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How Does Our Spinocerebellar Ataxia Treatment Benefit You?

The brain sends commands to all of our muscles and joints. The cerebellum is a component of the brain that absorbs information from the body's senses and then "gives" commands to the other bodily parts. These commands are sent from the brain to the spinal cord, which then sends them to the muscles that control the movement. When the connection between the brain (cerebellum) and the spine is disrupted. These commands from the brain do not reach the muscles in a timely manner, causing movement to be disrupted. Furthermore, a person is unable to walk normally (ataxia). Spinocerebellar Ataxia or Cerebrospinal Ataxia is the collective name for this disorder.
This is just a case of a lack of coordination. Cerebrospinal Ataxia is a degenerative condition that is caused by a genetic mutation. It isn't age-related. This syndrome is caused by a few genes, both dominant and recessive. It frequently manifests as a lack of coordination in verbal, hand, and eye movement. It can even make automatic motions like swallowing difficult. Sub-acute ataxias, congenital ataxias, and chronic progressive ataxias are examples of ataxias that mimic cerebrospinal ataxia but have distinct etiology.
We give therapy for spinocerebellar ataxia, and it works. The major goal of treatment is to keep the illness from worsening so that the patient does not become disabled and has a good quality of life.

Understand how we can help you with Spinocerebellar Ataxia .

Spinocerebellar Ataxia

The brain sends commands to all of our muscles and joints. The cerebellum is a component of the brain that absorbs information from the body's senses and then "gives" commands to the other bodily parts. These commands are sent from the brain to the spinal cord, which then sends them to the muscles that control the movement. When the connection between the brain (cerebellum) and the spine is disrupted. These commands from the brain do not reach the muscles in a timely manner, causing movement to be disrupted. Furthermore, a person is unable to walk normally (ataxia). Spinocerebellar Ataxia or Cerebrospinal Ataxia is the collective name for this disorder.
This is just a case of a lack of coordination. Cerebrospinal Ataxia is a degenerative condition that is caused by a genetic mutation. It isn't age-related. This syndrome is caused by a few genes, both dominant and recessive. It frequently manifests as a lack of coordination in verbal, hand, and eye movement. It can even make automatic motions like swallowing difficult. Sub-acute ataxias, congenital ataxias, and chronic progressive ataxias are examples of ataxias that mimic cerebrospinal ataxia but have distinct etiology.
We give therapy for spinocerebellar ataxia, and it works. The major goal of treatment is to keep the illness from worsening so that the patient does not become disabled and has a good quality of life.

Types of Spinocerebellar ataxia:

Acquired ataxia: Vitamin shortages, trauma, alcohol and drug misuse, and cancer are all examples of acquired ataxia.

Genetic ataxia: Genetic Ataxia is caused by a malfunctioning gene. When this gene spreads across a family, it poses problems for future generations. Because these genes have an effect on the cerebellum and spine's nerve cells.

Idiopathic ataxia: Idiopathic ataxia occurs when you haven't inherited a defective gene or had an illness or accident that may have caused your ataxia.

Ayurveda on spinocerebellar ataxia:

All movement-related illnesses are classified as Vata Vyadhi in Ayurveda. Vata is in charge of coordinating. Because all smooth and precise actions require coordination. When Vata is exacerbated, it creates issues with coordination and movement.

Cerebrospinal ataxia causes the same problems with coordination. When Vata isn't acting properly, the coordination of the body's motions is disrupted, causing problems for the sufferer. In the context of cerebrospinal ataxia, there are two things to keep in mind concerning the Vata dosha:

  • Because Vata aggravation promotes decay, the decay with Vata aggravation is always on the upper side.
  • Controlling the disease's progression is also a constant challenge.

Treatment for spinocerebellar ataxia:

Ayurvedic remedies and treatments can be used to treat Cerebral & Cerebellar Ataxia / Atrophy. This management is referred to as Samana Chikitsa and Shodhana Chikitsa. Shodhana chikitsa involves Ayurvedic Panchakarma Treatments and Samana chikitsa covers maintenance with internal drugs and exterior applications.

Tremor, stiffness, spasticity, sleep difficulties, muscular weakness, and depression (or frustration, sorrow, and rage) can all be treated with specialized drugs, treatments, therapies, and counselling.

How can Ayurveda help in the genetic condition of cerebrospinal ataxia?

The answer can be found in Ayurveda's initial thinking. According to Ayurveda, we are all susceptible to all ailments. And in Ayurveda, this is referred to as Prakriti.
Prakriti is concerned with the body's genes and interior environment.
Epigenetics is a new field of medicine that is being discussed in modern medicine. Gene expression alone cannot produce a problem, according to this new knowledge of the body's genetic constitution, unless it is triggered by diet and lifestyle.
As a result, we usually advise patients with Cerebrospinal Ataxia to maintain their food and lifestyle limitations for the remainder of their lives.

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