FSR

The Foundation for Sarcoidosis Research (FSR) is the leading international organization dedicated to finding a cure for sarcoidosis and improving care.

[FSR @StopSarcoidosis]

‼️ Registration is still open! ‼️
SARCOIDOSIS IN EVERYDAY CLINICAL PRACTICE
IDENTIFICATION & CARE MANAGEMENT

Join regional experts for a complimentary CME program focused on recognizing, diagnosing, and managing sarcoidosis in everyday clinical practice.

Designed for healthcare

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for sarcoidosis and improving care.

The Autoimmune Community Summit is a free, virtual event bringing together the autoimmune community for
three days of education, resources, and connection.
We hope to see you there!
Register for free: https://t.co/I10du8xwAI

[FSR @StopSarcoidosis]

We’re excited to be exhibiting at the Autoimmune Association’s Autoimmune Community Summit, October 14–
16!
Stop by our virtual booth to learn more about The Foundation for Sarcoidosis Research (FSR) and how we’re leading international organization dedicated to finding a cure

[FSR @StopSarcoidosis]

‼️ Registration is still open! ‼️
SARCOIDOSIS IN EVERYDAY CLINICAL PRACTICE
IDENTIFICATION & CARE MANAGEMENT

Join regional experts for a complimentary CME program focused on recognizing, diagnosing, and managing sarcoidosis in everyday clinical practice.

Designed for healthcare

[FSR @StopSarcoidosis]

Location: Sheraton Philadelphia Downtown

Register Here: https://t.co/qroZCJLbl3

@TJUHospital @Penn @TempleHealth

[FSR @StopSarcoidosis]

‼️ Registration is still open! ‼️
SARCOIDOSIS IN EVERYDAY CLINICAL PRACTICE
IDENTIFICATION & CARE MANAGEMENT

Join regional experts for a complimentary CME program focused on recognizing, diagnosing, and managing sarcoidosis in everyday clinical practice.

Designed for healthcare

[FSR @StopSarcoidosis]

professionals, this accredited CME program will provide practical, evidence-based education on recognizing, diagnosing, and managing sarcoidosis in everyday clinical practice.
Please note that this event is in-person
Date: Saturday, September 26, 2026
Time: 8:00 AM - 3:45 PM ET

[FSR @StopSarcoidosis]

SARCOIDOSIS IN EVERYDAY CLINICAL PRACTICE
IDENTIFICATION & CARE MANAGEMENT

Join regional experts for a complimentary CME program focused on recognizing, diagnosing, and managing sarcoidosis in everyday clinical practice.

Designed for healthcare professionals, this accredited

[FSR @StopSarcoidosis]

try; I rely on a dictionary myself—You’ll meet interesting practitioners and other sarc patients…” – Patient Stakeholder Reviewer, Anne Nissen

https://t.co/t3Woce4mXs

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Foundation For Sarcoidosis Research is proud to share our implementation of a Patient Stakeholder Reviewer Panel into our grant review cycle. This is a review process that brings the patient voice directly into evaluation of research proposals. It gives individuals living with

[FSR @StopSarcoidosis]

research and are ensuring that studies reflect the needs and desires of those living with sarcoidosis.

“The research is fascinating—You can help future sarc patients without leaving home, even while sitting down!—It’s a challenge but if you think you might be up to it, please

[FSR @StopSarcoidosis]

Sarc Fighter Podcast: https://t.co/WP7QkGsaUZ

#sarcoidosis #podcast #Raredisease

[FSR @StopSarcoidosis]

Kimberly Cleary lives in Chicago, where she is dealing with severe pulmonary Sarcoidosis. After a long path to diagnosis, she is working with her medical team to find a treatment that works for her. It has't been easy.

Listen to her story on the latest episode of the

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No one should have to navigate these challenges alone. Learn more about this new support program and how FSR is working to improve access to care:

Learn more: https://t.co/FnJJBSPbNo

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The Foundation for Sarcoidosis Research is working to better the experiences of patients so they can receive one-on-one support with:

-Insurance denials & appeals
-Prior authorizations
-Medicare & Medicaid enrollment
-Disability applications & appeals
-Financial barriers to care

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Whether you’re living with sarcoidosis or supporting someone as a care partner, your perspective can help build a clearer understanding of the needs of the Canadian Sarcoidosis Community

https://t.co/KRA4wPQ7gS

The survey takes approximately 5 mins to complete.

[FSR @StopSarcoidosis]

The Foundation for Sarcoidosis Research is working to better the experiences of people living with Sarcoidosis in Canada and we want to hear from you. The Canadian patient survey explore experiences with
- Diagnosis
- Treatment and care options
- Access to support and resources

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we’re talking about precision medicine.

💻 ILD Day is a one hour webinar presentation that you can join from anywhere. Our speaker is Dr. John Kim from UVA Health in Virginia.

Registration link: https://t.co/8DBOBlPaSc

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That’s the goal of precision medicine. 💊🫁

Most medical treatments are designed for the "average patient" as a one-size-fits-all-approach, which may be successful for some patients but not for others. Precision medicine, sometimes known as "personalized medicine" is an

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innovative approach to tailoring disease prevention and treatment that takes into account differences in people's genes, environments, and lifestyles.

And ILD has entered the precision medicine space! 💬🫁

📅 Our annual ILD Day returns on September 16 and this year,