Little Alisa beat the disease

"Like you, she never will be", said the doctors for mom of little Alisa. She will soon turn 2 years old, but she still cannot sit, crawl, eat, drink, walk and talk. Crumbs broken fine and gross motor skills, the girl also suffers from metabolic disorders. Meal for Alisa – the real hard labor: she has never liked to chew the girl doesn't know how, she often vomiting and weakness, she's underweight... 

It is difficult to imagine how a small child cope with the condition. After many consultations with different doctors, it became clear why Alice is so suffering. In the third trimester of pregnancy the mother of Alisa the bad news: premature aging of the placenta, the child has hydrocephalus and agenesis of the corpus callosum.

After the birth Alisa was immediately placed in intensive care. The baby did not eat, she was vomiting from the slightest drop of mom's milk, she put a dropper, fed through a tube... then the girl was sent to the capital "OKHMATDYT", where she stayed for a month and a half, then they and the mother were discharged home. But the story is not over. Later, alyssa was diagnosed with cerebral palsy, and genetic damage.

Since 8 months, Alisa is undergoing treatment in specialized rehabilitation centres and practices at home, these classes significantly improve the girl's condition. However, the young family through financial hardship not enough money for new courses of treatment. We urge you all to support the one that the doctors didn't believe since birth. "Like you, she never will be", said once the doctors for the young mother of Alisa. And it's true, she's not much better! She wins! She just needs a little help.

Name: Kravets Alisa, 24.05.2018

City: Kyiv

Diagnosis: cerebral palsy, spastic tetraparesis; duplication of the short arm of chromosome 8; agenesis of the corpus callosum, cerebellar worm hypoplasia; gastroesophageal reflux