As we observe Congenital Heart Defect (CHD) Awareness Week (February 7-14), we celebrate the healing of Roida (7 years, 10 days old) and Ramadhani (1 year, 8 months old), who are now recovering after undergoing open-heart surgeries.

Their healing journey has taken almost a year since they were first diagnosed with Tetralogy of Fallot (TOF) at Mbeya Zonal Referral Hospital in early March 2024 during our free children’s heart camp with Atul Prabhu, a pediatric interventional cardiologist and electrophysiologist from India.

Tetralogy of Fallot (TOF) is a complex congenital heart condition consisting of four heart defects that occur together, affecting blood flow between the heart and lungs.

Due to the severity of their cases, we initially planned to send them to India for open-heart surgery. However, we faced several challenges, including family issues, regulatory processes, and financial constraints.

We are deeply grateful to the Embassy of Tanzania in India, which provided crucial support in navigating regulatory requirements. Our first hospital of choice could not assist due to policy limitations, requiring us to seek alternative options.

The family had to travel from Mbeya to Zanzibar and back, covering a driving distance of more than 566 miles, and finally to India for treatment. Despite all these, our dedicated team at The One New Heart Tanzania, in collaboration with Atul Prabhu, Ministry of Health Zanzibar, Ark Associates Ltd, Container Concepts Limited, TANZANIA RED CROSS SOCIETY and Narayana Health Bangalore, made every effort to ensure their successful treatment.

Their corrective heart surgeries were finally performed in January 2025, marking a significant milestone in their journey to recovery. Indeed, it always takes many hearts to heal one little heart.

Congenital Heart Defect Awareness Week is observed annually to promote education and awareness about congenital heart conditions. CHDs are among the most critical and costly conditions, affecting individuals throughout their lives.

In Tanzania, nearly 8 in 1,000 live births are affected by CHDs, making them the most common type of birth defect and a leading cause of childhood mortality.

Given the prevalence and severity of this condition, it is crucial to increase awareness among medical professionals, researchers, families, and the general public. Greater awareness leads to early diagnosis, better treatment options, and improved survival rates for children born with heart defects.

Let us continue working together to support children with congenital heart defects and ensure they receive the care and treatment they need to live healthy lives.