CGD ASsociation of America
CGD ASsociation of America
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    • Home
    • Ways to Give
    • About Us
      • Who We Are
      • Partners and Sponsors
      • Mission & Accomplishments
      • Blog & E-Newsletter
      • Press Room
      • FDA PLS for CGD
    • Living with CGD
      • What is CGD?
      • Diagnosing CGD
      • Managing CGD
      • Treatments & Providers
      • X-linked CGD Carriers
      • For Clinicians
    • Getting Help & Support
      • CGDAA Zoom Calls
      • Financial Assistance
      • PC's for People
      • CGDAA Events
      • Carrier Connection
    • Contact
  • Home
  • Ways to Give
  • About Us
    • Who We Are
    • Partners and Sponsors
    • Mission & Accomplishments
    • Blog & E-Newsletter
    • Press Room
    • FDA PLS for CGD
  • Living with CGD
    • What is CGD?
    • Diagnosing CGD
    • Managing CGD
    • Treatments & Providers
    • X-linked CGD Carriers
    • For Clinicians
  • Getting Help & Support
    • CGDAA Zoom Calls
    • Financial Assistance
    • PC's for People
    • CGDAA Events
    • Carrier Connection
  • Contact

FDA Patient Listening Session for CGD

 

On August 11, 2025, several CGD patients and caregivers shared their experiences during a Patient-Led Listening Session with the U.S. Food and Drug Administration (FDA) so its members could learn more about the symptoms, treatment options, challenges in getting a diagnosis, as well as the complex care needed for a child with a rare disease and its impact on the child and entire family.


 

Thank you to our CGDAA community members who shared their personal stories, advocated for more treatment options, and provided valuable insights.

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