Huntington disease-a comparison between modern (allopathic) and Ayurvedic herbal treatment

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Die Huntington-Krankheit (HD), auch bekannt als Chorea Huntington, ist eine seltene, degenerative neurologische Erkrankung mit einer starken erblichen Komponente. Kinder mit einem betroffenen Elternteil haben eine 50-prozentige Wahrscheinlichkeit, die Krankheit zu erben. Die Symptome sind fortschreitender Natur und umfassen unwillkürliche, ruckartige Bewegungen, beeinträchtigte Muskelkoordination, Stürze, undeutliche Sprache, Schluckbeschwerden, Stimmungsschwankungen und Demenz. Die Symptome treten normalerweise im mittleren Alter auf, und der Tod kann zwischen zehn und dreißig Jahren eintreten. In seltenen Fällen können auch Kinder von einer juvenilen Form der Krankheit betroffen sein, die viel schneller fortschreitet als die Erkrankung im Erwachsenenalter. Die Basalganglien und die Hirnrinde sind die Teile, …
The Huntington disease (HD), also known as Huntington chorea, is a rare, degenerative neurological disease with a strong hereditary component. Children with an affected parent have a 50 percent probability of inheriting the disease. The symptoms are progressive in nature and include involuntary, jerky movements, impaired muscle coordination, falls, indistinct language, difficulty swallowing, mood fluctuations and dementia. The symptoms usually occur at middle age and death can occur between ten and thirty years. In rare cases, children can also be affected by a juvenile form of the disease that progresses much faster than the illness in adulthood. The basal ganglia and the cerebral cortex are the parts ... (Symbolbild/natur.wiki)

The Huntington disease (HD), also known as Huntington chorea, is a rare, degenerative neurological disease with a strong hereditary component. Children with an affected parent have a 50 percent probability of inheriting the disease. The symptoms are progressive in nature and include involuntary, jerky movements, impaired muscle coordination, falls, indistinct language, difficulty swallowing, mood fluctuations and dementia. The symptoms usually occur at middle age and death can occur between ten and thirty years. In rare cases, children can also be affected by a juvenile form of the disease that progresses much faster than the disease in adulthood.

The basal ganglia and the cerebral cortex are the parts that are most affected by the Huntington disease. The faulty Huntington gene produces abnormal triple dumplings, the sequence of which is repeated several times. Patients with HD have 36 or more repetitions (normal people have 26 or less); This causes the formation of an unusually large Hunting protein that is toxic and gradually causes a degeneration of the brain.

hd cannot currently be prevented or healed; However, several medications in modern (allopathic) system of medicine can help relieve the symptoms. Most medications work through the modulation of neurotransmitters, including Tetrabenazine and Duetetrabenazin. Useful medication also includes antipsychotics such as risperidone, olanzapine and haloperidol; Antidepressants such as citalopram, sertraline, fluoxetine and nortriptylin; and mood stabilizers such as lithium. In addition to medication, the long -term treatment of people with hunting tone includes graduated physical movement, correct nutrition and planned care.

In this scenario, the Ayurvedic herbal treatment of Huntington disease is of particular importance, since the treatment was observed as very effective within a short time. Treatment consists of oral drugs for regeneration and repair of damaged brain cells and to improve the function. Vegetable drugs that are well suited for Huntington treatment help to improve the metabolism, to reduce the faulty protein production and to reduce different nerve impulses due to the deposit of abnormal protein. All of this is aimed at the nerve and brain tissue (Majja).

Oral treatment is supplemented by special panchkarma techniques, including Shirobasti (medical oil that is kept in a cap on the scalp), Nasya (medical nasal drops), Sarvang Snehan and Swedan (full body oil massage with fomentation) and Basti (medical enema). These procedures are prescribed in combination courses; The medication used as well as the frequency and distance of the interventions can differ from patient to patient depending on the presentation and severity of the symptoms.

PANCHKARMA methods help reduce the number and dosage of oral drugs, which reduces the likelihood of long-term complications and increased compliance. The results are also faster and much more obvious; Patients with moderate or advanced symptoms can determine a significant improvement after only 7-14 treatment days! As soon as the symptoms have stabilized, further treatment can be planned as required, while the patient is carefully monitored in the long term. This reduces the treatment -free interval, which significantly reduces the financial burden and emotional stress for patients and nursing staff.

Ayurvedic herbal treatment therefore plays an important role in long-term treatment and management of Huntington disease.