Home Who & What is LDSA What is Down Syndrome Executive Committee Volunteers Contact Us
President: Randy Bilton  
Randy and his wife Dianne live near Belmont. They are the proud parents of Kyla, a beautiful girl with Mosaic Down Syndrome. Randy has been our President since March 2006 and the LDSA has benefited greatly from his unending efforts.
Vice-President:
Kym Hann Holdaway		  
Kym has been involved with the LDSA since 2005 and has contributed to many of our projects. Her efforts with regards to 'Building On Dreams' has made this event bigger and better every year. We are very happy to welcome Kym to our Executive Committee. Jamie (DS) is very proud to have Kym as her 'Auntie'.
Treasurer: Sandy Bogart  
Sandy joined the LDSA when her daughter Jamie (DS) was born. She has 20 years experience in book-keeping as well as personal and corporate income tax preparation. Sandy’s contributions to our association are heartfelt and committed. She is passionate about her position within the LDSA and aspires to be the best advocate possible for her daughter.
Secretary: Bev Bialik  
Bev lives in Lambeth with her husband Sean and their four daughters. Her youngest, Melissa, has Down Syndrome. Bev serves as the LDSA Secretary, is involved in the fundraising committee, and takes our information display to such events as the Health Unit's Prenatal Fair. Mellie and her big sisters manage to keep their mom and dad hopping, and they wouldn't have it any other way.
Editor: Ray Riviere  
Ray lives in London with his wife Jane their two daughters Sarah (DS) and Paige. Ray is the editor for the LDSA and is responsible for the quarterly newsletter's. During the summer he enjoys coaching with the Byron Challenge Baseball league in Byron.
Director at Large:
Paul Van Eyk		  
Paul is the father of three daughters; Sierra, Catrina and Monique. He and his wife Natalie, live in Lambeth. Sierra (DS) is their oldest child and was born in 1999. They support her and her sisters to become the best they can be.
Director at Large:
Jane Riviere		  

Jane is married to Raymond (Editor) and they live & work in London. They have two daughters Sarah 19yrs (DS) & Paige 15yrs. Jane and Ray are proud of both their daughters and all of their individual achievements. Jane has been the LDSA Teen contact since 2006 and is looking forward to also serving on the executive as a director.
Peer Representative: Heather Verdun  
Heather lives in London with her parents and two younger siblings. Having completed high school, she is currently taking some courses at Fanshawe College, working at a part-time job, and doing some volunteer work. As a peer representative, Heather feels strongly about advocating for herself and her peers, encouraging other young adults with Down Syndrome to be active in their communities, and make a difference!