CANAAF Board of Directors

Joined 2017

It is an honour to serve as CANAAF’s President. Connecting with many supportive individuals during CANAAF events & conferences has helped us tremendously in our journey with my daughter’s alopecia. I will do my best to help CANAAF grow as an organization.

Joined 2015

Hello from the East Coast! My alopecia journey began over 30 years ago and my son was diagnosed in 2014. CANAAF has been a welcome addition to our circle of support!

Joined 2014

My daughter was diagnosed with Alopecia in 2003. I joined the CANAAF Board to support other parents struggling to help their children live with this disease. I hope that I can help your family as CANAAF has helped mine.

Joined 2021

Hello! I’m a McMaster University student pursuing my Bachelor of Commerce. I developed alopecia universalis at age 13. CANAAF has been an incredible pillar of support in my journey. I strive to embrace kindness as our community continues to flourish.

Joined 2023

Hello! I first developed Alopecia Areata when I was 22 years old and have been wearing wigs ever since. I am honoured to be on the CANAAF Board to help spread awareness about Alopecia and hopefully connect others to the foundation.

Joined 2021

Hi, I’m a Microbiology and Immunology masters student at McGill. My Alopecia Universalis journey began when I lost all my hair, eyelashes and eyebrows at 7 years old. My mission is to make CANAAF accessible to francophones.

Joined 2023

Joined 2021

Hi, I’m a Microbiology and Immunology masters student at McGill. My Alopecia Universalis journey began when I lost all my hair, eyelashes and eyebrows at 7 years old. My mission is to make CANAAF accessible to francophones.

Joined 2023

I’ve had patchy alopecia since age 16. I wish I had a resource like CANAAF when I was first diagnosed! Through this role, I hope I can help other alopecians find support and community in their journey.