[Congressional Record Volume 156, Number 160 (Tuesday, December 7, 2010)]
[Senate]
[Pages S8597-S8598]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
NATIONAL ALZHEIMER'S PROJECT ACT
Mr. BAYH. Mr. President, I rise today to commend members of the
Senate Committee on Health, Education, Labor, and Pensions and Members
of the Senate for their support of the National Alzheimer's Project
Act, S. 3036. In particular, the committee was helpful in strengthening
the National Alzheimer's Plan and the annual reporting requirements to
Congress that include the articulation of goals, benchmarks,
priorities, recommendations, and tracking outcomes.
This legislation is focused on changing the devastating trajectory of
Alzheimer's disease for our families and our economy. Alzheimer's
disease is a debilitating illness that affects more than 5 million
Americans and their families every day. The growing number of Americans
expected to be affected by this disease, which is estimated to reach up
to 16 million people by 2050, will continue to place an enormous burden
on families and loved ones, not to mention the serious fiscal
consequences to consider if we do not act now to address this disease.
If nothing is done, studies report that Alzheimer's disease will cost
the United States $20 trillion over the next 40 years.
With no current plan to address Alzheimer's, this important piece of
legislation would lay the foundation to coordinate all Federal
Alzheimer's programs and initiatives, including research, clinical
care, institutional cared home- and community-based programs. The bill
also ensures that a national Alzheimer's plan will be implemented by
the agencies and Congress.
This bill will leverage existing leadership to offer real solutions
to the Alzheimer's crisis. The National Alzheimer's plan called for in
this bill will, for the first time, articulate what outcomes the
Federal Government is seeking to reduce the impact of this crisis. It
would allow Congress to assess whether the Nation is meeting the
challenges of the disease for families, communities, and the economy.
It
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would give all stakeholders an answer the fundamental question, ``Was
this a good or a bad year in the fight against Alzheimer's?''
The National Alzheimer's Plan will include appropriate performance
measures and benchmarks to allow legislators to evaluate progress in
the fight against Alzheimer's. The assessment and priority
recommendations will likely address issues such as the underinvestment
in Alzheimer's research. By addressing Alzheimer's disease and dementia
directly, the National Alzheimer's Plan will also call attention to the
many steps that can be taken to improve recognition, diagnosis and care
for people with these conditions, reduce symptom severity, support
family caregivers, and encourage ``healthy brain'' behaviors that may
reduce risk for these conditions.
With the leadership of the Federal Government and input from all
stakeholders, including Alzheimer's patient advocates, health cafe
prodders, State health departments, voluntary health associations, and
researchers, this bill would allow an opportunity for all worthy
entities addressing Alzheimer's, including organizations at the State
and at the national level, to come together on advisory council to make
recommendations and implement a national strategic plan to overcome
this dreadful disease. The advisory council will also ensure buy-in,
leadership, and coordination of all related Federal agencies conducting
Alzheimer-related care, services, and research.
One of the principal objectives of the advisory council is to
represent a broad range of expert stakeholders within the Alzheimer's
community to provide input and recommendations to the Federal
Government on a national strategic direction for combating Alzheimer's
disease. When crafting this legislation, the sponsors were careful to
include patient advocates, caregivers, and providers who serve at the
front lines of Alzheimer's care and who understand on a personal level
the toll of this disease on patients and their families. Additionally,
sponsors of S. 3036 included representatives of State health
departments and Alzheimer's researchers who have expertise regarding
the impact of this disease on public health as well as the state of the
science in discovering prevention methods, treatments, and cures.
Lastly, sponsors sought to include national voluntary health
associations on the council, who provide invaluable research, care,
support services, and advocacy tools for patients, caregivers, and
local organizations throughout the country. It is our intent that two
national organizations have representation on the council.
The threat that Alzheimer's disease poses to the health and wellbeing
of our Nation demands an aggressive and well-coordinated response. This
bill creates the first-ever national plan to combat Alzheimer's and
ensures that every dollar spent on the disease will be used to get the
best possible care for patients. At a time when medical research funds
are too scarce and we are struggling to provide quality health care for
all Americans, for the first time we will be able to assess all Federal
efforts related to Alzheimer's disease, ensure existing resources are
maximized, enhance the delivery of quality care, and support the kind
of research that will one day result in a cure for this devastating
disease.
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