Gunner entered this world like a whirlwind on New Year's Eve in 2004. He was three months ahead of schedule and weighed in at a whopping two pounds, eight ounces. Born with a rare condition called Amniotic Band Syndrome, Gunner had more problems than the ones associated with prematurity. He also had numerous orthopedic challenges including a club foot, webbing and amputation of some of his fingers, and the amputation of his right leg below the knee. With all the things Gunner has had to overcome, some of his most difficult struggles have been associated with his unilateral cleft lip. Gunner has had many surgeries in his short life, but his bone graft back in 2016 was, by far, the worst one he's ever had to tough through. Not only was the procedure rough, but the 90 day liquid diet that followed was absolutely brutal. Gunner has come a long way since his start as a tiny preemie! Now a sophomore in high school, he is taking all PreAP or AP classes. In his spare time, he loves to read or watch The Office or anything Star Wars-related. He’s also spending a little time behind the wheel. When COVID restrictions are loosened, he looks forward to spending time as a Junior Volunteer at Scottish Rite Hospital as well. Gunner's parents are incredibly proud of their warrior kid! We all know his future is bright, and we can’t wait to see where his path will lead!
WHERE ARE THEY NOW...................
"Mia Moo Fund made this difficult time so much more bearable by providing our family with much needed financial assistance. When Gunner needed us most, we were able to be solely focused on him and his recovery with no extra stresses or distractions from insurmountable medical bills. For that, our family is eternally grateful. In addition, Mia Moo gatherings have provided Gunner with the opportunity to meet, mingle, and relate to other kids who have also endured his struggles. It has benefited Gunner (and us his parents) so much to share experiences and fellowship with other families who really get it.” Brooke (Gunner's mom)