Who We Are

The Ethan James Wyne Organization has been a professional organization since October of 2013. We are a group of local professionals and close friends and family to Becky and Trevor Wyne, whom tragically lost their precious son, Ethan, on September 12, 2013.

Ethan was born with a very rare genetic disorder called Medium chain acyl-CoA dehydrogenase deficiency (MCADD). Children who are born with MCADD are either missing or born with a non-functioning enzyme that is responsible for the breakdown of fatty acids in consumed and stored food. These acids, once broken down, are the source of the energy we need to live. If caught early, children who are born with MCADD can live happy and healthy lives when diet and health are monitored very closely. Becky and Trevor knew right away that they needed to do something to raise awareness and education. Thus, this group of closely knit friends and family has been formed in Ethan’s honour.

To learn more about MCADD, please visit the WHAT IS MCADD TAB on this website or go directly to these very informative sites: