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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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

June 7, 2022June 7, 2022

CDH International Joins the Global Advocacy Alliance!

May 10, 2022May 10, 2022

CDH International Works With Rare Disease Advocates in the UK

August 29, 2022May 10, 2022

CDH International Fiscally Sponsors Patient Advocacy at the 2022 BioTechX Congress in Basel, Switzerland to Bring the Patient Voice to BioData and BioTech Research in Europe.

March 8, 2022March 8, 2022

Shannon Newby On This Week’s CDH Radio Show

February 22, 2022February 22, 2022

CDH International Joins RareConnect

February 22, 2022February 22, 2022

CDH International Joins NI Rare Disease Partnership

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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