Eva has ichthyosis. To protect her skin, she needs a special product

Eva, her dad and brother live in Simferopol. Eva was born in a cocoon, a thick film over her skin. She was born prematurely and this, according to the doctors, saved her. If the birth had been on time, the film would have turned into an impenetrable shell, and the girl would not have survived. Such people are called fish. They are born with scaly skin, which is constantly itching and peeling. There is no cure for ichthyosis, the disease is genetic. Due to a breakdown in the genes, the epidermis is disrupted, the skin is unable to retain moisture. Patients with ichthyosis do not receive any therapy from the state, because moisturizers are not considered medicinal products. Eva needs to take a bath with moisturizing oil three times a day, treat her skin and apply a special milk, Topicrem. He's the only one helping her. It is necessary to constantly monitor well-being, patients with ichthyosis do not sweat, they can overheat, especially in hot weather. And then the temperature will rise instantly. Eva needs 20 jars per month. Let's help together!