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Attorneys & Advocates

Learn more about Attorneys & Advocates | View General Legal & Advocacy Resources

Family Voices
1012 Pennsylvania AVE SE, Washington, DC
(202) 265-1432 (voice)

Family Voices is a national organization working in collaboration with various local organizations on behalf of Children and Youth with Special Health Care Needs (CYSHCN) . Family Voices provides parents of children with chronic conditions access to specialty healthcare resources and to other families.

NOTE: Family Voices and the Family-to-Family Health Information Center are separate programs. The latter is grant funded under various Family Voices affiliates.

Advocates for Justice and Education, Inc.
25 E Street, NW (on the 4th floor), Washington, DC 20001
202-678-8060 (voice)

Advocates for Justice and Education, Inc. educates and trains parents, teens, and young adults with disabilities about laws that govern public and special education or other conditions that impede learning. Training sessions are offered to achieve the following: clarify legal obligations; assist families to prepare for IEP and ITP meetings; provide training and courses to families on educational services; and help parents and transitioning students there are disagreements about educational plans

Advocates for Justice and Education, Inc. - DC Parent Information Network
1012 Pennsylvania AVE SE, Washington, DC 20003
202) 678-8060 (voice) | (202) 678-8062 (fax)

Under a grant from the D.C. Department of Health’s (DOH), Community Health Administration (CHA), AJE is to develop and implement a District of Columbia Parent Information Network (DC PIN). DC PIN is to provide area residents with special health care needs information on family navigation; care coordination; community education; and individual advocacy.  DC PIN will serve all families and children ages 0 to 21 within the District of Columbia.

Advocates for Justice and Education, Inc. - Parent to Parent Program
1012 Pennsylvania AVE SE, Washington, DC 20003
202) 678-8060 (voice) | (202) 678-8062 (fax)

Our Parent-to-Parent Program was created to provide parents with a supportive network of peers. This program offers parents an opportunity to develop leadership skills and offer parents in similar situations with support. Peer supporters are provided a comprehensive six-week training that focuses on educational advocacy, the laws supporting special education and related services, and leadership training.

American Association on Intellectual and Developmental Disabilities (AAIDD)
501 3rd Street, NW Suite 200, Washington, DC 20001
202-387-1968 (voice) | 202-387-2193 (fax)

AAIDD promotes progressive policies, sound research, effective practices, and universal human rights for people with intellectual and developmental disabilities.

AAIDD's goals are to:

  • Enhance the capacity of professionals who work with individuals with intellectual and developmental disabilities.
  • Promote the development of a society that fully includes individuals with intellectual and developmental disabilities.
  • Sustain an effective, responsive, well managed, and responsibly-governed organization.

AAIDD's principles* (or core values) that guide the achievement of its goals relative to its mission are to:

  • Cultivate and provide leadership in the field of intellectual and developmental disabilities that encompasses a diversity of disciplines, cultures, and perspectives.
  • Enhance the skills, knowledge, rewards, and conditions of people currently working in the field and encourage promising students to pursue careers in the field of intellectual and developmental disabilities.
  • Advance basic and applied research to prevent or minimize the effects of intellectual and developmental disabilities.
  • Advance the assurance of all human rights of people with intellectual and developmental disabilities, including equality, individual dignity, choice, and respect.
  • Promote genuine accommodations to expand participation in all aspects of life for people with intellectual and developmental disabilities, opportunities for choice and self-determination, and access to quality health, education, vocational, and other human services and supports.
  • Influence positive attitudes and public awareness to contributions of people with intellectual and developmental disabilities.
  • Establish partnerships and strategic alliances with organizations that share our values and goals.

ASAN's Toolkit for Advocates on Health Care and the Transition to Adulthood
PO Box 66122, Washington , DC 20035

ASAN is proud to announce the release of a comprehensive toolkit to empower people with disabilities and their families to manage their own health care as they transition to adulthood.

Transition to Adulthood: A Health Care Guide for Youth and Families provides people with people with disabilities and their families with information on how to choose a source of health care coverage, create a health care support network, integrate health care transition goals into their educational plans, and manage their health care. It includes useful guides and worksheets for keeping track of health care records, making doctor's appointments, and talking to doctors about health concerns.

The toolkit also includes Model Supported Health Care Decision-Making Legislation and its accompanying Questions and Answers resource. The model legislation, which ASAN developed in collaboration with the Quality Trust for Individuals with Disabilities, would enable people with intellectual or developmental disabilities to name a trusted person to help communicate with doctors, understand health care information, make informed decisions about health care, and/or carry out daily health-related activities. Advocates can use this model legislation when talking to their state legislators about ways to support people make independent health care decisions.

ASAN's policy brief, The Transition to Adulthood for Youth with ID/DD: A review of research, policy, and next steps, discusses the range of challenges facing youth with intellectual and developmental disabilities as they approach adulthood, including potential loss of health care coverage, barriers to obtaining adult-oriented care, and lack of support in making health care decisions. It outlines several policy recommendations to eliminate these barriers, including expanding access to income-based Medicaid coverage, increased education and awareness of the importance of transition and decision-making supports, and increased research on best practices in transition planning.

Bread for the City Legal Clinic NW
1525 7th St, NW, Washington, DC 20001
202-265-2400 (voice)

Volunteer and staff attorneys represent clients in landlord-tenant disputes, represent claimants who have been denied Social Security disability benefits, advocate in fair hearings for other public benefits, and represent clients in family law matters including child custody, civil protection orders, child support and divorce.

Crime Victims Compensation Program/The Superior Court of the District of Columbia Washington, DC
202-879-4216 (voice)

The Superior Court of the District of Columbia possesses experienced victim advocates, dedicated toward assisting innocent victims and their families who suffer hardship from extreme acts of violence. The Crime Victims Compenstation Program, CVCP, assists victims and their families, with crime-related expenses such as furneral and burial costs, medical and mental health costs, lost wages, loss of support and services, clean up of a crime scene and, for victims of domestic violence, the cost of temporary shelter.

Disabled American Veterans (DAV)

We are dedicated to a single purpose: empowering veterans to lead high-quality lives with respect and dignity. We accomplish this by ensuring that veterans and their families can access the full range of benefits available to them; fighting for the interests of America’s injured heroes on Capitol Hill; and educating the public about the great sacrifices and needs of veterans transitioning back to civilian life.

  • Providing free, professional assistance to veterans and their families in obtaining benefits and services earned through military service and provided by the Department of Veterans Affairs (VA) and other agencies of government.
  • Providing outreach concerning its program services to the American people generally, and to disabled veterans and their families specifically.
  • Representing the interests of disabled veterans, their families, their widowed spouses and their orphans before Congress, the White House and the Judicial Branch, as well as state and local government.
  • Extending DAV’s mission of hope into the communities where these veterans and their families live through a network of state-level Departments and local chapters.
  • Providing a structure through which disabled veterans can express their compassion for their fellow veterans through a variety of volunteer programs.

Disabled Veterans National Foundation (DVNF)
(202) 737-0522 (voice)

The Disabled Veterans National Foundation exists to provide critically needed support to disabled and at-risk veterans who leave the military wounded—physically or psychologically—after defending our safety and our freedom.

We achieve this mission by:

  • Providing an online resource database that allows veterans to navigate the complex process of seeking benefits that they are entitled to as a result of their military service, as well as additional resources they need.
  • Offering direct financial support to veteran organizations that address the unique needs of veterans, and whose missions align with that of DVNF.
  • Providing supplemental assistance to homeless and low-income veterans through the Health & Comfort program and various empowerment resources.
  • Serving as a thought leader on critical policy issues within the veteran community, and educating the public accordingly.

The Maryland Coalition of Families for Children’s Mental Health
10632 Little Patuxent Parkway, Suite 234 , Columbia , MD 21044
410.730.8267 (voice) | 410.730.8331(fax)

A grassroots coalition of family and advocacy organizations dedicated to improving services for children with mental health needs and their families and building a network of information and support for families across Maryland.

Mental Health and Mental Retardation Branch/DC Superior Court
Moultrie Courthouse 500 Indiana Ave, NW Room 4475, Washington, DC 20001
202-879-1040 (voice)

The Mental Health and Mental Health Retardation Branch of the Family Court processes matters relating to the hospitalization and continued treatment of persons adjudicated mentally retarded or in need of mental health services. Contact this branch for a court appointed attorney.

National Center for Autism Resources & Education (nCARE)


  • RESEARCH related to Autism and related neuro-developmental disorders,
  • PUBLIC AWARENESS about incidence of disorders and effective treatment,
  • ACCURATE INFORMATION dissemination of up to date, research based information to families, educators and medical professionals, and
  • EDUCATION of parents, advocates, clinicians, educators, lawyers and the community as to best practices and appropriate treatment. Promoting a collaborative, cross training approach.


  • BEING A SOURCE of accurate, up to date, research based information,
  • TRAINING families, educators and clinicians and lawyers, through community training programs,
  • SUPPORTING community programs that promote awareness about disabilities and support families and individuals with disabilities,
  • PROMOTING INDEPENDENCE through education advocacy, self advocacy, independent living and home and community based services for children and adults with Autism and related neuro-developmental disorders,
  • FUNDING of research that addresses the quality of life for parents and their children with Autism, and
  • SPONSORING quality Special Education Advocacy trainings through NSEAI, which provides on-site, on-line training, and conferences.

National Council on Independent Living (NCIL)
2013 H St.,NW, 6th Floor, Washington , DC 20006
202.207.0334 (voice) | 202.207.0341(fax) | 202.207.0340 (TTY)

NCIL represents thousands of organizations and individuals including: individuals with disabilities, Centers for Independent Living (CILs), Statewide Independent Living Councils (SILCs), and other organizations that advocate for the human and civil rights of people with disabilities throughout the United States.

National Disability Rights Network (NDRN)
820 1st Street NE, Suite 740, Washington, DC 20002
202-408-9514 (voice) | 202-408-9520 (fax) | 202-408-9521 (TTY)

The National Disability Rights Network (NDRN) works to improve the lives of people with disabilities by guarding against abuse; advocating for basic rights; and ensuring accountability in health care, education, employment, housing, transportation, and within the juvenile and criminal justice systems. NDRN is the nonprofit membership organization for the federally mandated Protection and Advocacy (P&A) Systems and the Client Assistance Programs (CAP) for individuals with disabilities. Collectively, the Network is the largest provider of legally based advocacy services to people with disabilities in the United States.

Native American Parent Technical Assistance Center (NAPTAC)
1600 San Pedro Dr.NE , Albuquerque, NM 87110
(888) 499-2070 (voice) | (505) 767-6631(fax)

NAPTAC is a project within Education for Parents of Indian Children with Special Needs (EPICS) to provide training and technical assistance to Parent Training Information Centers (PTI’s) and Community Parent Resource Centers (CPRC’s) nationwide on providing effective, culturally responsive services to Native American families of children with disabilities, as well as youth with disabilities. The NAPTAC will also provide differentiated, targeted and intensive technical assistance to parent centers requesting additional support to build their capacity to provide services to Native American parents of children with disabilities, as well as youth with disabilities. The staff and consultants of the NAPTAC are experienced professionals who are ready to provide each Parent Center with high quality services and supports. A Technical Assistance Specialist will be assigned a region as organized by the Regional Parent Technical Assistance Centers (RPTACs). EPICS is a non-profit entity providing training, advocacy and supports to families of Native American children with disabilities and special healthcare needs. EPICS houses the Community Parent Resource Center (CPRC) and the NAPTAC.

Quality Trust for Individuals with Disabilities
5335 Wisconsin AVE NW Suite 825, Washington, DC 20015
(202) 448-1450  (voice)

Quality Trust for Individuals with Disabilities is an advocacy organization that is an independent catalyst for change in the lives of people of all ages with developmental disabilities. Quality Trust advocates, monitors, provides legal education, training, and family navigation to residents of the District of Columbia.

1025 Vermont Ave, NW, Suite 300, Washington, DC 20005
202-540-9020 (voice) | 202-540-9019 (fax)

TASH is a civil rights organization for, and of, people with mental disability, autism, cerebral palsy, physical disabilities and other conditions that make full integration a challenge. Although TASH 's work is often on a global level, equally, if not more significant, is the direct support we provide individuals with disabilities and their family members. We serve as a clearinghouse for the daily reporting of treatment that is unjust or that limits opportunity. We provide information, linkage with resources, expert assistance toward fighting inequities, legal expertise, and targeted advocacy. We bring to the assistance of individuals in need, the backing of our thousands of members worldwide and the support of a national organization committed to social justice for all people.

David A. Clarke School of Law, Bldg 38, 2nd Floor, 4200 Connecticut Ave, NW, Washington, DC 20008
202-274-7400 (voice)

UDC School of Law students and faculty supervisors in the Juvenile and Special Education Law Clinic represent children and parents (or guardians) primarily in special education matters. Over the past sixteen years, the clinic faculty pioneered and developed a nationally-acclaimed approach to addressing the problems of delinquency by supplementing traditional delinquency representation with, where appropriate, advocacy to address the special education needs of the children who are the subject of those delinquency proceedings.

University Legal Services
220 I Street, NE, Suite 130, Washington, DC 20002
202-547-0198 (voice)

University Legal Services (ULS) is a private, non-profit organization that serves as the District of Columbia's federally mandated protection and advocacy system for the human, legal, and service rights of people with disabilities. Our services include information and referral; education and training; investigation of reported or suspected instances of abuse or neglect; individual advocacy; systemic litigation; and technical assistance regarding legislative and policy concerns. All services are offered free of charge to eligible individuals in accordance with ULS' available resources and policies.

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