Happy Rare Disease Day from the Stanford Center for Undiagnosed Diseases #RareDiseaesDay

‘When You Don’t Know, You Feel Alone in the World’ stanfordmag.org/contents/when-…

Beautifully written long form piece about some of our UDN families.

Check out this awesome piece on the life-changing work of Stanford CUD! So lucky to work with and learn from Matthew Wheeler and euan ashley, and thrilled to have Deni Ellis Béchard spend some time w us in the lab!

Uber-talented writer Deni Ellis Béchard profiles some of the patients and families who have received a diagnosis through Stanford’s branch of the NIH Undiagnosed Diseases Network: UDN, Stanford CUD. #GCChat #UndiagnosedDiseases #RareDiseases #NIH stanfordmag.org/contents/when-…

1/ Proud to share our paper with Matthew Wheeler out today in Genetic Counselors Journal of Genetic Counseling on outcomes of WES in patients with undiagnosed diseases facing prior insurance barriers #GCchat UDN tinyurl.com/yylyoy6f

1/ Excellent work by first author and GC extraordinaire Chloe Reuter out now in Journal of Genetic Counseling on outcomes of WES in patients with #undiagnosed diseases and prior insurance barriers tinyurl.com/yylyoy6f

Thank you, Stanford CUD for helping Carson and Chase. UDN is a wonderful program for #raredisease families.

#myheartcounts #scicd ⁦Stanford Health Care⁩ ⁦Stanford Medicine⁩ ⁦Stanford CUD⁩ #run #hearthealth

Hope for undiagnosed diseases; the economic woes of millennials; and using design thinking to make magic. These stories and more in the new issue of STANFORD: alu.ms/2ZYER0Y

This @StanfordMag feature highlights the impressive work of UDN, a research collaboration between Stanford CUD & 11 other academic institutions across the country aiming to solve the most challenging medical mysteries. bit.ly/2OeKdxU

It's the Sherlock Holmes of the medical world. The Undiagnosed Disease Program at the NIH pursues the challenges of diagnosing long-term mysterious conditions. bit.ly/2m7U5xH

Honored to lead off 2nd year of @stanford course led by Jason Hom: Diagnostic Odysseys in Medicine with @JenneferNoe at Stanford CUD discussing #undiagnosed to #diagnosed participant journeys

Grateful for the opportunity to share our story, promote the great work that UDN Stanford CUD do in #raredisease and create more awareness for MEPAN Syndrome.

Danny Miller (@sfcomms) shared his powerful story as a parent, advocate, and founder of the MEPAN Foundation, yesterday on Capitol Hill. The diagnostic odyssey is a challenging one - which is why programs like UDN are so critical. #FundNIH #fundscience ACMG

.Stanford CUD is one of UDN's 12 clinical sites across the country using innovative diagnostic therapies to solve the most challenging medical mysteries. bit.ly/2OeKdxU

Families find answers, and community, through the Undiagnosed Diseases Network scopeblog.stanford.edu/2019/10/01/fam…

There are over 7,000 recognized rare diseases and many more yet to be diagnosed. Stanford Medicine Magazine tells the story of four families, their quest for answers and the hope they found through Stanford's Center for Undiagnosed Diseases: bit.ly/2vpqPrc. #RareDiseaseDay

#RareDiseaseDay

Support rare diseases research this special rare diseases day Stanford CUD UDN National Organization for Rare Disorders (NORD) @MepanF