The Atypical HUS Foundation

NonProfit Status/Address


Foundation for Children with Atypical HUS

A 501(c)3 Organization

The Foundation for Children with Atypical HUS encourages patients and investigators to share information and explore options/resources as we work together to gain insight into this ultra-rare and complex disorder of the complement system. By increasing contact opportunities with researchers and medical personnel interested in helping the aHUS community, our stories foster a better understanding of atypical hemolytic uremic syndrome. Sharing information, inspiration and support for one another, we seek to gather together people and knowlege as we strive to improve the lives of patients and families dealing with aHUS.


Informational Site: Visit us at Bill Biermann, Webmaster ( )

Interactive Website: Visit us at Linda Burke, Webmaster ( )


Address Correspondence to:


Bill Biermann, Director

The Foundation for Children with Atypical HUS

One Campbell Plaza Suite 2B

St. Louis, MO 63139



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