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Idiopathic Pulmonary Fibrosis

Jeremy Feldman, MD

  • What is Idiopathic Pulmonary Fibrosis?
    • Idiopathic Pulmonary Fibrosis Definition
    • Symptoms of Idiopathic Pulmonary Fibrosis
    • Causes of Idiopathic Pulmonary Fibrosis
    • Who Gets Idiopathic Pulmonary Fibrosis
    • Gastro-Esophageal Reflux (GER) and Idiopathic Pulmonary Fibrosis
    • Interstitial Lung Disease vs. Idiopathic Pulmonary Fibrosis
    • Is Pulmonary Fibrosis Hereditary?
    • Research, Life Expectancy and Prognosis for Idiopathic Pulmonary Fibrosis
  • Diagnosing & Monitoring PF
    • Monitoring Progress of IPF
    • Idiopathic Pulmonary Fibrosis Diagnosis
    • Chest X-rays Used in IPF
    • CPET used in IPF
    • HRCT Scans Used to Evaluate IPF
    • Lung Biopsy To Diagnose IPF
    • Pulmonary Function Tests (PFTS)
    • Six Minute Walk Test To Monitor IPF
    • Stages of Idiopathic Pulmonary Fibrosis
    • Complications of Idiopathic Pulmonary Fibrosis
  • PF Treatment Options
    • Nerandomilast (Jascayd) Approved for IPF Treatment
    • Esbriet (pirfenidone) Used to Treat IPF
    • OFEV (nintedanib) Used to Treat IPF
    • Pulmonary Rehab for IPF Patients
    • Lung Transplantation for Pulmonary Fibrosis
    • Oxygen Used to Treat IPF
      • Update on Oxygen Use
    • Clinical Trials in Idiopathic Pulmonary Fibrosis
    • IPF & Leg Swelling
    • Pulmonary Hypertension and Idiopathic Pulmonary Fibrosis
    • IPF Exacerbation
  • PF Advocacy & News
  • FAQ’s
    • Respiratory failure, NSIP, diet
    • Leg swelling, lung biopsy, side effects & pets
    • FAQ’s Enzyme Therapy, Progression of IPF & Oxygen
    • FAQ: Diarrhea, Fibrosis Reversal, IPF Symptoms
    • FAQ: Oxygen Flow, Anesthesia & Genetics
    • FAQ: Contagious Cough? Stem Cells, Familial IPF, Flying
    • FAQ: GERD, Fatigue & Environmental Exposure
    • FAQ: How to Travel to Your Doctor’s Office with Oxygen
    • FAQ: Lung Biopsy with Pulmonary Fibrosis
    • FAQ’s: Alcohol, Clinical Trials, Pulmonary Function Testing
    • FAQs: Emphysema, Exercise & Lung Biopsy

I Have A Family History Of IPF, Do I Have IPF?

September 13, 2019 By Dr. Jeremy Feldman

dealing with emotions of having pulmonary fibrosis

This stressful question is on the minds of any patient who has a first degree relative with Idiopathic Pulmonary Fibrosis (IPF).  Our readers often ask how they can know for certain that they don’t have IPF if a parent or a sibling has the disease.   Most IPF Isn’t Familial  The majority of patients with IPF don’t have familial … [Read more...]

I Can’t Sleep – Dealing with Insomnia

August 28, 2019 By Dr. Jeremy Feldman

sleep

Difficulty with sleeping is a very common problem.  Hundreds of millions of people around the world struggle with poor sleep quality. The problem is even more common for people with health problems, including lung disease, pulmonary fibrosis and pulmonary hypertension. Insomnia, the technical term for trouble sleeping, can be divided into several categories.  Patients may … [Read more...]

Interstitial Pneumonia with Autoimmune Features

August 21, 2019 By Dr. Jeremy Feldman

symptoms of pulmonary fibrosis

Interstitial Pneumonia is a term used to describe a large family of non-infectious lung diseases. The most common entities include non-specific interstitial pneumonia (NSIP), hypersensitivity pneumonitis (HP), and idiopathic pulmonary fibrosis (IPF).  Less common members of this family include acute interstitial pneumonia (AIP), respiratory … [Read more...]

Scleroderma Associated Pulmonary Fibrosis: A New Study

July 8, 2019 By Dr. Jeremy Feldman

prescription for Ofev (nintedanib)

Idiopathic pulmonary fibrosis (IPF) is just one of many types of pulmonary fibrosis.  In patients with IPF, no other cause can be found and the disease has a typical radiographic pattern and when biopsied has a characteristic appearance under the microscope.   Scleroderma is a connective tissue disease characterized by skin thickening, esophageal … [Read more...]

6 Complications of IPF

May 30, 2019 By Dr. Jeremy Feldman

Patients with IPF often have to contend with multiple problems related to their lung disease. Cardinal symptoms are shortness of breath and cough.  These symptoms lead to evaluation that eventually includes a high resolution CT scan of the chest.  In some cases a lung biopsy is required to confirm the diagnosis and in others the diagnosis can be … [Read more...]

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Featured Blog Posts

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Recent Posts

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  • Interstitial Lung Disease and Progressive Pulmonary Fibrosis

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Popular Articles

IPF patient with doctor

Idiopathic Pulmonary Fibrosis Treatment Options

What is IPF?

  • What is Idiopathic Pulmonary Fibrosis?
    • Symptoms of Idiopathic Pulmonary Fibrosis
    • Causes of Idiopathic Pulmonary Fibrosis
    • Who Gets Idiopathic Pulmonary Fibrosis
    • Gastro-Esophageal Reflux (GER) and IPF
    • Interstitial Lung Disease vs. Idiopathic Pulmonary Fibrosis
    • Is Pulmonary Fibrosis Hereditary?
    • Research, Life Expectancy & Prognosis for Pulmonary Fibrosis

Diagnosing IPF

  • Idiopathic Pulmonary Fibrosis Diagnosis
    • Chest X-rays Used in IPF
    • CPET used in IPF
    • HRCT Scans Used to Evaluate IPF
    • Lung Biopsy To Diagnose IPF
    • Pulmonary Function Tests (PFTS)
    • Six Minute Walk Test To Monitor IPF
    • Stages of Idiopathic Pulmonary Fibrosis
    • Complications of Idiopathic Pulmonary Fibrosis

Treating IPF

  • Pulmonary Fibrosis Treatment Options
    • Esbriet (pirfenidone) Used to Treat IPF
    • OFEV (nintedanib) Used to Treat IPF
    • Pulmonary Rehab for IPF Patients
    • Lung Transplantation for Pulmonary Fibrosis
    • Oxygen Used to Treat IPF
    • Clinical Trials in Idiopathic Pulmonary Fibrosis
    • IPF & Leg Swelling
    • Pulmonary Hypertension and Idiopathic Pulmonary Fibrosis
    • IPF Exacerbation

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