Offer dietary tips for children with cerebral palsy

My daughter is 1 year and 5 months old and has been diagnosed with hypotonia-type pediatric cerebral palsy, accompanied by language disorders, drooling, inability to sit or stand independently. She also has strabismus and various symptoms. How should pediatric cerebral palsy be treated?

Treatment and Genetic Issues Related to Pediatric Cerebral Palsy

The treatment of pediatric cerebral palsy primarily focuses on rehabilitation training, combined with appropriate surgical intervention at the right time, and enhanced nutrition, especially the intake of proteins and vitamins, to promote brain development and strengthen the body’s resistance.

Pediatric cerebral palsy is a non-progressive condition that can be improved and developed through active treatment. In most cases, cerebral palsy does not inherit to offspring unless there is a family history of spasmodic paraplegia in the parents. However, the occurrence of cerebral palsy is related to various factors, including infections during pregnancy, maternal diseases, neonatal asphyxia, and neonatal jaundice, among others. Therefore, it is recommended to seek active treatment in the hospital as early as possible.

Explore the genetic aspect of pediatric cerebral palsy, offering professional medical insights to help parents understand the causes of the disease.

Hello, I would like to know if your hospital has effective treatment methods for pediatric cerebral palsy. Could you assist me, please?

How to identify the symptoms and manifestations of early pediatric cerebral palsy?

Understanding the Early Signs of Pediatric Cerebral Palsy

Early symptoms of pediatric cerebral palsy include hyperirritability, feeding difficulties, sensitive reactions, and motor abnormalities.