It's that time again—this month's edition of eNews is now available! Highlights from this month include that tickets are now available for Cool Comedy • Hot Cuisine, your impact on...
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"I learned about scleroderma when my mom had a mild case...Many people are misdiagnosed for years and there is not a lot of awareness or research funding." SRF Board Member...
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Rae is a medical researcher, a self-described nurturer and dreamer–and someone who lives with scleroderma. In our conversation with her, Rae talks about her journey to being diagnosed, how it...
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The Scleroderma Research Foundation’s 2020 Annual Report is now available online. This report demonstrates the many ways in which we drove our mission forward during a global pandemic, thanks to dedicated...
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Scleroderma advocacy began with Juliana’s diagnosis. “The minute I found out about my rare condition, I started advocating for my rights,” she says, “and I then founded 10 regional groups,...
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We're pleased to announce a new SRF-funded research study: Establishing a Spatially–integrated Transcriptomic, Epigenomic, and Histologic Signature of Fibrosis in Systemic Sclerosis, led by Michael Longaker, MD, and Howard Chang,...
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Participating in research is crucial to finding a cure for scleroderma. SRF Cure Crew member Melissa talks about just this in a new 23andMe blog post. She participated in 23andMe's...
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For #ThrowbackThursday, we’re remembering how Cool Comedy • Hot Cuisine spreads laughter and scleroderma awareness every year. And, we’re excited to host it virtually once again as a live broadcast on Sunday, October 17th! SRF...
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Supporters like you are at the core of everything we do at the Scleroderma Research Foundation. You make it possible for us to drive scientific research forward, helping to secure...
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