We are here to help
Histiocytosis Association of Canada (HAC) is dedicated to helping Canadians affected by all types of histiocytosis.
what we do
Donate
The importance of your support of the Histiocytosis Association of Canada cannot be underestimated.
With your help, we can continue our efforts in the fight against histiocytic disorders.
Our Mission
Histiocytosis Association of Canada is a vocal advocate to promote public and professional education, patient and family support, and stimulation and support of research.
Volunteer
Are you committed to joining the fight against histiocytosis?
Please contact us today to learn how you can get involved
Finding a cure for histiocytosis
The Histiocytosis Association of Canada is dedicated to improving the lives of Canadians affected by histiocytosis. We are focused on public and professional education, patient and family support, and stimulation of support of research.
We are an international group of parents, patients, physicians and friends in search of a cure.
We work closely with an international group of physicians, known as the Histiocyte Society, who are dedicated to studying the histiocytoses. Through this partnership, more has been learned and better treatments have been discovered.
If you or someone you love has been diagnosed with histiocytosis, and you are looking for help, contact us today at info@histio.ca. You are not alone.
Meet Our Team
Director
Dr. James Whitlock
President & Director
Aprile Duda
Director
Marlene Clune
Director
Claudio DiGirolamo
Director, Communications
Stephanie Landon
Past President
Teresa Hunt
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