The Sarcoidosis Research Institute understands that sarcoidosis patients and their loved ones often have to search for more information after their diagnosis. Sarcoidosis is not only rare, complex, and under researched, it presents itself in so many ways that patients and doctors alike struggle to make up-to-date information available. The SRI team is determined to provide the resources necessary for those directly and indirectly impacted by sarcoidosis to live an exceptional physical, mental, and emotional life.
SRI Webinars and Podcasts
Hear from our team on topics that directly affect those with sarcoidosis, such as its proximity to sleep disorders, treatment trends, and how it can relate to sickle cell disease. Under an hour yet full of relevant information, our podcasts and webinars give those that tune in a solid look into the most popular Sarcoidosis topics. We suggest starting with Dr. Judson’s podcast, “Is My Sarcoidosis Acting Up.” Dr Judson provides a high-level overview of sarcoidosis and discusses how to identify the difference between a sarcoidosis flare-up and other medical conditions.
View Podcasts & WebinarsSarcoidosis Videos
We’ve searched the web and compiled a fantastic group of videos on Sarcoidosis that could be helpful for Sarcoidosis patients and loved ones alike. If you’re looking for quick videos that provide a ton of great information, these are all under 20 minutes long and come from sources like the National Heart, Lung, and Blood Institute, the American Lung Association, and even Pfizer.
View Sarcoidosis VideosSarcoidosisUK – Patient Days Hub
SarcoidosisUK is a charity funded solely from personal donations, both monetary donations and volunteering. Their goal is to provide accurate and detailed information to people with sarcoidosis, their caretakers, and medical professionals. SarcoidosisUK also provides emotional support for people diagnosed with Sarcoidosis through phone calls, email correspondence, through social media, and in their support groups in the UK. A key way they achieve this is through Patient Days, where sarcoidosis patients, caretakers, and medical professionals have the opportunity to listen to speakers, have their questions answered, and be involved in the sharing of Sarcoidosis information.
Learn More About Patient DaysFSR Clinical Education
The Foundation for Sarcoidosis Research is dedicated to both finding a cure for sarcoidosis and improving care for sarcoidosis patients through research, education, and support. In an effort to do this, FSR hosts a clinical education and engagement series where sarcoidosis patients and their loved ones can engage with world-renowned medical experts and other clinicians who present research and case studies on the most current sarcoidosis topics. This program is completely free to attendees and takes place a few times each year.
Learn More About FSR Clinical Education