Our Team
Olya Vrublevsky - Executive Director
Location: Winnipeg, MB
I joined ASF Canada in 2024 with a passion for making a meaningful impact in the lives of AS Families. Having a personal connection through a best friend of mine and her son Kirill (diagnosed in 2020), I am committed to advancing the foundation’s mission and supporting individuals and families affected by Angelman syndrome. As the Executive Director of Angelman Syndrome Foundation Canada, I will continue building strong partnerships and develop innovative programs and initiatives that provide critical resources and immediate support to AS families across Canada. With a heartfelt focus on collaboration and compassion, my goal is to create a brighter future for those living with Angelman syndrome from coast to coast.
Bradley Schiele - President of the Board
Location: Saskatoon, SK
My daughter Ali was diagnosed at 18 months with Angelman Syndrome (Deletion). My wife Tracy and I attended our first CASS conference in Ottawa of 2014. We were welcomed into a community of families that truly understood the challenges we faced as parents of a child with special needs. Since then, I've worked hard to increase awareness of Angelman Syndrome and the difficulties faced by individuals living with it. I am proud to support CASS and help further the work of raising awareness, education, and research on Angelman Syndrome.
Christa Graham - Vice President of the Board
Location: Sharon, ON
I have a 16-year-old son with Angelman Syndrome and received tremendous support through the various Facebook groups and forums, which allowed me to connect with other parents in similar situations. I feel incredibly fortunate to have the support of these wonderful people who understand the joys and struggles that come with raising a child with special needs. Being a part of this community has been one of the greatest gifts of my life, and I am excited to be able to help other families in the same way.
Terry Singleton - Board Director
Location: Edmonton, ALB
Our son Daniel was the first person in Alberta to be diagnosed with Angelman syndrome. I have been involved with CASS/ASFC since 1996, having witnessed firsthand the progress and success of the organization in supporting families and raising awareness. As a parent, I’m grateful for the advances we’ve made in both research and support services, and I am committed to ensuring that more families like ours receive the help they need.
Gina Ciampa - Board Director
Location: Vaughan, ON
My twin daughters Samantha & Christina have Angelman Syndrome and were born in 1996. They received their diagnosis when they were 9 years old, and since then, I’ve worked tirelessly to ensure they have access to the care and support they need. As a mother and advocate, I’m committed to helping other families facing similar challenges. I know firsthand how hard it is, and I’m proud to be a part of CASS in its mission to raise awareness and provide critical support to families of children with Angelman Syndrome.
Amy Monk - Board Director
Location: Calgary, ALB
I am the proud Mom to Davis (UPD), who was diagnosed with Angelman Syndrome in 2020. I have been actively involved with the ASF Canada since Davis’ diagnosis, and have worked alongside other families to raise awareness and create opportunities for research. I’m thrilled to be part of an organization that supports our children and their families in so many ways. There is still so much work to be done, but I know we are making progress.
Audrey Rouleau - Board Director
Location: Quebec City, QC
I am mom to Zac, 20yo, who lives with Angelman Syndrome. I became a board member in January 2024 but was already helping the organization with English - French translations. I am passionate about ensuring that French-speaking families have access to the resources and support they need. My journey as a mother has led me to become deeply involved in advocacy, and I hope my work can make a difference for other families like mine.
Sarah Dupuis - Board Director
Location: Ottawa, ON
Our daughter, Alice, lives with Angelman Syndrome (Deletion +). I joined ASF Canada in 2023. I have a long standing passion for advocacy within the rare disease community, and I’m committed to bringing attention to Angelman Syndrome and raising awareness for this rare and often misunderstood condition. Through the ASF Canada, I want to ensure that families have the resources and support they need while also advocating for increased research and funding.
Melika Zamani - Board Director
Location: Vancouver, BC
I have a daughter that lives with Angelman Syndrome, and joined ASF Canada in December of 2023. I dream of a world where individuals living with Angelman Syndrome have access to the best care, treatment, and educational opportunities. I joined the board to advocate for more research, awareness, and inclusion, and to help others who are navigating the same journey I am with my daughter.