Wilms Cancer Foundation seeks to advocate on behalf of all children, families, healthcare organizations and the scientific/ research communities in order to assist them in tackling Wilms (Nephroblastoma) on a daily basis.  

 

The WCF actively attends, speaks and engages in professional groups and forums internationally in order to raise awareness of the disease and effect change where possible through collaboration, partnership and lobbying in order to; a) save lives and; b) advance the science in order to save lives. 

 

If you would like the foundation to advocate on your behalf or to attend an event you are attending or hosting please contact us at:

 

info@WilmsFoundation.org