Genetic path of growth

Little Hlib needs help so doctors can understand the true cause of his condition and choose the right way to support his development. He has autism spectrum disorder, speech and communication impairments, and epileptiform brain activity. Doctors suspect a genetic cause and recommend whole exome sequencing – a complex but crucial test that the family cannot afford on their own.

When Hlib was born, his development seemed typical: he sat, walked, and explored the world on time. However, around nine months of age, he began to lose previously acquired skills – his first words disappeared, eye contact faded, and repetitive behaviors appeared. After many examinations and consultations, he was diagnosed with autism, and later EEG tests revealed epileptiform activity. An MRI showed no structural brain damage, which led doctors to suspect a genetic origin of his condition. Genetic testing can help identify the cause, guide personalized treatment and rehabilitation, and prevent the loss of valuable developmental time.

This fundraiser is not just about a medical test – it is about giving Hlib a chance to communicate, develop, and live a fuller life. By supporting this project, you help a little boy gain a chance to be heard in this world.