#lungdisease

When is Chest Pain An Emergency? Shortness of Breath: Difficulty breathing or feeling winded. Nausea or Vomiting: Feeling sick to your stomach or actually vomiting. Sweating: Cold sweats or clammy skin. Lightheadedness or Dizziness: Feeling faint or unsteady. Pain in Other Areas: Discomfort in the arms, back, neck, jaw, or stomach. Rapid or Irregular Heartbeat: Palpitations or a racing heart. Anxiety or Feeling of Impending Doom: A sudden feeling that something is very wrong.

Pulmonologist in Patiala for Chronic Cough and Lung Diseases

Pulmonary Hypertension in Indians: Early Signs Many People Ignore

Pulmonary hypertension in Indians is often diagnosed late because the early symptoms look common at first. Breathlessness while climbing stairs, fatigue, dizziness, dry cough, chest discomfort, and ankle swelling are warning signs many people ignore for months.

Air pollution, chronic lung disease, sleep apnea, and delayed testing are increasing the risk in India. A simple 2D Echo test can help detect pulmonary hypertension before serious heart damage develops. Early diagnosis matters because treatment works best before the right side of the heart becomes weak. Read the full article: RealMedVision Note: This content is for educational awareness only and should not replace professional medical advice, diagnosis, or treatment.

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Encyclopedia of Respiratory Medicine (6 Volume Set, 2nd Edition) is a definitive and comprehensive reference covering the full spectrum of pulmonary and respiratory science. This multi-volume work integrates basic physiology, molecular biology, epidemiology, and clinical practice to address diseases of the airways, lungs, pleura, and respiratory muscles. With contributions from leading international experts, it provides in-depth coverage of asthma, COPD, interstitial lung disease, pulmonary infections, critical care, and emerging therapies. The encyclopedia is an essential resource for pulmonologists, respiratory scientists, intensivists, and advanced medical libraries.

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Imagine a condition that doesn’t announce its arrival — no sudden warning, no sharp beginning — just a gradual change in breath that many dismiss as tiredness or age. That’s the mystery of Idiopathic Pulmonary Fibrosis (IPF). The most intriguing part is that there’s no single starting point, no one trigger we can label as the cause. Instead, researchers see patterns forming from multiple possibilities. Ageing seems to make lung tissue more vulnerable, especially beyond midlife. Genetics may influence how well the lungs repair themselves. For some years of exposure to dust, fumes, or industrial pollution could be the quiet behind-the-scenes culprit. Smoking, chronic acid reflux and lifestyle factors may further contribute to repeated microscopic injuries. These tiny damages heal abnormally, forming scar tissue — slowly stiffening the lungs and making every breath feel heavier. IPF often develops from these layers of subtle harm rather than one event, which is why understanding risk factors becomes crucial. Early awareness can make the difference between a delayed response and a timely intervention.