Sardal received his first batch of medication!

Sardal has hemophagocytic lymphohistiocytosis. It is a very rare and severe genetic disease. The child's immune system attacks and destroys blood cells and organs. There are just over 50 patients nationwide with this diagnosis. The boy has a chance for a full recovery. His father will be the donor of his bone marrow transplant. But the success of the operation depends on the condition of the child. To help his immune system protect his body instead of harming it, Sardal needs to be treated urgently with a drug called Emapalumab. According to doctors, treatment with this drug is so far the only way to save Sardal. The drug is produced abroad and is not registered in our country, which means that it cannot be bought with budget money. Full course of 50 bottles of the drug costs more than 12 million rubles, which is an unaffordable sum for a family with many children. Let's help the Abdievs family save their son! With your help we can buy one bottle of the drug for Sardal. Translated with www.DeepL.com/Translator (free version)