Jace Halsell's Medical Support Fund

Craig and Andrea Halsell's son, Jace, who is only 11 years old, has been diagnosed with an "Arteriovenous Malformation" or AVM, located in the center of his brain.  Because of the location of the AVM, it is not surgically treatable!  The only true option they have is to monitor Jace  for the rest of his life and pray that the malformation never ruptures.  
Because of the severe nature of Jace's condition, "routine" doctor visits are no longer routine.  Something as simple as coughing and sneezing can be alarming enough to require extensive and expensive testing to ensure the AVM has not become worse.
The kinds of tests the Halsell family will have to pay for are very expensive and will come on short notice.  And because there are no doctors in Lubbock that have the expertise necessary, they will also be required to travel out of town or out of state in order to get the high level of medical treatment Jace will need.  Because of this, we are setting up a "GoFundMe.com" account where friends and family members can donate funds to assist Craig, Andrea and Jace during this tough time.  The burden is huge, but together we can help!