Tyler is absolutely amazing & has been a fighter since the day he was born. When he was 2 years old, we were told that he was Autism; in 2003 Autism wasn't a disability people were familiar with, all the doctors told us is that he would not progress in life like other "normal" children. We had no idea what the future had to hold for us as a family or for him. Kaelyn was born 2 weeks before Ty was diagnosed in October of 2003 and Ryan would come to join the family in August of 2009. In August of 2013, Tyler started to say that his legs were sore; I had taken him to the doctor who said he had "growing pains" and to take Advil. October 2013 comes along, Tyler is still doing gym at school and going about normal day to day's and still saying that he has pain in his legs, to the point where it was keeping him up at night. I went to his doctor to get an x-ray request for his legs, and on the day I went to pick it up, his school called me and he was screaming in pain. I took him to the Guelph General Hospital, they did an x-ray and determined that the left side of his pelvis was missing and we needed to be referred to Sick Kids Hospital in Toronto. After MRI's, CT scans, and a bone scan; Sick Kids has determined that Tyler has a rare form of bone cancer called Ewing's Sarcoma. Ewing's Sarcoma are tumors within the bone, it occurs in adolescents mainly, but can be diagnosed in older as well. Ewings Sarcoma is usually found in the long bones of the body; pelvis, femur, tibia. If the cancer is localized it is easier to treat, Tyler's was metastasized. Tyler's cancer was found from his brain to his toes and his prognosis wasn't good. Tyler was given 2 months to live. After 14 rounds of chemo, 36 rounds of radiation, and Cannabis Oil around the clock, Tyler is now NED (no evidence of disease) since 2015. Miracles do happen & doctors aren't always right. Follow your gut.