- About the CHS
- Provincial Chapters
- Our Stories
- Sylvie - When the branches of your family tree connect with your inherited bleeding disorder
- Karen - Survival and triumph
- Arizpe Family - Far from home but healthy for life
- Jason Leigh Stewart - The Story of J
- Stefan - Self-infusion: a thank you
- Shelley - Six generations of a VWD family
- Lyman Keeping - Living with factor XIII deficiency
- Judy - Eureka!
- Paul: My journey to a new life
- Kristy - How a bleeding disorder has affected my life
- Patrick4Life: Full Moon Wish
- Diane and Mackenzie: love at first sight
- Sarah
- Amber and Karine: A Harrowing Experience
- The “Bruise Brothers” play the blues
- Olivia
- Dilan
- A hemophiliac who plays rugby!
- Bleeding Disorders
- Women
- Inherited bleeding disorders affecting women
- Symptoms
- Diagnosis
- Inheritance
- Medical treatment options for menorrhagia and other symptoms
- Gynaecological treatment options for menorrhagia
- Precautions for pregnant women
- Staying healthy
- Bleeding disorder treatment centres
- Educational resources
- Stories from women and girls who bleed too much
- About the CHS
- Support and Education
- Educational Material
- Care and Treatment
- Safe, Secure Blood Supply
- Research
- International Development
- Treatment Centres
- HCV/HIV
- Youth Web
- Commemoration of the Tainted Blood Tragedy
- Media Room
- Links
- FAQ
To Support Us
As a not for profit organization, fundraising is the only means from which we are able to offer programs to our members.
Please contact our office for more information on how to support our chapter.





