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Disability |
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California's protection and advocacy system |
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ADVOCACY PLAN 2008-2012
Implementing Rights, Addressing Wrongs
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Disability Rights California www.disabilityrightsca.org
(800) 776-5746 |
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Adopted by Disability Rights California’s Board of Directors
September 2007
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Table of Contents |
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Disability Rights California Vision Statement Disability Rights California Mission Statement Stop discrimination, end institutionalization, and increase community living choices Eliminate abuse and neglect and improve quality of care Increase access to benefits, services, and health care Increase access to education, housing, transportation, and employment
Make sure the autonomy,
preferences, and choices of people with disabilities are respected Increase Culturally Competent and Geographically Accessible Services Examples of Problems We Can Help With Public Policy, Communication and Public Education Goals Goals to Expand, Enhance, and Improve the Effectiveness of our Services Advocacy Principles, Priorities, and Goals |
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Our vision is a barrier free,
inclusive world that values diversity, culture, and each individual.
In this world all people
with disabilities have: Equality, Dignity, Power, Freedom of choice, Freedom from abuse,
neglect, and discrimination. They have quality,
culturally responsive, safe, affordable, accessible: Housing, Education, Healthcare, Technology, Transportation, and Individual and family
supports that they choose and direct. People with disabilities
have the right to family, social, and intimate relationships. They are financially secure, can make life
choices, and have opportunities for satisfying work, recreation, spiritual
lives, and community service. |
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Our
Advance the rights of
Californians with disabilities. |
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Excluding
people with disabilities from the mainstream of community life has been a
civil rights issue in Over the
next five years, we will continue to advocate with and for people with
disabilities. We will work together to fight discrimination, promote autonomy
and choice, end abuse and neglect, and increase access to programs and
services that respect each client and his or her unique needs and culture.
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Our work
will be guided by the following principles: Stop discrimination, end institutionalization, and increase community living choices
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Stop discrimination and work for equal opportunities
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End institutionalization and increase access to culturally appropriate
and safe community living with supports chosen by the person with a
disability Eliminate abuse and neglect and improve quality of care
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Eliminate abuse and neglect
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Improve the quality of care and treatment in facilities and protect
rights, while working towards the goal of returning to the community Increase access to benefits, services, and health care
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Increase and maintain access to government benefits
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Increase and maintain access to public and private health programs
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Increase and maintain access to effective, client-centered, voluntary
community mental health services
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Make sure that people with developmental disabilities receive
Lanterman Act services based on their needs and choices Increase access to education, housing, transportation, and employment
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Increase children’s and youth’s access to appropriate education
services in the most integrated environment
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Increase the rights of people with disabilities to have work
opportunities consistent with their interests, abilities, and needs
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Increase the rights of people with disabilities to housing they can
use and afford
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Increase the availability of adequate, accessible transportation no
matter where they live and remove transportation barriers Make sure the autonomy, preferences, and choices of people with disabilities are respected
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Increase protections for the preferences, opinions, bodily integrity,
and privacy rights of individuals with disabilities
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Promote the rights of people with disabilities to direct their own
lives
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Expand services and protections for parents with disabilities
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Increase participation by people with disabilities on local and state
policy-making bodies and boards
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Make sure that voting systems and processes are accessible and barrier
free Increase Culturally Competent and Geographically Accessible Services
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Make sure that systems value disability, diversity, culture, and each
individual
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Make sure that there is equal provision of services in all geographic
areas
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Make sure that there is access to courts, administrative agencies, and
legal services so that individuals with disabilities can defend and enforce
their rights |
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1.
Tell people with disabilities about their many legal, civil, and service rights,
2.
Provide technical assistance, training, publications, and advocacy support for
Californians with disabilities, their families, and representatives,
3.
Advocate to make sure that laws benefit Californians with disabilities,
4.
Investigate complaints about serious physical or sexual abuse and neglect-related deaths
in institutions,
5.
Outreach to traditionally underserved ethnic and disability communities,
6.
Provide peer self-advocacy services for people with psychiatric or developmental disabilities,
7.
Provide patients’ rights advocacy for state psychiatric hospital residents, and technical
assistance and training for county advocates,
8.
Provide rights advocacy for clients with developmental disabilities who are receiving
services at regional centers,
9.
Bring impact litigation and act as amicus curiae in disability- related cases, and
10.
Represent individuals based on our priorities and case selection criteria.
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Examples of Problems we Can Help With We help
people with disabilities to solve disability-related problems. If you have a disability and qualify for
services, we can help you with problems like:
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Rights to basic support, personal care, therapy, and health care –
like Supplemental Security Income (SSI), In-Home Supportive Services (IHSS)
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Discrimination in housing, transportation, employment, and access to
public and private programs and services
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Abuse, neglect, and rights violations in an institution
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Least restrictive environment, dignity, privacy, choice, and other
basic rights
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Special education rights
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Mental health and support services that provide individualized
treatment
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Voting registration, vote casting, and accessible polling places
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Access to technology – like communication devices and power
wheelchairs If we can’t be of direct assistance, we refer people to
other sources of help. We also takes our services into the community, wherever
children, youth, and adults with disabilities live or go to school or obtain
services.
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We
provide advocacy help for Californians with disabilities. You could be eligible for our services if:
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You have a developmental disability
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You are a regional center consumer
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You have a psychiatric disability or emotional impairment
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You are a patient in a state psychiatric hospital
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You have a physical, learning, or sensory disability .
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You have a traumatic brain injury
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You need access to technology that you believe may help you live a
fuller, more independent life
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You receive SSI or SSDI and need help with employment issues or
keeping your benefits when you return to work
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You have questions about your right to vote In
deciding whether we can represent you directly, we will consider:
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The merits of your claim
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Your ability to advocate for yourself
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Other advocacy sources you could use
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Whether your problem falls within one of our priority areas
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Availability of our resources
If we
decide that we can not help you and you disagree, you can file a grievance. Each of
our grants and contracts has specific service eligibility criteria. If you want a copy of these criteria, the
complete case selection criteria, or a grievance form call (800) 776-5746.
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To ask
for our services anywhere in
1-800-776-5746
(Voice) 1-800-719-5798
(TTY) You can
also get help by contacting one of our regional legal offices:
916-488-9950
(Voice) 1-800-719-5798
(TTY) Bay Area Regional Office 510-267-1200
(Voice) 1-800-719-5798
(TTY) 213-427-8747
(Voice) 1-800-719-5798
(TTY) 619-239-7861
(Voice) 1-800-719-5798
(TTY) If you
are a regional center client, you may ask for help from the Office of
Clients’ Rights Advocacy (OCRA). Office of Clients’ Rights Advocacy 1-800-390-7032
(Voice) 916-575-1615
(Voice) 1-877-669-6023
(TTY) If you
are a patient at a state psychiatric hospital you may ask for help from the
Office of Patients’ Rights (OPR). Office of Patients’ Rights 916-575-1610
(Voice) You may
also access other advocacy services by contacting our Advocacy Unit. Advocacy Unit Legislation and Public Information
Unit (LPIU) 916-497-0331
(Voice) Communications/Media 510-267-1200
(Voice) 1-800-719-5798
(TTY) Peer Self-Advocacy Units 916-488-7787
(Voice) 1-800-776-5746
(Voice) 916-488-7715
(TTY) Collaborative Projects 916-488-7787
(Voice) 1-800-776-5746
(Voice) 916-488-7715
(TTY) |
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As a
disability advocacy organization, we are committed to implementing the
principles it advocates in its work place including employing people with
disabilities, implementing model employment practices including reasonable
accommodations and accessibility throughout the workplace, and involving
people with disabilities in decision making at all levels of the
organization. To demonstrate its
commitment, our Board of Directors adopts the following time-limited goals
to augment its merit-based selection and retention policies:
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The majority of staff employed by us should be individuals with
disabilities.
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The staff of each office and unit should reflect the disability
diversity of the communities they serve.
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People with disabilities should be employed at all levels of the
organization including directors, managers, advocacy staff, administrative,
and support staff.
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The staff of each office and unit should reflect the ethnic and
language diversity of the communities they serve.
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People of color should be employed at all levels of the organization,
including directors, managers, advocacy staff, administrative, and support
staff.
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Increase the number of multilingual staff, particularly those who
speak Spanish and Asian languages, based on the needs of the communities
served by our offices and units.
We
value diversity of life experiences and believe that employing individuals
whose life experiences are similar to those of our clients will make its advocacy
more effective. We seek out people with familiarity or contacts with
homelessness, the criminal justice system, people with substance abuse
issues, or the Lesbian Gay Bisexual Transgender, and Intersex (LGBTI)
community.
To
implement these time-limited goals, each office and unit will develop
periodic, time-limited Diversity Plans. Our staff
are our most valuable resource and make sure that we are able to effectively
serve Californians with disabilities.
In order to make sure that we are able to recruit and retain a highly
qualified, diverse workforce, we will strive to provide competitive salaries
and benefits.
Our
Board of Directors is committed to ensuring that the Board reflects the diversity of
The Board
will include public members on various Board committees as a way of ensuring
diverse perspectives are heard. The
Board will identify ways to include youth with disabilities in Board
committee work. We are
committed to ensuring that its services are accessible to individuals with
disabilities from ethnically and language distinct communities and that its
services are provided in a disability and culturally competent manner.
To
demonstrate its commitment, our Board of Directors adopts the following
goals:
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Make sure that the provision of advocacy services
reflects the language, and ethnic diversity of each office and unit service
area.
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Target advocacy services to individuals from
communities that are traditionally underserved by the office or unit. Underserved communities include: ethnic and
language distinct communities, immigrant communities, rural and low-income
communities, people who are homeless, individuals from the gay, lesbian,
bisexual, transgender and intersex community, individuals from distinct
disability communities, and children and youth in the foster care or juvenile
justice systems. To
implement these goals each office and unit will develop periodic Outreach
Plans. Public Policy, Communication and Public Education Goals Advance
our Advocacy Principles by:
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Developing an annual legislative platform
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Sponsoring or co-sponsoring select legislation or co-sponsoring
initiatives
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Advocating on select bills, initiatives, and budget issues
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Strengthening and increasing the effectiveness of our coalition
building activities with the disability rights movement and other civil
rights, social justice, and legal services groups
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Participating in task forces, ad hoc committees, meetings, and
coalitions
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Promoting our disability rights expertise to the community at large
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Promoting positive images of people with disabilities through
communications strategies including the media and our website
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Ensuring that media and communications strategies are part of all
aspects of our work including legislation, litigation, advocacy, and
communications
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Strengthening our communication tools and strategies including our
website and the use of other internet tools in order to tell others about our
work and advance our work.
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Informing and educating people with disabilities about our services
by:
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Publishing an Annual Report
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Making information about us available in other languages
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Informing and educating people with disabilities about laws, policies
and services that impact their rights by:
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Producing materials for people with disabilities and increasing the
accessibility of those publications by writing at appropriate literacy
levels, translating materials into languages other than English, and creating
alternative formats
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Providing training and other education activities for people with
disabilities, their families, their advocates, and organizations which target
traditionally underserved communities Goals to Expand, Enhance, and Improve the Effectiveness of our Services
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As resources become available, develop periodic plans which will
enable us to:
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Expand our current legal advocacy, peer/self advocacy, clients’ rights
and patients’ rights advocacy, and other advocacy services.
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Expand services to more remote and geographically underserved
communities.
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Increase our
ability to respond to emerging issues.
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Evaluate and
enhance current methods of providing and administering our services. |
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Advocacy Principles, Priorities, and Goals Our advocacy
will be zealous, dedicated, effective, creative, innovative, and daring. We will take on issues of importance to the disability
community even when the outcome is uncertain. We will integrate a variety of advocacy approaches in all of our
work, including self-advocacy, legal, non-legal, media, public policy,
legislative, and investigatory. We value diversity.
Our staff should reflect the ethnic, language, and disability
diversity, and demographic diversity of Our advocacy efforts will affirmatively address the needs
of traditionally underserved and under-represented communities through
partnership with such communities. Our advocacy will be of high quality regardless of the
type of service, the nature of the problem or who the client is. We will be honest, prepared, truthful, and
informed. All staff is expected to
contribute and their contributions will be valued and respected. When representing individuals:
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We will
do what the client wants – not what we or others think is best,
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We are
honest about our limitations, values, resources, and the likely outcome,
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The
client chooses the outcome and the method of achieving the outcome and the
client’s choices will be treated with respect, and
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The
client actively participates in every stage of the process. Advocacy Priorities We have
identified the following priority areas for the next five-year period:
Abuse and Neglect Discrimination Benefits Education for Children and Youth Lanterman Act Mental Health Peer and Self-Advocacy Collaborative Projects Patients’ Rights Advocacy Clients’ Rights Advocacy On the
following pages is an issue statement and specific goals for each of these
areas. People
with disabilities are much more vulnerable to abuse and neglect than others. 1. Reduce serious and life-threatening injuries caused by abuse and neglect in all facilities, including: · Institutions, · Hospitals, · Skilled nursing facilities, · Residential care facilities, and · Jails, prisons, and other correctional facilities. Improve how oversight agencies respond to reported abuse and neglect in these facilities. 2. Reduce serious and life-threatening injuries caused by abuse and neglect in community settings, including: · Schools, · Day programs and vocational training settings, and · Community living arrangements. Improve how oversight agencies respond to reported abuse and neglect in these settings 3. Eliminate the use of physical and chemical restraint, seclusion, other methods of containment, and aversives for people with disabilities. 4. Inform people with disabilities about their rights and give them the information and materials they need to advocate for themselves. 5. Monitor proposed state regulations about abuse and neglect, and identify those that impact people with disabilities. Comment on these proposed regulations as needed.
Benefits Government assistance and
health benefits, including assistive technology, provide the income support
and services people with disabilities need to live independently in the
community and have a good quality of life. But access to needed benefits is
often difficult because of rules and procedures that are complicated and
confusing, or because there is not enough funding. Because of this, many
people with disabilities are unable to get the services they need and have
the right to receive. 1. Preserve, increase, expand, and improve access to financial benefits, including: · Supplemental Security Income (SSI), · Social Security Disability benefits, · Cash Assistance Program for Immigrants (CAPI), and · Programs and services that maximize employment opportunities. 2. Preserve, increase, expand, and improve access to healthcare of good quality no matter where people live, including: · Medi-Cal, · California Children’s Services (CCS), · Genetically Handicapped Persons Program (GHPP), · Medicare, · Private health plans, and · Managed care plans. 3. Preserve, increase, expand, and improve access to programs in the community that provide the services and supports people with disabilities need to live, work, and participate fully in the community, including: · In-Home Supportive Services (IHSS), · Medi-Cal Personal Care Services, · Medi-Cal/Medicaid, including Home and Community Based Services Waivers (HCBS), and · Assistance Dog Allowance Program. 4. Make sure that people with disabilities are informed about their rights and have the information and materials they need to effectively advocate for themselves. 5. Monitor proposed state regulations about benefits, and identify those that impact people with disabilities. Comment on these proposed regulations as needed. People with disabilities
have the same human and civil rights as others. But Californians with
disabilities still face many barriers to full and equal participation in
society, including: · Attitudes, stigma, and stereotypes · Discrimination, harassment, and retaliation because of their disability and other protected categories · Inadequate and inaccessible transportation · Lack of affordable, accessible housing · Barriers to a full range of employment and self-employment opportunities · Inadequate training and supports necessary to enter and stay in the workforce · Lack of access to supports needed to participate fully in the community · Unnecessary segregation in institutions · Lack of reasonable accommodations, including assistive technology · Lack of education about their rights and how to enforce them · Architectural and policy barriers · Denials of rights to self-determination and choice · Restrictions on parenting rights · Barriers to voting and civic participation 1. End institutionalization by working to: · Change the policies and practices that unnecessarily segregate people with disabilities, and · Provide greater access and more options to live and participate in the community, and more information about these options. 2. Expand housing options for people with disabilities by working to: · Advance their rights to get, use, and keep housing, and · Keep and increase quality housing that is affordable and accessible 3. Fight discrimination and stereotypes about people with disabilities, and increase their rights and opportunities in the following areas: · Access to public, private, and government programs and services, including transportation, higher education, restaurants, stores, and businesses, · Employment of their choice, with or without supports, and · Directing their own lives, including rights to privacy, making choices, parenting, and other personal autonomy rights. 4. Make sure voting systems and election processes are accessible and barrier free, and increase the numbers of people with disabilities who vote. 5. Make sure people with disabilities know their rights and have the materials and information they need to effectively advocate for themselves. 6. Monitor proposed state regulations about discrimination, and identify those that impact people with disabilities. Comment on these proposed regulations as needed.
Education for Children and Youth Although children and
youth with disabilities have the right to receive appropriate special
education and supportive services in the least restrictive environment, it
does not always happen. They still face many barriers to getting education
services, including: · Failure to assess and address their intellectual, functional, academic, vocational, physical, mental health, sensory, and behavioral needs · Excluding children and youth from natural environments · Failure to provide supports and services, including assistive technology · Lack of compliance with processes required by law · Lack of information so that parents can participate in meetings and make informed decisions about their child’s education · Lack of local and state agencies’ compliance with the law · Failure to include students in their own IEP meetings 1. Provide equal access to education and related services for children and youth with disabilities. 2. Make sure that educational processes required by law are followed. 3. Make sure that students are educated in the most integrated and least restrictive setting. 4. Make sure that students with disabilities and their families are informed about their rights and have the information and materials they need to effectively advocate for themselves. 5. Monitor proposed state regulations about education, and identify those that impact children and youth with disabilities. Comment on these proposed regulations as needed. The Lanterman Act
guarantees people with developmental disabilities the right to choose and
receive the services and supports they need to be independent and productive
in their community. But they still face many barriers to fully participating
in society, including: · They are segregated in living situations, day programs, work, and social and recreational activities · They do not always have the information they need to make meaningful choices · They do not get adequate services and supports, including assistive technology · There are not enough innovative, integrated service alternatives · Services in different regional center areas are not comparable, including cultural/ethnic groups and rural areas · Service coordination is not always effective · Residential programs and other service providers may deny their rights · Services are often not culturally competent or individualized and each person’s needs are not heard · Due process procedures are not adequate · There is not enough money for quality services · The quality assurance system does not measure outcomes
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Regional centers are not always well monitored
by · Services and supports are often not culturally competent or individualized, and self-advocates are often not listened to · Self-determination and choice, including the right to parent and develop and maintain relationships, are denied 1. Increase access to: · Quality, culturally competent, inclusive community living options, · Innovative, integrated work, · Competitive employment, · Adult education, · Integrated social, volunteer, and recreational activities, and · Self-directed services where people control their own budgets, select their service providers, and select and manage their own personal assistants. 2. Expand culturally competent supports and services for people with developmental disabilities who want to live as independently as possible with their families or other people they choose. 3. Help people with developmental disabilities and their families better understand, exercise, and enforce their rights under the Lanterman Act and other laws, including rights to: regional center eligibility and services, privacy, personal autonomy, decision-making, and parenting. 4. Make sure that regional centers, the Department of Developmental Services (DDS), and service providers meet their obligations under the Lanterman Act and do not violate individual rights. 5. Make sure that people with disabilities and their families are informed about their rights, and that they have the information and materials they need to effectively advocate for themselves. 6. Monitor proposed state regulations about the Lanterman Act and related laws, and identify those that impact people with developmental disabilities. Comment on these proposed regulations as needed. Californians with mental
health disabilities often face discrimination and stigma. There is not always
timely access to the services, programs, and coordination they need to live
in the community, including client and family- centered programs. Children
and youth and people with multiple disabilities lack coordination of their
services. Because of these problems, people with mental health disabilities
often face unnecessary institutionalization. Once inside facilities, they are
denied adequate mental health services, physical health care, work, education,
social and recreational activities, choice, dignity, freedom, and respect.
They may also be denied self-determination and choice in their lives,
including the right to parent and to develop and maintain relationships. 1. Improve the quality of life for people with mental health disabilities in institutions, by protecting their rights and ensuring that they have effective, client-centered, culturally competent services that will help their transition into the community. 2. Help people with mental health disabilities direct their own lives and avoid institutionalization. This can be done by challenging laws, policies, and practices that violate civil and constitutional rights and lead to the unnecessary loss of freedom(s), or threaten their rights to privacy, making choices, parenting, and personal autonomy. 3. Make sure that people with mental health disabilities have prompt, unbiased access to voluntary, client-centered, culturally competent, community-based services and supports, including those through the Mental Health Services Act and those needed to keep children and youth at home or in the least restrictive placement possible. 4. Make sure that people with disabilities are informed about their rights and have the materials and information they need to effectively advocate for themselves. 5. Monitor proposed state regulations about mental health, and identify those that impact people with disabilities. Comment on these proposed regulations as needed. People with developmental,
mental health, and other disabilities face systemic barriers, discrimination,
and stigma. They are often not treated with respect. They may lack the
resources, support, and education they need to address barriers and
discrimination, and make choices that impact their lives, including:
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Culturally competent services and programs
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Health, mental health, and support services
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Public benefits
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Peer services
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Integrated education, employment, and housing
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Alternatives to homelessness
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Protection of rights
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Transportation
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Voting and civic participation
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Relationships and personal choice
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Support from peers and learning
how to advocate for one’s self through education, training, and collaboration
give people with disabilities powerful tools to break down these barriers and
fight discrimination. Peer and Self-Advocacy for People with Developmental Disabilities Goals 1. Provide effective peer/self-advocacy, support, education, outreach, and training to people with developmental disabilities to promote independence, empowerment, self-advocacy, and choice. 2. Work to transform systems and eliminate barriers, so the voices of people with developmental disabilities are heard, respected, and valued. Peer and Self Advocacy for People with Psychiatric Disabilities Goals 1. Provide effective peer/self advocacy, support education, outreach and training to people with psychiatric disabilities in order to promote independence, empowerment, and choice. 2. Work to transform systems by eliminating barriers, so that the voices of people with psychiatric disabilities are respected and valued. Different groups of people
with disabilities, including seniors with disabilities and people with
developmental, psychiatric, physical and/or sensory disabilities have
developed parallel advocacy efforts to address similar issues that impact
their lives. As a result, these efforts may be less effective and disability
groups may be in competition with one another. Goals 1. Help people with disabilities develop advocacy projects that foster collaboration and eliminate stereotypes between different communities, and address issues that are important to all groups. People with psychiatric
disabilities are vulnerable to abuse and neglect. Their rights may be
unreasonably and unlawfully denied. A patients’ rights advocacy system that
is independent of the service providers will help eliminate abuse, neglect,
and denial of rights and expand access to timely, appropriate, and culturally
competent treatment and services. 1. Protect and enforce the rights of people in state hospitals. 2. Provide access to an effective patients’ rights complaint process by investigating and taking action to resolve state hospital residents’ complaints. Also take action to resolve abuse, unreasonable denial of rights, and punitive withholding of rights that cannot be resolved by the county patients’ rights advocates. Make sure the patients’ rights advocacy system is accessible to patients. 3. Support county patients’ rights advocates by providing information, training, and reviews of their programs. People with developmental
disabilities served by the 21 regional centers are vulnerable to abuse and
neglect, and their rights are often not observed or protected. A clients’
rights advocacy system that is independent of the service providers will help
eliminate abuse, neglect and denial of rights and expand access to the
services and supports people with developmental disabilities need to live
independent and productive lives. 1. Protect the rights of regional center consumers, and help people with developmental disabilities pursue administrative and legal remedies. 2. Investigate and resolve complaints of abuse, unreasonable denial of rights, and punitive withholding of rights guaranteed by the Lanterman Act to residents with disabilities in licensed health and community care facilities. 3. Provide information, referrals, and training for regional center consumers and their families. |
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