Special Programs
 
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 Welcome to the Coordination of Rare Diseases at Sanford (CoRDS)!Based at Sanford Research, a not-for-profit research institution, CoRDS is a centralized international patient registry for all rare diseases. The goal of the CoRDS registry is to connect as many patients and researchers as possible to help advance treatments and cures for rare diseases. The CoRDS registry is free for patients to enroll and for researchers to access. We work with patient advocacy groups, individuals, and researchers to coordinate the advancement of research into the 7,000 rare diseases.
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Our SolutionHow does enrollment in the CoRDS Registry work?
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Twitter Updates on Sanford CoRDS
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RT @SmithSolve: Yesterday we had the opportunity to experience the cutting-edge research happening at Sanford on an amazing tour of the lab… -
RT @SanfordBenF: The topic of rare disease registries comes up often in the panel discussions at the #NORDSummit this week! They are valuab… -
RT @ataxiaandme: The topic of #RareDisease registries comes up so often in discussions They are valuable tools to advance #research and u… -
The topic of #RareDisease registries comes up so often in discussions They are valuable tools to advance… https://t.co/ywXZAEFAqJ -
RT @SanfordBenF: The topic of rare disease registries comes up often in the panel discussions at the #NORDSummit this week! They are valuab… -
The topic of rare disease registries comes up often in the panel discussions at the #NORDSummit this week! They are… https://t.co/6Sxw0hrR5a -
RT @SanfordBenF: Patient registries are valuable tools for interacting with researchers and the FDA. @SanfordCoRDS works with advocates to… -
RT @SanfordBenF: Patient registries are valuable tools for interacting with researchers and the FDA. @SanfordCoRDS works with advocates to… -
RT @SanfordBenF: Patient registries are valuable tools for interacting with researchers and the FDA. @SanfordCoRDS works with advocates to… -
RT @SanfordBenF: Patient registries are valuable tools for interacting with researchers and the FDA. @SanfordCoRDS works with advocates to… -
@SanfordBenF @SanfordCoRDS @ekeeleymoore -
Patient registries are valuable tools for interacting with researchers and the FDA. @SanfordCoRDS works with advoc… https://t.co/JTvka2DJoX -
Looking forward to a productive time at the #NORDSummit over the next couple of days! Let me know if you're intere… https://t.co/WaiUglXe8t -
@RareDiseases @SanfordBenF @SanfordCoRDS Awe thanks! @sueesherman is coming, so the @LAMFoundation will be well rep… https://t.co/mjGPqnvt9I -
@JensenKatieC @SanfordBenF @SanfordCoRDS We'll miss you this year, Katie!! Hope to see you next year! #NORDSummit