H.R.3015 - Pediatric, Adolescent, and Young Adult Cancer Survivorship Research and Quality of Life Act of 2011112th Congress (2011-2012)
|Sponsor:||Rep. Speier, Jackie [D-CA-12] (Introduced 09/22/2011)|
|Committees:||House - Energy and Commerce|
|Latest Action:||House - 10/05/2011 Referred to the Subcommittee on Health. (All Actions)|
This bill has the status Introduced
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Summary: H.R.3015 — 112th Congress (2011-2012)All Information (Except Text)
Introduced in House (09/22/2011)
Pediatric, Adolescent, and Young Adult Cancer Survivorship Research and Quality of Life Act of 2011 - Amends the Public Health Service Act to require the Secretary of Health and Human Services (HHS) to make grants to eligible entities to establish pilot programs to develop, study, or evaluate model systems for monitoring and caring for childhood cancer survivors.
Requires the Secretary to convene a Workforce Development Collaborative on Medical and Psychosocial Care for Pediatric Cancer to establish a plan to meet specified objectives relating to medical and psychosocial care workforce development, including: (1) disseminating to health care educators information relevant to providing medical and psychosocial services to persons with pediatric cancers; (2) adapting curricula for continuing education of the existing workforce; and (3) strengthening the emphasis on psychosocial health care in educational accreditation standards and professional licensing and certification.
Reauthorizes and expands the National Cancer Institute's pediatric cancer research and awareness program to include research on: (1) pediatric cancer survivors within minority or other medically underserved populations, (2) health disparities in pediatric cancer survivorship outcomes, and (3) follow-up care for pediatric cancer survivors.
Requires the Secretary to make grants to eligible entities to establish and operate a clinic for comprehensive long-term follow-up services for pediatric cancer survivors.