Family Appeals for Support to Save 5-Year-Old Boy Diagnosed with Rare Lymphatic Condition

By Sasuk Taban

The family of five-year-old Isaac Kamba is appealing to the public for financial assistance to enable him to receive specialized medical treatment in India after he was diagnosed with lymphangioma, a rare congenital condition affecting the lymphatic system.

According to the family, Isaac has suffered from swelling of the tongue since birth due to the condition, which has made treatment difficult.

Lymphangioma, also known as a lymphatic malformation, is a rare, non-cancerous condition caused by abnormalities in the lymphatic system. It is usually present at birth or develops during early childhood and commonly appears as fluid-filled swellings on the head or neck.

Isaac’s mother, Esther Hanan, said she has sought treatment for her son at several health facilities, including Usratuna Hospital, Freedom Hospital, Egyptian Hospital, Chinese Hospital, Al-Sabah Children’s Hospital, and Juba Teaching Hospital, but his condition has not improved.

“My son was diagnosed with lymphangioma at Juba Teaching Hospital and was referred to India for specialized treatment,” she said.

She explained that Isaac has been referred to Aarav Medicare Hospital in India, where the estimated cost of treatment is US$25,000.

Isaac’s aunt, Lily Arize, said the amount covers medical investigations, treatment, accommodation, feeding, and other related expenses during the child’s stay in India.

She added that the treatment and recovery period is expected to take approximately 38 days.

The family is appealing to well-wishers, humanitarian organizations, and members of the public to support Isaac’s treatment.

Those wishing to contribute can contact the family through the following numbers:

0929 111 554

0981 444 147

0921 505 496

E-mail: ariyelilyizi@gmail.com