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The Importance of the FSR Patient Registry
…complete the survey. FSR suggests for some it may take anywhere between 40-60 minutes, depending on your particular experience. And I was able to stop and come back to it…
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…complete the survey. FSR suggests for some it may take anywhere between 40-60 minutes, depending on your particular experience. And I was able to stop and come back to it…
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…research agenda and strategic vision that uniquely positions FSR to make the most impact for the sarcoidosis community. In addition, we have an extraordinary team of committed staff, Board of…
…both a practitioner and administrator. She provides executive leadership in managing the organization’s Community Impact Department which includes: Mental Health education to the community, support groups, a HELPLINE, and Anti-Stigma…
…poised to conduct multi-site trials – companies can come directly to FSR to propose studies and trials for the current eight sites, and save resources in the process. In addition,…
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…Mac died from complications from this disease. There is no prior history of Sarcoidosis in my family. My diagnosis came as a complete shock and disappointment. The dermatologist immediately began…
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…their local representatives to meet and discuss policy issues that face the rare disease community. FSR Patient Ambassador Sheron Williams of Michigan had numerous meetings scheduled throughout the month with…
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…global issue of respiratory health and the increasing challenges that individuals with respiratory complications face worldwide. The charter addresses environmental pollution and air quality, access to healthcare and education, and…
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…sarcoidosis community on The Mighty has grown, revealing the power of communication and the action that can follow. Several sarcoidosis survivors detail their individual experiences with the disease. They discuss…
…proud to partner with Inspire on the online Stop Sarcoidosis Support Community to provide a much-needed space for those living with sarcoidosis to come together and share experiences. Connect with…
…your community and/or nationwide (support groups, local sarcoidosis awareness efforts, etc.) Providing support for how to communicate with your healthcare provider Providing support for how to communicate with family and…