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The National Hemophilia Foundation’s Factor XIII Family Conference

October 10, 2018 - October 14, 2018

“Strength in Numbers”

This conference will be geared towards the families of those affected by factor XIII deficiency.

This event will feature educational sessions that will allow patients to learn more about this rare blood disorder.

Registration for the conference has not opened yet, so check the conference website for updates. More in-depth conference information should be available nearer the time. If you have questions, please email Meagan Richards.  (mrichards@hemophilia.org)





National Hemophilia Foundation
We believe rare disease patients are people, not a diagnosis. Through education, awareness and some humor, we help patients, caregivers and support persons by providing relevant and often inspirational news and stories.
Our goals are to share stories, cultivate strong community, provide the latest medical findings, connect people and pioneer production of patient worthy information. Help us attain these goals by telling us a little bit about yourself!

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