
Sarcoidosis Details
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.
Our Co-Sponsors

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.
Check out Sarcoidosis Moderator Regina Gordon’s Book!
Check out Sarcoidosis Moderator Regina Gordon’s Book!
To Hell with Sarcoidosis and Other Illnesses: Poetic Justice Journaling My Inner Thoughts
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.
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Meet our Moderators
Cathleen R. Terrano
Co-Founding Director: Roll Call Wheelchair Dance Long Island a 501 (c) 3 nonprofit organization
Chasta L. Posey
January 2005, the date she received the news of Sarcoidosis, was the moment life changed for the Posey’s!
Kevin McDevitt
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.
Regina Gordon
The author of 'To Hell with Sarcoidosis,' she champions sarcoidosis and rare disease awareness.
Rodney Reese
He founded the Sarcoidosis Awareness Support Group of Greater Baton Rouge and The Sarcoidosis Awareness Foundation of Louisiana, Inc.
Trina Massey Davis
Trina began advocating for better quality of life when she was faced with several chronic episodes.
Related Blog Posts
Rarity Life Magazine Featuring Rick Davis
Rarity Life Magazine interviews AnCan Founder, Rick Davis on the value of virtual peer support and how AnCan came to be,
CNTV’s “Best of the Nation” featuring Rick Davis
CNTV’s “Best of the Nation” featuring Rick Davis
AnCan welcomes Air Relief!
AnCan welcomes Air Relief – AnCan announces ‘new’ Executive addition
Resources
Past Recordings
If you’re curious about the format of a virtual support group, click HERE to see recordings of past groups.
Tax Deductible Donation Info
Our services are free, but if you benefit then please consider a tax deductible donation.
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.