FSR is grateful for our friends throughout the world who are dedicated to raising awareness and accelerating research for sarcoidosis! To learn how to host your own fundraising event, download our fundraising guide and email Angela Frelander at angela@stopsarcoidosis.org for help to get started. We’ll provide resources to make your event a success and help promote what you’re doing on FSR’s website.

 

April is Sarcoidosis Awareness Month

We will be working throughout the month to ensure the voices of sarcoidosis sufferers everywhere are heard! In addition to the Kick In to Stop Sarcoidosis (K.I.S.S.) 5K Run/Walk in Nashville, TN, volunteers will be bringing walks to their own hometowns on April 22, 2017. Search for a walk near you using the search function below. If you can’t find an event near you, learn about how you can become a walk leader and raise awareness in your own community!

Sat 08

Ohio

On July 8th Marie and her husband Jack, a neurosarcoidosis patient, will be at the Cornerstone Meeting & Event Center in Grove City, Ohio for an expo to raise awareness and funding for sarcoidosis research. The expo will host local businesses and include amazing prizes donated from vendors! Entry is free and raffle tickets will be sold at the door, 1 ticket for $3.00 or 4 tickets for $10.00. Before the end of the expo, Marie and Jack will draw raffle winners! What is neurosarcoidosis? Sarcoidosis is an inflammatory disease that can affect almost any organ and in Marie's husband's case, has affected...
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Sat 29

Washington

Please join the Foundation for Sarcoidosis Research and internationally recognized physicians in Seattle, Washington to gain valuable insight into sarcoidosis. Patients and loved ones will have the opportunity to learn about FSR’s research initiatives, sarcoidosis treatment options, and clinical care with experts in the field. This event provides the chance to network with patients, physicians, and researchers to share your experience, identify and discuss needs, and gain a better understanding of sarcoidosis. Each attendee requires an individual registration – please complete the form below and refresh the page to register additional attendees. More information on the venue and parking are available below. Information on exact locations, speakers, agenda,...
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Sat 29

Georgia

Put on your favorite white outfit and come join the Sarcoidosis Support Group of Atlanta when they host their annual All White Party on July 29th from 6:00p.m.-9:00p.m.! The Sarcoidosis Support Group of Atlanta is a 501(c)3 non-profit organization dedicated to raising sarcoidosis awareness and promoting health and wellness in their community. The annual All White Party is one of the awareness events they plan in order to continue their mission to raise awareness, provide additional resources and education to patients, their families and friends. The event is open to the public and everyone in the area has been encouraged...
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Sat 30

10:00 am - 3:00 pm

Please join the Foundation for Sarcoidosis Research and internationally recognized physicians in Ann Arbor, MI to gain valuable insight into sarcoidosis. Patients and loved ones will have the opportunity to learn about FSR’s research initiatives, sarcoidosis treatment options, and clinical care with experts in the field. This event provides the chance to network with patients, physicians, and researchers to share your experience, identify and discuss needs, and gain a better understanding of sarcoidosis. Each patient attendee requires an individual registration – please complete the form below and refresh the page to register additional attendees. Information on exact locations, speakers, agenda, etc. will be updated regularly. If you have...
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Sat 11

FL

Please join the Foundation for Sarcoidosis Research and internationally recognized physicians in Jacksonville, FL to gain valuable insight into sarcoidosis. Patients and loved ones will have the opportunity to learn about FSR’s research initiatives, sarcoidosis treatment options, and clinical care with experts in the field. This event provides the chance to network with patients, physicians, and researchers to share your experience, identify and discuss needs, and gain a better understanding of sarcoidosis. Each patient attendee requires an individual registration – please complete the form below and refresh the page to register additional attendees. Information on exact locations, speakers, agenda, etc. will be updated regularly. If you have immediate...
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