The Coalition plays a key leadership role and is a member of several external broad based public policy initiatives that work to advance the access and quality of care for people with serious illness. Below is an example of the cross-cutting policy initiatives the Coalition currently supports.
The National Academies of Sciences, Engineering, and Medicine convened the Roundtable in 2016 in response to the ground-breaking and seminal report Dying in America Improving Quality and Honoring Individual Preferences Near the End of Life (hyperlink to report) which continue to influence health care policy for those with serious illness and at the end of life. The Roundtable fosters an ongoing dialogue about critical policy and research issues to accelerate and sustain progress in care for people of all ages with serious illness. The NCHPC Executive Director represents the Coalition on this Roundtable.
The National Academies of Sciences, Engineering, and Medicine – Roundtable on Quality Care for People with Serious Illness
Financing and Payment Strategies to Support High-Quality Care for People with Serious Illness
A Workshop | November 29, 2017
Featured Coalition members:
Edo Banach, JD, President and CEO, National Hospice and Palliative Care Organization (NHPCO)
Diane Meier, MD, Director, Center to Advance Palliative Care (CAPC)
The Patient Quality of Life Coalition was formed to advance the interests of patients and families facing serious illness, including survivors. The Coalition includes more than 40 nongovernmental organizations (providers, patient advocacy organizations, health systems and other external stakeholders) dedicated to improving quality of care and quality of life for these adults and children. The Coalition has developed a consensus-based agenda aimed at promoting public policy that will improve and expand access to high-quality palliative care. NCHPC Executive Director represents the Coalition on the Steering Committee of this broad based Coalition.
The State Pain Policy Action Network is an association of leaders, representing a variety of health care and consumer organizations and individuals, who work together in a cooperative and coordinated fashion to effect positive pain policy on the state level—policy that guarantees access to comprehensive and effective pain care for all people living with pain.
The Pain Care Forum is a coalition of diverse organizations with a stake in improving pain care. This group convenes monthly to discuss topics of concern in pain management, and foster consensus development and action when possible.