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Cystic Fibrosis Treatment

Overview

Studies suggest that the incidence of CF in India is lower than in many other countries, with an estimated incidence of 1 in 30,000 to 1 in 100,000 live births. In India, CF has been reported in various populations, including individuals of European, Indian, and mixed ancestry.

Cystic fibrosis (CF) is a genetic disorder that affects the cells that produce mucus, sweat, and digestive juices. People with CF have a defective gene that causes a buildup of thick, sticky mucus in the lungs, pancreas, and other organs. This can lead to serious health problems such as lung infections, difficulty breathing, digestive issues, and malnutrition.

Ayurvedic treatment of cystic fibrosis focuses on working on the root cause of the disease and reduces persistent cough and shortness of breath. Ayurvedic treatment also focuses on the adverse symptoms such as salty skin and infertility. Ayurved improves the quality of life by treating the disease and has no side effects.

Research

Jain’s cow urine therapy clinic aims for a happy and healthy life by integrating ancient Ayurvedic knowledge with modern technology. Our therapy means cow urine including Ayurveda works on a person’s three doshas that are- The Vata, Pitta, and Kapha. These tri-energies maintain our health, any imbalance in these doshas, is responsible for human’s health and disease. We are glad to say that we have seen so many positive results through our treatment. Thousands of people got rid of many diseases after taking our treatment.

Our patients not only put an end to their disease but also live a disease-free healthy life forever. This is the reason why people are getting attention towards our therapy. Our years of research in Ayurvedic treatments have helped us advance our methodology. We aim to reach as many people as we can to build a healthy and happy society all over the world.

Effective treatment by cow Urine Therapy

Jain’s Cow Urine Therapy promotes Ayurvedic remedies, treatments and therapies that are known worldwide for their efficient results.

Jain’s Cow urine therapy helps in the treatment of cystic fibrosis by reducing the following symptoms and also cow urine therapy is an effective way to get rid of the disease without any side effects -

  • Works on the throat and reduces persistent cough
  • Slows down the metabolism as patients
  • Improves stamina and promotes fertility
  • Reduces lung congestion and improves shortness of breath

BRONKOL+ LIQUID ORAL

KOFNOL+ CAPSULE

TONER (NASAL DROPS)

FORTEX Pak

Key herbs which makes the treatement more effective

Adusa

Adusa (Justicia adhatoda) is an herb commonly used in traditional Indian medicine. It has been studied for its potential therapeutic effects in a variety of conditions, including respiratory disorders like asthma and bronchitis.

Mulethi

Mulethi, also known as licorice root, is a plant commonly used in traditional medicine. It has been suggested that mulethi may have anti-inflammatory properties and may help to loosen mucus in the respiratory tract, which has led to some interest in its potential use in the treatment of cystic fibrosis.

Haldi

Haldi, also known as turmeric, is a spice commonly used in traditional Indian medicine for its anti-inflammatory and antioxidant properties.

Sirish

Sirish, which is also known as ivacaftor, is a medication that is used to treat a specific mutation of CF called the G551D mutation. It works by increasing the activity of the defective protein that causes the mutation, which helps to improve lung function and reduce the frequency of pulmonary exacerbations.

Tulsi

Tulsi, also known as Holy Basil, is a medicinal herb commonly used in Ayurvedic medicine. While there is some evidence to suggest that tulsi may have antioxidant, anti-inflammatory, and antimicrobial properties, there is currently no scientific evidence to support its use in the treatment of cystic fibrosis.

Sonth

Sonth, also known as dried ginger, is a traditional medicinal herb commonly used in Ayurveda to treat various ailments, including respiratory diseases.

Kali Mirch

Kali Mirch, also known as black pepper, is a common spice used in Indian cuisine and traditional medicine. While there is some research on the potential benefits of Kali Mirch in treating various health conditions.

Kakra singhi

Karka Singhi (also known as black horn) is a type of sea snail found in the Indian Ocean and is sometimes used in traditional medicine for various purposes including cystic fibrosis.

Nausadar

Navasadar (also known as Navasardar or Navasarjan) is an Ayurvedic medicine that is commonly used in India and other parts of the world for the treatment of respiratory disorders, including asthma and chronic obstructive pulmonary disease (COPD).

Pippli

Pippili, also known as Piper longum, is a plant that has been used for medicinal purposes in traditional Indian Ayurvedic medicine for centuries. There is some evidence to suggest that it may have therapeutic benefits in the treatment of cystic fibrosis.

Kapoor

It includes tannins, flavonoids and coumarins like chemicals. These chemicals tend to minimize chest inflammation (swelling).

Gojala

We use gojala in our cow-urine therapy, basically it means cow-urine extract, the main component in our medicine. This extract is made of the urine of the indigenous breeds of cow. Gojala has its own benefits because it’s beyond the possibility of any kind of contamination. It has high quality and is abundant. When gojala mixed with ayurvedic herbs it becomes more effective to treat any disease and favourable to the consequence of the particular disease. This extract is superimly tested and that’s why it’s more trustable and beneficial as well.

Causes of Cystic Fibrosis

Here are the causes of cystic fibrosis listed in points:

  • Cystic fibrosis is a genetic disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
  • The CFTR gene provides instructions for making a protein that is involved in the production of mucus, sweat, and digestive juices.
  • When the CFTR protein is not functioning properly due to mutations in the CFTR gene, it can lead to the production of thick, sticky mucus in the lungs, pancreas, and other organs.
  • This mucus can cause a range of symptoms and complications, including difficulty breathing, frequent lung infections, poor growth and weight gain, and digestive problems.
  • Cystic fibrosis is an autosomal recessive disorder, which means that a person must inherit two copies of the mutated CFTR gene (one from each parent) in order to develop the condition.
  • People who inherit only one copy of the mutated gene are carriers of the condition and do not typically experience any symptoms.


 

Prevention from cystic fibrosis

Cystic fibrosis is a genetic disorder that cannot be prevented, but there are some measures that can help manage the symptoms and reduce the risk of complications. Here are some preventive measures for cystic fibrosis:

  • Genetic counseling: Individuals with a family history of cystic fibrosis can undergo genetic counseling to determine their risk of having a child with the condition.
  • Newborn screening: All newborns in many countries are screened for cystic fibrosis shortly after birth, allowing for early diagnosis and prompt treatment.
  • Vaccinations: Vaccinations against infectious diseases such as influenza and pneumonia are recommended to prevent lung infections in individuals with cystic fibrosis.
  • Regular checkups: Regular checkups with a healthcare provider who specializes in cystic fibrosis can help monitor symptoms, prevent complications, and adjust treatment plans as needed.
  • Nutritional therapy: Nutritional therapy, including a high-calorie, high-fat diet and pancreatic enzyme replacement therapy, can help individuals with cystic fibrosis maintain a healthy weight and prevent malnutrition.
  • Exercise: Regular exercise can help improve lung function, reduce the risk of infections, and improve overall health in individuals with cystic fibrosis.

Symptoms of Cystic fibrosis

Cystic fibrosis (CF) can affect multiple systems in the body, leading to a range of symptoms. The severity of the symptoms can vary widely from person to person, and they can change over time. Some common symptoms of cystic fibrosis include:

  1. Respiratory symptoms:
  • Frequent coughing with thick, sticky mucus
  • Shortness of breath, wheezing or difficulty breathing
  • Repeated lung infections, such as pneumonia or bronchitis
  • Nasal congestion, sinus pain or pressure
  1. Digestive symptoms:
  • Poor weight gain and growth in children
  • Abdominal pain and bloating
  • Excessive gas or constipation
  • Fatty or foul-smelling stools
  • Pancreatitis (inflammation of the pancreas)
  1. Other symptoms:
  • Salty-tasting skin
  • Delayed puberty or infertility in males
  • Osteoporosis (weak bones)

 

Types of cystic fibrosis

Based on the severity of the mutations, cystic fibrosis can be classified into different types, including:

  • Classical CF: This is the most common and severe form of CF, associated with two severe mutations in the CFTR gene.
  • Non-classical CF: This form of CF is associated with one severe mutation and one mild or moderate mutation in the CFTR gene.
  • Cystic fibrosis carrier: A person who has one CFTR gene mutation but does not have the condition themselves is called a carrier.

Stages of Cystic fibrosis

This classification system is known as the CF Foundation Staging System and includes the following stages:

  • Stage 1: This stage is characterized by normal or near-normal lung function, with little or no symptoms.
  • Stage 2: This stage is marked by the onset of respiratory symptoms, such as coughing, wheezing, and shortness of breath. Lung function is still relatively preserved, but there may be some mild lung damage.
  • Stage 3: In this stage, lung function continues to decline, and symptoms become more severe. Individuals may experience frequent infections, worsening cough, and difficulty breathing.
  • Stage 4: This stage is characterized by severe lung damage and advanced respiratory symptoms. Individuals may require supplemental oxygen and may experience frequent exacerbations, hospitalizations, and decreased quality of life.

 

Complications from Cystic Fibrosis

Cystic fibrosis (CF) is a chronic disease that can affect multiple systems in the body, leading to a range of complications. Some common complications associated with CF include:

  1. Respiratory complications:
  • Chronic lung infections, which can cause progressive lung damage and lead to respiratory failure
  • Bronchiectasis, which is a condition where the airways become enlarged and damaged, making it difficult to clear mucus from the lungs
  • Pneumothorax, which is a collapsed lung due to the accumulation of air in the chest cavity
  • Respiratory failure, which is a life-threatening condition where the lungs can no longer provide enough oxygen to the body
  1. Digestive complications:
  • Malnutrition, which can result from poor absorption of nutrients in the intestines
  • Pancreatitis, which is inflammation of the pancreas, causing abdominal pain and difficulty digesting food
  • Liver disease, including cirrhosis and fatty liver disease
  1. Other complications:
  • Diabetes, which can develop as a result of damage to the pancreas
  • Infertility in males, which can be caused by blockages in the reproductive system
  • Delayed puberty, which can be caused by hormonal imbalances

Recognitions

GMP Registration

 

IP Rights Registration

 

World Book of Records