Expanding Access to Community-Based Palliative Care

By Kristofer L. Smith, MD, MPP — Elea Institute Board Member

I recently joined colleagues from across the country, moderating a convening hosted by the Coalition to Transform Advanced Care (C-TAC) and sponsored by The John A. Hartford Foundation (JAHF). Our goal was to bring together industry leaders and identify concrete ways to measure and expand access to community-based palliative care. The conversations reinforced what so many of us know to be true, patient-centered serios illness care can improve outcomes for patients and families.

The gathering also reinforced Elea Institute’s daily mission to bolster hospice and palliative care on a national level, and ensure access is available to patients and caregivers.

Recognizing the Power of Community-Based Care

Throughout the discussion, I was struck by how often success stories came from local, community-driven models. When we meet patients where they are, care becomes more personal and effective. To continue broadening access and improving patient outcomes, states need the flexibility to adapt models that fit their populations, community resources, and workforce. At Elea Institute, this concept is the heart of our mission. We partner with local entities to fund community specific needs and pinpoint opportunities they need support.

A Path Forward

Expanding access to community-based palliative care requires collaboration across providers, policymakers, and communities. Elea Institute is actively engaged in the partnership efforts to convene industry leaders, both in the U.S. and beyond. Through our grants and relationships, Elea Institute aims to spark impactful conversations that result in tangible growth in the field.