In only our third year, we welcomed over 650 guests who helped us raise over $60,000 for Prader-Willi Syndrome (PWS) research. We were honoured to have representatives from across Canada and the US, including Joanne Taylor and Cheryl Gagne from BCPWSA and Dr. Theresa Strong and Alice Viroslav from the FPWR. Our increase of almost 50% in fundraising along with the international attendance demonstrates the growing momentum behind uniting Canada to eliminate the challenges of Prader-Willi Syndrome. The gala, held at the luxurious Terrace Banquet Centre in Vaughan, was both an emotional and entertaining evening.
My little sister is 8 and has PWS for videos go to my videos andwatch m prader willi video..
sasa11698 1 year ago
My son 2 years has Prader Willy syndrom.
It is my Little sunshine.
medodonny 2 years ago