In June 2016 our lives changed forever. We welcomed our son Cooper to the world and in less than a week he was suspected to have cystic fibrosis. We were shocked! At the time we knew nothing about the progressive disease or how it would impact our family. Since his diagnosis we have had amazing support from family, friends, and different agencies in and around our community. Cooper has a fiery personality, he handels his daily treatments and medications like a champ.
After coming to terms with Cooper’s diagnosis and learning what life can be like with a child with a chronic illness we had a longing to give back. Sweating for Swag was started as a way to help raise money and awareness for different charities across the United States.