Help baby Weston get medical services

As many of you know, my husband LT and I have been searching for an answer to Weston's health complications and global, developmental delays. We have taken him to see doctors from Mississippi to Florida, performed every test imaginable, and paid countless medical bills, with still no answer. He is currently enrolled in therapy through Early Intervention and outpatient therapy at Thomas Hospital. Recently, we were informed that one the leading experts in mitochondrial disorders (Weston's "recessive" gene deletion, FBXL4) and other rare diseases lives in the southeast in Roswell, GA, which happens to be very close to my hometown where some of my family still lives. She has an extensive resume, including teaching pediatric medicine at Harvard University and now Emory in Atlanta! We were excited to hear this news! She is very willing to see our son, but insurance does not cover this expense. We are asking that you help us raise $1000 so that Dr.  Fran Kendall can help us find a diagnosis in order for Weston to receive the medical services he needs! THANK YOU.

http://vmpgenetics.com/dpc/