Biography
Terry Pirovolakis is a rare disease crusader and the father of Michael, who has spastic paraplegia type 50 (SPG50), a slow progressing neurodegenerative disorder. Mr. Pirovolakis fight to find a cure for his son could also transform the way that rare diseases are treated. Shortly after Michaels diagnosis, Terry began researching, reading scientific jounals and meeting with gene therapy expert. A month later he signed a contract to start a gene therapy program. It took over a dozen research institutions and laboratories working throughout the globe to develop a treatment for Michael. Then, last December Health Canada formally granted regulatory approval for the clinical treatment that would, hopefully, save the life of Michael and all those affected by SPG50. Mr. Pirovolakis was so moved by this ordeal that he wants to change the way rare diseases are approached at the national level. He's hosting free monthly gene therapy courses (Genes 101, Genes 103, and Genes 103) to help other families advance their own discovery programs.
Track Co-Chairs:
Yael Weiss, Mahzi
Peter Marks, FDA