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 gain clarity from both sides as to what the underlying issues might be. We found out that life insurance is something that people living with HIV think about today, but few folks know that it’s an option. And, for the few people living with HIV who are aware that Manulife and Sun Life are offering life insurance options, many people wondered what is offered and were curious about where to go for more information or to apply. Some wanted to know what the “catch” might be.
The PositiveLite.com team (from left to right): Rob Olver, Wayne Bristow, John McCullagh and 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.
Depuis 2009, la Saskatchewan figure en tête des provinces canadiennes ayant le taux le plus élevé de nouvelles infections au VIH et la plus importante proportion de personnes vivant avec le VIH. L’épidémie de VIH dans cette province est unique par rapport aux autres juridictions du Canada, car plus des trois quarts de nos nouvelles infections surviennent chez les personnes qui utilisent des drogues injectables (la moyenne canadienne se situe sous la barre des 14 %).
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 woman living with HIV
Le Blogue de CATIE présente des perspectives et opinions des personnes et organismes qui travaillent ou collaborent bénévolement à la réponse du Canada au VIH et à l’hépatite C.