Open Heart Surgery for Jaxon Anderson

Meet Awesome Jaxon.  He was born with an extremely rare heart condition called ebsteins anamoly.  His doctors have always told his parents he has a mild case and would not need any surgery till he was a young adult.  Unfortunately, heart failure has a mind of its own and Jaxons heart is not handling him growing like we had hoped.  After sending his records to an EA specialist, Jaxons parents have found out that he is in need of open heart surgery right now.  To give Jaxon the best chance at living a normal life with a healthy heart, their family needs to travel to the Mayo Clinic in Rochester MN for surgery.  They have been told to plan for a 2 week stay if everything goes smoothly.  As a fellow heart mom, I  know how terrifying it is to travel across the country and try to figure out how to pay for a hotel, food, car, medical bills and the other millions of extras that always pop up during these types of emergencies.  Please help us lighten this burden for Jaxons parents so they can focus on whats important, keeping their little boy healthy and strong so he can fly through surgery and get to experience life as a little boy without heart complications.
Kendra