What We Do
The Canadian Alopecia Areata Foundation supports those affected by Alopecia Areata, promotes awareness and education of this auto-immune disease, and raises funds for research.
Our Mission
CANAAF offers a supportive community where we connect, learn, and celebrate together to journey through our Alopecia with confidence.
Our Vision
To be a nationally recognized, locally-focused pillar in the overall support network for the alopecia community.
Board of Directors
CANAAF is led by a volunteer Board of Directors who know the impact of Alopecia Areata.
Our History
We founded CANAAF on a bucket full of tears, a huge heart, and an incredible, unstoppable desire to assist and protect our children. This incredible rollercoaster ride literally started as a grass roots endeavor at a picnic gathering.
– Jim Makris, Co-Founder of CANAAF
What We Do
The Canadian Alopecia Areata Foundation supports those affected by Alopecia Areata, promotes awareness and education of this auto-immune disease, and raises funds for research.
Our Mission
CANAAF offers a supportive community where we connect, learn, and celebrate together to journey through our Alopecia with confidence.
Our Vision
We aspire to be a nationally recognized, locally-focused pillar in the overall support network for the
alopecia community.
Board of Directors
CANAAF is led by a volunteer Board of Directors who know the impact of Alopecia Areata.
Our History
We founded CANAAF on a bucket full of tears, a huge heart, and an incredible, unstoppable desire to assist and protect our children. This incredible rollercoaster ride literally started as a grass roots endeavor at a picnic gathering.
– Jim Makris, Co-Founder of CANAAF
What We Do
The Canadian Alopecia Areata Foundation supports those affected by Alopecia Areata, promotes awareness and education of this auto-immune disease, and raises funds for research.
Our Mission
CANAAF offers a supportive community where we connect, learn, and celebrate together to journey through our Alopecia with confidence.
Our Vision
We aspire to be a nationally recognized, locally-focused pillar in the overall support network for the alopecia community.
Board of Directors
CANAAF is led by a volunteer Board of Directors who know the impact of Alopecia Areata.
Our History
We founded CANAAF on a bucket full of tears, a huge heart, and an incredible, unstoppable desire to assist and protect our children. This incredible rollercoaster ride literally started as a grass roots endeavor at a picnic gathering.
– Jim Makris, Co-Founder of CANAAF