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

URGENT: Patient Support Group Survey

WE NEED YOU Specifically we need your opinions in our confidential survey. We hope to hear from as many of you a...

Rare Disease Day in Ontario

The Canadian Organization for Rare Disorders is hosting Breakfast Reception at Queen’s Park in celebration of I...

MDS App Manager

Are you interested in participating in a study for MDS patients? The MDS Manager™ is a health and life manage...

2018-2019 Nursing Grant Recipient

AAMAC and the Canadian Nurses Foundation (CNF) are pleased to announce the 2018-2019 Nurse's Scholarship has bee...