That all Canadians with hereditary (HAE) and related angioedema achieve optimal health and well-being while living attack free lives.

Provide support, education, and resources to our community, and advocate for exceptional disease management and equitable access to treatment.

Improve our ability to achieve our mission and goals by engaging and empowering our members; developing our Board; training our volunteers; and by collaborating with our stakeholders and partners.

Equip patients, caregivers, family members and healthcare providers with the information, tools and resources needed to ensure that those with HAE and other related angioedema live healthy and productive lives.

Convey relevant information, about HAE and other related angioedema, to those in the community.

Enhance our ability to advocate for our members by communicating our mission; lobbying and influencing governments; by educating people; and by promoting awareness of the issues faced daily by those with HAE and other related angioedema.