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COPAA’s mission is to protect and enforce the legal and civil rights of students with disabilities and their families.  Our primary goal is to secure high quality educational services and to promote excellence in advocacy

For over a decade, ADAMS ESQ has represented students from the ages of 3 through 22 who qualify or should qualify for special education and related services provided by their local school districts. Working as a team with parents and caregivers, we obtain school and medical records, prepare and file due process hearing requests, provide representation at early resolution sessions, mediations, and administrative hearings, and provide representation on Federal Court appeals.

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As a service to our special needs community, we also organize and participate in workshops and seminars at no charge to parent and student oriented groups. ADAMS ESQ has published numerous articles in local periodicals to further educate the special needs community regarding their rights and responsibilities.

The Autistic Self Advocacy Network seeks to advance the principles of the disability rights movement with regard to autism. ASAN believes that the goal of autism advocacy should be a world in which autistic people enjoy equal access, rights, and opportunities. We work to empower autistic people across the world to take control of our own lives and the future of our common community, and seek to organize the autistic community to ensure our voices are heard in the national conversation about us.

The Disability Rights Education and Defense Fund (DREDF), founded in 1979, is a leading national civil rights law and policy center directed by individuals with disabilities and parents who have children with disabilities.

Founded in 1975, Disability Rights Legal Center (DRLC) is a 501C-3 non-profit, public interest advocacy organization that champions the civil rights of people with disabilities as well as those affected by cancer and other serious illnesses. DRLC is a leader in bringing cutting-edge cases to court and in winning victories to protect and to expand the rights of people to help eliminate discrimination and other legal barriers.

Some states require insurers to provide coverage for the treatment of autism. However, opponents to this approach argue that care for individuals with autism is the responsibility of parents and the school systems. Others have raised concerns that mandating coverage for autism will significantly increase insurance premiums. . .

We provide and maintain up-to-date information and resources to assist families so they can make informed choices for their children, and to educate professionals and the community-at-large in order to promote inclusion and understanding. 

CASE advocacy staff, thoroughly trained in special education law, helps families and school districts work together when designing appropriate special education programs for students with disabilities, who are at risk for school failure, so they can succeed in school, get a job and become productive members of their community. CASE provides these basic services:

• Free technical assistance consultations to families and professionals on special education rights, responsibilities and services regarding specific special education students or issues; 

• Direct representation by attorney and non-attorney advocates at Individual Education Program (IEP) meetings, due process mediations, and administrative hearings if necessary on behalf of students with disabilities and their parents; and, 

• Training on special education rights and services to parents so they to can better advocate for appropriate special education programs and services on behalf of children with disabilities.

The goal of ParentAdvocates.org is to put tax dollar expenditures and other monies used or spent by our federal, state and/or city governments before your eyes and in your hands.

Through our website, you can learn your rights as a taxpayer and parent as well as to which programs, monies and more you may be entitled...and why you may not be able to exercise these rights.

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Across the Nation there are those willing to help you advocate for your child's rights. Click here to see listings of helping agencies across the nation.

This booklet is for the parents, caregivers, or representatives of children younger than age 18 who have disabilities that might make them eligible for Supplemental Security Income (SSI) payments. It is also for adults who became disabled in childhood (prior to age 22), and who might be entitled
to Social Security Disability Insurance (SSDI) benefits. (We call this SSDI benefits a “child’s” benefit because
it’s paid on a parent’s Social Security earnings record.)

This booklet will help you decide if you, your child, or a child you know, might be eligible for SSI or Social Security. 

EMPOWERING FAMILIES of Children with Special Needs to successfully Understand and Access the systems that serve them

Advocate, educate, investigate and litigate to advance and protect the rights of Californians with disabilities.

We envision a barrier-free, inclusive, diverse world that values each individual and their voice. In this world, all people with disabilities enjoy the power of equal rights and opportunities, dignity, choice, independence and freedom from abuse, neglect and discrimination.

Families for Early Autism Treatment, Inc. (FEAT) is a non-profit organization of parents, family members, and treatment professionals, designed to help families with children of all ages who have an Autism Spectrum Disorder (ASD), which includes Autistic Disorder, Pervasive Developmental Disorder, Not Otherwise Specified (PDD-NOS), and Aspergers’s Disorder (AS).  It offers a network of support where families can meet each other to discuss issues surrounding autism and treatment options.  

TASK is a nonprofit organization that specializes in special education and assistive technology support for the families of children with disabilities and the professionals who serve them