Thanks to you Khalima has medicine and special nutrition.

Halima has a rare genetic disease called tyrosinemia. The body does not break down tyrosine, toxins accumulate and destroy the liver.

To save her life and health, Halima needs the drug Nidorfan, which blocks the formation of toxins, and a specialized TYR Anamix Infant formula — it completely replaces regular milk, which is dangerous with this diagnosis.

The family has already overcome the first difficulties thanks to the help of loved ones, but they cannot continue to cope with expensive treatment on their own. Mom is on maternity leave, Dad is a soldier.

We've already helped Halima before, but we're running out of supplies. Therefore, we have opened a collection to purchase medicine and food for Halima. Please support the family — this is a chance to keep the child healthy.