Myeloma Alberta Support Society has no input to survey content nor receives any data collected, MASS simply provides access to these Myeloma Canada surveys as a service to members.
Myeloma Canada collects data through surveys and the Patient Advisory Council. Patient and caregiver opinions and input can provide valuable information in getting new drugs funded and available. Myeloma Canada invites myeloma patients and caregivers to complete brief online surveys. Links to current Myeloma Canada surveys are found below.
There are no surveys currently.