Helping Hands For Jace Halsell
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The EIA Customer Appreciation Fall Festival will feature a charitable cause that's close to our hearts. We will be raising money to support a very special kid named Jace Halsell. Here is his story:
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.
Jace's story has touched all of us at EIA. He is truly a special kid. Through all of the tests, trials, appointments, and doctors visits, Jace keeps a smile on his face. He's an inspiration to us all.
We created this page to help to the Halsells with their medical expenses. Our goal is to raise 1,000 in support of Jace's Journey. Jace's Journey
Jace needs your help and prayers. Please consider making a donation of $5 or more to help the Halsells and Jace get the treatment he needs.
Your support means the world to Jace and his family. Together, through helping hands, we can make a difference in his life.
Thank you in advance,
- EIA
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.
Jace's story has touched all of us at EIA. He is truly a special kid. Through all of the tests, trials, appointments, and doctors visits, Jace keeps a smile on his face. He's an inspiration to us all.
We created this page to help to the Halsells with their medical expenses. Our goal is to raise 1,000 in support of Jace's Journey. Jace's Journey
Jace needs your help and prayers. Please consider making a donation of $5 or more to help the Halsells and Jace get the treatment he needs.
Your support means the world to Jace and his family. Together, through helping hands, we can make a difference in his life.
Thank you in advance,
- EIA
Organizer and beneficiary
Jenna Royall
Organizer
San Antonio, TX
Craig Halsell
Beneficiary
