Support the Tanzanian Albinism Society

In Tanzania, 1 in every 1,500 people is born with albinism — one of the highest rates in the world. Albinism is a rare genetic condition characterized by an absence of pigmentation in the skin, hair, and eyes. Beyond the physical challenges of extreme sun sensitivity and visual impairment, people with albinism in Tanzania face severe social stigma, discrimination, and even violence rooted in harmful superstitions and witchcraft-related beliefs.

For decades, myths have circulated that body parts of people with albinism bring luck, wealth, or protection. These false and devastating beliefs have placed an already vulnerable community in danger — making albinism not just a genetic condition, but a daily struggle for safety and dignity.

Every child is born into the world cradled by a promise—that their life matters, deserving protection and freedom from fear. Yet in Tanzania, being born with albinism can mean living under constant threat of violence and persecution. Since 2000 there have been many violent actions against people with albinism, and additional murder cases. Driven by superstition and greed, brutal attacks against individuals with albinism reveal a tragic betrayal of humanity’s most fundamental promises.

Many children born with albinism are forced to live hidden indoors, excluded from education and community life. Without access to basic protective materials like sunscreen, hats, sunglasses, or long-sleeved clothing, they are exposed to life-threatening skin cancer at a young age. In rural regions, treatment is nearly impossible to access, turning a preventable condition into a deadly one.

This fundraiser supports the Tanzanian Albinism Society, a nonprofit organization based in Dar es Salaam that has worked tirelessly to promote safety, awareness, and equal rights for people with albinism. Funds raised will go directly toward providing essential protective items, education, and community outreach programs that allow children and families to live freely and safely.

The Tanzanian Albinism Society has the vision and dedication — but they need international support to make lasting change. Every contribution, no matter how big or small, helps protect lives, empower children, and bring visibility to one of the world’s most overlooked human rights challenges.

All funds will be collected through a US based NGO A-2nd-Chance and then transfer to Tanzania society through an NGO-to-NGO transfer.

Your generosity can help ensure that no child with albinism has to live in fear or isolation again.

Thank you for standing with the Tanzanian Albinism Society. Together, we can bring light, safety, and hope.

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