Undiagnosed Diseases Network Foundation Promotes Access and Equity for Undiagnosed and Ultra-Rare Disease Patients
Washington, DC – Today, a group of undiagnosed and ultra-rare diseases patients and their family members, medical providers, and advocacy partners announced the launch of the Undiagnosed Diseases Network Foundation (UDNF). The organization aims to improve access to diagnosis, research, and care for all with undiagnosed and ultra-rare diseases.
For more information visit udnf.org
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