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 2020-2021 Annual Report, detailing our accomplishments for this for this year.

Go to 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

Promising Research in MDS

The Video Journal of Hematological Oncology (VJHemOnc) is a global, open-access video journal, dedicated to prov...

MDS Patient engagement collaboration opportunity

AAMAC has teamed up with Dr. Brett Houston and Nora Choi. They looking to organize a group of 5 MDS patients to ...

PNH Patient Recruiting Support

NFA Health, a Toronto-based creative agency, is looking for people diagnosed with PNH to participate in a resear...

Better Living with PNH, Day by Day!

Discover the comprehensive guide with a holistic approach to Better Living with PNH, day by day, from the Ca...