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Working Together

How compassion is built together.

Co-design, transparency, consent, and shared discovery. The practice of compassionate research.

The future of compassionate care is not built by any one team. It is built by a community — clinicians, researchers, patients, families, caregivers, ethicists, and the organizations that hold them — working together with patience, honesty, and care.

The collaborations below describe how we work, not just what we work on. They are commitments, not capabilities. If your organization, institution, or community shares these commitments, we would welcome a conversation about what working together could look like.

Way 01

Clinical collaborations

Working alongside clinicians, nurses, social workers, and chaplains in active palliative care settings. Every clinical collaboration begins with listening to the people who do this work — and ends with what they ask for, not what we assume they need.

  • Co-design sessions with palliative care teams
  • Embedded observation (consented, anonymized)
  • Clinical advisory roles in every design decision
  • Outcome measurement developed with clinicians, not for them

Way 02

Research collaborations

Partnering with academic institutions, research networks, and methodologists. Research here is conducted in the open — protocols published before enrollment, findings published after, including what does not work.

  • Co-authored studies with university partners
  • Open-data sharing where consent permits
  • Pre-registered protocols and endpoints
  • Honest publication of null and negative results

Way 03

Community collaborations

Listening to the people this work is ultimately for — patients, families, caregivers, and the communities that hold them. Community voice is not an advisory layer. It is the foundation.

  • Lived experience advisory council
  • Community-led story sharing (consented)
  • Public review of every major design decision
  • Community representation in governance

Way 04

Ethics collaborations

Inviting independent ethicists, governance bodies, and patient advocates into every stage of the work. Ethics is not a checkpoint. It is a partner.

  • Independent ethics review of every model deployment
  • Patient advocacy representation in governance
  • Public publication of every ethics decision
  • Right of withdrawal honored within 24 hours

Our commitments

What every collaboration promises.

  • 01Every collaboration begins with listening — not presenting.
  • 02Every partner is credited openly for what they bring.
  • 03Every finding — positive or negative — is published.
  • 04Every participant can withdraw at any time, for any reason.
  • 05Every decision is documented and reviewable.
  • 06Every voice — especially the quietest — is heard.

Imagine what we could discover together.

Begin a collaboration