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The Cade R. Alpard Foundation for Pediatric Liver Disease

Racing to Cure Pediatric Liver Disease

The Cade R Alpard Foundation for Pediatric Liver Disease, INC. (Cade’s Foundation) is a non-profit 501(c)(3) organization established in 2003 by Scott and Jennifer Alpard for the purpose of supporting and funding the various programs that will make a difference in the lives of children with liver disease. Cade’s Foundation was started when Cade was diagnosed with biliary atresia, a form of liver disease whose only cure is liver transplantation. Cade received his new liver at the age of 1. During this time and after much research we found there was no foundation or organization dedicated solely to pediatric liver disease.

Cade’s Foundation focuses its activities in the following areas:

  • Funding and supporting research directed at identifying the cause of, a cure for, and means to prevent pediatric liver disease.
  • Being the vital link for patients and their families to information and education programs
  • Heightening awareness to the nature of these diseases and the efforts of Cade’s Foundation in order to stimulate volunteerism, scientific and health care community activism, and public support essential to the fight against pediatric liver disease.

This foundation is very dear to my heart as I, Nancy Anderson, personally know the family and felt their pain as they went through the diagnosis and uncertainty while waiting for a transplant. A family that did not stop at make my son better, but went beyond what most others would do and said let us help ease the pain and suffering of others with what we have learned in our own experience. To find out more or make a donation visit www.cadesfoundation.org

 

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