The National Fabry Disease Foundation (NFDF) is pleased to announce its 2024 virtual education meeting series.  We will have one or two meetings per month, on weekdays at 7pm ET for your convenience.  

Learn more about our schedule, speakers, and register for our meetings HERE

Recordings will be posted to our youtube channel

Primary attendees for this group of virtual meetings are individuals with Fabry disease, family members, and caregivers. The intended audience will vary from U.S. only to global participation depending on the applicability of each topic or resource. Primary attendees are encouraged to ask questions and participate in our prize drawings. 

Other attendees, such as healthcare providers and industry partners, can attend to learn about the resources currently available to the Fabry community.

Most of the webinars will be recorded and available online a week or two after the meetings. 

Please share this announcement with adult family members with Fabry.

Subscribe to our e-newsletter at https://tinyurl.com/NFDF-news.

We look forward to seeing you there! 

The NFDF Team (Jerry, Casey, and Susan)

Thanks for your support!

As an IRS 501(c)(3) non-profit charitable organization we rely on donations from organizations and individuals to provide meaningful programs and services to people/families with Fabry disease.                      Please give generously!  

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Thank you to our corporate/business sponsors as well as our many individual donors. Contributions of all sizes add up to make a tremendous difference.

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