Eszter Hars, Ph.D., President and CEO, SDS AllianceOct 22, 2021SDS Patient Stories and NewsNora's SDS Story with a Twist: Our Quest for a Cure
Eszter Hars, Ph.D., President and CEO, SDS AllianceOct 10, 2021SDS Alliance News2021 Annual Global Virtual Fundraiser - Two Million Steps Closer to #CureSDS - Huge Success
Eszter Hars, Ph.D., President and CEO, SDS AllianceSep 30, 2021SDS Alliance NewsElevating Shwachman-Diamond Syndrome's Standing
Eszter Hars, Ph.D., President and CEO, SDS AllianceSep 25, 2021SDS Alliance NewsBringing Shwachman-Diamond Syndrome to the Forefront
Eszter Hars, Ph.D., President and CEO, SDS AllianceJul 24, 2021SDS Patient Stories and NewsBetty's SDS Story and Journey through Bone Marrow Transplant
Eszter Hars, Ph.D., President and CEO, SDS AllianceJul 7, 2021SDS Alliance NewsMouse Model Project: Meet the Scientists!
Eszter Hars, Ph.D., President and CEO, SDS AllianceJun 13, 2021SDS Alliance NewsAdvocating for SDS Research at Rare Drug Development Symposium
Eszter Hars, Ph.D., President and CEO, SDS AllianceMay 29, 2021SDS Alliance NewsThe SDS Alliance Launches Mouse Model Project with The Jackson Laboratory
Eszter Hars, Ph.D., President and CEO, SDS AllianceApr 30, 2021SDS Patient Stories and NewsWhitner's SDS Story and Journey to Bone Marrow Transplant
Eszter Hars, Ph.D., President and CEO, SDS AllianceApr 24, 2021SDS Patient Stories and NewsKim and Harrison's SDS Story from the UK
Eszter Hars, Ph.D., President and CEO, SDS AllianceApr 23, 2021SDS Patient Stories and NewsRyker's SDS Story and Journey to Bone Marrow Transplant
Eszter Hars, Ph.D., President and CEO, SDS AllianceJan 15, 2021SDS Alliance NewsA Cure for SDS: Our Mission
Eszter Hars, Ph.D., President and CEO, SDS AllianceAug 12, 2020SDS Patient Stories and NewsHealing Henley. An SDS Story told by Henley's mom, Jess
Eszter Hars, Ph.D., President and CEO, SDS AllianceAug 12, 2020SDS Patient Stories and NewsCarter and Skye's Story: A short video for Maddie Riewordt's Vision
Eszter Hars, Ph.D., President and CEO, SDS AllianceAug 12, 2020SDS Patient Stories and NewsGracie van Brunt – singer, songwriter, and rare disease advocate – shares her story in a podcast.
Eszter Hars, Ph.D., President and CEO, SDS AllianceJun 19, 2020SDS Patient Stories and NewsMax's Story: A short insight as part of the 2020 Jeans for Genes
Eszter Hars, Ph.D., President and CEO, SDS AllianceMay 23, 2020SDS Patient Stories and NewsGracie's Story: Finding my voice and insights into my BMT
Eszter Hars, Ph.D., President and CEO, SDS AllianceFeb 21, 2020SDS Patient Stories and NewsAbout a mother's relentless quest for a cure for SDS
Eszter Hars, Ph.D., President and CEO, SDS AllianceJan 27, 2020SDS Research UpdatesBone marrow-on-a-chip provides new research directions for Shwachman-Diamond syndrome
Eszter Hars, Ph.D., President and CEO, SDS AllianceDec 20, 2019SDS Research UpdatesThe North American SDS Registry celebrates its 10 year anniversary by giving back to the community
