Five PFF Scholars Receive $100K Grants to Advance Pulmonary Fibrosis Research
Five PFF Scholars will each receive a $100,000 research grant over two years to improve the understanding of pulmonary fibrosis and advance successful treatments.
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Five PFF Scholars Receive $100K Grants to Advance Pulmonary Fibrosis Research
Five PFF Scholars will each receive a $100,000 research grant over two years to improve the understanding of pulmonary fibrosis and advance successful treatments.
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Guidance for Diagnosis and Treatment of Pulmonary Hypertension Related to ILD
The Pulmonary Fibrosis Foundation and Pulmonary Hypertension Association have developed a position statement that addresses gaps in the diagnosis and treatment of patients living with pulmonary hypertension related to interstitial lung disease.
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7 New Sites Join PFF Care Center Network
The Pulmonary Fibrosis Foundation announced that seven medical centers have joined the PFF Care Center Network as clinical associate members, a new membership option.Â
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Cleveland Clinic Pulmonologist Takes Helm at Pulmonary Fibrosis FoundationÂ
The Pulmonary Fibrosis Foundation announced Franck Rahaghi, MD, MHS, FCCP, as its incoming president, CEO, and chief medical officer, effective Sept 15.
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PFF Urges Patients to Use Only FDA-Approved Oxygen Devices
The medical advisory board of the Pulmonary Fibrosis Foundation issued a position statement on non-prescription supplemental oxygen.
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Pulmonary Fibrosis Research on Access, Quality of Care
Important research results from five studies examining access to care and outcomes for patients living with pulmonary fibrosis and interstitial lung disease (ILD) are being presented at ATS 2022.
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A Spotlight on the Pulmonary Fibrosis Foundation Care Center Network
The Pulmonology Advisor interviewed experts to learn about how the Pulmonary Fibrosis Foundation’s PFF Care Center Network can advance research.
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Pulmonary Fibrosis Awareness Month Celebrates PF Heroes
September is Pulmonary Fibrosis Awareness Month. This year the Pulmonary Fibrosis Foundation is celebrating PF Heroes who are raising awareness of the disease.
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PFF Summit Awards Highlight Pulmonary Fibrosis Research
The Pulmonary Fibrosis Foundation’s recent PFF Summit has announced winners for its poster sessions.
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Pulmonary Fibrosis Drug Development Pipeline Launched
The PF Foundation has launched a new PF Drug Development Pipeline tool to help the pulmonary fibrosis community search for different treatment options.
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PF Foundation Reaffirms Caution Over Stem Cell Therapies for PF
The Pulmonary Fibrosis Foundation strongly cautions patients with PF against using stem cell treatments outside of an approved clinical trial.
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Pulmonary Fibrosis Foundation Releases Information Guide
The guide provides patients and families with up-to-date information about pulmonary fibrosis and treatment options.
Read MorePFF Expands Patient Registry and Care Center Network
The Pulmonary Fibrosis Foundation is expanding its Patient Care Network and Patient Registry, which it formed in late 2013 to improve the quality of life for patients with all types of pulmonary fibrosis, including idiopathic pulmonary fibrosis.
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FDA to Host Meeting on IPF Drug Treatment
In September, the Food and Drug Administration will host a meeting on patient-focused drug treatment of idiopathic pulmonary fibrosis (IPF), according to an announcement from the Pulmonary Fibrosis Foundation.
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