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CODEROUGE 2018
Our Stories
Rob - Unspeakable: a story that needs to be told
Miranda - I'm not perfect ... but I sure am special!
Christian - Cultivating happiness
Meet Vincent Dumez: A model of perseverance and community involvement
Rhys - Breaking the ice: Life of a youth with hemophilia north of 60
Milena - Hemophilia Mother
Eric - Freedom on wheels!
Gilbert - Living with factor X deficiency
Jen and Sheri - The cure is near— let’s all help make it happen
Arnaud in the land of dreams
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
The “Bruise Brothers” play the blues
Amber and Karine: A Harrowing Experience
Dilan
Olivia
A hemophiliac who plays rugby!
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Bleeding Disorders
Hemophilia A and B
What is hemophilia
The history of hemophilia
The clotting problem in hemophilia
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Von Willebrand disease
Preface
Acknowledgements
An Introduction to von Willebrand disease
Types of von Willebrand disease
Heredity of von Willebrand disease
Symptoms of von Willebrand disease
Diagnosis of von Willebrand disease
Treatment options for von Willebrand disease
Introduction
Recommended Treatments for Men and Women
Not Recommended Treatments
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Living with von Willebrand disease
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Other factor deficiencies
Factor I deficiency (Fibrinogen deficiency)
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HIRT?
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variant Creutzfeldt-Jakob disease (vCJD)
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CHS - Novo Nordisk Psychosocial Research Program
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Past research programs
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Fellowship Research Project Funded in 2006
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Fellowship Research Project Funded in 2009
Fellowship Research Project Funded in 2010
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coderouge 2012
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Canadian Blood Services - November 23, 2017
André Picard - November 28, 2017
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