Teaching Researchers to be Clinically Relevant
BioCanRX provides research assistants, postdocs, graduate students, and technicians with the tools needed to make their science more clinically relevant.
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Category: Stories
Stories
How to Help Patients to Contact Their Health Minister: A Case Study with PHA Canada
Pulmonary Hypertension Association of Canada (PHA Canada) and Scleroderma Canada’s camapign to empower patients to advocate themselves.
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Huntington Disease Youth Mentorship Program
Jody Mitchell, daughter and granddaughter of persons with Huntington disease, talks about the benefit the program has brought as both a mentee and a mentor.
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The Three I’s of Caregiving
At the Huntington Society of Canada’s National Conference in Kelowna, we talked with Peter Rosenberger, author of the books ‘Hope for the Caregiver’ and ‘7 Caregiver Land Mines’.
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The Origins of Giving Tuesday
Giving Tuesday – a day where many people give generously to their favourite charity or charities. But are you aware of the origins of Giving Tuesday?
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Keeping Canadian Workers Healthy: With or Without a Chronic Condition
Health Partners brings together employers with various patient focused charities for the purpose of helping to keep Canadians as healthy as possible in the workplace.
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Huntington Disease Youth Organization (HDYO)
At the Huntington Disease National Conference held in Kelowna, B.C, we talked with Chandler Swope of the Huntington’s Disease Youth Organization (HDYO) about their organization.
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Want to Fix the Power Imbalance? Start Paying Patient Advocates
Parent advocate Isabel Jordan, co-founder of the Rare Disease Foundation talks about that imbalance of power between advocates and doctors, researchers, pharmaceutical executives, public relations personnel, and many others.
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