Ayaulym is a joyful little girl from the small town of Aktobe, Kazakhstan. However, a congenital spinal condition—spina bifida—severely limits her mobility and progressively worsens her health. She urgently needs our help.

Ayaulym was born via a scheduled C-section. Her condition was diagnosed immediately after birth, as a lump was detected in her lower back. Doctors performed emergency surgery to remove it. Unfortunately, over time, her condition deteriorated. She began experiencing severe pain, which made it difficult for her to sleep, and her left foot became deformed. Rehabilitation sessions have provided some relief, but her condition continues to worsen.

At just five years old, Ayaulym still cannot walk. She can only move by crawling. While she can sit, she is unable to stand, and any physical activity causes her significant pain, forcing her to spend most of her time lying down. This has greatly impacted her physical development. She is also battling progressive scoliosis. The disease is mercilessly stealing her childhood, but there is hope—a chance to change her life and prevent permanent disability.

Israeli Professor Shimon Rochkind, a specialist in spina bifida treatment, is ready to perform micronurosurgical surgery on Ayaulym at Assuta Hospital. This procedure could stop the progression of her condition and preserve the functionality of her legs and pelvic organs.

Ayaulym is raised solely by her mother, as her father abandoned the family. It is impossible for her mother to raise the €52,440 needed for the surgery on her own. She desperately needs our support.

Please click the "Help" button and contribute whatever you can to help Ayaulym.
Together, we can сhange her life!