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L-150783
David
TITLE
Over the years, there has been the struggle for persons with
disabilities to be integrated into mainstream society. They are often set to
the side and treated as objects of policy-making and charity; they are often
denied opportunities to participate in public domains or to politically
organize. More often than not policies are developed for them, instead of
policies that encourage their direct participation, thus leads to the feeling of
less self-efficacy, and the belief that they do not have the capacity to impact
the political system1. Until today, persons with disabilities still experience
inequalities in public and private establishments, transportation facilities,
and in most aspects of the policymaking process that include lobbying,
voting, and even performing as a public servant2.
According to the World Health Organization, about 15% of the worlds
populationor an estimated number of 650 million peoplehave disabilities,
and one in every six people in poverty areas are affected by moderate or
severe disability. Given that disability is extremely diverse, it is also
extremely difficult to cater to the needs of people with disabilities. However,
as much as everyone else is entitled to mainstream health care services, so
should be persons with disabilities. This veers into the discussion of disability
not being a topic of medicine or charity but an issue of human rights.
In order to counter the medical model was the social modelit
maintained that persons with disabilities continue to be excluded and
discriminated against from direct participation in mainstream society. The
advocacy for the rights of the disabled flourished as the social model became
the foundation of the disability movement that provided the gravitas that
supported disabled persons organizations (DPOs) to negotiate with their
governments for a rights-based approach toward disability. The rights-based
approach also asserted that existent resources should be distributed
equitably, thereby ensuring that the most vulnerable and marginalized
1 David L. Braddock & Susan L. Parish on An Institutional History of Disability, in
HANDBOOK OF DISABILITY STUDIES (Albrecht, et al., 2001);
2 Sarah Parker Harris et al., Civic Engagement and People with Disabilities: The Role
of Advocacy and Technology, 5 JCES 1 (2012)
is the declaration that the term to be used in all sections of the same act in
reference to disabled persons shall be changed Persons with Disabilities
(PWDs). In the third section, R.A. 10070 also stated:
Within three (3) years after the effectivity of this Act, appropriate agencies,
headed by the Department of Social Welfare and Development (DSWD), in
consultation with the NCDA and relevant NGOs and POs, shall review its
implementation and recommend to Congress the need to mandate the
establishment of a PDAO in fourth (4th), fifth (5th), and sixth (6th) class
municipalities.
6 Artha Kira Paredes et al., THE RIGHT TO VOTE: FILIPINOS WITH DISABILITIES AND THE 2013
ELECTIONS, (Luz Rimban & Yvonne Chua, eds.) (2014)
7 Bradley Lewis, A Mad Fight: Psychiatry and Disability Activism, in THE DISABILITY
STUDIES READER, (Lennard J. Davis ed. 2010)