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X-WR-CALDESC:Events for National Scleroderma Foundation
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DTSTART;TZID=America/New_York:20260923T190000
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DTSTAMP:20251001T211529Z
CREATED:20250910T233024Z
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UID:10001486-1790190000-1790197200@scleroderma.org
SUMMARY:LGBTQ+ Scleroderma Support Group
DESCRIPTION:If you are interested in learning more\, please email\, LGBTQ@scleroderma.org\, with questions. \nClick here to register in advance. A link to the meeting will be made available after registration.
URL:https://scleroderma.org/event/lgbtq-support-group/2026-09-23/
LOCATION:Zoom
CATEGORIES:National Support Groups,Support Groups
ATTACH;FMTTYPE=image/png:https://scleroderma.org/wp-content/uploads/2025/09/LGBTQ-Support-Group-1.png
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DTSTART;TZID=America/New_York:20260923T190000
DTEND;TZID=America/New_York:20260923T210000
DTSTAMP:20260910T135418Z
CREATED:20260910T134022Z
LAST-MODIFIED:20260910T135418Z
UID:10003232-1790190000-1790197200@scleroderma.org
SUMMARY:The 20%: A Virtual Support Group for Males Living with Scleroderma
DESCRIPTION:Scleroderma diagnoses are less common amongst men. In fact\, only 20% of the patient population is made up of males. We’ve designed a support group especially for males with scleroderma. \nThis 20% Mens support group meeting is being held jointly with the Florida/Puerto Rico Chapter and our speaker will be Dr. Yen Chen\, a post-doctoral researcher at the University of Michigan scleroderma center; she will talk on brain fog. \nPlease click here to register in advance. A link to the meeting will be sent to you after registration. 
URL:https://scleroderma.org/event/the-20-support-group-for-males-living-with-scleroderma-2/
LOCATION:Zoom
CATEGORIES:National Events,National Support Groups,Support Groups
ATTACH;FMTTYPE=image/jpeg:https://scleroderma.org/wp-content/uploads/2025/09/20-support-Group-2.jpg
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