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.

The cornerstone of our efforts is to advocate for access to early diagnosis and appropriate treatments. We amplify the patient voice and raise awareness of the daily challenges encountered by those living with HAE and related angioedema to educate change- makers and influence policies.

We commit to a more accessible and supportive environment for all. We engage our members to understand and accurately represent their unique, diverse needs.

Involves cross-pollination of ideas and collaboration beyond our immediate community to drive change and improve outcomes for all.

We provide our members with access to tools and resources aimed at fostering strength, confidence, and autonomy to advocate for their own health and well-being.

We are committed to equipping and connecting the HAE community with current information, best practices, and resources.

Achieve our mission, goals, objectives, and commitments, and to sustain HAE Canada through:

• Membership Growth & Retention
• Human Resources (Staff & Volunteer)
• Financial Capacity / Sponsorship
• Accreditation Alignment & Governance