Comron has undergone radiation therapy. Thank you for your help!

Comron has a rare genetic disorder called neurofibromatosis. Multiple tumours in his body squeeze nerve endings. This can lead to loss of hearing, vision, walking skills. It all depends on where the tumour forms. There is a risk of malignancy. It is still impossible to completely cure the disease, but it is possible to eliminate the symptoms of pathology and prevent the development of complications. It is important to carry out treatment in time. Last year Comron began to complain that he could see worse. The left eye became noticeably more bulging. His parents went to the doctor. Unfortunately, they were unable to help the boy at home in Tajikistan. His father brought his son to Russia to see more experienced specialists. The Foundation helped Komron undergo his first course of radiation therapy this spring. Doctors at the Burdenko Neurosurgery Centre managed to reduce the size and growth of the ocular nerve neoplasm. The boy could have gone blind, but thanks to the treatment his vision was preserved. Now the nine-year-old boy needs our help again. The growth of the tumour in the ear canal threatens hearing loss and other serious complications. Despite the seriousness of the disease, Comron is not discouraged. He goes to school, watches cookery shows and dreams of becoming a chef. To make his dream come true, he needs our support. Treatment for Komron, as for a foreigner, is only paid. Dad works as a loader and his salary is enough only for the essentials. The family really needs help in paying for the treatment!