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Rare & Neglected Conditions

Working with communities facing chronic neglect to rethink access, research priorities, and care pathways.

Systemic Problem

Conditions are not only biologically rare or common; they are socially prioritized or neglected. Many diseases remain under-researched, underfunded, and poorly integrated into health systems, despite their heavy individual and collective burden. Neglect is produced by a combination of weak data infrastructures, low political visibility, fragmented care pathways, and limited patient representation.

Our Approach

We work with affected communities to redesign research priorities, data infrastructures, and care pathways. We treat neglect as a systemic phenomenon, not as an accident.

What We Build

Participatory disease observatories, equity-aware research infrastructures, patient-led registries, and evidence-generation tools.

Stakeholders

Patient organizations, clinical centers, public health authorities, researchers.

How We Evaluate

We assess not only clinical outcomes, but also visibility, inclusion, governance quality, and policy traction.

Collaboration

We collaborate with actors willing to rethink what counts as legitimate evidence and who gets to define research priorities.