Author: CATIE | Page 21

HIV and life insurance: A welcome change but questions remain

May 8, 2018 • By Wendy Porch and Jeff Potts

Historically, people living with HIV in Canada have been excluded from access to life insurance. In recent years, however, both Manulife and Sun Life have started accepting applications from people living with HIV, now that HIV is widely recognized as a manageable chronic illness. Nevertheless, this significant change in policy is not well-known within the HIV sector. How can we change that and how can we facilitate access to life insurance for people living with HIV? With these two questions in mind, we at Realize and the Canadian Positive People Network (CPPN) surveyed our members and the insurance sector to...

PositiveLite.com: It’s gone, so what next?

April 9, 2018 • By Bob Leahy

It’s not surprising that PositiveLite.com —what we called Canada’s online HIV magazine but it was, I’d argue, so much more —came to an end on March 31. It had been going for nine years. It was a unique model run by people living with HV for people living with HIV. Most people thought we had big offices; in fact, we operated out of our own homes. We were independent in all senses of the word.

Learning from Saskatchewan’s HIV emergency

March 19, 2018 • By Susanne Nicolay

Saskatchewan has led the country in the rate of new HIV infections and the proportion of people living with HIV since 2009. The HIV epidemic in this province is unique from other jurisdictions in Canada in that more than three-quarters of our new infections occur in people who use injection drugs (the Canadian average is less than 14%).

Beyond stigma: Challenging STBBI stigma in the classroom

March 5, 2018 • By Brittany Neron and Makeda Zook

Sex education is a largely stigmatized and often politically volatile subject, even though access to comprehensive sexuality education is enshrined in international law as a human right.

Love Positive Women: why a fulfilling sexual life with HIV matters

February 13, 2018 • By CATIE

By Allison Carter, Jessica Whitbread and Angela Kaida “I went through a long period, seems like ancient history now, but I remember when I was first diagnosed, I felt so dirty. Like everything about me was, I suppose, unsafe and unclean and my blood was just full of crap. Just the whole thing was very internalized… For the most part now, I feel loveable. I feel good about myself. I just feel like I’ve still got a lot to offer and give and that I can be part of a strong, healthy relationship, despite the difficulties, I suppose.” —Anonymous quote by a...

Indigenizing research: the Wise Practices conference

February 6, 2018 • By Laurie Edmiston

This past year the Canadian Aboriginal AIDS Network (CAAN) held its annual gathering, on the theme of “transforming wholistic approaches to Indigenous health.” It’s a gathering of First Nations, Métis and Inuit people, combining a business meeting, a gathering of Aboriginal people with HIV/AIDS, and the ‘Wise Practices’ research conference. But more importantly, it is a gathering of colleagues who have become friends, clients who have become peers, people with HIV who have become community leaders, and an extended family. Also present are elders welcoming delegates to their traditional lands, and children – the younger ones mostly playing with each...