Details of our 2009 Advocacy Agenda
Expanding the geriatric workforce
Click here to read a coalition letter urging the Senate Committee on Health, Education, Labor and Pensions to include S. 245 in health care reform.
Adding a care coordination benefit to Medicare
What AFA is doing: Studies have shown that coordinated care for this population can reduce healthcare expenditures, improve quality of care and enhance health outcomes. AFA is urging Congress to support S. 1004 (Lincoln), H.R. 2307 (Green), “The Reaching Elders with Assessment and Chronic Care Management and Coordination Act” or “RE-Aligning Care Act,” and/or S. 1131 (Wyden), H.R. 2560 (Markey), the “Independence at Home Act of 2009.” These approaches would create a new benefit under Medicare for care coordination and annual geriatric assessment.
Mandating transparency in nursing homes
What AFA is doing: AFA believes S. 647 (Kohl/Grassley), (House bill not yet introduced), the “ Nursing Home Transparency and Improvement Act of 2009,” will increase public transparency of nursing home owners and operators by requiring nursing homes to disclose their corporate owners and the affiliated entities that operate, manage or control them. By implementing reporting requirements that show direct care costs and nurse staffing levels and turnover patterns, the no-cost bill will provide families and policymakers critical new information to evaluate the quality of services provided in nursing homes across the country. The bill will also make other quality-related information available to consumers; make it easier for family members to file complaints about poor care; and develop a model for independent government monitoring of nursing home chains. S. 647 also would require facilities to include dementia management and abuse prevention training as part of pre-employment training.
What AFA is doing: AFA urges Congress to support S. 697 (Kennedy), H.R. 1721 (Pallone), the “ Community Living Assistance Services and Supports Act” or the “CLASS Act.” This bill would create a disability insurance program financed through voluntary payroll deductions for adults who become unable to perform at least two activities of daily living. The measure would provide a cash benefit to help obtain services and supports, while providing disabled individuals more choices and opportunities to live and participate in their communities.
Click here to learn more about the issue.
Background: Comparative Effectiveness Research (CER) compares treatments and strategies to improve health. This information is essential for clinicians and individuals to decide on the best course of care.
What AFA is doing: As an advocate for CER, AFA is a member of the Alliance of Comparative Effectiveness Stakeholders (ACES) coalition. The ACES coalition supports CER as part of health care reform, but urges Congress to consider the following: 1) to be truly effective, CER must include research on at-risk and under-served populations, individuals with disabilities and the chronically ill; 2) any CER initiative must include a formal structure to ensure broad public input and transparent decision-making as recommendations are determined; and 3) Congress should bar this research from being used to make coverage decisions by Medicare, Medicaid or any other public program.
Click here to read a letter from the ACES coalition to the Senate Finance Committee.
Providing advance planning education and resources
What AFA is doing: AFA backs S. 1263 (Warner), H.R. 3172 (Baldwin), the “Senior Navigation and Planning Act of 2009,” which would create a new transitional care benefit through hospice. This would include palliative care consultation services, patient and family counseling, respite services and in-home caregiver training, while also allowing for the continuation of curative treatments. The bill requires physicians to provide information on advanced care planning for individuals specifically diagnosed with certain conditions; provides incentives for accreditation and certification in hospice and palliative care; requires more comprehensive discharge planning; and increases public awareness about the importance of advance planning.
Expanding Medicare coverage for adult day care
What AFA is doing: Adult day centers serve as an effective source of relief to family caregivers and provide quality care options for our nation's elderly population, which is about to dramatically increase with the aging of the baby boomer generation . AFA is urging Congress to support H.R. 3043 (Linda Sánchez), (Senate bill not yet introduced), the “Medicare Adult Day Care Services Act of 2009,” which would include adult day care as a covered provider of post-acute services under Medicare. This bill would pay adult day care providers 98 percent of the Medicare-certified home health rate and give seniors the option to choose adult day care or in-home care. Services at adult day care may include: nursing, physical, occupational and speech therapy, dignified assistance with activities of daily living, nutrition therapy, health monitoring, social interaction, stimulating activities and transportation. These care hours and additional services are critical to keeping individuals healthier and at home. In addition, the social aspects of adult day care may offer some relief from the isolation and depression that often accompany chronic illness and disabilities.
Click here to read a letter of support for H.R. 3043 signed by AFA and more than 85 other national and state and local organizations .
2) More resources for treatment and caregiver support services related to Alzheimer’s disease
What AFA is doing: AFA supports the re-introduction of the “Alzheimer’s Treatment and Caregiver Support Act,” which was sponsored last year in the 110th Congress by Representative Maxine Waters. This legislation would provide grants to public and non-profit organizations to improve treatment for individuals with Alzheimer’s disease, and expand training and support services for caregivers. AFA is the lead organization in support of this legislation and enlisted the support of more than 65 national and local organizations and 117 House co-sponsors in the 110th Congress . It is expected to be re-introduced in the 111th Congress this year.
Click here to read a copy of H.R. 1032, the bill from the 110th Congress.
Background: It is estimated that 60 percent of individuals with Alzheimer's disease are likely to wander at some point during the progression of their illness. Wanderers are vulnerable to dehydration, weather conditions, traffic hazards and individuals who prey on people who are defenseless. Up to 50 percent of individuals with Alzheimer’s disease who wander will become seriously injured or die if they are not found within 24 hours.
What AFA is doing: AFA has been collaborating with Project Lifesaver International, a national nonprofit organization that features rapid response technology, to reauthorize and double the funding for the Missing Alzheimer’s Disease Patient Alert Program, a Department of Justice grant program that provides funding to non-profit organizations for the identification and search and rescue of missing persons with dementia. AFA supports H.R. 908 (Waters), (Senate bill not yet introduced), “ Missing Alzheimer's Disease Patient Alert Program Reauthorization of 2009,” which would reauthorize this program and provide competitive grants to multiple organizations. H.R. 908 passed the House in February 2009, and AFA is working to secure a Senate sponsor for a companion bill. AFA and Project Lifesaver International also support efforts to pass S. 557 ( Martinez), H.R. 632 (Doggett), the “National Silver Alert Act of 2009,” which would create an alert system for missing adults; the House has passed the bill and the Senate has referred it to the Committee on the Judiciary.
Click here to read a letter in support of H.R. 908, which reauthorizes the Missing Alzheimer’s Disease Patient Alert Program, and click here to read a letter that supports the 2010 fiscal year funding for the program.
Background: According to surveys conducted by AFA, Hispanic caregivers were significantly more likely (33 percent) than caregivers of other races (23 percent) to believe that Alzheimer’s disease is a normal part of aging and were also significantly more likely (67 percent) to dismiss the symptoms of Alzheimer’s disease as old age than respondents of other races (53 percent). The resulting delay in diagnosis can likewise delay treatments that can help hurt slow progression of symptoms, and it can increase stress on family caregivers.
What AFA is doing: AFA urges Congress to support H.R. 2987 (Linda Sánchez), (Senate bill not yet introduced), the “ Cure and Understanding through Research for Alzheimer’s Act of 2009,” or the “La CURA Act of 2009,” which would increase funding to the National Institutes of Health (NIH) and the Centers for Disease Control and Prevention for adequate Alzheimer’s research, outreach and education in all communities. La CURA would authorize an education and outreach program to promote public awareness and risk reduction with respect to Alzheimer's disease (with particular emphasis on education and outreach in Hispanic populations), as well as address diversity deficiencies in research by encouraging increased participation by Hispanics in NIH clinical trials and epidemiological studies.
Background: According to the Lifespan Respite Task Force, the nation’s estimated 50 million family caregivers provide about 80 percent of long-term care . Respite care, the most frequently requested family support service, has been shown to provide family caregivers with the relief necessary to maintain their own health, bolster family stability, keep marriages intact, and avoid or delay more costly nursing home care placement.
What AFA is doing: AFA and our coalition partners at theLifespan Respite Task Force are urging Congress to appropriate the full authorized amount for grants under the “Lifespan Respite Care Act of 2006.” The act authorizes competitive grants to state agencies through Aging and Disability Resource Centers in collaboration with public or private non-profit organizations to make quality respite accessible to family caregivers regardless of age or disability. The act was signed into law in 2006 and will receive first-time funding of $2.5 million in current 2009 fiscal year. The law authorizes Congress to spend up to $71.11 million in the 2010 fiscal year—the full amount AFA and its partners are pressing for.
Click here to read a coalition letter of support requesting full funding for the Lifespan Respite Care Act.
Background: Despite being largely preventable, falling is a common cause of unintentional injury among people with dementia. Overall, the Centers for Disease Control and Prevention (CDC) reports that one in three Americans aged 65 and older falls each year. As well, in 2005, the latest year for which CDC has statistics, 1.8 million older adults were treated in emergency departments for nonfatal injuries from falls, 433,000 were hospitalized and nearly 16,000 died from their injuries. CDC confirms that $19.2 billion annually is spent on treating the elderly for the adverse effects of falls.
What AFA is doing: AFA is part of the Falls Free Coalition, a group of national organizations and state coalitions working to reduce the growing number of falls and fall-related injuries among older adults. The coalition is advocating for $10 million in federal funding for the CDC’s National Center for Injury Prevention and Control to address the very costly, but preventable problem of falls among older adults.
Background: According to the National Research Council, between one million and two million Americans aged 65 or older have been injured, exploited or otherwise mistreated by someone on whom they depended for care or protection. The frequency of elder mistreatment will undoubtedly increase over the next several decades as the population ages.
What AFA is doing:: AFA supports S. 795 (Hatch), H.R. 2006 (King), the “ Elder Justice Act of 2009,” which aims to make communities safer for older Americans by developing new strategies and requiring prompt reporting of crimes in nursing homes. If enacted into law, the Elder Justice Act would provide federal resources to state and community officials who currently grapple with elder abuse with scarce means and fragmented systems. Mechanisms for identifying and tracking elder abuse indicate that many instances of injustice are not reported for appropriate prosecution. This legislation has been endorsed by the Elder Justice Coalition, a national membership organization comprised of 584 groups, including AFA, that are dedicated to eliminating elder abuse, neglect and exploitation in America.
Click here to learn more about the legislation and the coalition.
Background: In recent years, a growing number of long-term care facilities have required individuals—often unwittingly—to agree prior to admittance to arbitration as the only method for dispute resolution during their residency. Such agreements involve the waiver of a fundamental constitutional right and prevent a resident from having malpractice and other claims heard by an impartial judge or jury.
What AFA is doing: AFA supports S. 931 (Feingold), H.R. 1020 (Johnson), the “Arbitration Fairness Act of 2009,” which declares that no pre-dispute arbitration agreement shall be valid or enforceable if it requires arbitration of an employment, consumer or franchise dispute, or a dispute arising under any statute intended to protect civil rights. This would include disputes involving long-term care facilities. AFA also supports S. 512 (Martinez), H.R.1237 (Linda Sánchez), the “Fairness in Nursing Home Arbitration Act of 2009,” which applies specifically to long-term care facilities and would end the practice that requires families, during the stressful process of admitting a loved one to a nursing home or assisted living facility, to forgo the right to sue the facility if the resident is injured or dies because of the facility's neglect. AFA signed on in support of both bills and is working with a number of other national organizations to increase support.
Alzheimer's Foundation of America 866.232.8484