By Nancy Seyden(1) and Bob Robert(2) A rich history lies behind the development of In-Home-Support Services (IHSS) and Public Authorities (PAs) in California. The history is filled with vision, struggle, drama, and the voices of many people. Advocates sought to address the needs of people who are disabled, blind, and elderly who require assistance with personal care and/or domestic services. The people wanted to live independently at home, in homes of their choosing, and to participate in their communities with the hands-on assistance of others. They wanted to have a say in the services provided. With adequate support and assistance from others, they knew independent living could be achieved. Herewith begins the story about independent living, the experience of disabled people who live with assistance from others and who receive public assistance. Many post-polio and respiratory dependent individuals lived at Rancho Los Amigos in the 1950s, a rehabilitation facility in Downey, California, where the story begins. To save money, local administrators decided in 1953 to move about 100 patients into the community. This bold move was only made possible because the March of Dimes offered to pay for the attendant care. The March of Dimes decided to discontinue its support of the program after the anti-polio vaccine had been developed and was successful. Several people who were affected by the cuts went to the California legislature to request funding for their desperate situation. The legislature responded positively with the Attendant Care program but only provided very limited funding. In the 60s and very early 70s, the Aid to the Totally Disabled (ATD) program provided a monthly cash payment of up to $300/month to disabled persons who needed attendant care. Recipients would then hire and pay their provider. The attendant care program came later to be part of the Social Services system instead of the medical system. This distinction is very important because the person is viewed very differently under each of these systems. Essentially, advocates argued this was a social issue where the person with a disability is seen as needing routine care in the community rather than being viewed under the medical system as being sick and needing to be cured where the problem resides with the person who needs specialized care. In January 1974, Supplemental Security Income (SSI) was implemented. It gave a flat grant to recipients for basic living costs. It did not cover costs for attendant care. Since the ATD program was ending, California was forced to create a new program. The home health industry wanted services provided by contract agencies to ensure quality control. Disabled individuals, however, wanted to retain flexibility, control, and independence. They made many visits to the Capitol and stressed the importance of users maintaining full control over their attendants. The new program that was created was called the Homemaker-Chore program which later became In-Home-Supportive Services (IHSS). This program emphasized consumer control. The development of IHSS during the 70s and 80s parallels the rise of the Independent Living Movement. Statewide Independent Living Centers, the World Institute on Disability, and Senior Advocacy Groups were the early supporters and advocates who emphasized the concept of consumer directed services. In 1991, there was a huge budget deficit in California. The World Institute on Disability and the California Foundation for Independent Living Centers (CFILC) advocated that Medicaid funding should be brought into the IHSS program. Their recommendation was adopted. New federal funding was acquired that led to a shift of funding from a Social Services block grant to Medicaid. There were problems for some IHSS recipients who were no longer eligible for Medicaid funding. The State responded by dividing the program into two parts: 1) the Personal Care Services Program for people who were eligible for 50% Medicaid funding, and 2) the IHSS Residual Program for people not eligible for Medicaid funding.