![]() |
|
![]() |
|
|
|
Governmental Affairs
The government has a profound effect on all of our lives and it is important to stay informed of the current issues and legislation being discussed and voted upon. People with developmental disabilities and their families are directly impacted by the decisions made by our governing officials. Therefore, it is imperative to stay abreast of public laws and legislation pertaining to disability issues and to use this vital information to educate our representatives on the unique needs of people with developmental disabilities.
For current legislative bills of interest see “Tips for writing a letter or emailing your senator”. Tips for Writing a Letter or E-mailing Your Senator
Name of Senator and District # To use the Legislature's web-site – www.unicam.state.ne.us
The Rights & Responsibilities You Have
Advocating For Our Children You and the Legislature When you have a child with disabilities born into your family, you realize that part of raising that child involves accessing current and updated information. You may find yourself responsible for doing things to benefit your child/family that you have never had to do in your life before. You may get connected with agencies, organizations and educated experienced people that can help you figure it all out. Many of you who have a family member with a disability already advocate on a daily basis for things your family needs. So I am always a bit surprised when I hear people ask "Why is it still necessary to advocate or be an activist for people with disabilities today—you have services, people are much better off than they were say 30 years ago! Yes it is true that we have services today. Historically we as a nation have come far in the field of developmental disabilities and wonderful things have been accomplished by parents and professionals in regard to developmental disabilities. Over the years parents and disability advocates have seen the inequities and taken up the charge of ensuring the best for people with disabilities. They have done this through the disability civil rights movement, through agenda's that have worked to establish education, medical and financial services for the people that need them. They have brought about change for people. Great change! So why is it that we need to still advocate? Why be an Activist when it comes to disability issues?
Advocacy and Activism are still needed. Parents and our family members with disabilities are the stakeholders that are affected when their needs cannot be met. With the help of informed sources and information sharing, advocating for your child does not have to take up a huge chunk of your time, but continues to be necessary. We must protect the rights we already have and continue to move forward towards equal rights for people who cannot always advocate for themselves. If you would like to get updated or educated on legislative or governmental issues that may affect your family you can receive information by signing up to be on a legislative e-mail list-serve or receive information in the mail. To do this you may call Annie Anderson or Cleo at 346-5220 to be added to the list-serve. Here are some things that have been happening legislatively on both a federal and state level that you may be interested in... In the state of Nebraska, there is currently a bill called LB 623. This bill would codify the rights of individuals with disabilities to make autonomous decisions about their services. This supports that allowing people with developmental disabilities to make decisions about his or her own life gives them the same rights as ordinary citizens in our society. It recognizes that service delivery should be based on the consumer and his or her needs. People with disabilities should be able to live in the most integrated community settings that are appropriate to their individual support requirements and their preferences. They should have the right to exercise meaningful choices about the services they receive, the types of support they can use etc. Governors and State Legislatures are proposing sweeping changes to trim Medicaid by the billions. They have devised proposals to curb the rapid growth of Medicaid. Under the new proposals, some individuals who receive Medicaid would have to pay more for care and states would have more latitude to limit the scope of services. The proposals provide guidance to Congress, which just recently proposed a budget blueprint that would cut projected Medicaid costs by 10 billion over the next five years. The state officials say their goal is not to save money, but to avoid wholesale cuts in coverage like those in Tennessee, which is dropping more than 300,000 people from its Medicaid rolls—Missouri is dropping 90,000 people. These proposals have a substantial chance of becoming law. President Bush has a new initiative called "Competitive Sourcing" which worries workers with disabilities. David Goodman, a clerk at the National Institute of Health in Bethesda, is caught between two conflicting federal policies, one that helped him get his federal job 14 years ago and another that soon may take it away. Goodman, 34, has Autism. He landed his job at Occupational Health and Safety Division in 1991 as a Schedule A appointee, the beneficiary of a long-standing government policy that promotes employment of people with disabilities in federal agencies. Goodman loves his job. Last month his family learned that Goodman is among tens of thousands of federal employees whose agencies are evaluating whether their jobs could be performed better and more cheaply by a private contractor. This is a part of Bush's "competitive sourcing initiative which requires civil servants across the government to prove they can do their work more efficiently than private contractors, or risk seeing the work outsourced. The initiative has thrown a scare into many workers who are anxious about whether or not they will be forced to go to work for a private contractor or find themselves without a job at all. This new policy is especially vexing for employees with disabilities and their advocates. They fear that a strict economic comparison puts such workers at a decided disadvantage because they often require more supervision and extra help, and therefore cost more to employ. Timothy J. Wheeles the federal manager in charge of competitive sourcing at NIH, said, "The agency values the diversity of its workforce, and many mangers and colleagues are worried about what competitive sourcing will mean for employees with disabilities. Legislative/Governmental Affairs Links
|
1941 South 42nd Street / Suite 122 / Omaha, Nebraska 68105 |