Polycystic kidney disease allows the cysts to form in the parts of the kidneys. These cysts over time get filled with fluid causing obstruction in the kidney function. Quite painful, the cysts grow large by 0.5 inches or larger thereby increasing the size of the kidneys. Unlike simple kidney cysts, PKD is an innate condition and is caused by alterations in the genes a child receives from his parents.
PKD may also allow the formation of cysts in the liver and anywhere else in the body. Certain lifestyle changes and polycystic kidney disease ayurvedic treatment may allow the kidneys to have a normal kidney function once again. Allopathy considers no permanent cure for PKD but only the complications can be cured with medicines. On the other hand, Ayurvedic science has a different viewpoint of disease and so does the polycystic kidney disease ayurvedic treatment. The herbal medicines proffer natural diuretic, anti-bacterial, and anti-hypersensitive properties which help to release toxins in and out of the body.
Is PKD a common disorder?
PKD is a common disorder that affects individuals of all age groups and is not gender-biased. It is the fourth leading cause of kidney failure.
What other organs besides the kidneys are affected by PKD?
PKD can affect many organs besides the kidneys. The cysts may grow anywhere in the liver, pancreas, spleen, ovaries, and bowel. The cysts may or may not cause any serious complications and may also affect the heart or brain. When it affects the brain it causes brain aneurysm that may even result in death or stroke. Its effect on heart can be a change in the heart valves resulting in a heart murmur in some patients. So, it is crucial to mend it with the help of polycystic kidney disease ayurvedic treatment.
What are the types of PKD?
The two main types of PKD are:
- Autosomal dominant PKD
- Autosomal recessive PKD
Autosomal dominant PKD or ADPKD means a child can get a gene mutation only from one parent. There are two different gene mutations involved in the occurrence of ADPKD, i.e. PKD 1 and PKD2. Most people with ADPKD may have PKD 1 gene while only 10% of the cases of PKD have PKD2 gene triggering mutation.
This form of PKD appears later in life with signs appearing after 30 years of age. People with the PKD1 gene usually progress more quickly to kidney failure than people with PKD 2 gene although how quickly the condition progresses is dependent on person to person.
The common signs may appear at the time of ADPKD may include:
- Pain
- It may arise because of cysts in the liver or kidney and,
- kidney cyst infection
- bleeding or burst kidney cysts
- urinary tract infection
- kidney stones
- tissue stretching around the kidney due to cyst
- Persistent headaches
- High blood pressure
High blood pressure may arise because of fluid and waste deposited in the blood.
Hematuria
Those with ADPKD may have blood in the urine.
Autosomal recessive PKD
Autosomal recessive PKD means for the child to have this disorder, both the parents must have gene mutations. If only one parent has the genes, the child will not be borne the disease rather becomes the carrier of the disorder and can only pass the gene mutation to the next generation.
ARPKD can be diagnosed as soon as the baby is born or even before the baby is born. The sooner it is diagnosed, the sooner you can start with the treatment. Good prenatal care is important along with the polycystic kidney disease treatment in Ayurveda longevity.
The common signs that may appear at the time of ARPKD include:
- Enlarged size of the kidneys
- Growth failure
- Low levels of amniotic fluid
PKD ayurvedic treatment
Patients may seek the help of PKD ayurvedic treatment that supports kidney disease with their natural therapeutical potential herbal medicines. Along with the treatment, patients are also advised to follow a diet based on tridosha levels. This will help to channelize the energy of the mutravaha srotas so that signs and causes are cured.
For more information on polycystic kidney disease ayurvedic treatment, you can consult us at Karma Ayurveda.
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