Our team would like to show our support to our community. We are reaching out and building awareness about a child in need of help. His name is Max, most call him Mighty Max. He received the diagnosis of Spinal Muscular Atrophy type 2, a rare and debilitating disease. The way to maximize length and quality of life is to seek Zolgensma - a gene therapy that as of December 2020 has been approved for use in Canada but is not funded by Health Canada, a drug that must be administered before he reaches a certain weight. The cost is $2.8 million CAD. The family is seeking help from our community. We have attached the GoFundMe link below. We will be making contributions on every order placed. If you are able to offer additional support Max and his family would greatly appreciate it.