Page:United States Statutes at Large Volume 124.djvu/4128

 124 STAT. 4102 PUBLIC LAW 111–375—JAN. 4, 2011 (B) initial recommendations for priority actions to expand, eliminate, coordinate, or condense programs based on the program’s performance, mission, and purpose; (C) initial recommendations to— (i) reduce the financial impact of Alzheimer’s on— (I) Medicare and other federally funded pro- grams; and (II) families living with Alzheimer’s disease; and (ii) improve health outcomes; and (D) annually thereafter, an evaluation of the implementation, including outcomes, of the recommenda- tions, including priorities if necessary, through an updated national plan under subsection (d)(2). (6) TERMINATION.—The Advisory Council shall terminate on December 31, 2025. (f) DATA SHARING.—Agencies both within the Department of Health and Human Services and outside of the Department that have data relating to Alzheimer’s shall share such data with the Secretary of Health and Human Services, or the Secretary’s des- ignee, to enable the Secretary, or the Secretary’s designee, to com- plete the report described in subsection (g). (g) ANNUAL REPORT.—The Secretary of Health and Human Services, or the Secretary’s designee, shall submit to Congress— (1) an annual report that includes an evaluation of all federally funded efforts in Alzheimer’s research, clinical care, and institutional-, home-, and community-based programs and their outcomes; (2) an evaluation of all federally funded programs based on program performance, mission, and purpose related to Alzheimer’s disease; (3) recommendations for— (A) priority actions based on the evaluation conducted by the Secretary and the Advisory Council to— (i) reduce the financial impact of Alzheimer’s on— (I) Medicare and other federally funded pro- grams; and (II) families living with Alzheimer’s disease; and (ii) improve health outcomes; (B) implementation steps; and (C) priority actions to improve the prevention, diag- nosis, treatment, care, institutional-, home-, and commu- nity-based programs of Alzheimer’s disease for individuals with Alzheimer’s disease and their caregivers; and (4) an annually updated national plan.