Living Life Fulfilled
we believe that children and families affected by Inherited Genetic Diseases (IGDs) deserve to live productive, fulfilling lives β regardless of where they are born. We work to raise awareness, expand access to quality health care, and nurture holistic character development for every child impacted by genetic disease.
Why We Care
𧬠Attention
Inherited Genetic Diseases (IGDs) often receive little attention within health care systems, leaving many children undiagnosed or untreated. We work to shine a light on these hidden challenges.
π Access
Even with global advances in genetic medicine, children in low-income regions still struggle to access care. TJI bridges this gap through partnerships, education, and advocacy.
π Aspiration
We believe that every child, regardless of background or condition, deserves the chance to live fully β to learn, play, dream, and contribute to their communities.
Our Work
We take a holistic approach to improving the lives of children and families affected by IGDs.

Awareness & Education
Promoting community understanding of IGDs through campaigns, workshops, and school programs.

Access to Health Care
Building partnerships with hospitals, genetic counselors, and health ministries to improve care delivery.

Character Development
Empowering children through mentoring, counseling, and skill-building programs that foster confidence and resilience
Driven by Compassion. Guided by Science. Inspired by Hope.
Founded in 2022, The Jason Initiative (TJI) is a non-profit organization born out of a deep conviction that no child should be left behind because of a condition they inherited.
We are committed to ensuring that children with Inherited Genetic Diseases β and the families who love them β can live meaningful, empowered lives through education, advocacy, and care.
βEvery child should grow up healthy and become a responsible citizen in his or her community.β
Understanding Inherited Genetic Diseases (IGDs)
Inherited Genetic Diseases (IGDs) are caused by changes (mutations) in a personβs DNA β the biological instructions that make us who we are. These mutations can pass from parent to child and may lead to various health conditions that affect physical, mental, or developmental well-being.
Common IGDs Include:
- Sickle Cell Disease β affects red blood cells, causing pain and fatigue
- Hemophilia β prevents normal blood clotting
- Cystic Fibrosis β causes lung and digestive system complications
- Down Syndrome β impacts development and learning
- Thalassemia β leads to low hemoglobin and anemia

Jude Anyati
Support Staff

Simon Edwonu
Support Staff

Catherine
Support Staff

Beatrice Ecuru
Support Staff
Become a volunteer
Get involved
Together, we can create a future where every child β no matter their genetic condition β has a fair chance at life.
- Volunteer: Share your time and talents.
- Donate: Help us fund life-saving initiatives.
- Partner: Join hands with us as a medical, educational, or advocacy partner.
