The CSPA Board of Directors is composed of patients, skin-health professionals, educators, and members of industry. The group meets face-to-face once a year at the Annual General Meeting and has regular conference calls throughout the year. Board members are elected and serve a two-year term.
The board, which has representation from across Canada, sets the mandate for the organization and oversees staff to ensure financial and human resources are allocated appropriately to best serve Canadian skin patients.
The current Board of Directors:
Christena Baker (Co-Chair), Ontario
Barbara-Anne Hodge (Co-Chair), Manitoba
Barbara-Anne Hodge is an Occupational Therapist who worked on the Burn Unit at the Health Sciences Centre in Winnipeg, MB for 27 years. Inspired to support and nurture the burn survivor community, she helped found the Mamingwey Burn Survivor Society and has served as Chair since 2003. She is also a founding member of the Canadian Burn Survivors Community and is currently on the board of the Winnipeg Firefighters Burn Fund Inc. She has been involved with the Canadian Skin Patient Alliance since 2008 and is currently the President of the Board.
Sanjay Bhatt, Ontario
Sanjay Bhatt is a leading IT professional. He has held several excutive Director level positions with MNC IT companies. In 2003, he started his own IT company. As Founder & CEO, he grew the company to over 580 software professionals with over 270 Million Dollars in revenue. Sanjay maintains an IT blog covering new innovations, IT technology trends and is a member of IEEE.
Gena Brumitt, Ontario
Gena Brumitt is the daughter of Pat Barbrey, an incredible woman who suffered from the rare genetic skin disease, Recessive Dystrophic Epidermolysis Bullosa, Severe (Hallopeau Siemens) subtype. Gena is the founder of International EB Awareness Week, in memory of her late mother, and a founding member and 2-term Executive Committee member of DEBRA International as well as past president of DEBRA Canada. Gena is currently a regional ambassador for DEBRA International's EB Without Borders as well as board member of the Canadian Organization for Rare Disorders (CORD), in addition to proudly serving on the board of CSPA.
Sandy Burton, Ontario
Sandy was diagnosed with Rare Skin Disease (Darier's) at 3 years old. She has experienced many flareups and experimental medications but feels she is a survivor. She has an amazing Dermatologist and his Mother before him(Dr.Rikki Schachter and Dr,Dan Schachter) who she is so thankful to. She is honoured to be a Director on CSPA Board and is proud to be a voice in helping people with skin conditions.
Kyla LaHaye, Alberta
Besides being involved with the CSPA as a Board Member, Kyla is a full time stay at home mother to two little boys, as well as a skin patient.
Recently, Through specialized testing, Kyla was finally officially diagnosed with a rare disorder called Autoimmune Progesterone Dermatitis. As well as having APD, she also tested positive for being photo sensitive/allergic to UVB light. An official diagnosis however for the photo sensitivity has not yet been given. She is closely working with her doctors and is just in the beginning process of being seen by medical genetics department in Calgary Alberta.
In her spare time, Kyla enjoys working out, traveling, singing and spending quality time with her family.
Morris Manolson, Ontario
Morris F Manolson is a Professor and Associate Dean at the Faculty of Dentistry with a cross appointment in the Faculty of Medicine at the University of Toronto. His research focuses on preventing the excessive bone loss associated with osteoporosis, inflammatory arthritis and periodontal disease.
Munish Mohan, Ontario
Hansi Peiris, Quebec
Hansi Peiris is a Clinical Research Coordinator from Montreal, Quebec with a B.Sc. in Psychology from McGill University. She is passionate about dermatological research and advocating for skin patients. Hansi wishes to pursue her higher education to further advance clinical trial research while continuing to promote and protect the health of skin patients from across the globe.
Julie Powers, Ontario
Julie Powers has her Post Graduate Diploma in Event Management, and currently is the Director of Member Relations and Events for a Private Fishing Club in Mt. Albert, Ontario. She is a co-founder of The Canadian Alopecia Areata Foundation, CANAAF, which has grown from a small group picnic in a park, to an organization with successful independence. When not volunteering on the CANAAF Board, or participating and facilitating the annual conference, she enjoys being with her 2 teenagers and her stubborn but loveable French bulldog.
Ashutosh Sharma, Quebec
Jacqueline Sigurdson, Manitoba
Executive Committee: Barbara-Anne Hodge, Julie Powers, Munish Mohan, Christena Baker