About Liverev

An emerging organisation with a large ambition.

Liverev is a Nigerian health group focused on improving care for Sickle Cell Disease (SCD). We are just getting started—and we are proud to be open about that.

People gathered during a Liverev community health activity

Our starting point

Build trust before building scale.

Liverev works with local communities, partner organizations, and people with sickle cell disease (SCD) to see what help is missing and test useful solutions.

Why we exist

Beyond diagnosis, the system offers little structured support for the transition from paediatric to adult care, limited local research infrastructure, and few pathways connecting warriors to innovation, funding or policy influence.

Liverev exists to close these gaps — not by duplicating what already works, but by identifying what's missing and building the connections that let existing efforts, new solutions, and the people they're meant to serve actually reach each other.

Our approach

We start from a documented gap, not an assumption. We test small, learn in public, and only scale what's demonstrated to work. We treat people living with SCD as partners and co-creators, never only as beneficiaries or research subjects.

We are honest about our current stage. Where a programme is still an idea, we say so. Where it's in early testing, we say so. We'd rather build trust slowly and accurately than appear more established than we are.

Liverev community outreach promoting sickle cell awareness

Liverev community outreach encouraging genotype awareness

Our current stage

What we've demonstrated so far

Community outreach

Two SCD/genotype sensitisation and testing outreaches held in 2026, including a World Sickle Cell Day event in Jikwoyi, Abuja, and a testing drive in Kurudu reaching 300+ people.

Collaborative support

Support for partner organisations including Hope at Dawn Foundation's Warriors' Voice conference, and participation in collaborative SCD activities with Beulah Sickle Cell Foundation and other Sickle Cell Foundations.

MySickleStory

An early research and evidence-generation initiative exploring lived experience and genotype awareness — the first demonstration of Liverev's research function.

Our principles

How we hold ourselves to account

Evidence over claims

We don't publish figures, partnerships or outcomes we can't verify. If a number isn't confirmed, it doesn't appear on this site.

People as partners

Warriors are never framed only as beneficiaries. They shape what we build, from needs assessments to programme design.

Alignment, not duplication

Where government or established frameworks already exist — such as paediatric-to-adult transition guidance — we work to strengthen access to them, not compete with them.