Shortly after Noemi was born, her parents noticed that she was unable to swallow milk due to a congenital tongue defect. To save her life, she was fed through a feeding tube, ensuring she received the necessary nutrition to grow and reach the age for critical medical intervention.

Now one year old, Noemi is experiencing speech delays and breathing difficulties caused by her condition. Her family is in a financially difficult situation and cannot afford the medical expenses required for her treatment.

She now urgently needs a genetic test (WES), which costs 500,000 AMD. Only after this test can doctors provide an accurate diagnosis and begin the appropriate treatment.

Support Noemi today, stand by her family, and help change the course of her life.