Milana Pshenko

Milana Pshenko is a young girl diagnosed with severe spinal muscular atrophy (SMA) type I. Her condition was identified at just two months old, and her parents fought tirelessly to raise $2.2 million for the life-saving gene therapy Zolgensma. Following the treatment, Milana has shown remarkable progress, developing new skills such as sitting independently and beginning to speak, showcasing her strength and determination.