About Myeloma Canada

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Who we are

Myeloma Canada is the only national charitable organization created by, and for, Canadians impacted by multiple myeloma. We are driven to improve the lives of those affected by this disease by empowering our community through awareness, education, and advocacy programs, and by supporting clinical research to find a cure.

We are committed to making myeloma matter, and have been since our founding in 2005 by two gentlemen who were living with myeloma, Aldo Del Col and John Lemieux.

A grandmother and young grandaugher seated in a garden looking at one another

Our mission

To improve the lives of and empower all Canadians affected by myeloma and accelerate access to the best care while supporting the pursuit of its cure and prevention.

Our equity, diversity, and inclusivity pledge

We pledge to cultivate and maintain an inclusive environment for our community and our organization. This includes respecting and addressing the diverse needs of all people—First Nations, Métis, and Inuit; underrepresented and marginalized populations; the LGBTQIA2S+ community; cultural, racial, and ethnic minorities—in all that we do.

Our commitment to you

Myeloma Canada is proud to have attained Imagine Canada Level 2 Accreditation, having successfully completed a rigorous peer review of our operating and governance practices. Our accreditation lets our volunteers and donors formally know that when they support Myeloma Canada, their goodwill is in good hands, further solidifying the bond of trust and confidence you’ve already placed in us.

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Find support

Myeloma touches the lives of tens of thousands of Canadians. Whether you’re living with this disease or caring for someone who is, there are many support options available to you where you can meet and exchange with people who understand the journey you’re on.

We have an ever-growing network of volunteer-run and -led local support groups across Canada, online special interest Facebook support groups, and peer-to-peer support programs. Each helps to create a sense of belonging and community for people with myeloma and their families.

Making myeloma matter

Myeloma Canada is a patient-driven, patient-focused grassroots organization that unifies and represents the voice of the Canadian myeloma community. Together, we are committed to improving the lives of those impacted by myeloma. We do this by:

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Providing free educational resources to people living with myeloma, their families, and caregivers

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Increasing awareness of the disease and its effects on the lives of those it touches

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Facilitating access to new therapies, treatment options, and healthcare resources

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Advancing clinical research and promoting access to new drug trials in Canada

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Empowering Canadians impacted by myeloma through community so that no one feels as if they are going through their journey alone

Photo of Aldo Del Col and John Lemieux

What our co-founders Aldo Del Col and John Lemieux created has since evolved into a leading, internationally respected and innovative organization. In their honour, and in honour of the thousands of Canadians living with this 2nd most common form of blood cancer, we will continue to empower every Canadian touched by myeloma. We are focused on the future and on fulfilling our promise to our myeloma community.

Making Myeloma Matter: Strategic Plan 2025–2029 goes into more detail about Myeloma Canada’s strategic goals and our plans to achieve them.

Read our annual publications

Your gift to Myeloma Canada today helps improve the lives of thousands of Canadians living with this complicated and as of yet incurable disease. See the real impact of your donations in our 2024 Myeloma Canada science and research impact report. Learn why your donations are so vital in our Case for Support brochure.

Learn more about myeloma and how we can help in our mini pamphlet.

Order a printed copy

Our five-year strategic plan

Looking forward to a life uninterrupted by myeloma.
Making Myeloma Matter: Myeloma Canada’s strategic plan for 2025–2029

Myeloma Canada’s five-year strategic directions plan not only addresses our vision for Myeloma Canada but for myeloma in Canada as well.

In order to create our five-year plan, we needed to understand where we were yesterday, where we are today, and, more importantly, where we want to be tomorrow. We did a full evaluation and analysis of our values and mission statement, our direction, goals, and objectives to make sure they were aligned with and representative of who and where we want to be by 2029 for our community and as an organization.

Myeloma Canada’s continued leadership and work on behalf of the broader myeloma community is focused on four strategic goals. Each of the goals has people living with myeloma at the heart of what we do.

Our strategic goals: putting the person first

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No one left behind:
Meet the needs of the Canadian myeloma community

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Bring out of the best in our people:
Invest in our team to better support our community

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Mobilize and empower:
Bring on meaningful change to improve treatment and care

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3

Invest in science and research:
Ensure the research that matters most to Canadians living with myeloma gets done

Learn more about our goals and how we’ll know we’ve succeeded in “Looking forward to a life uninterrupted by myeloma.”

The Myeloma Canada team

We believe in the strength of our people and in ensuring an inclusive, responsible, and transparent organization that is able to adapt to the needs of our community.
Martine Elias, Executive Director

Martine Elias
Chief Executive Officer

Alysa Batzios
Director of Major Gifts and Planned Giving

Photo of Gabriele Colasurdo, Director of Science and Research

Gabriele Colasurdo
Director, Science & Research

Rania Gamal
Patient Education and Digital Resource Manager

Guy Gaudet
Myeloma Information Specialist

Vesper Guthrie

Vesper Guthrie
Digital Platforms Coordinator

Photo of Shaneika Heslop, Senior Administrative Assistant

Shaneika Heslop
Senior Executive Assistant

Photo of Muriel Ingrassia, Director of Operations

Muriel Ingrassia
Director of Operations

Digital Engagement and Communications Specialist Leigh Kinch-Pedrosa

Leigh Kinch-Pedrosa
Digital Engagement and Communications Manager

Photo of Michelle Oana, Director of Development and Community Relations

Michelle Oana
Chief Mission Officer

Weronika Poziemska
Community Engagement Coordinator (French Canada)

Jessy Ranger
Director, Patient Programs, Health Policy & Advocacy

Ruben Riley
Fundraising and Events Coordinator

Photo of Aidan Robertson, Advisor, Health Policy & Advocacy

Aidan Robertson
Advisor, Health Policy & Advocacy

Myeloma information specialist, Stephanie Valkenier

Stephanie Valkenier
Myeloma Information Specialist

Photo of Chantel Wicks, Regional Community Engagement and Development Manager

Chantel Wicks
National Manager of Community Outreach and Resources

Myeloma Canada Board of Directors

Myeloma Canada is governed by a board of directors whose role is to provide leadership, guide the strategic direction of the organization, and ensure that it fulfills its mission. Central to this is the reinforcement and development of our five pillars: Community empowerment, Education, Awareness, Advocacy, and Science & research.

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Bill Paine
Chair

Bill Paine

Chair

Bill Paine holds an MBA and has over 30 years of experience as a senior executive and board member with Canadian public companies in the energy industry, and has also held board and senior management roles within community and national charitable organizations. His expertise includes building businesses in more than 20 countries. Bill currently serves on the boards of a TSX-listed Canadian energy company, and two international energy companies. He previously focused on fundraising from corporate, community, and governmental sources for a not-for-profit in Vancouver. Bill has been actively involved with Myeloma Canada in corporate fundraising, community support groups, and the Myeloma PSP Steering Committee. He and his wife, who has myeloma, are enjoying full and productive lives in Vancouver with their new puppy, Cooper.

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Lorelei Dalrymple
Vice-Chair

Lorelei Dalrymple

Vice-Chair

Lorelei works as a Team Lead for Alberta’s largest credit union. Since her 2009 diagnosis, she has been extremely active in the Canadian myeloma community, holding roles on the Myeloma Alberta Support Society Board, including President for three years, and Myeloma Canada’s Patient Advisory Council where she has been Chair since 2016. Lorelei has been instrumental in Myeloma Canada’s Support Group Leader and Advocacy Summits, the Myeloma Awareness Day at the Alberta Legislature, and the Myeloma Canada Early Diagnosis program. She is a member of the Board of the Myeloma Canada Research Network and a steering committee member of Myeloma Canada’s Myeloma Priority Setting Partnership for research in Canada. Lorelei is thrilled to join the Myeloma Canada Board and ensure the voices of myeloma patients are represented.

Photo of David Niebach, Secretary

David Niebach
Secretary

David Niebach

Secretary

David has extensive experience in Accounting, Finance, Enterprise Risk Management, Strategy Development and Execution, and Leadership Development and Coaching. He is a Fellow of CPA Alberta, holds a BBA from SAIT, an MBA from Laurentian University, Canadian Risk Management designation with GRMI, is FMVA certified from the Canadian Finance Institute, and has passed the Exempt Market Proficiency Course with IFSE.

David has worked for industry-leading organizations during high-growth and recessionary cycles and has held leadership positions in large-scale enterprises. Currently, he is CFO for a group of privately owned companies operating in logistics, warehousing, and wholesale tire distribution.

David is passionate about and conducts post-secondary and corporate courses in Leadership Development. He sits on various boards including the Government of Alberta Internal Audit Committee, St. Albert Economic Development Advisory Board (past-chair), chair of the NAIT Accounting Advisory Committee and serves on the CPA Alberta Nomination Review committee, and volunteers with post-secondary institutions as well as CPA Alberta.

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Nancy Gray
Treasurer

Nancy Gray

Treasurer

Nancy Gray is a chartered professional accountant who has worked in the fields of health and post-secondary education for over 30 years in Ontario. Nancy has extensive experience in managing financial processes, risk, policy, and governance as a staff and board member in not-for-profit and charitable organizations. In July 2021, Nancy retired from her position as Executive Director, Financial Affairs, at McMaster University. Nancy is proud of her work in leading the Hamilton Myeloma March since 2018, and especially proud that their September 2020 Zoom/in-person March raised over $53,000. Nancy’s husband has been living with myeloma since 2017.

Photo of De'Shanel Childs, Director

De’Shanel Childs
Director

De’Shanel Childs

Director

De’Shanel Childs is a seasoned healthcare leader with extensive experience in benefit administration, operations management, and customer experience. De’Shanel is currently the State Operations Director of operations for Consumer Direct Care Network where she is accountable for the successful delivery of the state’s operational performance, ensuring state’s contractual requirements were consistently met. She graduated from the University of Washington with an undergraduate degree in health care leadership and from Western Governors University with an MBA in health care administration and management.

John Dirks
MD, Director

Photo of Phillip Eappen, MD, Director

Philip Eappen
Director

Philip Eappen

Director

Dr Eappen is an experienced Health Care Executive with over a decade of healthcare management and operations experience. Dr Eappen is an Assistant Professor at Cape Breton University and an Assistant Director of Clinical Services at the Breton Ability Center. Before teaching at Cape Breton University, Dr Eappen taught at the University of Toronto, Southern Alberta Institute of Technology, and Fanshawe College. Before moving to Canada, Dr Eappen also worked as the Director of Health Services and Chief Administrator of the Health Center and taught as an adjunct faculty at the American University and various other universities. Dr Eappen is also on various director boards, including Myeloma Canada, Aplastic Anemia, and Myelodysplasia Association of Canada.

Kim Groff

Kim Groff
Director

Kim Groff

Director

Kim is a business owner and certified Business Coach from Saskatoon, Saskatchewan. He’s been married to Valarie since 1987, and they have two adult daughters and four grandchildren. Since his diagnosis in 2024, Kim has been active with the local Myeloma Support Group, participating in the annual Marches and other endeavours to increase public awareness. As a dedicated board member of Myeloma Canada, he is committed to advancing support, education, and research for Canadians affected by multiple myeloma. He brings a strong background in governance, strategic planning, and community engagement, with a focus on improving patient outcomes and amplifying patient voices.

Paola Neri
MD, Director

Paola Neri

MD, Director

Dr Paola Neri, MD, PhD is an Associate Professor of Medicine, attending physician in the Hematology division at University of Calgary, and member of the Arnie Charbonneau Cancer Institute. Since January 2019 she has been the Scientific Director of the Cancer Translational Research Core, a clinically accredited laboratory located at the Arthur Child Comprehensive Cancer Center in Calgary. She is very active both in preclinical and clinical trial research in Multiple Myeloma.

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Vijay Ramakrishnan
Director

Vijay Ramakrishnan

Director

Dr. Ramakrishnan is currently an Associate Director for Oncology Biomarkers at Labcorp. Prior to that he was an Assistant Professor at the Mayo Clinic, Rochester, MN where he worked on basic and translational multiple myeloma research. He has published several papers and secured funding from extramural and intramural sources to support his research while at the Mayo Clinic. He is delighted to be a part of the board of directors and is very much looking forward to serving in this role to support MM Canada’s mission and help patients and families impacted by multiple myeloma.

Annie Roy, Director, Myeloma Canada Board of Directors

Annie Roy
Director

Annie Roy

Director

Annie is an experienced business leader with over 25 years of expertise. She began her career in the insurance industry before transitioning to entrepreneurship, where she played a pivotal role in building three companies with national reach.

In 2020, after a two-year search for answers, Annie was diagnosed with multiple myeloma at age 48. She underwent extensive treatments, including radiation, chemotherapy, an autologous stem cell transplant, and later, an allogeneic stem cell transplant, which brought her three years of remission. In 2024, her fight with multiple myeloma resumed, and she continues to face each challenge with exceptional courage and resilience.

Photo of. Sandor Sajnovics, Director

Sandor Sajnovics
Director

Sandor Sajnovics

Director

Sandor is an experienced regulatory lawyer and accountant. He has worked as a lawyer in the resource development sector, provincial government, and non-profit health sector in both Alberta and British Columbia.

Additionally, Sandor has experience as a board member for the Schizophrenia Society of Alberta and as a committee member for the Law Society of Alberta’s Audit and Finance Committee. Sandor has extensive experience in advising clients on business decisions and regulatory matters.

Sandor holds a Bachelor of Commerce, a Bachelor of Arts, and a Bachelor of Law all from the University of Manitoba. He also holds a CPA-CGA designation.

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Julie Stakiw
MD, Director

Julie Stakiw

MD, Director

Dr. Stakiw is a malignant hematologist and stem cell transplant physician with a special interest in myeloma. She is based at the Saskatoon Cancer Centre and is an associate professor at the University of Saskatchewan. An active member of the Canadian Myeloma Research Group (CMRG), she also sits on the CMRG Database steering committee. Her research interests include health equity, with a specific focus on First Nations and Metis patients with myeloma. Julie recently finished her term as the Medical Director of the Saskatoon Cancer Centre and was previously the Provincial Head of Hematology for Saskatchewan.

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Keith Taylor
Director

Keith Taylor

Director

Keith studied at the University of British Columbia, Cambridge University, and Sheffield University. He has worked as a police officer in London, UK, and with the Vancouver Police Department, as well as in research, planning, and management with the Calgary Police Service, the Justice Institute of BC, and Canada Post. He has served on several boards and committees and is currently Partner in a consulting firm specializing in police, justice, governance, and community issues.

An accomplished photographer, he enjoys short-course triathlons, hiking, and biking. Keith was diagnosed with myeloma in 2012. As a Director on Myeloma Canada’s Board, he is grateful to give back to the myeloma community for what he describes as the superb care he receives as a patient.

Darlen Thibault, Director, Myeloma Canada Board of Directors

Darlene Thibault
Director

Darlene Thibault

Director

Ms. Darlene Thibault is currently Senior National Program Director with the Industry Initiatives and Partnerships segment of BMO Bank of Montreal. She is responsible for building and growing commercial banking strategies and programs supporting selected industries for the North American Commercial Bank. Ms. Thibault was formerly a Senior Relationship Manager, Diversified Industries in the Corporate Finance Group and previously Regional Director and Team Lead of BMO Equipment Finance.

Ms. Thibault was formerly with the Bank of Nova Scotia from 2005 to 2015 her last role being a Regional Director and Group Lead in the Specialized Financial Services Group. A graduate from McGill University with a Bachelor’s degree in Economics and Political Science, her 25-year career in the financial services industry has included positions at HSBC Bank, Bombardier Capital Ltd., AT&T Capital Canada Inc., and Pitney Bowes Leasing. Ms. Thibault was appointed to the Board of Directors of Export Development Canada in January 2010 and was Chair of the Board Risk Management Committee from 2015 to 2021. Ms. Thibault is also a member of the Institute of Corporate Directors.

Alissa Visram
MD, Director

Alissa Visram

MD, Director

Dr Visram earned her MD at the University of Toronto in 2014. She completed her internal medicine training at the University of Ottawa in 2017, followed by hematology training at Dalhousie University in 2019. She further completed fellowship training at the Mayo Clinic, including an advanced hematology clinical fellowship, followed by a research fellowship, focused on understanding the epidemiology of precursor plasma cell disorders. She also completed a Master of Public Health and Clinical Epidemiology at Harvard University. Prior to joining McMaster University, Dr Visram was a staff physician in the Division of Hematology at the Ottawa Hospital and Assistant Professor in the Department of Medicine, University of Ottawa. 

Dawn Wilson

Dawn Wilson
Director

Dawn Wilson

Director

Dawn is a senior executive with extensive leadership experience across the health, regulatory, and not-for-profit sectors. She currently serves as Chief Executive Officer of a national oral health accreditation agency, where she leads the development and oversight of national accreditation and standards that support excellence in dental education and practice.

She brings significant expertise in governance, accreditation, and working with boards, regulators, and professional bodies. Prior to her current role, Dawn was CEO of Speech-Language & Audiology Canada and has held leadership positions with several national medical organizations, including the Canadian Association of General Surgeons, the Canadian Hernia Society, and the Royal College of Physicians and Surgeons of Canada.

Dawn is recognized for her collaborative leadership style and her ability to advance complex, multi-stakeholder initiatives. Her accomplishments include leading national organizational integrations, securing major funding partnerships, launching a national entry-to-practice examination, and supporting the development of professional and manufacturing standards.

She has served on the Board of St Mary’s Home for over five years and is a Certified Association Executive. Originally from Scotland, Dawn trained as a nurse and now lives in Ottawa with her family.

Two women signing a paper at a Myeloma Canada event, with Myeloma Canada representatives

Get involved

Volunteers are the foundation of Myeloma Canada, and we are always looking for people in communities across Canada who wish to give their time and energy to make myeloma matter.

Myeloma Canada Patient Advisory Council (PAC)

In 2014, Myeloma Canada’s Board of Directors created the Patient Advisory Council (PAC). The Council’s primary objective was, and continues to be, to advise the Board of Directors on important issues for patients, caregivers, and support groups, while providing the patient perspective on national and regional issues. The PAC also works closely with the Myeloma Canada professional team to provide patient-focused advice and feedback on the organization’s many activities.

The PAC is committed to the well-being of the Canadian myeloma community. We will continue to focus on embedding the patient perspective in all Myeloma Canada activities.

Meet the PAC members

Rinat Avitzur
Chair

Rinat Avitzur

Chair

Rinat was born in Israel and moved to Toronto in 2009 with her husband and three daughters.

Rinat studied accounting and economics at Tel-Aviv University and has a CPA (Isr) designation. She worked for over 30 years in the financial industry in finance and risk management, focusing on adopting new regulations, developing and implementing policies, and supporting management and front-line employees to manage business and operational risks.

Rinat was diagnosed in February 2020 and underwent tandem stem cell transplants in July and October. Rinat is currently in remission, keeping an active and healthy lifestyle. Since learning about multiple myeloma Rinat has been increasing awareness through fundraising and is an active member of Myeloma Toronto Support Group.

Photo de Shawn Crossman, Représentant du Canada atlantique

Shawn Crossman
Vice Chair & Atlantic Provinces Representative

Shawn Crossman

Vice Chair & Atlantic Provinces Representative

Shawn Crossman is husband to Bev Dawson and proud father to Isabelle Crossman. Shawn stated his own sales and marketing company in 1999 and continues today to enjoy working with so many businesses across Atlantic Canada. Shawn continues to keep in close contact with the community by volunteering with Minor Hockey, Crossman Community Centre, local church, local youth groups, and business development. He loves playing golf, riding his bike, and walking, however is no longer able to play adult hockey due to Multiple Myeloma.

Shawn was diagnosed with Multiple Myeloma on July 1, 2018, after being admitted to hospital due to back pain. It was then discovered that Shawn had a crushed vertebrae and was showing signs of kidney failure. After back surgery he started a 16-week chemo treatment schedule. After a successful treatment schedule, he was prepared for a stem cell transplant in January 2019. Since his stem cell transplant, Shawn has continued to enjoy remission while experiencing a new quality of life.

Shawn hosted the first Moncton Myeloma March in 2019, 2020, and 2021 and has been honoured with the 2019 and 2020 Nathalie Allard Memorial Award. Shawn also started the Moncton Myeloma Support Group, which continues to be a very active group: listening, supporting each other, and offering a new quality of life during our personal Multiple Myeloma journeys while continuing to learn about Multiple Myeloma.

Barb Beaton
Representative for the Great North

Barb Beaton

Representative for the Great North

Barb was born in Toronto, Ontario and moved to Yellowknife in 1993 for a six-month adventure to work as a Pediatric Occupational Therapist and travel throughout the North. Here, she met her husband Gene, and they are the proud parents of Johanna.

In addition to occupational therapy, Barb has worked as an early childhood consultant and now works with a multi-disciplinary pediatric team as coordinator/case manager.

She enjoys walking/hiking, snowshoeing, gardening, going for coffee, cooking and has recently taken up rug hooking.

Barb was diagnosed with multiple myeloma in 2020 and is grateful for the excellent care she continues to receive in the Northwest Territories and Alberta.

She is one of the co-support group leaders in the newly formed Northern Support Group. Barb is excited and honoured to be the first Northern Canada representative on the Patient Advisory Council.

Bev Dunn
Representative for the Prairies

Bev Dunn

Representative for the Prairies

Bev is a retired Legal Assistant/Paralegal and a dedicated lifelong learner who has completed numerous courses in business organization and human resources management. She has extensive experience serving on the boards of various non-profit organizations. Bev is the past president of the Southern Alberta Myeloma Patient Society in Calgary and currently serves on the Board of Directors of the Health Coalition of Alberta. She is also an active member of the Myeloma Canada National Advocacy Committee.

Bev resides in Calgary, Alberta, with her husband and their Maltese dog, Sophie. She enjoys cycling, camping, travelling, reading, and a variety of crafts. She and her husband spend as much time as possible with family and friends, cherishing every opportunity to be with their grandchildren, Raevyn and Ezra.

Following her diagnosis with multiple myeloma in 2018, Bev chose early retirement to focus on her health and recovery. Since then, she has devoted herself to patient advocacy and volunteer work, contributing her skills and experience to support others affected by myeloma and to advance patient-centered care.

Photo de Manon Veilleux, Vice-présidente, Représentante du Québec

Manon Veilleux
Quebec Representative

Manon Veilleux

Quebec Representative

Born in Montreal and also living on Orleans Island near Quebec City, Manon started her studies in Business Administration at HEC in Montreal and ended them in the Quebec region at Laval University, with a major in Finance. She then chose to become a financial planner because she likes numbers, meeting people and accompanying them through their financial health.

Now retired, she finds it important to be engaged in the numerous activities of Myeloma Canada to help the people touched by multiple myeloma live better. This includes creating the Quebec Support Group, with the precious help of Julie Martel. It is also a sign of appreciation towards the engagement of the Myeloma Canada team for this cause.

She loves to learn new languages, because it allows her to discover a new world every time. Already bilingual since kindergarten, she added Spanish and Italian through the years. She loves reading, travelling with her husband Albert, and both are good walkers, accomplishing approximately twenty kilometres weekly.

Susan McLean
Western Canada Representative

Susan McLean

Western Canada Representative

Susan is a retired high school English teacher who has studied at many universities: UBC, University of Ottawa, University of Saskatchewan, and McGill. She was also the president of the BC Teachers of English Language Arts and worked with the BC Ministry of Education to help write the new English curriculum. Living in Nanaimo, BC, she enjoys an active outdoor life, yoga, swimming, gym workouts, and playing in an ensemble at the Nanaimo Conservatory of Music. She and her husband enjoy spending time with their children and grandchildren, travelling, and have lived in five different Canadian provinces!

Susan was diagnosed with multiple myeloma in 2016 and has been in remission for nearly two years. She is the co-support group leader for the Nanaimo Support Group, helped start the first Vancouver Island Multiple Myeloma March, as well as the first Cinco de Mayo fundraising dinner.

Crystal Morris
Ontario Representative

Crystal Morris

Ontario Representative

Crystal Morris, a resident of Ottawa, Ontario, joined the PAC in December of 2025. A diagnosis of Multiple Myeloma in October 2024, at the age of 47, came as a complete shock. While relatively new to the journey of living with multiple myeloma, her motivation to join PAC includes representing younger females and mothers, and bringing forward the voice of all living with myeloma who reside in Ontario.
Crystal is a registered Occupational Therapist and presently works as a clinical manager for several outpatient mental health programs at The Ottawa Hospital. Her clinical experience has included leading and implementing many projects, developed in partnerships with patients, that have improved care and service delivery. She looks forward to representing those living with multiple myeloma.
Crystal enjoys baking, pilates, crocheting, spending time with her husband Stephen and children Calvin and Agnes, walking the trails in Ottawa and sharing a good laugh with friends over a delicious meal.

Gisèle Fournier
Quebec Representative

Gisèle Fournier

Quebec Representative

Gisèle Fournier joined the PAC as the second representative for Quebec at the end of 2024. Originally from the Montreal region, Gisèle has been an active member of several myeloma support groups since September 2020 when she was diagnosed at the age of 61. Her story was shared in the Spotlight section of Myeloma Canada’s e-newsletter last October.

A nutritionist by training, Gisèle worked in health communication and education for her entire career—19 years in Canada and 20 years in Europe. Gisèle loves teamwork, outdoor activities, cooking for family gatherings, and… Swiss chocolate, among many other wonderful things in life!

Tanya Zigomanis 2024. -PAC Co-chair

Tanya Zigomanis
Ontario Representative

Tanya Zigomanis

Ontario Representative

Tanya Zigomanis was diagnosed with Multiple Myeloma at 37 years old. She is a mom of two young girls and has been married for 11 years to her long-time best friend, Adam Koroneos. They live in Vaughan, Ontario, and have enjoyed travelling down south and exploring Ontario’s cottage country in the recent years.

Tanya is currently on leave but is an insurance defence litigation lawyer at a boutique firm in Toronto, with a specialty in WSIB law. She attended Osgoode Hall Law School and worked in government before heading to private practice.

Tanya was diagnosed with multiple myeloma in May 2019 and had a stem cell transplant in Toronto in September 2019. She achieved a very good partial remission and is hoping her maintenance therapy will help her reach a complete remission.

From June 2019 to September 2020, Tanya has raised over $40,000 for Multiple Myeloma research, mostly through the Multiple Myeloma March in Newmarket. She is determined to spread awareness and raise funds to further myeloma research in Canada.

Learn more about the Patient Advisory Council and what they do in the 2024 Year in Review.

Myeloma Canada Ambassador Network (MCAN)

The MCAN aims to amplify the voices of those impacted by myeloma and represent Myeloma Canada at various public forums, initiatives, and events. This role also offers a chance to contribute to community engagement by offering valuable feedback to enhance services and initiatives as needed. Ambassadors help support the organization’s outreach by building connections with key individuals, such as community leaders, healthcare professionals, and potential partners.

Who can become a Myeloma Canada Ambassador?

The Myeloma Canada Ambassador Network is open to:

  • people living with myeloma,
  • caregivers, family members, and advocates,
  • Healthcare professionals with a strong interest in myeloma,
  • individuals passionate about advancing Myeloma Canada’s mission and supporting the myeloma community.

MCAN ambassadors are appointed for an initial two-year term, with the possibility of renewal based on mutual agreement, their involvement and contributions.

We are not accepting submissions at this time.

Multi-Disciplinary Advisory Council (MDAC)

The Multi-Disciplinary Advisory Council (MDAC) advises Myeloma Canada’s Board of Directors on broad policy and program considerations.

The MDAC:

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has a strategic focus, highlighting multi-disciplinary trends in the global multiple myeloma community

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advises on emerging issues, threats, and opportunities pertaining to the five strategic pillars of the Corporation, and provides invaluable input to the Board of Directors in responding to the challenges faced by Canadians impacted by myeloma.

Two women signing a paper at a Myeloma Canada event, with Myeloma Canada representatives

Get involved

Volunteers are the foundation of Myeloma Canada, and we are always looking for people in communities across Canada who wish to give their time and energy to make myeloma matter.