named programs · 2 · from sources
What they call their work
End-of-Life Research Initiative
Conducts scholarly research on legal, ethical, and medical aspects of end-of-life care and decision-making
Public Education Campaign
Provides educational resources to the public on patient rights, advance directives, and healthcare autonomy
activities · 1 group
What they do
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Palliative and End-of-Life Care Education 2 activities
- Conducts research on end-of-life issuesEngages in research focused on end-of-life care and decision-making to inform policy and practice around patients' rights.
- Public education on patients' rightsProvides educational initiatives to raise public awareness and understanding about patients' rights, particularly in the context of end-of-life care.
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financials · form 990 · fy2024
revenue
Total revenue$2.25M
Contributions & grants$2.25M100%
Program service revenue$00%
Investment income$500%
Other revenue$0
expenses
Total expenses$1.23M
Program expenses97%
Admin / overhead1%
Fundraising2%
Salaries & benefits$0
Grants paid out$761K
Largest expense lineProfessional Fees
balance sheet
Total assets$1.31M
Cash$1.31M
Investments$0
Liabilities$63K
Net assets$1.24M
Liquid reserves12.7 mo
4 years on record · 2020–2024 · YoY revenue +31.3%
leadership · form 990 part vii · fy2024
Who runs it
paid leadership · 1
| Name | Title | Hours/wk | Compensation |
|---|---|---|---|
| MATTHEW VALLIERE | EXECUTIVE DIRECTOR | 20 | $157K |
board members · 8
- DR ALAN CARVER — DIRECTOR
- FREDERIC CLARK — TREASURER
- FREDERICK J WHITE MD — SECRETARY
- GREGORY PFUNDSTEIN — CHAIRMAN
- MARIA ALVARADO — DIRECTOR
- MARTHA REICHERT — DIRECTOR
- MOLLY PERRY — DIRECTOR
- SHERMAN GILLUMS — DIRECTOR
strategies · 1
How they approach the work
Named approaches extracted from this org’s sources. Where others share an approach, follow it to see the full set of orgs running it.
- Research and Public Education on Patient Rightsmethodology: research_and_public_educationBy conducting research on end-of-life issues and coupling it with public education, the organization advances patient rights because informed public discourse leads to greater awareness, policy change, and individual empowerment in healthcare decision-making.