This web site is designed to be a resource -  your resource. 

If you have information or links that you think would be a useful addition to this web site, please email:

webmaster@beckwith-wiedemann-nz.org

Page last updated on:

7/06/2006 9:56 p.m.

Assisting individuals and families affected by BWS

The Beckwith-Wiedemann Children’s Association of New Zealand

Amber, September 2004, aged three months. 

 

A beautiful little BWS angel.

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The Beckwith-Wiedemann Children’s Association of New Zealand (BWCA NZ) is a non-profit organization created for New Zealand parents, professionals, and others who are interested in the Beckwith-Wiedemann Syndrome.

The major goals of BWCA NZ are:

· To increase public and professional awareness of Beckwith-Wiedemann Syndrome (BWS) in New Zealand.

· To provide information and peer support to individuals and families in New Zealand affected by BWS.

· To provide social and educational resources for those who are affected by BWS, and for the medical professionals who treat them.

 

Please note that this site is under construction.  If you need information urgently, please feel free to contact us directly.

 

THIS PAGE IS UNDER CONSTRUCTION - MORE TO FOLLOW LATER