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Pulmonary Fibrosis Foundation launches new website

The website features resources and user-friendly tools for patients

The Pulmonary Fibrosis Foundation (PFF) has launched a new website, pulmonaryfibrosis.org, for the more than 200,000 Americans impacted by pulmonary fibrosis (PF), a group of debilitating lung diseases. The site features educational resources and tools to help patients learn more about their diagnosis and to locate care, clinical trials, and support. In addition, healthcare professionals will find continuing medical information materials and research opportunities on the site. The new website was funded through a grant from Three Lakes Foundation. 

“Pulmonary fibrosis is a devastating diagnosis and our new website is designed to help patients, their caregivers, and loved ones navigate their disease journey with trusted information and resources,” said William T Schmidt, President and CEO, PFF. “Our goal is for the PF community to use this site to easily access what they need to empower them to become more knowledgeable and to achieve a better quality of life with PF.” 

Patient resources on the new site include disease education videos and webinars, fact sheets on the types of pulmonary fibrosis, and a pulmonary rehabilitation toolkit. A medical care and support group finder provides users with the closest PFF Care Center Network sites and support group locations. The Clinical Trials section offers a searchable tool for users to identify relevant and feasible clinical trials. Users can read about the latest news from the PFF and learn about ways to donate and volunteer with the Foundation. 

Researchers and healthcare providers will find valuable clinical resources at the site to help inform their care for patients and research interests. Position statements on genetic testing, stem cell therapy, and other topics are also available. In addition, research opportunities including the PFF Scholars and the PFF Registry are accessible. 

“We are proud to support the PFF in the development of this outstanding new website for the PF community,” said Dana Ball, Executive Director, Three Lakes Foundation. “Patients and caregivers must have a comprehensive resource to help them navigate the many needs of living with PF, and the PFF has provided just that through this new site.”

 

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