therapy
Research Unit (NaMTRU) at the University of Melbourne conducted a
qualitative study by collecting various reports of those involved, such
as the NDIA, and the Australian Music Therapy Association (AMTA), as
well as selected participants of the scheme or families of the
participants. The study aimed to: (a) better understand the needs and
capacity for contribution of each stakeholder involved, and (b) generate
knowledge for each stakeholder regarding requirements and objectives of
both the scheme and music therapy access options.
Literature Review
The practice of music therapy in the field of disability has a long
and contested history that has been documented since the 1940s (Aigen,
2014). Literature exploring the therapeutic application of music for
people with disability has typically been focused on person-centred
goals that are identified by professionals to address perceived needs of
the service recipients. Recent research in this area clearly supports
the effectiveness of music therapy in school and institutional contexts
and documents outcomes in social (Darrow, 2014; Pienaar, 2012), physical
(Dieringer, Porretta, & Gumm, 2013; Klaphajone et al., 2013; Wang et
al., 2013), communicative (Dunning, Martens, & Jungers, 2015;
Krikeli, Michailidis, & Klavdianou, 2010; Pienaar, 2012; Stevenson,
2003), psychological (Krikeli et al., 2010) and wellbeing or quality of
life domains (Curtis & Mercado, 2004; Shiloh & Lagasse, 2014).
Whilst music therapy services have been used for decades to support and
facilitate expert-determined goal attainment for people with
disabilities, there is currently limited understanding of the ways in
which music therapy can address the self-identified needs of people with
disability in the community. This distinction is key to the ideology
underpinning the NDIS which is built on the social, rather than medical
model of disability.
Within a medical model of disability, having a disability is
considered to be an individual's problem that requires medical
attention by an expert. Within a social model of disability, having a
physical, intellectual, or mental disability is understood as being part
of the diversity of human experiences and a responsibility of the
society to allow for the active participation of all citizens (Carson,
2009). The social model that originated from Scandinavian countries in
the late 1970's initiated a deinstitutionalisation movement across
the world, and people with disabilities whose lives had been managed in
large institutions and organisations were moved back into the community,
often in sheltered housing. Values such as community participation and
social inclusion were critical in this movement. This paradigm shift
visibly influenced the field of music therapy in the 21st century
(Ansdell, 2002), with the emergence of contemporary music therapy models
such as community music therapy (Stige & Aaro, 2011) and resource
oriented music therapy (Rolvsjord, 2010) also emanating from
Scandinavia. Other equity oriented approaches such as feminist music
therapy (Hadley, 2006) and anti-oppressive music therapy (Baines, 2013)
have shaped contemporary music therapy practices and research worldwide
(Aigen, 2014; Kenny & Stige, 2002).
Community music therapy research and theory has been most clearly
aligned with the disability rights movement worldwide (Stige & Aaro,
2011; Stige, Ansdell, Elefant, & Pavlicevic, 2010), endorsing a
focus on empowerment and community participation that is aligned with
the rhetoric of the NDIS on choice and control. Congruently, action
research projects in this field have shown how people with the most
profound disabilities can make choices within and about music therapy
(Warner, 2005), participate in community music therapy groups, such as
choirs (Elefant, 2010), as well as music festivals (Stige, 2010). More
critical approaches have also been emerging around the globe, with a
focus on ableism, neurodiversity and broad questioning of assumptions
about what people with disabilities want from music therapists as
captured in the journal VOICES special edition on music therapy and
disability studies (Hadley, 2014). Local scholars in the Asia Pacific
region have been prominent in this discourse, including Daphne Rickson
(2014), Hiroko Miyake (2014) and Melissa Murphy (2018), whose recent PhD
presented a critical analysis of young people's access to music as
they transitioned from child to adult disability services. While
promoting these consumer-driven forms of practice, the NDIA appears to
apply principles from the medical model when funding therapeutic
services, which demands a focus on measurable, evidence-based practices
rather than participants' rights and choice to access music in many
forms (Cameron, 2017; McFerran, 2016). This inconsistency has caused
confusion for people with disabilities, their families, and service
providers, as well as those involved in the planning process, including
the NDIA staff (McFerran, 2016).
Music therapy practices in Australia have also been changing slowly
to embrace the social model of disability. Although Registered Music
Therapists (RMTs) often embrace humanistic approaches in the field,
medical model practices such as neurologic music therapy (NMT) (1) have
also become popular in a range of fields including the disability
sector. This treatment model emphasis may serve as a point of
distinction between the work of RMTs and community musicians in the same
sector and is surprisingly well matched to the demands of the NDIS, who
often seek evidence whilst also promoting choice.
To better understand the relationship between different service
providers, McFerran (2008) conducted a mixed methods research project to
compare the practices of RMTs and community musicians in one adult
disability service. Some distinctions between the programs were
apparent, with the community music program being described as
"being about energy and expression" and seemed more targeted
towards those with mild and moderate disabilities, while the music
therapist was seen as facilitating "meaningful interactions and
self-expression at a personalised level" (p.22) better suited to
people with severe and profound intellectual disability. Despite
differences between the programs that were readily identified to the
researchers, many of the carers felt that both programs offered
participants an opportunity to transcend their disability and connect
with others joyously, socially and musically. This matches closely with
Stige's (2009) description of practice in the disability field when
visiting Australia, when he said "music as a social phenomenon is
both a very common thing and a very special thing." The role of
music therapy can therefore be understood as the provision of
professional and qualified services that address agreed
psycho-social-emotional goals, whilst it is important to note that this
occurs within a landscape of other music services that serve musical
outcomes.
One recommendation arising from the comparative study (McFerran,
2008) was to consider more bridging options into community. However, a
decade later, Murphy and McFerran's (2016) critical analysis of 27
articles describing music programs in the disability sector showed that
the majority of programs were still conducted in closed groups for
people with disabilities. Once again, the emphasis was on social
encounters and music therapists focused on building connections between
group members within expert driven models. For example, Lee's
research (Lee & McFerran, 2012) revealed a similar emphasis on
expert models, with findings of improvements in communication being
fostered through the provision of consistent song-choice opportunities
for individuals with Profound Intellectual and Multiple Disabilities
(PIMD). However, Lee's (2014) subsequent research, involving
interviews with five RMTs who worked with individuals with PIMD on a
long-term basis, moved towards the social model by acknowledging that
the improvements were not just in the skills of the RMTs, but also in
the increasing depth of the relationship between therapist and client,
which also allowed the therapist to better understand the client's
communication.
This emphasis on building relationships within long-term therapy
was also reported by Cameron (2017), who described an array of benefits
for four adults she had worked with over many years in areas such as:
communication and self-expression, choice and control, social contact
and ameliorating deterioration, and development of skills. She explained
how these benefits were achieved through careful and sophisticated
therapeutic facilitation at critical moments, and explored the
importance of qualified professionals providing music therapy services
under the NDIS scheme.
In summary, it is evident that service provision in the disability
field is changing ideologically, although this change is inconsistent
and diversely understood, both around the globe and locally. A
bio-psychosocial model is adopted by the World Health
Organisation's International Classification of Functioning,
Disability and Health (ICF) (2001) to encompass elements of biological,
social and individual perspectives of health and to integrate both the
medical and social models of disability. This model may be relevant for
RMTs who flexibly adjust their practices to suit the perceived resources
and needs of participants in distinct contexts. Whilst funding and
services continue to change under the NDIS, we determined that it would
be useful to attempt to better understand music therapy access from
multiple perspectives by interviewing stakeholders whose involvements
with the NDIS were different during the first two years in the trial
sites. Ethical approval was granted by the University of Melbourne
(Ethics ID: 1545407.1) and data for this study was collected in October
and November, 2015.
Method
Study Design
A qualitative approach was employed to address the research aim
which sought perspectives of parties involved with the roll out of the
NDIS. Rather than undertaking a large-scale survey to collect relevant
data, in-depth interviews with a smaller number of key stakeholders were
used to produce rich descriptions of their lived experiences, leading to
subjective insights into how each person constructed that particular
view from their position. Specifically, Interpretative Phenomenological
Analysis (IPA) (Smith & Eatough, 2007; Smith, Flowers, & Larkin,
2009) was utilised since it was developed to interpret how participants
make sense of experiences in their personal and social world (Smith
& Eatough, 2007). IPA also allows the researcher to take an active
role in contributing to meaning making using the techniques such as
epoche, which is different to descriptive phenomenology with strict
limitations on the researcher's personal involvement with the data
(Giorgi, 2009). By using IPA, the researchers aimed to understand the
phenomenon from the multiple perspectives by incorporating and making
connections between the descriptions.
Recruitment
This study was conducted in partnership with the research office of
the NDIA and the AMTA, and funded by the University of Melbourne.
Purposive sampling (Creswell & Plano Clark, 2011) was used to
recruit people who had experiences with the NDIS through the
study's partnering organisations. The AMTA Board invited RMTs
already working in NDIS trial sites through their membership base. The
NDIA's research office manager invited some NDIS planners and other
staff to participate in the study. Once RMTs and NDIA workers were
invited, we used a snowball recruitment method in which the RMTs and the
NDIA workers identified others, including persons with a disability
and/or their families who have used the scheme to fund music therapy
services. All the participants were required to be competent to provide
informed written consent, and we sought a balance of NDIA staff, RMTs,
and persons with a disability and/or family in the scheme, although this
was not achieved.
Study Participants
A total of nine people, consisting of three NDIA staff, five RMTs,
and one mother of an eight-year-old boy with a functional disability,
agreed to participate in the study. Most of the participants had been
involved with the NDIS since the beginning of the trials in July 2013
and represented trial sites in three states: New South Wales (NSW),
Victoria (VIC), and Australia Capital Territory (ACT). Information about
each participant is presented in Table 1, including the names of the
participants (pseudonyms) and the number of clients who accessed music
therapy under the NDIS scheme, since these were further analysed.
Data Collection
The same researcher conducted all nine interviews. Due to issues
with distance to these regional trial sites, the three NDIA staff and
parent participated in phone interviews, and all five RMTs were
interviewed via Skype. All participants were offered the option of
either medium. The participants all agreed to their interviews being
audio-recorded, and each interview lasted no more than an hour.
Open-ended questions were asked as follow:
1) In your own words, please explain the NDIS.
a. Who does it support?
b. What are its primary objectives?
2) In your experience, how does the development of support plans
for participants of the scheme (people with disability) take place?
3) How is eligibility for service provision determined?
4) What kinds of music-based services do you know about that are
available through the scheme?
5) What is your understanding of the purpose and use of music-based
services for people with disability?
6) What has been your experience of working with the NDIS?
Data Analysis
Having gathered the data from nine participants, four stages of
analysis were undertaken, following key principles of IPA suggested by
Lakin and Thompson (2012).
Stage 1: Immersing in the data and extracting key statements from
the interview transcripts.
The interviews were transcribed into text line by line. After
becoming familiar with each participant's perspective, key
statements relevant to the research questions were identified and
extracted in an Excel-spread sheet for further analysis. Each statement
was coded with labels such as 'Alice_3,' which means it was
Alicia's 3rd statement.
Stage 2: Conducting an idiographic level of analysis, concerning
the person-in-context.
Attending to each participant's data, a researcher then
performed double hermeneutics which enabled her to attend to each
statement and try to make sense of what the person was making sense of
his/her own experience (Smith, 2007). More specifically, with each
statement, the researcher first asked "What matters to the
interviewee?" from the person's perspective, and then
interpreted this perspective from the researcher' point of view by
trying to interpret "What that means to the interviewee?" The
researcher interpreted the participant's inner thoughts and
feelings based on the description of the experiences (Larkin &
Thompson, 2012). An example of this idiographic process is presented in
the Appendix 1, with all the other analyses recorded in an Excel form.
Stage 3: Developing Emergent Themes by gathering similar
perspectives across the nine participants.
As the current study interviewed people representing three groups
in relation to the topic, it was apparent that similar perspectives were
observed within the same group of people. For example, in the following
two statements, the two NDIA staff explained how all their decisions to
fund music therapy should have been justified:
* I've only funded it (music therapy) 2 or 3 times and all
sort of different reasons. So, I've funded it for one 15-year-old
with a lot of behavioural problems. He had autism, was nonverbal and
found it very difficult to self-regulate. Mum was a single parent
finding it very challenging. And there'd been some music therapy at
school that had been, well they anecdotally said that it had been
successful. So, we put that in the plan to look at that sort of
self-regulation: breathing and calming. (Alicia_3)
* Goals always need to be linked back to the disability and
justified from that perspective. (Bryce_6)
Based on these two statements, an Emergent Theme was developed,
"it's important for me to justify my decision to fund music
therapy," and a code N1 was given to this theme as well. N refers
to NDIA staff, indicating that this theme was dominantly reported by the
NDIA staff. In this way, R represented RMTs and P represented Parents.
By looking across the similar interpretations of nine participants'
perspectives in this way, a total of 14 Emergent Themes were identified.
Table 2 shows how each Emergent Theme was developed, typically based on
at least two interviewee's statements. Two themes (e.g. N5 and P1,
see Table 2) comprised only one person's opinion but were included
because those nuanced statements were critical in forming the Final
Themes. Moreover, in phenomenological analysis, not only the agreed
perspectives across the participants are valued, but also critical
individual perspectives are valued (McFerran & Grocke, 2007). Hence,
including these two themes was appropriate.
Stage 4: Searching for connections across Emergent Themes by
abstracting and integrating themes and revealing Final Themes.
By further examining the various perspectives captured in the
Emergent Themes, three Final Themes were developed. For example, of the
14 Emergent Themes, the following four themes appeared closely related:
* N1: It's important for me to justify my decision to fund
music therapy
* N2: I have personal belief about the certain benefits of music
therapy
* N5: I should be careful in supporting music therapy because not
everyone is convinced about the effectiveness of music therapy
* R7: It is not about only the choice of services but also how to
make a good argument for that choice. NDIA planners should understand
music therapy more but RMTs also need to use the right language for
effective communication.
While the first three themes reflect the NDIA staff's inner
thoughts while making decisions about whether to fund music therapy
services, the last theme is based on two RMTs' experiences and
these further explained that the choice to access music therapy did need
to be argued on the basis of a solid justification and using accepted
language. Accordingly, this Final Theme was named "The
decision-making process of the NDIA planners revealed." Two more
Final Themes were developed in this way and are presented in the result
section. To ensure the credibility of the analysis, each stage of
analysis was recorded transparently and traceable by other researchers
in the university team, and each outcome was reviewed by co-researchers.
Findings
Final Theme 1: The decision-making process of the NDIA planners
revealed (Emergent Themes N1, N2, N5, & R7).
Initially, most RMTs and the parent expected that music therapy
would be easily funded upon request during the planning process, as it
was included on the NDIS providers' list. However, in the
interviews, all the NDIA staff explained how complicated it could be for
them to make a decision on whether to fund music therapy or not, and if
they decided to fund, justifying their decisions to fund music therapy
became crucial (N1). The planners we interviewed held a range of beliefs
about the potential benefits of music therapy and they were more able to
agree to funding if the request aligned with those beliefs (N2). For
example, one planner strongly believed that music therapy would be
beneficial for a child who had difficulties with speech, indicating that
she would fund music therapy only for the speech goals. This revealed
that most of the NDIA staff we interviewed had limited knowledge of the
breadth and scope of music therapy.
It was also understood that there were many other elements to
consider when planners made decisions for a participant, and they had to
justify their decisions to a higher authority or colleagues in the NDIA.
As not everyone in the NDIA was convinced about the effectiveness of
music therapy and s/he felt impelled to care about other planners'
opinions on music therapy, at least one planner felt that she should be
careful or cautious in supporting music therapy (N5). With regard to
this issue, two RMTs with years of experiences with the NDIA suggested
that the NDIA planners needed to better understand music therapy, and
that RMTs need to use the right language for effective communication.
One of the RMTs explained that being on the NDIS providers' list
did not mean that all the requests would be accepted, and each request
needed to be submitted with an accepted justification which linked back
to the client's disability and goals (R7).
In order to understand who made the decision to provide access to
music therapy and how it was justified, ten cases of participants who
were able to access music therapy through the NDIS funding were further
analysed. The details of each case are presented in Appendix 2 and Table
3 to show the result of the analysis.
Out of these ten examples, five were child clients who were under
10 years of age (case example no. 3, 4, 5, 8, 9) and receiving
Transdisciplinary Early Intervention Packages (TEIP). Surprisingly, one
client (example 8) was given access to music therapy even though the
parents did not request it and did not know what music therapy was. The
main goals for these children in early intervention were improving their
functional abilities and skills in relation to their developmental needs
such as improving speech, communication, physical skills,
self-expression and articulation of emotions.
Among the other five examples, four school aged children were aged
between 14 and 15 years and attending school (case example no. 1, 2, 6,
10), and two could be described as noteworthy in their uniqueness.
Example 2 was reported by the NDIS Planner Alicia, and she explained
that the 14-year-old boy who was born without eyes needed extra support
in accessing adapted print music in order to participate in a community
band. Therefore, the planner supported the boy to have practical support
from a RMT. She further explained that his parents were paying for the
trumpet lessons, which is an expense expected to be paid by any parent,
regardless of whether their child has a disability. However, the extra
cost for the adapted printed music was a special need resulting from
this boy's disability, so the planner supported this cost.
Similarly, Example 6 appeared to be quite a special case where a
teenage boy with autism was participating in ongoing music sessions with
a community musician prior to entering the NDIS. Although the main focus
of their sessions was expanding song-repertoire and singing together,
the NDIS considered it as fulfilling Occupational Therapy (OT) needs and
funded this musician as if he was an OT assistant. Under NDIS
arrangements, an RMT was funded to twice observe their sessions and
provide an assessment. The rationale for funding the other two teenagers
was behavioural problems (Example 1) and mental health issues (Example
10), and in both cases, the families were finding it challenging to
manage their child's behaviours and therefore ongoing music therapy
was supported.
Only one adult client was funded to participate in on-going music
therapy (case example no. 7). This 30-year-old woman had been working
with a music therapist for many years before entering into the NDIS. Her
family argued that music therapy played an important role in supporting
their daughter to share her life experiences with family and relatives
living overseas because she would write songs to share with them.
Final Theme 2: The impact of the NDIA's decisions on both
participants and RMTs' practices was revealed, and RMTs expressed
desires to better understand the NDIS approval process (P1, RP6, NPR4,
R3, R5, & R1).
The parent participant in this study reported that the outcomes of
her music therapy funding requests across several planning processes
depended on the planner's knowledge of music therapy. This resulted
in inconsistent outcomes (P1) and these inconsistent outcomes negatively
impacted on her son. This mother's experience was also confirmed by
other RMTs who described how planners limited the amount and frequency
of music therapy which sometimes caused issues related to therapeutic
closure (R6).
While most people believed that the RMTs' reports were crucial
in the planning processes (NPR4), two RMTs found that the NDIA did not
approve the recommendations made in their reports. In particular, one
RMT described how the NDIA did not follow through on her six monthly
progress reports and never responded to her suggestions for a client to
access community music programs (R5). Some RMTs described that
communicating with the NDIA was often a very slow and complicated
process and RMTs felt out of their control at times (R3). Accordingly,
most RMTs hoped to be better informed about how the NDIA is structured
and actually works (R1).
Final Theme 3: This is an important time to raise awareness of
music therapy and RMTs can be active in this process to advocate for
music therapy as a necessary service (N3, PR2, R2, & R4).
The three NDIA staff hoped that other planners might get more
information about music therapy and RMTs in general, and expected RMTs
to actively communicate with the planners to provide knowledge and
information about music therapy (N3). They explained that the NDIA
planners have mandatory trainings every fortnight and that this might be
a useful place for RMTs to start the promotion of music therapy and
education of the NDIA planners. Likewise, the parent participant and one
RMT thought RMTs should have more active roles in educating and
promoting music therapy as a reasonable and necessary service to both
planners and parents/families of persons with disabilities. It was also
understood that being acknowledged by other allied health professionals
was helpful and having these professionals write recommendation letters
for music therapy might be extremely important in relation to the NDIS
(P2).
Most RMTs agreed that awareness of the benefits of music therapy
needed to be increased and some believed it was now an important time to
raise awareness in collaboration with the NDIS, since some planners had
actively recommended music therapy to families (R4). Since the request
for music therapy should come from participants of the scheme and/or
their parents' voices, RMTs believed they might need to prompt and
inform participants to do so in the future (R2). Some RMTs expected AMTA
to take an active role in more formal aspects of advocacy, and to
provide publicly available information and tools, which has since
occurred. Formal advocacy from AMTA has included animated videos for
social media as part of a broader public relations campaign, an online
training course on the NDIS, the establishment of an NDIS sub-committee
who has had several meetings with the NDIA, and an active Facebook page
that is monitored by that committee. Together with the RMT community,
many parents and other professionals have been active in contributing to
greater understandings about the benefits of music therapy during this
time of transition.
Discussion and Conclusion
Since the inception of the NDIS in July 2013, there have been many
ongoing changes. These interviews were conducted in October and November
2015 and the focus on individual stories means that there is no basis
for generalisation. Therefore, results and findings of the current study
should be understood and interpreted appropriately. Following up the
participants in music therapy at the time of data collection and
investigating their journey in a longitudinal study could provide
additional insights in the future.
Music therapy is recognised by the NDIS as a reasonable and
necessary therapeutic service. As the scheme unfolds, there have been
cases where families, clients and the NDIA staff have not clearly or
consistently understood what it is or how it could be funded under the
scheme. Similarly, other allied health and creative arts therapies, have
anecdotally reported similar experiences of misunderstanding. The
results of this study also suggest that RMTs have found it difficult to
understand the scheme at times, showing that the confusion can flow in
both directions. This study revealed that the inclusion of music therapy
on the NDIS list did not secure families' rights to access music
therapy services and there is no guarantee that people's choices to
receive music therapy will always be enabled by the scheme.
As the roll out of the NDIS continues in the coming decade, RMTs
will be required to demonstrate their professional skills and draw on
their ethical obligations to advocate for participants' rights to
access music therapy services. This study shows that individual RMTs may
have different experiences and face diverse demands as individual
planners learn about the kinds of services that participants in their
scheme want and desire. During this time, it will be essential to
continue to respond to current information about the NDIA and its
decision-making processes and it may be useful to engage in research
that better explains what music therapists do. Ongoing connection to the
Australian music therapy community may serve as one conduit for RMTs in
facilitating this ongoing communication, as well as a sensitivity to the
desires of people accessing the NDIS and a careful distinction between
our own desires to serve and an openness to what people are truly
requesting. This kind of ongoing reflexivity will benefit Australian
society as we embrace the social model of disability, and all the
bio-psycho-social models that come next, ensuring that our actions are
in keeping with the famous dictum that heralded the beginning of the
critical disability movement: Nothing about us, without us.
Acknowledgements
This research was conducted with a grant from The University of
Melbourne Engagement Grant and support of the
Australian Music Therapy Association and the National Disability
Insurance Agency.
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Appendix 1.
An example of an idiographic analysis in stage 1
Alicia/NDIS Planner What matters to
Alicia?
1 It's making their goals and working with them Finding the right
to look at what supports they have currently supports for the
and looking at the support, not just funded participant
support so we also look at their informal
support network and how they can assist
with achievement of the goals, as well as
looking at what's out there in the mainstream
and community... looking at how mainstream
services and community supports can get by
that participant in helping them meet their
goals and then we look at funded support
after that, after we've exhausted what's out
there already.
2 They get to have choice and control of it, the Finding the right
participant, and lots of the modality and support for the
therapy that they want to choose. And often participants to
they'll come to us and say "well what else can achieve the goals
you give me? Or what would someone like
me... what else is there?" But we don't really
look at it like that. We look at what your
goals are and we look at what supports we
can put in place around those goals. So, we
don't throw the whole catalogue of supports
at you and say tick tick tick like a shopping
list, pick what you'd like. Some parents do
come in with that list. They've been through
the catalogue and they are aware of what
can be funded under NDIA so they want
everything that they can get for their child
which is understandable. So it can work both
ways a bit but primarily it's just developed
around their goals.
3 I've only funded it (music therapy) 2 or 3 times Whether funding
and all sort of for different reasons. So, I've music therapy
funded it for one 15 yo with a lot of behavioural will be
problems. He had autism, was non-verbal and beneficial to the
very difficult to self-regulate so mum was a participant to
single parent finding it very challenging. And achieve the goals
there'd been some music therapy at school that
had been, well they anecdotally said, that it had
been successful. So we put that in the plan to
look at self-regulation: breathing and calming.
4 There was a 14-year-old boy born without any Whether funding
eyes so I funded Music Therapy (MT) for him music therapy
because he participated in bands and he will be
wasn't able to access the music. It was not beneficial to the
typical MT I funded, but I funded a RMT to help participant to
him access print music so they're adapting the chieve the goals
print music into a suitable format for him. He
can then memorise the music cause that's how
he learns it. His parents paid for trumpet lessons
each week--if it's something that all parents
would be expected to pay for, then it's not
something that we'd fund.
5 We wouldn't, or I wouldn't consider music Whether the
lessons. To me that would be an ordinary request of a
cost of parents. It's just expected that certain service
parents would cover any cost of music is directly
lessons. So that's one our principles in related to his
looking at a reasonable and necessary /her disability
support, is whether it's a day to day living or not
cost by a parent. So even though it might
be related to a disability, if it's something
that all parents would be expected to pay for,
then it's not something that we'd fund.
6 You can amend the plan in that 12 months Whether the
if you get a progress report saying they've participant was
made these amazing gains and we've still gaining outcomes
got these goals... we're looking at these to get more
goals for the next 10 sessions, then you funding for
might look at funding another 10 sessions if music therapy
you think it's reasonable and necessary.
But yeah, it doesn't mean that it's only 10
necessarily for the entire 12 months. But
maybe it does keep it accountable that there
is progress being made, and the therapist
needs to get back to you with those
outcomes.
7 I think I'd like info on music therapy as well Making a right
and when we might actually implement it and decision when to
when we might not. Because it is, music fund music
therapy is a bit of a grey area. It's not therapy or not.
requested very often.
What that means to Alicia?
1 Identifying goals to achieve is more important than finding services
and support
2 Identifying goals to achieve is more important than finding services
and support
3 Justifying my decision to fund music therapy is important.
4 Justifying my decision to fund music therapy is important.
5 Making decisions according to our principles regarding funding
reasonable and necessary supports is important.
6 Making decisions whether to continue the funding is up to the
participants' outcomes.
7 Alicia feels she needs to be informed more to make right decisions.
Appendix 2.
Ten funded music therapy cases as described by participants
Case Interviewee Age/ Diagnosis
reporting the Gender
case of the
client
1 Alicia/NDIS 15/M Autism, Non-verbal, Difficulties to
Planner self-regulate
2 Alicia/NDIS 14/M Born without eyes
Planner
3 Diana/RMT 2/M Born premature resulted in developmental
delays
4 Diana/RMT 8/M Functional Disability resulted from
Cancer - one of his eyes removed
5 Emma/ 3/F Not specified
RMT
6 Emma/ Teen /M Autism
RMT
7 Emma/ 30's/F Not specified
RMT 2
8 Florence/ 5/F Not specified
RMT
9 Florence/ 6/M Speech Delay
RMT
10 Florence/ 15/F Mental Health Issues/Obsessive Compulsory
RMT Disorder (OCD)
Case Interviewee Age/ Other Personal Circumstance
reporting the Gender
case of the
client
1 Alicia/NDIS 15/M Mother is a single parent finding it
Planner challenging and previous music therapy
history at school reported to be
successful so planner was happy to put
music therapy in the plan.
2 Alicia/NDIS 14/M He participated in bands but wasn't able
Planner to access the music (sheets). His parents
paid for trumpet lessons each week. If
it's something all parents would be
expected to pay for, then it's not
something that we'd fund.
3 Diana/RMT 2/M Family visited RMT's group session
conducted in an organisation and noticed
the child was positively responding to
music.
4 Diana/RMT 8/M When they got NDIS funding, his mum
asked for music therapy and then I got
contacted. But NDIA had already put on
the plan for group music therapy but we
were unable to provide group music
therapy so we ended up only providing a
shorter amount of sessions because they
wouldn't give us more funding for
individual sessions. So that was a bit
of a different process because we really
had to advocate for him and say that "no,
we thought that individual would still
work."
5 Emma/ 3/F She was having music therapy before she
RMT joined the NDIS a couple of years ago,
so obviously her parents just came in
and said we really like music therapy
and we'd like it to continue. So that
was easily done. They may have asked me
for a report.
6 Emma/ Teen /M A musician who was working with a lad
RMT who has autism. And I don't know what
funding stream... oh Occupational Therapy
(OT) I think. I do know that this
musician is not being paid same as an OT,
they stretched the funding but it's under
the OT line, whatever they call it. That
was quite a long time ago now and I've
done it twice. So, what they've asked is
that they have a music therapist write
a report about what's going on in the
sessions and then they claim it through
OT.
7 Emma/ 30's/F Those songs written in music therapy
RMT 2 sessions are all recorded onto a cd and
she gives them to her family and
extended family that are also overseas,
so it's a way for her to connect with
all sorts of people that she doesn't see
very often - her family don't live
nearby.
8 Florence/ 5/F On the one hand, I had a client who rang
RMT me saying, "we have music therapy on
our plan, what is it?" so then I told him
what music therapy was and then, just
based on what he had told me about his
daughter, what I might possibly be able
to work on with his daughter. And he
said "Oh that sounds perfect. When can
we start?" But I've only had that once
and it does seem unusual.
9 Florence/ 6/M One of my clients has been under an
RMT organisation doing all sorts of early
intervention stuff. Then they come up for
NDIS so they go "well we're happy with
this organisation we want to stay with
them." They're an organisation that is
registered with NDIS to be a provider.
Obviously, there is communication with
the family as well but there is someone
from that organisation who I think also
is in the planning meeting and helping
develop the plan. Then that organisation
is given a bulk amount of money or
funding to then provide OT, speech,
physio, whatever it is.
10 Florence/ 15/F She's got a lot of insight and she's
RMT quite articulate but when it comes to
connecting, she finds what's happening
physically and emotionally a bit tricky.
This girl has OCD and she won't touch
any instruments so we do a lot of
singing. Self-expression, self-esteem
and confidence are important because she
also suffers with depression and low self
-esteem so her family are very keen to
have opportunity for achievements and
positive experiences.
Case Interviewee Age/ Music Therapy Goals
reporting the Gender
case of the
client
1 Alicia/NDIS 15/M To promote self-regulation through
Planner breathing and calming
2 Alicia/NDIS 14/M To help him access print music so they're
Planner adapting the print music into a suitable
format for him and then memorise the
music cause that's how learns it.
3 Diana/RMT 2/M To improve speech, working on to begin
with any words and then two words and
now it's putting the word on the end of
a song
To upskill parents and grandparents to
share musical activities with him at home
4 Diana/RMT 8/M To build coping skills like reducing
anxiety and dealing with negative
emotions such as frustration through
song-writing
To express emotions through keyboard
playing and improvisation
To provide creative emotional outlet and
build confidence by leading and
directing music-making process
To use music with mother at home
throughout daily routines
5 Emma/ 3/F To exercise choice and control by
RMT indicating her preference of song,
instrument or activity through head
movement, pointing, reaching out or
vocalising
To maintain and increase body awareness
and tactile experiences through different
types of touch and active movement
To maintain and increase her non-verbal
communication
To increase gross motor control through
playing instruments
To have opportunities for increased self
-expression and communication
6 Emma/ Teen /M To fulfil some OT needs by building up
RMT an repertoire of songs which they sing
together
7 Emma/ 30's/F To expand her repertoire in music by
RMT 2 playing keyboard and learning new songs
To articulate and express different
aspects of her life through song-writing
To increase confidence through shared
music-making
To create an expressive outlet through
song-writing and recording
To extend non-verbal communication
To increase self-awareness, control and
autonomy
To gain independence in music-making
outside the sessions
8 Florence/ 5/F Not specified
RMT
9 Florence/ 6/M To improve speech and motor skills
RMT To improve emotional expression and
articulation of emotions and experiences
10 Florence/ 15/F To reduce anxiety through relaxation and
RMT breathing techniques
To gain looking at emotional expression
and emotional understanding and
articulation as well as body awareness
in relation to emotions
To discuss about emotions expressed in
music through active listening to music
Case Interviewee Age/ NDIS Funding
reporting the Gender
case of the
client
1 Alicia/NDIS 15/M Not specified
Planner
2 Alicia/NDIS 14/M Not specified.
Planner
3 Diana/RMT 2/M 20 individual sessions funded
4 Diana/RMT 8/M Initially got four individual sessions
and then we had to write a progress
report. Then I think he got ten. And
then now we've just had 20 funded for
him. But they've been a lot more, this
was earlier on and they didn't want to
fund as many as 10 individual sessions.
5 Emma/ 3/F Music therapy is part of an
RMT interdisciplinary package she's got.
6 Emma/ Teen /M 2 music therapy assessment sessions
RMT
7 Emma/ 30's/F Ongoing regular sessions over several
RMT 2 years and the RMT has been submitting
report every 6 months.
8 Florence/ 5/F Initially 10 hours funded for music
RMT therapy assessment.
Then I've just written a report for them
so that can get reviewed and then they're
planning to have more music therapy.
9 Florence/ 6/M Transdisciplinary Early Intervention
RMT Package. When it came to me doing music
therapy with him because music therapy
wasn't listed separately, NDIS told me
that I had to go through this
organisation and that it would come under
their funding. This is extra admin for
us so how about we charge you like 10%
or something.
10 Florence/ 15/F Not specified
RMT
Appendix 3.
The participants' statements
Final Theme 1: The unknown decision-making process of the NDIS planners
revealed
Emergent Theme N1: It's important for the NDIS planners to justify
their decisions to fund music therapy.
There was a 14-year-old boy born without any eyes so I funded Music
Therapy (MT) for him because he participated in bands and he wasn't
able to access the music. It was not typical MT I funded, but I funded
a RMT to help him access print music so they're adapting the print
music into a suitable format for him. He can then memorise the music
cause that's how he learns it. His parents paid for trumpet lessons
each week--if it's something that all parents would be expected to pay
for, then it's not something that we'd fund. (Alicia 4)
Emergent Theme N2: The NDIS planners have personal beliefs about the
certain benefits of music therapy.
If a child has speech delay I would say music therapy. The goal would
be something like 'be assisted by speech pathologist and music
therapist to help with learning to speak'. I mean that's just... I
wouldn't word it like that but that's how I would link the goal to the
service. I think for music therapy... the only time I've put music
therapy in a plan is when it's speech delay, cos that's where I see it
as an amazing type of therapy for children with speech delay. (Cheryl 6)
Emergent Theme N5: The NDIS planners should be careful in supporting
music therapy because not everyone is convinced about the effectiveness
of music therapy
We'd all under plans I guess, work together if someone's got expertise
in an area. We talk amongst each other to get some idea of how to put
the plans together for different cohorts. (Cheryl_1)/As I said,
planners don't recommend therapies. I did once recommend music
therapy--I just said "I've heard it can be really great for speech
delay" and they were really interested. But as we discussed it's not
the general approach. I think getting the information to planners as
well would be great because there's so much debate or controversy about
supports." (Cheryl_9)
Emergent Theme R7: It is not about only the choice of services but also
how to make a good argument for that choice/NDIA planners should
understand music therapy more but RMTs also need to use right language
for effective communication.
It (allocated financial amount) does matter but it's on a needs basis.
So if you can put forward a really good argument for something you can
have... I know some people seem to have a huge plan. I'm working with
one 3 yo, and her parents think that she may have the biggest plan yet!
But within that, it seems that there are some limitations as well. So I
think they have to put forward a good argument and that family are
really arguing strongly for as many services as they can for their
child. (Emme_3)/I guess a lot of confusion on both parts, like the
planners not really understanding music therapy, not really
understanding what we can offer. Also me trying to find the right
language to communicate to them in a way that they're going to
understand what we're talking about as well. Because often if they've
not heard it before they get a bit confused or lost. (Diana_19)
Final Theme 2: The impact of the NDIA's decisions on the participants
and the RMTs' practices was revealed and RMTs expressed desires to have
more channels of communication with the NDIS
Emergent Theme P1: Depending on the planner's knowledge about music
therapy, funding outcomes are different and inconsistent.
If your planner is clear enough to know how the different disciplines
work and what they try to achieve and are cluey enough to sit there and
go "Right. Sounds like William's struggling with that. Why don't we get
an assessment done on this and say whether or not therapy would be
worthwhile?" Then, it's great. It gives you a hint of where to start.
But for the everyday person, there's no way. If it was not something
that they've been familiar with before. The planners certainly use it.
Subsequent to that I've now got a different planner, and that planner
hasn't offered or suggested anything different. (Iris 10)
Emergent Theme PR6: The planner's lack of understanding of music
therapy negatively impacted William's access to music therapy
So every time at the end of that block then, like the plan comes to an
end and you have to provide a progress report so it's always uncertain
about whether music therapy is going to continue and that's also
something that I've raised with the planner. Because last time before
this child got 20 sessions, we only had one session left and mum was
due to have her plan reassessed in a month, and we'd been meeting
fortnightly and so I contacted the planner and said that's the
likelihood of this continuing? You know we've only got one session left
and the mum knew that she had flexible support so the mum thought that
she could actually take some from speech that she hadn't used and use
it for music therapy... But the planner was like we won't know until
the day of the plan and I'm talking about, but that's not appropriate
for closure. I've been working with this child for so many sessions
now, he's really engaged, mum's saying he wants more music, he's saying
he wants more music - where do we sit? And she's like just have the
final session or hold onto one of your sessions until we know. And I
said but that's still not actually enough, because I started these
discussions when I still had a couple and then it took that long. And
then I had that discussion with them and said that actually for
therapeutic closure, that's not appropriate for a child who's highly
anxious and had all that trauma in his life. And then so she said she
was going to take that up to NDIA but I haven't heard anything back. So
that's a big issue as well. The new plan meeting happened after the
first plan ended. There was like a lapse. (Diana 9)
Emergent Theme NPR4: Reports are important and RMTs should be
thoughtful and clear about what they write in reports.
I guess cos we 're not, like most planners aren't therapists or if they
are, only in a specific area generally, I always say... if a
participant says "I want music therapy or I want my child to have music
therapy" I don't say... I don't have any knowledge of whether it would
be a good thing or not so I would put in an assessment for music
therapy. So I'd put in probably 10 hours and say, "If I could get a
good assessment from the music therapist as to why this is a good
support, and how many hours they think is required, then I would go off
the report." I would make the determination myself. (Cheryl 3)
Emergent Theme R3: Getting into NDIS system was a slow and complicated
process for RMTs.
When you are trying to chase up, like I've been trying to find out if
this person does have funding before I've provided the service, like
the communication between myself and the NDIS is quite slow. They say
about 5 business days to answer any email... most of the time when I've
rung up, the person on the phone is more just a general call centre
sort of person, and if they're not aware of individual cases they'll
say well send an email to whoever is dealing with it from that end. So
when you have clients that are waiting for a service or if you have
issues with looking up their funds and stuff it can be quite a slow
process. (Gabriella 6)
Emergent Theme R1: RMTs need to know how the NDIS works.
With this next client, I've got coming on I'm thinking I'm gonna try
sorting things out a bit further... I mean I don't really care how
it's, I mean if I get paid at the end of the day that's fine like I
don't really care. But the way it's set up in terms of when it's on
their plan separately and I just keep invoicing NDIS, it's so simple
and it works really well. And this other system through the
organisation works as well now that we've got it set up. Like I just
invoice them and they pay me. Now that we've done that it probably will
be okay with the second client. But I'm also thinking well, with any
clients I'm advising them that if you want music therapy try and get it
as separate item on your plan - that's much simpler. (Florence_8)/Not
everybody gets a copy of the NDIS plan. I purposely went out of my way
to request them. Because you really need them to know whether you're
helping them achieve their goals. So I had to request them (Hannah 9)
Emergent Theme R5: RMTs reports and recommendation about the amount of
sessions were not respected by the NDIA.
There's been no input or request from the NDIA at all from me. Except
for formally but they don't even seem to follow up with that. They say
they want a report every 6 months and I've been doing that fairly
consistently but they've never chased me for it. So I've just written
what I always write for reports which is goals and what's happening in
the session and the outcomes. (Emma_15)/During school terms once a
week. I think I asked for forty sessions. She came back and said they
do either 48 (half an hour) or 24 (an hour). The other thing I got to
ask her which I was just assuming but hadn't clarified with anyone, was
... It's by the hour.... And I said "is that inclusive of chatting to
mum, doing the reports, doing an assessment, admin type stuff as well?"
Because I assumed it was. And she said that it was, she clarified that
it was. (Florence 16)
Emergent Theme 3: This is an important time to raise awareness of music
therapy and RMTs can be active in this process to advocate for music
therapy as a necessary service
Emergent Theme N3: The NDIS planners hope the other planners get some
information about music therapy and RMTs.
Communities of Practice--setting up groups with differing levels of
expertise for knowledge management and transfer of knowledge across the
NDIA. Music Therapy and therapy services is probably one of those areas
that would fit quite well with that sort of approach. (Bryce_7)/We do
have training sessions... well we're meant to have them anyway
fortnightly. People from various organisations that provide certain
supports come and speak to us. So you could get in touch with the
Engagement Teams in different sites and just say if it's possible, we'd
like to come and have a chat with the planners about the benefits of
music therapy. And that could very well be something that they'd be
interested in cos we are meant to have regular training on different
supports.(Cheryl_10)/I think I'd like info on music therapy as well and
when we might actually implement it and when we might not. Because it
is, music therapy is a bit of a grey area. It's not requested very
often. (Alicia 7)
Emergent Theme P2: Therapists' active role in educating and promoting
music therapy and being acknowledged by other allied health
professionals are extremely important.
Unless where the therapists are engaged they are able to communicate
with those parents, "Look, you've got to get on the NDIS site. You
should consider it." I'm not sure. I sort of think also, perhaps align
disciplines for example. Diana does with William's coordination skills
and things like that that he struggles with, like it's an Occupational
Therapy (OT) goal, but Diana works on that with him as well. She brings
out the keyboard and gets him to attend to his left-hand side using the
keyboard. So yes, we're doing emotional relief, that was the main
purpose of having her, but she's also been able to get him to move
fingers and all sorts of stuff. in terms of increasing a profile, then
we'll also be working with just making yourself really well known, as
to what music therapy can do to support another discipline, so that
when the therapist is writing their recommendation for what services
you might need, that they're suggesting it as well. That's probably how
you get it into the plan. (Iris 11)
Emergent Theme R2: Decisions should be informed by parents' voices and
RMTs might need to prompt and inform them.
It sounds like their hands are ties, like it has to be all from the
parents' voice. I don't even think they can say "look we've had other
people with this diagnosis and they're benefited from you know, x, y,
z." I don't think they can do that at all. So it's sort of I figure out
what they're needing and then I help them jump through the hurdles. So
I pass the message on to the head clinician and I've got to kind of
whisper to her "look you need to inform the parents that they need this
if you want to get it approved" (Hannah 12)
Emergent Theme R4: Awareness of the benefits of music therapy should be
increased in the future.
I believe that they're supposed to click on 'find a provider' and they
can search for what's available. But I'm guessing in general, probably
the awareness of music therapy is probably not quite as high as
awareness of say speech therapy or OT. So they're probably going to
search for those sorts of things before they would search music
therapy. And other than that, unless individual planners are aware of
it and suggest it, then I don't really see the NDIS as kind of
sprouting it. (Gabriella 9)
Juyoung Lee, Kate Teggelove, Jeanette Tamplin, Grace Thompson,
Melissa Murphy and Katrina Skewes McFerran
Faculty of Fine Arts and Music, The University of Melbourne,
Australia
Address correspondence to:
Juyoung Lee
[email protected]
To cite this article: Lee, J., Teggelove, K., Tamplin, J.,
Thompson, G., Murphy, M., & McFerran, K. (2018). Whose choice?
Exploring multiple perspectives on music therapy access under the
National Disability Insurance Scheme. Australian Journal of Music
Therapy, 28, 91-115. Retrieved from
https://www.austmta.org.au/journal/article/whose-choice-exploring-multiple-perspectives-music-therapy-access-under-national
In plain language:
This research study investigates how different stakeholders
perceived access to music therapy under the National Disability
Insurance Scheme (NDIS) in the trial sites between 2013 and 2015. Nine
people who had the lived experience of the matter such as NDIS planners,
Registered Music Therapists (RMTs) and a parent of a boy with a
disability were individually interviewed. Interpretative
Phenomenological Analysis reveals that everyone believed that music
therapy was not fully understood or received well by everyone, and RMTs
need to take more active roles in educating and promoting music therapy
to staff in the National Disability Insurance Agency (NDIA), allied
health professionals, as well as parents of people with disabilities.
(1) NMT involves "the therapeutic application of music to
cognitive, sensory, and motor dysfunctions due to neurologic disease of
the human nervous system" (Thaut & Volker, 2014, p.2).
Table 1.
Participant information
Name Participated Gender Region Involvement Description
as a with NDIS of Music
since Therapy
Client
Alicia NDIA Planner F NSW-Hunter 2013 2 Clients
Bryce NDIA Plan M VIC-Barwon 2014 N/A
Support
Coordinator
Cheryl NDIA Plan F ACT 2014 N/A
Support
Coordinator
Diana RMT F VIC-Barwon 2013 2 Clients
Emma RMT F VIC-Barwon 2013 3 Clients
Florence RMT F NSW-Hunter 2013 3 Clients
Gabriella RMT F NSW-New 2013 2 Clients
Castle
Hannah RMT F ACT 2013 2 Clients
Iris Parent of an F VIC-Barwon 2013 Her Son
8-year-old
boy
Table 2.
The 14 Emergent Themes
N1 It's important for the NDIA planners to justify their decisions
to fund music therapy.
N2 The NDIA planners have personal beliefs about the certain benefits
of music therapy.
N3 The NDIA planners hope other planners get some information about
music therapy and RMTs.
NPR4 Reports are important and RMTs should be thoughtful and clear
about what is included in reports.
N5 The NDIA planners should be careful in supporting music therapy
because not everyone is convinced about the effectiveness of music
therapy
P1 Depending on the planner's knowledge about music therapy, funding
outcomes are different and inconsistent.
PR2 Therapists' active role in educating and promoting music therapy
and being acknowledged by other allied health professionals are
extremely important.
R1 RMTs need to know how the NDIS works.
R2 Decisions should be informed by parents' voices and RMTs might
need to prompt and inform them.
R3 Getting into the NDIS system was a slow and complicated process
for RMTs.
R4 Awareness of the benefits of music therapy should be increased in
the future.
R5 RMT reports and recommendations about the amount of sessions were
not respected by the NDIA.
RP6 The planner's lack of understanding of music therapy negatively
impacted clients' access to music therapy
R7 It is not about only the choice of services but also how to make
a good argument for that choice and RMTs also need to use right
language for effective communication.
(*) N: NDIA Staff, P: Parent, R: RMT
Table 3.
Reasons for funding music therapy and decision-making process during
NDIS planning
Example Reasons for Funding Music Who Made that Decision?
No. Therapy
1 To support a single mother of Planner found a good
a son who has behavioural justification in a unique
problems and whose previous situation
music therapy participation
at school was successful
2 To adapt print music for Planner found a good
community participation justification in a unique
situation
3 To support a boy born Family accessing
premature that resulted in Transdisciplinary Early
developmental delays and Intervention Package (TEIP)
required early intervention
4 To support a boy with NDIA not providing sufficient
functional disability session amount requested by
resulting from cancer to family and didn't regard music
learn coping skills therapy as therapy but a group
activity
5 To support ongoing music Family accessing TEIP
therapy that has been
conducted previously for a
3-year-old girl as part of a
TEIP
6 To fund a music therapist Planner found good
to conduct assessment of justification in unique
sessions provided by a situation
community musician
focused on OT needs
7 To support the client to Planner found good
communicate with her family justification in unique
living overseas, music was situation
found to be effective in this
so her sessions have been
funded regularly on an
ongoing basis for more than
several years now.
8 To support a 5-year-old girl NDIA (parent didn't know of
with developmental delays Music Therapy but it was given
in TEIP (parents had no idea as part of TEIP)
about music therapy)
9 To support a 6-year-old boy NDIA happy to offer TEIP to an
with speech delays in TEIP organisation
10 To support a 15-year-old Planner found good
girl with mental health justification in unique
issues such as anxiety situation
and Obsessive Compulsory
Disorder
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