The Canadian Consensus Statement. Sign it. Use it. I have and here’s why.

 September 13, 2016 •  By Glenn Betteridge

Many of you may have noticed the ebb and flow of the community-based HIV movement, influenced by medical and scientific breakthroughs, funder priorities, community activism and larger political, social and economic forces.  Throughout my 20-plus years in HIV community-based work and volunteering, I have tried to ground myself in a few bedrocks as a way of anchoring my work. The essential connection between health and human rights. The need for policies, programs and services grounded in evidence and lived experience. Recognition of the central role played by the social determinants of health. And a commitment to social justice and taking...

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Indigenous Youth Leaders are Taking Action on HIV in their Communities!

 September 6, 2016 •  By Sarah Flicker and the Native Youth Sexual Health Network

Taking Action II is a community-based action research project about building and supporting Indigenous youth leadership in the HIV/AIDS movement. We are a group of Indigenous youth leaders, Indigenous community-based organizations and university-based researchers. We wanted to create awareness around HIV, sexual health, and decolonization in First Nations, Métis, and Inuit communities across Turtle Island (also known as Canada).

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How intimate partner violence affects women living with HIV

 August 2, 2016 •  By Sandra Ka Hon Chu

A global study released last year revealed alarming figures concerning women living with HIV and violence. Among 945 women living with HIV from 94 countries who participated in the study, 89 per cent reported having experienced or feared violence before, since and/or because of their HIV diagnosis. Violence they experienced was reported to be higher after HIV diagnosis from their intimate partner and others in their social network.

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National survey reveals information habits of people living with HIV

 July 19, 2016 •  By David McLay

From its beginning, CATIE has shared information with people living with HIV so that they can take better care of their health. In Fall 2015, we undertook a national online survey to better understand the information needs of people living with HIV today. The survey results may confirm what you already know about your clients’ information needs. Or perhaps they contain a surprise or two. Whatever the case, the results help guide all of us in how we can best serve our clients.

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Lessons learned from the HCV Symposium Part 2: Equal access, equal representation

 July 5, 2016 •  By Sarah Cloutier and Yung-Wo Jao

On February 27, 2016 CATIE had the opportunity to host another Learning Institute (LI) at the 5th Canadian Symposium on HCV in Montreal, Quebec. Learning Institutes are exciting knowledge-exchange and capacity-building opportunities for stakeholders engaged in Hep C prevention, treatment and care across Canada. Our 15 rapporteurs learned about current research and worked together to summarize that information and bring it back to their communities.

In part two of this two-part blog series, two rapporteurs reflect on their experiences at the LI.

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