The KTeam
WHY DO WE WALK?
9/11/11.. almost THIRTEEN years ago and just 3 short months into parenthood, we experienced our most frightening moment as parents... we learned that our baby had a condition that had no cure. That the only treatment option would require immediate brain surgery. That this surgery wouldn't cure his condition, but would treat it. That he could potentially need more brain surgeries throughout his lifetime. That the extent of damage to his brain was unknown. Every question we asked was answered with "at this point, we'll have to wait and see.." Thinking back during this time.. ALL OF YOU, our family and friends, prayed for our baby! And we know you have been praying for him since. We are forever grateful. He came out that day with a successful surgery and has been overcoming obstacles related to this condition ever since. He is our greatest blessing ever and is a true testament of God's healing power.
This condition that I write about is Hydrocephalus. And while we and those close to us hear the term and learn more about it daily, we want to teach others about how this condition affects Khoy, and other children and adults like him. Without awareness, there will be no funding.. without funding, no research.. and without research, no cure... WE NEED A CURE! Our daily prayer is that a cure or better treatment option is found before Khoy needs another brain surgery. Help us raise awareness! Please consider donating to our cause today. If you are unable to donate, a share of our page is just as helpful! And if you're in the DMV area, please join our team and walk with us on Saturday, September 21st at the Sylvan Stage (base of the Washington Monument) in DC as we WALK to raise awareness!
Please join me and The K-Team and WALK with us to End Hydrocephalus!
Thank you!
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