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Who Are We?

This support group is for patients and caregivers of a Sarcoidosis patient. We are all
patients supporting one another.

Sarcoidosis (pronounced SAR-COY-DOE-SIS) is an inflammatory disease characterized by the formation of granulomas—tiny clumps of inflammatory cells—in one or more organs of the body. When the immune system goes into overdrive and too many of these clumps form, they can interfere with an organ’s structure and function.

This disorder affects the lungs in approximately 90% of cases, but it can affect almost any organ in the body. In some cases, the disease goes away on its own. In others, the disease may not progress but individuals will still suffer from some symptoms that challenge their quality of life. The rest of patients—up to a third of people diagnosed with the disease—will require long- term treatment. Sarcoidosis is considered chronic in people whose disease remains active for more than 2-5 years; in this population sarcoidosis can be debilitating and life-threatening.

When and Where

Our video chat virtual group meets on the 2nd Wednesday of each month at 7 pm Eastern, 6 pm Central, 5 pm Mountain and 4 pm Pacific in the AnCan Schmier Room. You can join online or by phone at +1 646 749 3127 Access # 656-182-845. See the Joining Instructions Panel above right for more information and other Country Access codes.

Our Co-Sponsors

Instructions for Joining a Group

 

Click HERE to learn how to connect with your computer or phone. No downloads required.


Click HERE to sign up for email reminders on virtual groups that interest you.

All of our groups are FREE...

and you can drop in at any time!

 

 

Upcoming Sarcoidosis Groups

Sarcoidosis

With this national online support group you will be able to do a video chat with others who are affected by sarcoidosis and their caregivers: if you don’t feel comfortable with video, you will be able to call-in also, but we do ask that we are able to put your first name in the room so we know who is talking.

May
8
Jun
12
Jul
10
Aug
14

Meet our moderators

cathleen headshot
Sarcoidosis Moderator
Co-Founding Director: Roll Call Wheelchair Dance Long Island a 501 (c) 3 nonprofit organization
chasta headshot
Sarcoidosis Moderator
January 2005, the date she received the news of Sarcoidosis, was the moment life changed for the Posey’s!
Regina headshot
Sarcoidosis Moderator
The Founder of Sarcoidosis Fort Wayne Support Group
Rodney headshot
In Memoriam - Sarcoidosis Moderator
He founded the Sarcoidosis Awareness Support Group of Greater Baton Rouge and The Sarcoidosis Awareness Foundation of Louisiana, Inc.
Trina standing with her hand in a fist
Sarcoidosis Moderator
Trina began advocating for better quality of life when she was faced with several chronic episodes.
Sarcoidosis Moderator
He was diagnosed with sarcoidosis in 2010 in his lungs and lymph nodes. In January 2020,  after a motor vehicle accident, the sarcoidosis spread to his heart. 

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Radionuclide treatment for prostate cancer is at least 10 years old – does that surprise you? Bayer’s Xofigo was approved in 2013 but adoption has been slow until recent FDA approvals of theranostics (treatment) viz. Pluvicto, and diagnostics (scans) like Illucix and Posluma.

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Our services are free, but if you benefit then please consider a tax deductible donation. You can also support us by signing up to Amazon Smile and nominating Answer Cancer Foundation at no cost to you.

AnCan does not provide medical advice – we do empower you to manage your own care.

Our calls are recorded and posted on this website for later listening; please note we are a peer-to-peer support group and not subject to HIPAA compliance.