Sickle Cell Awareness Group of Ontario (SCAGO) is a membership based patient association. SCAGO puts patients and families affected by Sickle Cell Disease (SCD) first, by advocating on their behalf with the government, schools and healthcare community. It understands the challenges faced by people with SCD and their family members.
To address some of these challenges, it developed various programs including Learning for Life Seminars, and Peers and Parents Support Network. It also contributes to the educational advancement of students with SCD by providing scholarships and grants. In addition, SCAGO established the impactful Lunch and Learn Program to support knowledge translation among care providers. Through numerous activities, SCAGO provides support (mental, emotional and physical) to patients and their families and raises awareness in the community to reduce the number of new SCD births.

According the By-Law of the SCAGO, members of the organization determine its direction. As such, members have voting rights among other privileges. If you are an individual or family with SCD; medical or allied health professional, advocate and general community member or corporation, we encourage you to join SCAGO and be a part of our future Please complete Membership form Here

Sickle Cell & Thalassemic Disorders Act
SCAGO is a proud member of the Sickle Cell Disease Association of Canada (SCDAC). Founded in 2012, SCDAC is the national body regulating patient advocacy and support in Canada. It currently has 6 member organizations.