Three programmes, and the line between them.

Direct grants to patients, and to the hospitals and patient-support organisations treating them, against costs treatment alone does not cover: transfusions, chelation and other long-course medication, diagnostics, and travel to the centre that can treat the condition. Grants are made to institutions wherever possible, so the money is applied against an actual invoice rather than reimbursed after the fact.

Materials, and access to medical knowledge and resources, for patients, their families and the people caring for them. For chronic conditions the caregiver carries most of the management between clinic visits, and the quality of that management is decided by what they were given to work with.

Raising awareness of acute, chronic and life-threatening illness, and advocating for patient rights in underserved communities — including where a condition is common enough to be routine and still not resourced.

We are not a treatment provider and we hold no clinical facility. We do not fund research. We do not solicit or hold patient medical records. Where a grant supports a named patient, it is administered by the treating partner, not by us.