Category: Mental Health

March 15, 2023

Hypokalemic Periodic Paralysis Treatment By Herbal Remedies

ABSTRACT

Hypokalemic periodic paralysis is a genetic condition that is associated with muscle weakness and paralysis. Genetic condition comes into context when someone inherits an altered gene from their parents and there is an increase in developing that particular condition too in them. Genes are the proteins in the body that play an important role in transferring any kind of information in the body that is needed to control the body’s growth, development and functioning. So if there is a defect in any of the genes then the definite thing is to develop any condition in the body. Many conditions run into the families and one of them is Hypokalemic Periodic Paralysis. Now we are going to discuss in this article about this condition in detail and the management of this particular condition with the help of ayurvedic remedies.

Hypokalemic Periodic Paralysis

INTRODUCTION

Hypokalemic periodic paralysis, a condition associated with low levels of potassium and includes episodes of severe muscle weakness that generally begins in childhood or at the adolescent age. Mostly these episodes include temporary inability in moving muscles of the arms and legs. There are several attacks almost every day. Particularly this condition occurs rarely but is considered as very severe in nature. Although the exact prevalence of this condition is unknown, hypokalemic periodic paralysis has an estimate to affect 1 in 100,000 people. Men are more prone to experience the symptoms of Hypokalemic periodic paralysis than women. To know more let’s study the causes and symptoms of Hypokalemic periodic paralysis.

CAUSES

It is one of the genetic disorders in which there is a mutation in the gene named CACNA1S and SCN4A. These are the essential genes that provide command for making proteins which play an important role in the skeletal muscles for maintaining their functions. The normal movement of the body is conducted by contraction and relaxation of the skeletal muscles in a coordinated way. The contraction of the muscles are activated by flow of some positively charged ions in the muscle cells. Both the previously mentioned genes form channels which control the flow of that positively charged ions. The CACNA1S transports the calcium ions and the channels of SCN4A helps in transporting the sodium ions. If the mutation occurs in both the genes they alter the functioning and structure of sodium and calcium channels. Thus causes alteration in the contraction of the skeletal muscles which alters the movement of the muscles and leads to the severe muscle weakness and paralysis in episodic periods which is known as hypokalemic periodic paralysis.

SYMPTOMS

As it is a genetic disorder the one who suffered from this condition may experience the symptoms at the age of 10-14 years. The periods occur randomly and get more triggered by some factors like exercise, food items etc. After waking from sling time sleep it’s very habitual to experience. The severity of the attacks vary from forbearing muscle weakness to remarkable paralysis. The episodes may last between several hours to several days and their frequency also varies from human to human. Some of the humans may experience the episodes daily and some may experience a few times a year. With the growing age the episodes of paralysis become fewer and are known as abortive attacks which refers to general weakness that lasts for a longer period of time. Beside all this one may experience the following symptoms:

  • Weakness in muscles
  • Cramping in muscles
  • Heart palpitations
  • Most oftenly the muscles involved are shoulders, arms, legs and hips
  • Paralysis

DIAGNOSIS

This condition is even hard to diagnose as there is not such specific test for this condition. Also we cannot diagnose this condition with the symptoms rather the attack will occur. So if any of you may experience the significant symptoms of Hypokalemic periodic paralysis then it’s a must to visit the physician nearby. The physician will ask you your symptoms, at which time you may experience the symptoms and after that the diagnosis may be clear but it’s difficult to diagnose. If someone have family history then the diagnosis is more clear and at the time of diagnosis if someone experience symptoms then the following diagnostic techniques may be done to clarify the diagnosis:

  • Blood tests for potassium levels
  • Examination of muscle reflexes if they are reduced
  • Electrocardiography if a patient may experience any symptoms related to heart

So above mentioned are some of the diagnostic steps that a physician may perform to diagnose Hyperkalemic periodic paralysis.

AYURVEDIC VIEW

As we read earlier the condition is hereditary and there is a mutation in the genes named CACNA1S and SCN4A. As per ayurveda the hereditary condition is correlated to beej dushti, so let’s discuss what beej dushti is? Beej dushti is the defect in beejbhaga that is the sperm and ovum. Ashuddha shukra (defected sperm) and ashuddha artava (defected ovum) are the main causes of beej dushti. If there is any defect in the gametes (sperm and ovum) of parents then the child should inherit the disease. If we see on the side of dosha pacification then there is the vitiation of vata dosha as it is responsible for any movement and functioning control in the body. Hypokalemic Periodic Paralysis is a genetic condition so we should not cure it but will manage the symptoms of this condition with certain herbal remedies and improve the quality of the patient.

HERBAL REMEDIES BY PLANET AYURVEDA FOR MANAGING HYPOKALEMIC PERIODIC PARALYSIS

Planet Ayurveda is a GMP certified clinic which formulates various herbal supplements for maintaining the overall health as well as alleviating any kind of health issue. The formulations produced by Planet Ayurveda are produced under the strict observance of M.D. Ayurveda practitioners. All the herbal supplements are free from any kind of preservatives, additives, fillers, color, starch, resins and other synthetic material. For the purpose of managing the symptoms of Hypokalemic Periodic Paralysis Planet Ayurveda provides 7 herbal remedies that we will discuss further in detail.

  1. RASARAJESHWAR RAS
  2. ASHWAGANDHAGHAN VATI
  3. MUSLI STRENGTH CAPSULES
  4. GANDHAK RASAYAN
  5. AMRIT KALASH
  6. BRAHMA RASAYAN
  7. GREEN ESSENTIALS

PRODUCT DESCRIPTION

1. RASARAJESHWAR RAS

Ras Rajeshwar Ras is an ayurvedic formulation that has been used for maintaining the health of the nervous system. It consists of ingredients like swarna yukta rasraj ras, ashwagandha (Withania somnifera), guggul (Commiphora mukul) and some others. The ingredients of this formulation contain miraculous vata pacifying balya (strengthening) properties. Due to its properties Rasarajeshwar Rasa aids in promoting the normal functioning of the nervous system as well as strengthening the weakened muscles in case of Hypokalemic Periodic Paralysis.

Dosage: 1 tablet twice daily to be chewed.

2. ASHWAGANDHAGHAN VATI

Ashwagandhaghan vati is a formulation by Planet Ayurveda which is available in tablet form. These herbal tablets consist of Ashwagandha herb (Withania somnifera) that is an effective adaptogenic herb in nature. The adaptogenic properties of ashwagandha helps in reducing stress in the body which further prevents the damage at cellular level. So for preventing the damage of muscle cells Ashwagandhaghan vati is useful in the management of Hypokalemic Periodic Paralysis.

Dosage: 2 tablets twice daily with plain water after meals.

3. MUSLI STRENGTH CAPSULES

Musli Strength Capsules by Planet Ayurveda is a herbal remedy which consists of the standardized extract of two herbs that are safed musli (Chlorophytum borivilianum) and gokshura (Tribulus terrestris). The capsules consist of various properties such as antioxidant, adaptogenic, strengthening, immune boosting and rejuvenating. All these properties make these herbal capsules effective in managing the symptoms of Hypokalemic Periodic Paralysis. It strengthens the weak muscles, promotes the functioning of the skeletal muscles, prevents the degeneration of the skeletal muscle cells as well as prevents from the stage of paralysis.

Dosage: 1 capsule twice daily with plain water after meals.            

4. GANDHAK RASAYAN

Gandhak Rasayan is an ayurvedic formulation that is formulated by Planet Ayurveda under the strict observance of M.D. Ayurveda practitioners. It consists of shuddha gandhak (purified sulphur) which has been used since ancient times in the field of ayurveda for managing several disorders. It is a natural immunity booster, so by boosting the immunity levels this remedy assists in alleviating the muscle weakness associated with Hypokalemic Periodic Paralysis.

Dosage: 2 tablets twice daily with plain water after meals.

5. AMRIT KALASH

Amrit kalash is an ayurvedic formulation that is one of the best rasayana (rejuvenators). Rasayana are the ones that are believed to enhance the resistance of the body towards various infections as well as diseases. Rasayana are considered as effective in enhancing the longevity of life by promoting overall health. Amrit kalash promotes nervous health by pacifying vata dosha and helps in promoting the functioning of skeletal muscles. This rasayana formulation alleviates the weakness of muscles by increasing the reduced contraction, so it is quite effective in the management of Hypokalemic Periodic paralysis.

Dosage: 1 tsp twice daily with plain water after meals.  

6. BRAHMA RASAYAN

Brahma Rasayan is one of the best ayurvedic health supplements which is available in lehya (jam) form. Usually this ayurvedic health supplement is used in various nervous disorders and associated conditions such as anxiety, cognition issues, lack of concentration, etc. As in case of hypokalemic periodic paralysis there is the reduction of contraction of skeletal muscles which leads to their weakness and if not treated later on leads to paralysis of skeletal muscles. The consumption of Brahma Rasayan increases the contraction of skeletal muscles which further reduces the weakness in the muscles.

Dosage: 1 tsp twice daily with plain water twice daily.

7. GREEN ESSENTIALS

Green essentials is a herbal remedy formulated by Planet Ayurveda in capsule form under the observance of M.D. Ayurveda practitioners. These capsules are polyherbal and consist of standardized extracts like grape seed (Vitis vinifera), wheat grass (Triticulum aestivum), spirulina (Spirulina platensis) and some others. These capsules are considered as one of the best immunity booster due to mention of ingredients. Also the antioxidant properties present in these capsules prevent the damage of nerve cells and muscle cells which further prevents paralysis of the skeletal muscles.

Dosage: 2 capsules twice daily with plain water after meals.

CONCLUSION

CONTACT PLANET AYURVEDATO PROVIDE YOU THE COSTING / ORDERING AND DELIVERY INFORMATION AT – COSTING.PLANETAYURVEDA@GMAIL.COM OR CALL AT +91-172-5214040

Hypokalemic periodic paralysis, a condition associated with low levels of potassium and includes episodes of severe muscle weakness that generally begins in childhood or at the adolescent age. It is one of the genetic disorders in which there is a mutation in the gene named CACNA1S and SCN4A. In this case a person may experience weakness in muscles, cramping in muscles, heart palpitations, most oftenly the muscles involved are shoulders, arms, legs and hips and at last paralysis. As per ayurveda the hereditary condition is correlated to beej dushti in which there is a defect in beejbhaga that is the sperm and ovum. Don’t worry the condition is manageable with ayurvedic medications and for this purpose Planet Ayurveda provides various herbal remedies that are free from any kind of additives and preservatives. So without worrying you can start taking treatment from Planet Ayurveda and while consuming remedies if you have any query then you can share your query on www.PlanetAyurveda.com

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January 17, 2023

Fragile X Syndrome – Ayurveda Herbal Treatment

Herbal Remedies for Fragile X Synndrome

Abstract

Fragile X syndrome is an inherited genetic disease which is passed down from parents to children which causes developmental and intellectual disabilities. Fragile X syndrome is also known as Martin-Bell- syndrome. Fragile X syndrome is the genetic condition which causes a range of developmental problems which includes cognitive impairment and also includes learning disabilities. Commonly, males are more prone than females. Most of the males with this disease have mild to moderate intellectual disability and about one-third of affected females are intellectually disabled. Let’s discuss this disease in detail.

Introduction

Fragile X syndrome is the genetic condition involving changes in a person’s X chromosome which triggers several developmental challenges such as cognitive impairment and learning disabilities. Children with fragile-X syndrome may include anxiety and hyperactive behaviour such as impulsive actions and fidgeting. The disease is caused by the reduction of expression of fragile X mental retardation protein and also associated with the variety of behavioural, medical and physical problems which are managed through the supportive treatment. Fragile X syndrome is an X-linked disorder which affects approximately 1 in 4000 males and females. The disease in Ayurveda is correlated with the Beejja dushti (ova and spermatozoa). In Fragile X-syndrome during fertilisation, all Tridoshas (Vata, Pitta and Kapha) are aggravated in which Vata dosha mainly vitiates and  results in this disease.

Fragile X Synndrome

Facts

  • It is a genetic disorder and causes developmental and intellectual disabilities.
  • Fragile X syndrome is also known as Martin-Bell syndrome.
  • This disease in Ayurveda occurs due to Beejha dushti (dysfunction of sperm and ovum), in which Vata dosha mainly aggravates.

Sign and Symptoms of Fragile X Syndrome

  • Seizures
  • Difficulty in sleeping
  • Hyperacidity
  • Impulsiveness
  • Stuttering
  • Autism
  • Attention difficulties
  • Depression
  • Anxiety (both social and general)
  • Developmental delays: Taking longer time to talk,walk and sit
  • Social issues like: Disliking being touched and not making eye contact with others.

Some People with Fragile X Syndrome Also Includes Physical Abnormalities

  • Flat feet
  • Elongated face
  • Protruding ears, chin and forehead
  • Flexible or loose joints
  • Large ears and forehead with prominent jaw

Causes of Fragile X Syndrome

Fragile X syndrome is mainly caused by the change to the gene on X-chromosome called FMR1 GENE. The gene produces protein which helps the brain to function normally. If the gene is altered or changed in any way then, it can not produce its normal protein, which may result in Fragile X syndrome.

Diagnosis

In the diagnosis of Fragile X syndrome the main diagnosis is:

Blood test

DNA testing : This  procedure is recommended for:

  • Women or Men over 50 with balance or gait problems, dementia or tremor.
  • People who have a history of Fragile X syndrome or intellectual disability.
  • Women with problems of early menopause and fertility.
  • Women with family history of primary ovarian insufficiency.

Management of Fragile X Syndrome

The disease is not completely treated but the symptoms and condition of Fragile X syndrome can be managed. The management of this disease includes sensory integration, special education, speech therapy, occupational therapy and behavioural therapy. Some of the medications are used in different conditions which includes: Anticonvulsants are used to control seizures, antidepressants are helpful in mood disorders, anxiety and in obsessive compulsive disorders. Antipsychotic helps in, if there’s a presence of aggressive behaviours or self-injury.

Ayurvedic Overview Of Fragile X Syndrome

Fragile X syndrome is a genetic disorder and also known as Martin -Bell syndrome. As we all know that Ayurveda is a science which has the capability to manage all types of diseases. The disease occurs due to genetic disorder and in Ayurveda all the genetic disorders occur due to the Beeja dushti (which means injury or damage to sperm or ova). In genetic disorders all three doshas are vitiated during fertilisation but in this disease aggravation of Vata dosha mainly occurs, which results in fragile X syndrome. During fertilisation shukra and shonita (sperm and ovum) vitiated because of aggravated tridoshas and later on domination of Vata dosha results in Fragile X syndrome. The disease is genetic and hence can not be diagnosed properly but symptoms of this disease can be managed by taking the remedies which are given below:

Herbal Remedies For Fragile X Syndrome By Planet Ayurveda

Planet Ayurveda offers best herbal remedies for Fragile X syndrome by which the symptoms of the disease can be managed. This disease is not prevented properly but symptoms of the disease are manageable. These formulations have their great results in controlling the symptoms of  Fragile X syndrome and these remedies also boost the immune system of the body. All the herbal remedies are formulated under MD Ayurveda experts and have no side effects. The formulations did not contain any type of chemicals, colours, dyes and preservatives etc.

Product List:

  1. VAT GAJANKUSH RAS
  2. TELOMERE BOOSTUP
  3. CURCUMIN 95%
  4. BRAHMI VATI GOLD
  5. KUMAR KALYAN RAS
  6. ASHWAGANDHADI GHRIT

Product Description

1. VAT GAJANKUSH RAS

Vat Gajankush ras has its nice results in this disease, the formulation balances the aggravated dosha. Ingredients involved in this formulation are: Shuddha haratala (Arsenic trisulphide), Long pepper (Piper longum), Shrungi (Citrullus colocynthis), Black pepper (Piper nigrum), Juice extract of Nirgundi (Vitex negundo) and  Juice extract of Mundi (Sphaeranthus indicus) etc. Vat Gajankush ras pacifies the aggravated Vata dosha and is effective in neurological health.

Dosage: 1 tablet twice daily with plain water after meals.

2. TELOMERE BOOSTUP

Telomere boost up mainly functions on and stops its accumulation. This formulation includes ingredients :Giloy (Tinospora cordifolia), Amla (Emblica officinalis), Grapeseed (Vitis vinifera), Moringaii (Moringa oleifera) and Ashwagandha (Withania somnifera). In Fragile X syndrome this formulation maintains the overall health of the body and increases immunity.

Dosage: 1 capsule twice daily with plain water after meals.

3. CURCUMIN 95% CAPSULES

This formulation helps in overall health of the body The main ingredient of this capsule is Haridra std. Ext. (Curcuma longa 95% CStd. Ext.). It helps in pacifying of Vata dosha and also useful in neurological problems. As per ancient texts it is an amazing antiseptic and antiviral in nature.

Dosage: 1 capsule twice daily with plain water after meals.

4. BRAHMI VATI GOLD

Brahmi vati gold is an classical formulation and ingredients involved are: Laung (Syzygium aromaiculum), Dalchini (Cinnamomum verum), Saunf (Foeniculum vulgare), Akik bhasma and Manikya bhasma etc.This formulation is very useful fragile X syndrome and works on depression, anxiety and other conditions.

Dosage: 1 tablet once daily with plain water after meals.

5. KUMAR KALYAN RAS

Kumar kalyan ras is very useful to boosts up the immunity, ingredients of this formulations are: Abhrak bhasma (Bhasma of purified Mica ), Makshika bhasma (bhasma prepared from iron), Ras-sindoor (Shuddha parda), Kumari rasa (Aloe-vera extract juice) and Loha bhasma (Bhasma prepared from iron) etc. The formulation works on the healthy neurological condition and maintains overall health.

Dosage: 1 tablet twice daily with plain water after meals.

6. ASHWAGANDHADI GHRIT

This formulation is very effective in neurological conditions, in Ashwagandhadi ghrit the ingredients involved are: Bhibhitaki (Terminalia bellirica), Cow’s milk and Ashwagandha (Withania somnifera) etc. The formulation is useful in general weakness and gives strength to the body.

Dosage: ½ tsp twice daily

Contact Planet Ayurveda Support Team to provide you the costing/ordering and delivery information at – costing.planetayurveda@gmail.com or Call at 0172-521-4040 (India), +91-172-521-4040 (Outside India) or Whatsapp at (+91) 842-749-4030.

CONCLUSION

Fragile X syndrome is the genetic disorder which causes a range of developmental problems which includes cognitive impairment and also includes learning disabilities. The disease is not completely preventable but symptoms of the diseases are manageable. In Ayurveda the disease occurs due to Beeja dushti (dysfunction in ovum and sperm), during fertilisation tridoshas are vitiated and laterally Vata dosha mostly aggravates which results in Fragile X syndrome. In simple words the dosha which is mostly aggravated during the process of fertilisation results in this particular disease. So Planet Ayurveda offers best remedies for this disease which manages the symptoms of the disease. This disease is not completely preventable but we can manage the symptoms of the diseases by taking these formulations, which are pure, natural and have no side effects.

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