Get Cutting Edge Medical Treatment for Muscular Dystrophy and Cerebral Palsy

Posted by eliteinternet on May 21st, 2018

Cerebral Palsy is a neurological condition which is caused by injury to the brain or a malformation while the brain is still developing. It affects muscle coordination and movement.  Children with Cerebral Palsy are children with impairment, but are still healthy. It is believed that the appropriate management of the Cerebral Palsy enables the individuals to live an active, quality and engaged lives.

There is no such Cerebral Palsy cure, but it can be managed. It is considered that finding a cure for Cerebral Palsy requires research on the following:

  • Understanding cause and causal pathways
  • Intervention measures to thwart brain injury and malformation
  • Preventing brain injury and brain malformation to occur
  • Repairing brain cells to restore function to the damaged areas of the brain.

It is believed that a research is carried upon, so as to ascertain, whether the damaged brain cells can be fixed or replaced. The avoidance of risk factors before conception, during pregnancy, and after birth helps them to prevent a child from Cerebral Palsy.

Every individual can be prone to Muscular Dystrophy especially if it is genetic. The Muscular Dystrophy doctors recommend treatments such as fetal stem cell therapy which will aid in relief from the pain and suffering of this illness.

Muscular Dystrophy is a group of diseases causing progressive weakness and the loss of muscle mass. There are numerous types of Muscular Dystrophy. Most of its symptoms begin well into childhood. The individuals, who have Muscular Dystrophy, lose their ability to walk. Some of the individuals face problems in swallowing and in breathing.

The main sign of this illness is progressive muscle weakness. There are therapies as well as medications which help in managing symptoms, as well as slow the course of the disease. It has been seen that Muscular Dystrophy occurs in all sexes, ages and races. The most common variety of the Muscular Dystrophy takes place in boys. The individuals with family background of Muscular Dystrophy have higher possibilities of having the illness.

Doctors who specialize in this condition begin with a physical examination and a medical history. After this the doctor may recommend the patients do the following:

  • Enzyme tests: Damaged muscles release enzymes.
  • Genetic testing: For some mutations, blood samples can be examined and testing for different types of muscular atrophy.
  • Lung monitoring tests: These tests are primarily used for lung infections.
  • Heart monitoring tests: Always recommended for close monitoring of function.
  • Muscle biopsy: A small piece of muscle is removed for intense examination.

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eliteinternet
Joined: February 13th, 2018
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