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November 22, 2024

Government of Canada establishes a committee of experts to make recommendations on national pharmacare

The Honourable Mark Holland, Minister of Health, announced the establishment of the Committee of Experts which will recommend options on how to operate and finance a national, universal, single-payer pharmacare program in Canada. The Committee will include: Dr. Nav Persaud (Chair); Dr. Stéphane Ahern; Amy Lamb; Dr. Steve Morgan; and, Linda Silas. Over the next year,[…]

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November 21, 2024

Talquetamab not recommended for reimbursement 

On October 31st the pan-Canadian Oncology Drug Review Expert Review Committee (pERC) of Canada’s Drug Agency (CDA-AMC) decided not to recommend TALVEY (talquetamab) for reimbursement.  The pERC’s draft decision states that due to the limited data available for their review and the nature of its side effects, public drug plans should not fund[…]

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November 19, 2024

Cancer Action Now Alliance (CANA) releases survey results on diagnostic and treatment wait times in Quebec

CANA’s survey of 300 Quebecers living with cancer highlighted the long wait times respondents experienced. The study, supported by Coalition Priorité au Québec and conducted by Léger, found that more than half of Quebecers living with cancer wait on average 3-5 months for their first treatment. The survey also revealed[…]

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October 2, 2024

The changing landscape of multiple myeloma – Toronto Star

September is Blood Cancer Awareness Month — an important time to spotlight the impact of blood cancers on the lives of Canadians. While many people are familiar with blood cancers like leukemia, they may not know that multiple myeloma is the second most prevalent blood cancer in Canada and is predicted[…]

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October 2, 2024

“I knew something was wrong”: A Terrebonne woman has to go back to the doctor six times to be diagnosed with blood cancer – Journal de Montreal (in French only)

A Terrebonne woman who had to go to the doctor six times before being diagnosed with blood cancer in 2013 is using her remission to raise awareness of this insidious disease and prevent other sufferers from being ignored. “I didn’t have a family doctor at the time and had to go[…]

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September 19, 2024

The Government of Canada introduces the Connected Care for Canadians Act 

On June 6, 2024, the Honourable Mark Holland, Minister of Health, introduced Bill C-72 the Connected Care for Canadians Act. This Act is about enabling Canadians to securely access their own health data, which will empower patient’s decision-making and improve the care they receive from health providers in Canada. This Act outlines[…]

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Myeloma Canada updates

 

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September 24, 2024

Multiple myeloma: research update

Myeloma Canada, along with thousands from the global hematology community, had the privilege of following the American Society of Clinical Oncology (ASCO) Annual Meeting (May 30 – June 3) and the European Hematology Association (EHA) Hybrid Congress (June 13-16) to hear from leading myeloma experts about the latest progress in[…]

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September 19, 2024

Myeloma Canada at the CDA-AMC Symposium 2024

Canada’s Drug Agency (CDA-AMC) Symposium 2024 is a 3-day hybrid event in Ottawa (ON) that gathers leaders from across Canada with expertise in policy, industry, health technology assessment, patient advocacy, medicine, public health, and communications. Representing Myeloma Canada were Martine Elias – CEO; Jessy Ranger – Director, Health Policy, Advocacy[…]

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July 17, 2024

Letter to the Editor: The best of science and the worst of bureaucracy

We invite you to read our opinion letter, written by Jessy Ranger, Director, Patient  Programs, Health Policy & Advocacy at Myeloma Canada, and Christina Sit, Manager, Community and Strategic Partnerships at The Leukemia & Lymphoma Society of Canada, on the issues of access to treatment and care. As the country’s[…]

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July 16, 2024

Advocacy activities recap 2023

At first, engaging in advocacy initiatives involving government bodies, officials, drug agencies, and various stakeholders invested in improving the healthcare system or treatment accessibility may appear abstract or a little daunting. Nevertheless, numerous organizations, such as ours, are inherently suited to negotiate, influence and persuade those who have the authority[…]

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June 21, 2024

Martine Elias summarizes Real World Evidence (RWE) session at 2024 Myeloma Patients Europe Masterclass 

As proud members of Myeloma Patients Europe (MPe), Myeloma Canada attended – and presented at – MPe’s annual Masterclass this past May. The Masterclass is a one-and-a-half-day educational program designed to: increase the knowledge and skills of MPe’s members;  share the latest updates on myeloma and amyloidosis diagnosis, treatment and care;  discuss the[…]

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May 2, 2024

A round of applause for Martine and her new role! 

It is with great joy and pleasure that we announce the advancement of our well-regarded Executive Director, Martine Elias, to the distinguished position of CEO at Myeloma Canada.  Martine has been the driving force behind numerous achievements and advancements that have shaped Myeloma Canada into the leading organization it is today.[…]

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