Ellada underwent a course of sanatorium treatment for ichthyosis!

Hellas is 22 years old. At the age of 2, the girl developed a rare genetic disease that greatly affected her health. Sulfatase deficiency with ichthyosis is the name of her disease. Medicine cannot offer a cure. It is only possible to maintain an acceptable quality of life and reduce the painful manifestations of the disease. The girl's musculoskeletal and nervous systems are damaged, and her internal organs are affected. Mom feeds her eldest daughter baby cereals and mixtures. The body does not perceive anything else. The skin damaged by ichthyosis turns into a painfully itchy, dry, cracking surface, similar to hard scales. From severe pain, burning and itching, as after a burn, only regular mud treatments, special peels and physiotherapy procedures are available outside the sanatorium. The family does not have the means to pay for sanatorium treatment. Hellas has a younger sister who has no one to leave with when her parents take Hellas for treatment. Let's take care of the family and pay for a sanatorium for Hellas, mom and sister.