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Twitter Updates on Sanford Research
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RT @SanfordBenF: Connecting patients with researchers is our mission at @SanfordCoRDS. To witness such a passionate and inspiring group mee… -
RT @JFCConsultants: #raredisease @EparentConnect @PPALSorg @teaminspire If you haven't heard about @SanfordCoRDS then you need to watch thi… -
Great story! #PPI #raredisease #science #research https://t.co/SGVdCpBwjc -
RT @SanfordHealth: “When you meet these young warriors that are singing to Frozen, singing Disney songs and their parents are just starting… -
@SanfordCoRDS I was recently connected with Anna. She’s such a great advocate for Alagille Syndrome and the rare disease community. -
@EparentConnect @ComplexChildMag @PPALSorg Check out the @SanfordCoRDS video on the #raredisease #alagillesyndrome.… https://t.co/wUeBDZfymU -
RT @JFCConsultants: #raredisease @EparentConnect @PPALSorg @teaminspire If you haven't heard about @SanfordCoRDS then you need to watch thi… -
@NAF_Ataxia @SanfordCoRDS This form is too hard to fill out. -
RT @SanfordHealth: “When you meet these young warriors that are singing to Frozen, singing Disney songs and their parents are just starting… -
“When you meet these young warriors that are singing to Frozen, singing Disney songs and their parents are just sta… https://t.co/cbn01fPFwA -
RT @shamy27: #RareDiseaseResearch @SanfordCoRDS @SanfordHealth is something spectacular. They work in such a collaborative environment! It… -
@SanfordCoRDS @ORDIndia Thanks for the retweet! 😁 -
RT @SanfordCoRDS: CoRDS connects patients and researchers. Here's one video from a group of patients from the Alagille Syndrome Alliance me… -
#RareDiseaseResearch @SanfordCoRDS @SanfordHealth is something spectacular. They work in such a collaborative envir… https://t.co/WtI42oV4Ov -
RT @shamy27: As far as opportunities of a lifetime go, this is one of them.@spicylilAnna & I are so grateful! I urge you all to watch this…