rare disease Archives - CDH International - A Global Initiative to Stop Congenital Diaphragmatic Hernia

CDH International is a registered charity in the US, UK, Netherlands, Hong Kong, Singapore, Canada and Switzerland.

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March 1, 2024February 29, 2024

CDHi Teams Up with Beyond The Diagnosis

December 6, 2023December 6, 2023

CDH International Attends Rare Fair 2023

December 3, 2023December 3, 2023

CDH International Signs On To IRA Community Letter to Congress

December 3, 2023December 3, 2023

CDH International Attends the UN Global Health Summit

December 3, 2023December 3, 2023

CDH International Attends the 2023 World Orphan Drug Congress in Barcelona

October 12, 2023October 12, 2023

CDH International Attend the 2023 Rare Fair

July 9, 2023July 9, 2023

CDH International Signs On To Letter To Congress to Protect the Orphan Drug Act and Pass the RARE Act

July 9, 2023July 9, 2023

CDH International Signs Letter Of Support for the Accelerating Kids’ Access to Care Act

March 27, 2023March 10, 2023

Gulf Beacon at Gulf Tower and Koppers Building Lights Up For CDH Awareness

March 14, 2023February 26, 2023

Louisiana Proclaims April CDH Awareness Month

November 15, 2022November 15, 2022

CDH International Attends the 2022 BioTechX Conference

June 14, 2022June 14, 2022

CDH International Signs Letter with NORD and 85 Other Rare Diseases Nonprofits for Research Legislation and Funding

Founded in 1995 as CHERUBS, CDH International is a global non-profit working to help over 6500 patient families in 74 countries through support services, raising awareness and funding and conducting CDH research

CDHi is a registered non-profit in the United States, Canada, United Kingdom, Switzerland, Hong Kong, Singapore and the Netherlands.

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