Patient Foundation with GGC Ties Awarded Funding through Chan Zuckerberg Initiative to Drive Progress Against Rare Diseases


The Chan Zuckerberg Initiative (CZI), created by Dr. Priscilla Chan and Mark Zuckerberg in 2015, announced $13.5 million in funding to 30 patient-led organizations
that are working to find treatments and cures for rare diseases. These grants are part of CZI’s Rare As One Project,
aimed at supporting and lifting up the work that patient communities are doing to accelerate research and drive progress in the fight against rare

Rare diseases are anything but rare: as many as 7,000 rare diseases affect 400 million people worldwide. The vast majority of these diseases are
not well known or understood, and fewer than five percent have any FDA-approved therapy. The knowledge and learnings of patients suffering from
these diseases are key to driving breakthroughs in research and treatment, but a lack of funding and infrastructure to support such patient-led
research is holding that progress back.

The family-led Snyder-Robinson Syndrome Foundation is one of 30 grantees selected to participate in the
Rare As One Network. The Foundation will receive $450,000 over two years, along with resources including training, community mentorship, and capacity-building
services to assist them in establishing a network of researchers and clinicians, convening their community, and developing a research agenda. The
hope is that these organizations will share feedback with and learn from one another, and identify how to best address the most pressing needs
across a spectrum of rare diseases.

The Greenwood Genetic Center (GGC) has a close relationship with the Snyder-Robinson Foundation and a long-standing interest in this condition that
causes hypotonia (weak muscle tone), developmental delay, intellectual disability, seizures, and orthopedic problems.

The gene causing Snyder-Robinson syndrome was discovered in 2003 by GGC’s then-Director of Research, Charles Schwartz, PhD and his team. He convened a workshop at GGC in 2017 including clinicians, scientists, pharmaceutical representatives, and families to launch a
collaborative effort to develop a treatment for Snyder-Robinson syndrome which initiated several promising research partnerships. Schwartz retired
from GGC in 2018 but continues his work with Snyder-Robinson syndrome as Chair of the Foundation’s Medical and Scientific Advisory Board.

“I am so proud that the Snyder-Robinson Foundation has been selected for this transformational award,” said Schwartz, who was recognized by the Foundation in 2015 for his commitment to improving the lives of patients. “They have done extraordinary things to mobilize families from around the world who are
impacted by this rare condition, and with this grant and their perseverance, I have no doubt that we will find an effective treatment and eventually
a cure.”

GGC’s current work on this condition includes a project funded by the University of Pennsylvania’s Million Dollar Bike Ride program to study biomarkers for an early diagnosis, as well as an NIH-funded project with the University of Miami investigating mechanisms of neurological
disease in patients with Snyder-Robinson syndrome.

Michael Raymond helped start the Snyder-Robinson Syndrome Foundation after his son was diagnosed, and at the time, only two other US families had been
identified with the condition.

“The Snyder-Robinson Foundation hopes that its participation in the Rare As One Network will help advance research to improve the lives of SRS patients
and those with related disorders,” said Raymond. “The organization aims to build on the momentum gained over the last few years so that it may
deliver safe and effective treatments to all patients who need them.”

“No one is more committed to finding cures for rare diseases than the patients and families of those affected by these disorders,” said Priscilla Chan,
Co-Founder & Co-CEO of CZI. “We are proud to support patient-led organizations as they pursue diagnoses, information, and treatment options
in partnership with researchers and clinicians.”

About the Chan Zuckerberg InitiativeFounded by Dr. Priscilla Chan and Mark Zuckerberg in 2015, the Chan Zuckerberg Initiative (CZI) is a new kind of philanthropy that’s leveraging technology to help solve some of the world’s toughest challenges — from eradicating disease, to improving education, to reforming the criminal justice system. Across three core Initiative focus areas of Science, Education, and Justice & Opportunity, we’re pairing engineering with grant-making, impact investing, and policy and advocacy work to help build an inclusive, just and healthy future for everyone. For more information, please visit


Meet the Shenal Family

Our daughter, Ryleigh, was diagnosed with a rare chromosomal deletion shortly after she was born in 2010. Since we received her diagnosis, the Greenwood Genetic Center has become part of our family. They made certain that we did not feel alone, and they continue to provide ongoing, compassionate care for our child. The impact they have had on our family and others across the globe everyday is immeasurable. We can't imagine walking this journey without...

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