Supporting Canadians

With Bone Marrow

Failure Diseases

Supporting Canadians

With Bone Marrow

Failure Diseases

What We Do

The Aplastic Anemia & Myelodysplasia Association of Canada (AAMAC) is a leading funder of research into bone marrow failure diseases in Canada. Our volunteer-run organization supports patients and caregivers across the country who are living with aplastic anemia, myelodysplastic syndrome (also called MDS or myelodysplasia) and paroxysmal nocturnal hemoglobinuria (PNH).


To provide a seamless support network for every Canadian patient, family member, friend, and concerned healthcare provider dealing with aplastic anemia, myelodysplasia and paroxysmal nocturnal hemoglobinuria.


To support all Canadians and their families and friends through diagnosis, treatment and remission stages of these diseases.

Annual Report

We are pleased to announce our 2021-2022 Annual Report, detailing our accomplishments for this for this year.

Click here for more information and to download the report

It's in ME to WIN!

Click here to order or download a copy of AAMAC's children's book.

Latest News

Paroxysmal nocturnal hemoglobinuria (PNH) Study

Sorry, this entry is only available in French.If you are interested in participating and sharing your experience...

Marrow Failure & Myelodysplasia (MFM) Patient and Family Conference

SAVE THE DATE! Join Sick Kids for a virtual Marrow Failure & Myelodysplasia (MFM) Patient and Family Confer...

Severe Aplastic Anemia (SAA) Survey – Eltrombopag

We are looking for individuals with severe aplastic anemia (SAA) and individuals who have been treated with eltr...

Addressing PNH unmet medical needs: a policy roadmap to aspire for change

Below is a  recording of a multi-stakeholder online conference held on December 7, 2022 and organised by Partner...