Everyone had beads on, but certain colors. If you had red, you were a family member of a chiarian, gold was friend, orange for volunteer, purple was that you had chiari, blue was syringomyelia, and other colors that stood for related conditions....
We all had teams we were walking for, and took team photos
From left to right: Liz, Daniel, Dad, Mom, Abby, Kaylie, Mason, Ben Me, Sabrina, & Matt |
Hi, my name is Amber Barnes. My 6yr old daughter was
diagnosed with Chiari 1 Malformation this past March. Like most chiari
patients, she suffered from a slew of symptoms, but her big 3 were daily
headaches, ear and eye pain. After much research, and finding the right
neurosurgeon for our family, she went through Posterior Fossa Decompression,
Duraplasty, and a C1 Laminectomy. A world of emotions changed our lives
forever, the day we found out about Kaylie. But that same day, I told myself I
would not let Chiari conquer us, we would conquer chiari!
We will Conquer Chiari. As we stand here today as passionate
patients, parents, siblings, grandparents and other family & friends, we
will push the awareness that is needed. We will raise money for research and we
will better educate our medical community. I thank god everyday that I found
this great group of people in Oklahoma, every one of you means the world to me.
Thanks for your support.
In all it was great, I met a lot of new friends, and friends from my FB groups. There was over 300 participants, and they raised over 10K. Amazing. Jenna, Stephanie, and Karen did a great job coordinating the event. Way to go ladies! I want to thank my family for coming out, it means the world to me!!! Much love to you all!
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