Airindya Bella K Assessment3
Airindya Bella K Assessment3
Airindya Bella K Assessment3
Student ID : 34586288
Under this human rights-based framework, persons with disabilities are acknowledged as having
the right to health, essential for leading independent lives, pursuing education, and engaging in
employment. This right is not just a theoretical concept but translates into tangible policies and
actions that impact the daily lives of those with disabilities. The law's recognition of these rights
underscores the importance of providing support structures that enable individuals with
disabilities to live fulfilling, autonomous lives.
In alignment with this commitment, the Indonesian government, both at the central and regional
levels, is mandated to establish Disability Service Units (Unit Layanan Disabilitas – ULT). These
units are a critical component in the practical realization of the rights of persons with disabilities.
They are envisioned as hubs of support, providing essential services and facilitating access to
resources necessary for persons with disabilities to thrive in society.
According to Article 55 of Law No. 8 of 2016, ULT is formed and funded through regional
budgets, ensuring that local governments play a direct role in addressing the needs of their
disabled constituents. This decentralized approach allows for tailored solutions that reflect the
unique contexts and challenges of different regions, thereby enhancing the effectiveness of the
services provided.
One of the primary responsibilities of these units is to ensure the availability and acquisition of
assistive devices for persons with disabilities, tailored to their specific needs and the type of
disability (Ministry of Social Affairs [MSA], 2020). These assistive health devices are crucial
tools that optimize the functionality of body parts for individuals with disabilities, based on
medical recommendations. They are not mere gadgets but are lifelines that enable persons with
disabilities to navigate their environments more effectively, enhancing their independence and
quality of life.
The financial support for these assistive devices varies according to regional government
regulations. This indicates an understanding that the needs of persons with disabilities may differ
significantly across regions (MSA, 2021). Thus, local governments are best positioned to
determine the appropriate level of financial assistance required. This decentralized approach,
while allowing for contextualized support, also raises questions about the uniformity and
equality of support across different regions.
Nevertheless, there was a startling disparity in four major cities; Bandung, Solo, Makassar, and
Kupang. Approximately 91% of persons with disabilities in these cities had never received any
assistive devices from their local governments (Indonesia Corruption Watch [ICW], 2019). This
statistic is a glaring indicator of the policy's ineffectiveness in ensuring equitable access to
essential resources for persons with disabilities.
Moreover based on the state-owned Health Care and Social Security Agency (BPJS) Law no.7
(2018) about the management of health facility claims administration, the process of acquiring
AT requires the involvement of healthcare facilities and professionals to determine the specific
needs of each individual based on their disability type. This step is crucial for the provision of
appropriate and functional assistive devices. The healthcare system itself is generally
commendable in its services for the broader population but falls short in adequately addressing
the special needs of persons with disabilities. Facilities often lack essential features like
handrails, wheelchairs, computers with number-reading capabilities, Braille letters, accessible
toilets, and special counters or lanes for persons with disabilities (ICW, 2019). These deficits,
quantified in significant percentages, underscore the gaps in the healthcare infrastructure that
directly impact the effectiveness of disability policies.
A further complicating factor is the readiness of healthcare workers (HCWs) to handle the
specific needs of persons with disabilities. A staggering 74.1% of HCWs are reported to be
inadequately prepared for this task (ICW, 2019). This is particularly concerning given that
medical assessments and evaluations from doctors are prerequisites for receiving assistance in
obtaining AT (MSA, 2021). The disconnect between the policy's intentions and the healthcare
system's capacity to support it creates a bottleneck in service delivery.
A major challenge is the inconsistency in data from key national surveys like the National Socio-
Economic Survey (Susenas) and the Basic Health Research (Riskesdas). As highlighted in the
SMERU Research Institute report (2020), this discrepancy leads to a fragmented understanding
of the real number of persons with disabilities and their needs, impacting service delivery and
device provision. Without accurate data, policy implementation can be misdirected, failing to
meet the actual needs of the disabled community.
Another significant issue is the lack of coordination across different sectors involved in disability
services, such as health, education, and social services. This often results in operational silos,
leading to inefficiencies and redundancies that weaken the impact of disability policies (Tuti, R.,
& Lisa, A., 2020).
Financial constraints also pose a challenge. The limited budget for social rehabilitation programs
for persons with disabilities restricts the reach and effectiveness of these services, especially in
providing essential assistive devices. Adequate funding is vital for expanding and sustaining
these services (ICW, 2021).
Furthermore, there is a shortage of skilled social workers with expertise in disability issues,
leading to suboptimal service delivery. This gap in skilled personnel affects the quality of support
provided to persons with disabilities (Tuti, R., & Lisa, A., 2020).
The planning and budgeting for assistive device procurement also fall short of the required
strategic and responsive approach. Insufficient planning and budget allocations often lead to
delays or inadequacies in providing essential tools for daily living and social participation (Tuti,
R., & Lisa, A., 2020; ICW, 2021).
Beyond systemic issues, societal attitudes pose significant barriers. Social stigma around
disability results in a lack of understanding and support, limiting the provision of adequate
assistive devices and excluding persons with disabilities from societal participation. This stigma
not only affects physical access to services but also creates psychological barriers, discouraging
individuals from seeking support (Adioetomo, 2014).
Administrative hurdles further impede access to services and devices. Many persons with
disabilities are not registered on family cards, essential for obtaining IDs, thus barring them from
accessing government-provided assistive technology and services (Tuti, R., & Lisa, A., 2020).
Age limitations on assistive device recipients, restricting aid to those under 59, and eligibility
criteria based solely on poverty line thresholds also hinder access. These criteria exclude older
persons with disabilities and those with slightly higher incomes but facing increased living costs
due to their disability (Tuti, R., & Lisa, A., 2020).
Conclusion
Indonesia's journey towards inclusive healthcare and social welfare for persons with disabilities,
particularly in Assistive Technology (AT) provision, highlights significant disparities and
challenges. Despite progressive legislation like Law No. 8 of 2016, which marks a paradigm
shift from a charity-based to a human rights-based approach, practical implementation reveals
gaps between policy and practice.
Implementation challenges stem from inaccurate and outdated data, lack of coordination across
sectors, insufficient funding, a shortage of skilled social workers, and inadequate planning for AT
procurement. Societal stigma and bureaucratic hurdles further exacerbate these issues, limiting
access to services and assistive devices.
To address these challenges, Indonesia needs to establish national technical regulations for
inclusive AT provision, maximize individual-based services, formulate regulations for inclusive
health facilities, and implement effective monitoring and evaluation mechanisms. These
recommendations aim to enhance the effectiveness of policies, ensuring they are inclusive,
equitable, and responsive to the needs of persons with disabilities. Such comprehensive measures
are crucial for building a more inclusive society, where AT serves as a bridge to opportunity and
dignity for all.
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