Eva is a joyful 6-year-old girl who loves learning, singing, drawing, and dreams of one day being able to walk. At just six months old, Eva was diagnosed with spinal muscular atrophy — a severe genetic condition that damages motor neurons, gradually weakening the muscles and making movement increasingly difficult.

As the disease progresses, it can lead to life-threatening respiratory and orthopedic complications, as well as difficulties with swallowing and eating.

In recent years, gene therapies and innovative medications have become available worldwide, making it possible to significantly slow down — and in some cases even halt — the progression of the disease when taken continuously. Eva needs the medication Evrysdi (Risdiplam), which costs 610,000 AMD per month. Unfortunately, her family cannot cover this expense on their own.

This year, Eva started attending school with great enthusiasm. She loves learning and shows excellent academic progress. Eva is the youngest child in her family and has two older brothers. One of them, already an adult, has the same condition and is no longer able to move due to complications of the disease.

Eva deeply needs all of our support.

Together, we have already managed to provide Eva with a six-month supply of her medication, but this condition requires continuous treatment.

Even the smallest contribution can become a new source of hope for her recovery. Let us help Eva take steps toward her dream of walking.