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Responsum Health is harnessing the promise of the Internet to better inform and engage patients with chronic conditions. Join us!

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Email: info@responsumhealth.com
Phone: +1 (949) 264 2277
Headquarters Office: Washington, DC
Operations Office: Irvine, CA

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Great News For Pulmonary Fibrosis Patients

Great News for Pulmonary Fibrosis Patients

Today is the day we begin to change the way patients use the Internet forever.

Today is the day when everyday patients begin to gain the ability to use the world wide web to inform and empower themselves with current, meaningful, and trustworthy information about their health and their lives.

The Pulmonary Fibrosis Foundation (PFF), a leading patient advocacy group for pulmonary fibrosis, announced that it will bring its unmatched knowledge base and reputation to build a powerful partnership with Responsum Health—a leading innovator in online patient information and engagement.

Through this partnership, Responsum Health and the PFF have created a first-of-its-kind technology resource for patients with pulmonary fibrosis (PF).

Headshot for Andrew Rosenberg, CEO and Founder of Responsum Health

“No longer will doctors feel the need to warn their recently diagnosed patients against unvetted online searches…

No longer will PF patients be forced to sift online through overwhelming amounts of inaccurate, outdated and overly scientific information…”

Andy Rosenberg

This new knowledge platform—Responsum for Pulmonary Fibrosis—does the searching for patients. We only include information that the PFF says is valid, we summarize it, and we send it to our patients’ personal Newsfeeds The information is easy-to-read and delivered right to your inbox, as well as categorized so that patients can effortlessly search for articles in our extensive Link Unit Library (LUL).

The internet offers patients the promise of unfettered access to massive amounts of information. We understand, however, that patients can easily find themselves overwhelmed by too much—or underserved by inaccurate, inappropriate, and/or overly complex content.

Responsum for Pulmonary Fibrosis solves that problem. At the end of the day, a better-informed patient makes for better outcomes, and that is our number one goal. We’re very excited about this partnership with the PFF, and we believe that, together, we can change healthcare.

If you or a loved one has PF, I hope you’ll consider signing up today. If you want to help us improve the way patients harness the Internet to better their health, we hope you’ll follow us.

Andy Rosenberg
Founder and CEO, Responsum Health

This Post Has 5 Comments
  1. I look forward to reading and expanding my knowledge about pulmonary fibrosis. Particularly interstitial pulmonary fibrosis. I was diagnosed in March of 2020.
    I was told that there is no cure and nothing that will slow progression for the type I have. I continue to seek information. I have discovered that walking is important to maintain oxygen level . I have read that there are breathing exercises and some therapy . Very interested in expanding my knowledge.

    1. Hi, Jean! Thank you for taking the time to share with us. Have you joined the Responsum for PF platform yet? If not, I strongly encourage you to sign up, as you’ll find information, resources, and other people with PF to talk about your experience with. If you have any other questions or concerns, please don’t hesitate to ask! – Chief Content Editor, Responsum Health

    1. Hi, Patsy! We appreciate you taking the time to share your experience with us. According to a number of different medical studies, “up to twenty percent of patients with sarcoidosis develop pulmonary fibrosis.” Thus, sarcoidosis is not a form of pulmonary fibrosis (PF), but it can lead to PF in some cases. If you have any other questions or concerns, please don’t hesitate to ask! – Chief Content Editor, Responsum Health

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