Story about Leukodystrophy .

Tadan Charles Foss

Aug 7, 2017

By: Todd


page:U269

In 2009 a 3 year old boy was diagnosed with a terminal ill disease, called Vanishing White Matter Leukodystropy, 2 1/2 years later the little boy passed away. His name was Tadan Charles Foss, my son.

 

This foundation was based on a promise a father made to his son when he visited him after he passed on. The father promised his little boy that his death from a terrible disease would not go unnoticed but would live forever and somehow help other parents and children with their life changing event. There are many resources that will help a family through this event, but the biggest is the drive and compassion from a father keeping his promise to his son. This promise was made to Tadan Charles Foss from me, his father. God Bless. Todd A. Foss, President, Tadan's Touch Foundation

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