Supporting Canadians

With Bone Marrow

Failure Diseases

Supporting Canadians

With Bone Marrow

Failure 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.

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.

Latest News

Research Update

AAMAC is very pleased to have recently approved funding for a project at B.C. Children’s Hospital entitled: Sing...

MDS Alliance Webinar Translation Project

The MDS Alliance has translated a few patient-centric webinars. Three webinars, which were kindly gifted by t...

Engagement on the Disability Inclusion Action Plan

The Government of Canada is engaging Canadians on how to improve the lives of Canadians with disabilities. Your ...

Global PNH Patient Registry

The Aplastic Anemia and MDS International Foundation (AAMDSIF) and the National Organization for Rare Disorders ...