“Finally! Discover The All-Natural Blood Pressure Lowering Techniques That Can Help You Lower Your Blood Pressure Without Prescription medications or Pharmacy Drugs, and Suffering Through Dangerous Side Effects!”

“Natural treatment for Hypertension (high blood pressure)” is a powerful, yet simple and easy guide that I wrote with most honest intention to provide help to you and to many others like you because I already have been there and I know how is it … My point is to bring to your attention the fact that alternative treatments are gaining widespread acceptance… more and more people are looking for alternatives to high priced, harmful, side-effect-plagued prescription medications.

All About Pulmonary Arterial Hypertension (PAH)

Pulmonary Arterial Hypertension (PAH), as the name suggests is a lung disorder. When the blood blood pressure levels in the pulmonary artery, vein, or capillaries is increased, it causes to the disease known as the lung vasculature, which in turn is leading to fainting, dizziness, shortness of breath or other various symptoms. They all are exacerbated by exertion. It is erious and incurable, though fortunately rare. In order to establish the cause, whether the disease might be familial, the physician will generally conduct a detailed family medical history.

It can essentially be divided categories:

1. Primary Pulmonary arterial hypertension (PPH), which cannot be attributed ny specific cause
2. Secondary Pulmonary arterial hypertension (SPH), where there is a known cause, like bronchitis or emphysema.

PPH is sometimes referred to as pulmonary arterial high blood pressure or by another recent name, Idiopathic Pulmonary Arterial Hypertension (IPAH). Each year in the United States, an estimated 500 to 1,000 new cases are diagnosed, most of them women between the ages of 20 and 40.

However, both genders and any age can develop PPH. According to the American Lung Association, there were 3,065 deaths attributed to PPH in 2000. Basically this lung disorder negatively impacts the flow of blood from the lungs to the heart and results in high blood pressure in the pulmonary artery, which is responsible in carry low-oxygen blood from the right ventricle of the heart to the lungs.

The net effect of this increased blood pressure may tighten the interior passageway of the arteries, which constricts the arterial flow. The arterial walls may become thick resulting in scar tissues, which further narrows the arteries. Blockages result from the blood clots and in extreme cases the right ventricle ceases to function in the right way causing heart failure and eventual death of the patient. P.A.H. may also be accompanied by left ventricular dysfunction.

In a study entitled “Severe left ventricular dysfunction secondary to primary pulmonary high blood pressure” conducted by BRAUCHLIN Andreas E. et al., and published in The Journal of heart and lung transplantation 2005, vol. 24 issue: “When right ventricular failure develops secondary to primary pulmonary hypertension, right-left ventricular interaction may lead to severe impairment of left ventricular function. In such cases, many experts favor combined heart-lung transplantation by fear that the left ventricle may not recover after transplantation of the lungs alone.”

As with any dangerous and life-threatening disease, diagnosis of pulmonary high blood pressure calls for detailed counseling for all those who are involved in the patients’ family. The pulmonary hypertension prognosis as well as all information related to pulmonary high blood pressure treatment including therapy options available and the required lifestyle changes are usually shared for the future well being of the patient.

Moreover, as high blood pressure is difficult to identify, Pulmonary Arterial Hypertension PAH affects 1 of 3 adults in the United States alone. Unfortunately, PPH has no known cure. There are a large variety of very specialized P.A.H. treatment options available, which are effective in reducing Pulmonary High Blood pressure symptoms by enhancing daily activity, reducing blood pressure, and most importantly, which would increase the patients’ life expectancy. PAH symptoms include dizziness, tiredness, breathing difficulty, fainting, inflammation of legs and ankles, bluish lips and chest pain.

Unfortunately Pulmonary Hypertension prognosis is poor and there is no known cure for this condition, though some methods like lifestyle changes, medication and lung and heart transplants have been effective in pulmonary high blood pressure treatment. Treatment also includes use of anticoagulants, which bring about some improvement of quality of life of patients suffering from PAH. Over and above the anti-clotting medication prescribed by doctors, there are some other drugs used in pulmonary hypertension treatment. These include calcium channel blockers and vasodilators. Recently the use of Viagra (Sildenafil) has been seen to provide satisfactory improvement to conditions of PAH, but it is still awaiting approval for formal use in the treatment of the condition.

Usually, Pulmonary Hypertension causes remain unknown but generally attributed to genetic or familial factors, diseases of the immune system or over exposure to drugs/chemicals. There are several drugs like cocaine, amphetamines and diet drug Fen Phen have been associated with causing PAH. Even a couple of decades ago PPH meant definite death. Today with advancements made in the field of new therapies for the condition, life expectance of people suffering from the condition has increased. Untreated, the survival rate is about 68% at one year, 48% at three years, and 34 % at five years, according to the University of North Carolina at Chapel Hill Pulmonary & Critical Care Medicine. With treatment, life expectancy can increase on average 3-5 years.

There has been keen interest in the area of understanding the link between Pulmonary Hypertension and thyroid problems like cancer. In one study carried out by the Mayo Clinic in Jacksonville, USA they studied 358 people over a 14-year period and it was concluded that those suffering from P.H. are at a greater risk of acquiring thyroid problems. Though there was a high rate of presence of thyroid disease in many of the subjects there still seemed no correlation between the disease and the severity of P.H. The direct link between Pulmonary High Blood Pressure + thyroid cancer is not very clear but there seems to some link anyway.