FSR's Blog — Page 58 of 112 — Foundation for Sarcoidosis Research

VIDEO: Birmingham Conference Recording

Feb 7, 2019

Here at FSR, part of our mission is to bring educational experiences and knowledgeable physicians to as many patients as possible. That’s why we’re proud to be hosting a record of nine patient conferences all across the country this year. We know it’s difficult for...

Topics: FSR Events/ Online Educational Content

Life as a Sarc Warrior: Making Our Medical System Work for You

Feb 1, 2019

Life with sarcoidosis can be hard. This is why we reached out to you, our patients, for advice on how to deal with our medical system.

Topics: Patient Voices

Add Your Voice – Treatment Survey

Jan 16, 2019

FSR is partnering with pharmaceutical companies and biotechs to build a strong pipeline of potential treatments for patients with sarcoidosis and we want to hear your story. Has your doctor ever suggested you take Infliximab (remicade) for your sarcoidosis? Please...

Topics: Other

Patient Survey Leads to New Treatment Guidelines

Jan 14, 2019

Early last year, we asked our community to tell us which treatment outcomes are most important to sarcoidosis patients. You and hundreds of other patients around the world responded! The survey, developed by a European Respiratory Society (ERS) working group which...

Topics: News

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VIDEO: Birmingham Conference Recording

Life as a Sarc Warrior: Making Our Medical System Work for You

Add Your Voice – Treatment Survey

Patient Survey Leads to New Treatment Guidelines

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