welcome to the histiocytosis association of canada


Being a Histio survivor, I fully understand the needs of patients and families as I was diagnosed with Langerhans cell histiocytosis in 2007. I want you all to know that I am committed to serving the Canadian histio community and look forward to working with all of you to ensure that we find the cure for this disease while supporting one another.


Please do not hesitate to contact me at info@histio.ca


Thank you,


Teresa L. Hunt

President