Stay up-to-date on FSR’s latest activities and learn about the ways that FSR is driving progress and accelerating research towards a cure.
FSR launched the Ignore No More: ACTe Now! Campaign (Advance Clinical Trials for Equity in Sarcoidosis) to address the underrepresentation of Black Americans in clinical trials. As part of the campaign, FSR conducted the first of its kind, IRB-approved national patient survey for Black Americans to better understand the challenges and experiences Black Americans with sarcoidosis face as it pertains to clinical trials and their disease journeys. FSR also conducted a Key Opinion Leaders Thought Workshop (KOL) and Patient Focus Group to explore the findings in greater depth and to identify recommendations for how to improve clinical trial access and overall care of Black sarcoidosis patients.
Some recommendations that emerged include building a blueprint for clinical trial design that increases access and supports diversity, clinical trial navigation and support specifically targeted for Black patients, and educational toolkits to better educate patients and physicians about trial opportunities and engagement. Though this campaign was specific to Black Americans with sarcoidosis the learnings are relevant to improving access to clinical trials for all Black Americans.
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FSR Blog
Life as a Sarc Warrior: Advice on Friends and Family
Life with sarcoidosis can be hard and no one knows that better than our patients. This is why we reached out to you, our patients, for advice.
Ask The Ambassadors: How to Navigate Medical Expenses
We reached out to our patient ambassadors and asked for their advice on navigating the medical expenses that come with sarcoidosis.
Understanding Cardiac Sarcoidosis
Cardiac sarcoidosis is diagnosed in 2-5% of patients with systemic sarcoidosis. However, some reports are showing that the incidence of cardiac sarcoidosis in the US may be as high as 20-30% in sarcoidosis patients.
For the patients who go undiagnosed, the repercussions can sometimes be fatal. Wendy Ullmer, a 36-year-old from Wisconsin was unfortunately one of those cases, leaving her husband and their four young boys devastated by her loss. Read her story and learn the signs and symptoms that indicate you should talk to you doctor about screening for cardiac involvement.
What is an FSR Patient Ambassador?
All of our patients ambassadors have a different experience and a different reason for becoming an ambassador. Find out in their own words what our patients ambassadors do and why they became involved with this program.
Team KISS is Going to New Orleans!
We have big news! FSR’s sixth annual Team KISS 5K Run/Walk will take place in New Orleans, Louisiana!
Ask The Ambassadors: Developing a Healthy Lifestyle
We reached out to our patient ambassadors and asked for their advice on developing a healthy lifestyle while dealing with sarcoidosis.
Want to Make an Impact This Summer? Join Team KISS!
Summer isn’t over which means now is the perfect time to soak up the extra sunlight and mild weather while you fundraise with Team KISS!
Ask The Ambassadors: Hard Conversations with Friends and Family
We reached out to our patient ambassadors and asked for their advice on having hard conversations with friends and family about sarcoidosis.
Healthy Eating Habits: Heart and Lungs
Developing healthy eating habits while dealing with sarcoidosis can be hard. Here are some diet tips to help keep your heart and lungs healthy.
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