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TBRS Community Receives Rare As One Grant

  • Written by: Erin Rooker
  • Last update by: Erin Rooker
  • First posted: 11/3/2021 5:37:41 PM
  • Last updated: 11/3/2021 5:37:56 PM

The TBRS Community is thrilled to announce the Chan Zuckerberg Initiative has selected our organization to be part of the Rare As One Network, a collection of ambitious, patient-led organizations that are driving progress toward understanding and treating rare diseases. The award provides $600,000 in funding over three years to support the TBRS Community’s efforts to support families, advance research, and improve diagnosis and access to resources.

“The Rare As One grant is an incredible opportunity to help us fulfill our mission to find treatments for TBRS,” said Jill Kiernan, the executive director of the TBRS Community, who founded the organization in 2017. Jill’s daughter was one of the first 13 people in the world to be diagnosed in 2014. “We have come so far in developing a truly supportive, global community of families, doctors, and researchers in a few short years, and now we will be able to push ahead at an even faster rate.”

The TBRS Community is among 50 rare disease organizations in the Rare As One Network, which launched in February 2020. In addition to financial support, the Network provides training in strengthening community, building capacity, and promoting collaboration. The Rare As One Network provides opportunities to collaborate with other rare disease organizations.

The TBRS Community advocates for individuals with Tatton Brown Rahman Syndrome, a rare disease caused by variants in the DNMT3Agene. To date, around 250 individuals have been diagnosed with TBRS globally. In 2021, the TBRS Community launched a patient registry to gather medical and developmental information into a single database that will be accessible to researchers—a much-needed resource that aims to help answer fundamental questions about the syndrome.

The TBRS Collaborative Research Network, formed in 2020, represents the world’s top clinical and scientific experts on TBRS. Driven by the priorities of our community members, the TBRS Community partners with these investigators to further research on DNMT3A and TBRS, with the ultimate goal of identifying potential interventions for TBRS.

“For biomedical research in rare diseases to advance quickly and effectively, patients must be full partners with scientists and clinicians in research,” said CZI Head of Science Cori Bargmann. “We’re proud to expand our cohort of Rare As One grantees and further support the rare disease ecosystem as we work towards diagnosis, treatments, and cures together.”

“It is an honor to be among the organizations in the Rare As One Network and to learn from each others’ accomplishments,” said Kacee Richter, the president of the TBRS Community and the mother of seven-year-old Lucas, who has TBRS. “The impact of this grant is immeasurable to patient-led organizations like ours.”

https://tbrsyndrome.org/news/tbrs-community-receives-rare-as-one-grant