Six-year-old Eva is a joyful little 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 (SMA) — a severe genetic disease that damages motor neurons, causing muscle weakness and gradually making movement more 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, the world has gained access to innovative gene-therapy treatments and new-generation medications that can significantly slow — and in some cases even halt — the progression of SMA when taken long-term.
Eva urgently needs the medication Evrysdi (Risdiplam), which costs 610,000 AMD per month. Her family cannot afford this treatment on their own.

This year, Eva has joyfully started school. She loves learning and is showing excellent progress. She is the youngest child in the family and has two older brothers. One of them, now an adult, has the same condition and can no longer walk due to severe complications.

Eva truly needs the support of all of us.
Even the smallest contribution gives her a new hope for healing.

Let’s help Eva take a step closer to fulfilling her dream — the dream of walking.