Dee Lawson Trip to See Specialist

Dee has Klippel Feil Syndrome. A rare genetic disorder that effects the spine, major organs, muscles, limbs, eyes, hearing and causes chronic daily pain. She also has Autism and is nonverbal. Her insurance won't pay for her to see a specialist in California that works with KFS. So this is a effort to raise money for that. I am Dee's Mom, Janey, I had the blessing of adopting Dee near birth. She was born at 23 weeks(1 lb 11 in) and not expected to live, she was meth exposed and had 2 heart surgeries & 4 eye surgeries, she stayed in the hospital most of her first two years. She us now 6, attending school, in regular classroom & making good grades. Unfortunately,, Dee continues to battle major health problems due to her KFS. Your help is deeply appreciated!!!! This fundraiser is to help her get to Sacremento, CA to see a Specialist about her disorder.