Update on the COVID-19 pandemic

Information regarding COVID-19 is in constant change, as is the situation regarding vaccination and prioritization for immune-compromised individuals.

If you have any COVID-19-related questions, we’ve created a specific COVID section on our website that can be accessed by clicking here or by selecting the “News & Events” tab from our homepage. In this section, you’ll find the latest news and information about the pandemic in Canada from trustworthy and reliable sources.

Any specific questions that you may have regarding the COVID-19 vaccination, delays between vaccine dosing, and prioritization within your province are best answered by your healthcare team. They’re the ones who know you and your particular situation and are therefore in a position to best address your unique concerns.

Created by, and entirely focused on, Canadians impacted by myeloma, Myeloma Canada is the only national charitable organization committed to providing you with the most up-to-date and reliable information on myeloma. Some of the ways we do this is through our monthly e-newsletter, “Myeloma Matters”, as well as through our social media platforms.

Please don’t hesitate to contact us at contact@myeloma.ca or toll-free at 1-888-798-5771 with any questions regarding our programs and services.

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Myeloma Canada Patient Advisory Council

Early in 2015, the Myeloma Canada Board of Directors approved the creation of the Patient Advisory Council (PAC). The primary purpose of the PAC is to function as an advisory to the Board of Directors on matters important to patients, caregivers and support groups, providing the patient perspective on national and regional issues to the Board.  

One of the major accomplishments of the PAC in 2016 was a national online survey conducted for myeloma patients and caregivers across Canada. The purpose was to gain insight from respondents on the programs and services currently offered by Myeloma Canada and provide suggestions for the future. We would like to thank the PAC for preparing this important survey, the Support Group Leaders for assisting with the distribution of the survey and the hundreds of patients and caregivers who responded with their valuable input.    
The 2016 Support Group Leader's Summit in Edmonton

The PAC also participated and assisted in the planning of several Myeloma Canada events including: the National Conference, Scientific Roundtable, Support Group Leader and Advocacy Summits, the Awareness Day, and the Family Medicine Forum. Most notably however, was the development of the Support Group Leader toolkit, which has been enthusiastically received by Support Group Leaders across the country.

 

The PAC members are as follows:

Glenn Hussey, Chair 

Glenn, a Newfoundlander, studied at Memorial University before moving to Ottawa where he completed his studies at Carleton University.

He worked for the federal public service for 40 years focusing on policy, strategic planning and client service. Following Glenn’s retirement in 2015, he acted as a caregiver for his wife who was in complex, continuing care until her passing in 2017. Glenn discovered that he had the markers for multiple myeloma in 2008, but didn't require treatment until 2017.

Following back-to-back stem cell transplants in 2018, Glenn is currently medically stable. He is a writer, a fitness lover, and has been an active community volunteer for youth sports (soccer and figure skating).

Glenn continues to share his passion for soccer, especially Manchester United, with family and friends. He was awarded the Commemorative Medal for the 125 th Anniversary of the Confederation of Canada for his contribution to his community.

Email: helene-glenn@rogers.com

Susan McLean, Vice Chair & 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.

Email: mclean@shaw.ca

Phil Harbridge, Western Canada Representative

Phil Harbridge is husband to Kay, father to Charissa and Nicolette, father-in-law to Austin and grandfather to Teal (born Feb. 11/20). He has worked extensively (39 years) with youth and young adults as; pastor, teacher, writer and professor. Currently Phil enjoys serving with Christian Journeys (helping schools, churches and community groups experience Lands of the Bible), Capernwray Bible School Thetis Island (teaching) and The Chapels Group (officiating weddings).

Phil was diagnosed in February 2019 and had his stem cell transplant in July. Phil’s response to treatment has been significant and he’s continuing to see positive results from the maintenance therapy.

He enjoys listening to peoples’ stories, running, cycling, swimming, tennis, sunshine, coffee and the Edmonton Oilers. Phil has been involved in several Myeloma Canada events (1st Place Team at 2019 Vancouver Multiple Myeloma March), conferences, webinars, and he’s an active member of the Surrey Support Group. 

Email: pharbridge@telus.net.

Rinat Avitzur, Ontario Representative

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.

Email: rinatavitzur@hotmail.com

Tanya Zigomanis, Ontario Representative

Tanya Zigomanis who 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.

 Email: tzigomanis@gmail.com 

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 weekly approximately twenty kilometres.

Email: veilleux.manon@videotron.ca

David McConkey, Atlantic Canada Representative  

David is the Support Group Leader with Myeloma NL. He is a person living with myeloma and committed to living life fully on Change Islands and in St John's Newfoundland & Labrador. David worked as a counsellor for over 30 years and was known as a long-distance runner. He is currently actively involved with aspects of family, community and the environment as well as artistic pursuits.

Email:  sunshyneontherock@hotmail.ca