Deputy Minister of Health, Dr. Florence Samizi, has urged Tanzanians to abandon stigma and support people living with epilepsy, noting that many patients struggle to get help from their families and communities. This lack of understanding often delays treatment, leading to worsened health outcomes.
Dr. Samizi made the remarks today, February 6, 2026, during World Epilepsy Day celebrations at Muhimbili National Hospital (MNH).
She said the Ministry of Health is developing guidelines and procedures to ensure that epilepsy patients live in safe, supportive, and dignified environments.
“Globally, nearly 50 million people live with epilepsy, with six million new cases diagnosed every year, according to the World Health Organization (WHO). People with epilepsy face three times higher risk of death, and in Africa, the rates are four to six times higher. Over 80 percent of the global burden falls on low- and middle-income countries, including Tanzania,” Dr. Samizi said.
Acting Chief Executive Officer of MNH, Dr. Julieth Magandi, said stigma remains a major barrier, as some communities still believe epilepsy is caused by curses, witchcraft, or hereditary factors beliefs that are not true.
She emphasized that epilepsy is a medically treatable and manageable condition, and communities should provide patients with respect and the care they deserve.
Professor William Matuja, President of the Epilepsy Association of Tanzania, stressed that public education is key in the fight against epilepsy.
“When communities are properly informed, patients are more likely to seek early treatment and live normal, productive lives,” he said.
The event highlighted the need for increased awareness and societal support to ensure that epilepsy patients are treated with dignity and given timely medical care.