Two Lloydminster residents rallying support around child's rare disorder treatment
Two Lloydminster residents rallying support around child’s rare disorder treatment SHARE ON: Max Sych was diagnosed with Spinal Muscular Atrophy type 2 in November 2020. A treatment option, Zolgensma, is available in the United States for $2.8 million and must be administered to the child before he turns two years old. (Supplied Bowden Sych, GoFundMe) A Fairview toddler needing a life-altering gene therapy is getting a helping hand from people across the province here in Lloydminster. Max Sych, who has the affectionate nickname Mighty Max, was recently diagnosed with Spinal Muscular Atrop...