Aslifat has tuberous sclerosis. She needs rehabilitation for development.

Aslifat has tuberous sclerosis—a rare genetic disease. Her seizures began when she was eight months old. Based on the results of the MRT, we were diagnosed with TS. In addition to tubers in the brain, this disease affects the eyes, heart, and kidneys; fibromas appear on the face, and intellectual disability is observed. Every year, it is necessary to undergo an MRT, an EEG (every 6 months), tests for drug concentration, and other examinations. To overcome developmental delays, Aslifat urgently needs rehabilitation. However, the family's financial situation is difficult, and they cannot pay for this course on their own. Let's help Aslifat complete this important rehabilitation course!