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

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...

PNH Rare Disease Month Campaign launched

WHAT IS RARE DISEASE DAY? Rare Disease Day is the official international awareness-raising campaign for rare di...

MDS Alliance – MDS Global Survey

Thank you in advance for agreeing to complete this survey for the MDS Alliance. As someone who has been diag...