There is no single myeloma experience
Myeloma touches the lives of tens of thousands of Canadians. Whether you are living with the disease, caring for someone who is, or are connected another way, your experience and your story are important. We strive to share stories representing the multitude of experiences myeloma can bring.
Filter these stories by topic, or scroll through them chronologically.
Personal stories
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Person living with myeloma, Support Group Leader, Advocate, and Patient Advisory Council Representative for Québec (Quebec City, QC)
April, 2020
I had a stem cellThe basic unit of any living organism. transplant in 2014 and found Myeloma Canada then. I also had another stem cell transplant in 2018, and again went to Myeloma Canada for information. When I was first diagnosed, I had ordered books from the USA and around the world.
Person living with myeloma, Support Group Leader, Past Patient Advisory Council Chair, Myeloma Canada Board Member (Edmonton, Alberta)
March, 2020
When I was diagnosed with myeloma in 2009, my doctor gave me this wonderful patient handbook that was done by Myeloma Canada.In the handbook, I remember having all the information a person could want. It gave me the opportunity to reach out and connect wi
Hematologist, supporter of Myeloma Canada, member of the Myeloma Canada Scientific Roundtable
February, 2020
I first became involved with Myeloma Canada in a very interesting way! I was attending the American Society of Hematology (ASH) meeting in 2005 and I was getting on a bus, a shuttle, that was taking me to my hotel. A man sat down beside me, looked at my n
Patient, strong advocate, volunteer, and Support Group leader
January, 2020
Spotlight on Quebec Ambassadors: Seeking Access to Innovation
December, 2019
Spotlight on Lynn Hoffman: Accepting Cancer
October, 2019
Spotlight on Véronica Gill: Living With Myeloma
September, 2019
Spotlight on Jean-François Couture: Never Give Up
August, 2019
Spotlight on Yolanda Brunson-Sarrabo : Bringing Awareness to Racial Diversity Within the Multiple Myeloma Community
July, 2019