Emma Krall's Continuing Journey

Emma was born 9 weeks premature and has Campomelic Dysplasia. Because of this, she has countless health struggles- collapsing airway, need for a trach & ventilator, scoliosis (need for spinal fusion and halo), severe hearing loss, floppy muscles, cleft palate, bowed legs, club feet (need for casts), g-tube fed, and others. The money from this charity will be spent on gas money to and from Seattle Children's Hospital, medical bills, orthopedic items, physical therapy toys, and specialized medical equipment. Emma has a continuing journey throughout her life that will need to be sustained as much as we can! More of her story can be found at her blog:
https://van09001.wixsite.com/mysite-1

Update March 2020-
Emma is continuing to improve! She has 2 surgeries in the next couple of months- cleft palate repair and removal of overies due to chance of cancer. We are also in the process of ordering physical therapy equipment, such as a stander and other activity chairs to strengthen her muscles. Insurance does not cover these items, but they are absolutely necessary for her growth .