We are a society of patients, parents, and friends supporting patients affected by Thalassemia; with a mandate to advocate and support patient care and development.

Over the years, we have found success in collaborating with medical staff and government to secure vital treatments for patients in British Columbia.  Our purpose is to provide a network which can deliver many forms of assistance to patients and their families.

We wish to raise awareness of this disorder among the public, by promoting screening, prenatal diagnosis, and enough information to couples to help them bear healthy children and eventually eradicate the disorder from their family gene pool.

if you have a friend or family member who has the disorder, we invite you to become a member of the societies support group.