Je n’aime pas trop fréquenter les espaces médicaux. Pour moi, ce ne sont pas seulement des espaces essentiels à ma santé. Ce sont aussi des espaces d’exclusion et de traumatismes.
Combien de fois ai-je entendu parler de refus de soins chez des gens de mes communautés? Une migraine chronique est blâmée sur les hormones. Une plaie ouverte n’est pas pansée parce qu’on « n’a pas les connaissances pour traiter avec ce genre de personne. » Et que dire des questions déplacées, des mauvais noms sur les dossiers, ou encore de morinoms lus dans la salle d’attente, devant tout le monde?
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
Every year on July 28, we mark World Hepatitis Day with an event to educate, gather together, and also remember those we have lost from the hepatitis C community. This year, we should have much to celebrate: in early 2017, medications that had previously been unavailable were finally added to some formularies, including Ontario’s. This means that people with certain types of hepatitis C who have been waiting years to access safe, effective medication will finally be able to start treatment and be cured. For many, being cured means avoiding potentially fatal outcomes like liver failure and liver cancer. It also means shedding the burden of carrying a highly stigmatized illness that is often met with ignorance, ostracism and discrimination.
Je me vois souvent contraint de commencer mes billets sur le travail du sexe en parlant du Grand Prix de F1 de Montréal.
Chaque année, dans la foulée du Grand Prix – et particulièrement l’année dernière, en juin – les médias se font un plaisir, sinon un devoir, de prendre d’assaut ce qu’ils perçoivent comme une violente augmentation de l’exploitation sexuelle et de la traite des femmes dans le cadre de ces évènements sportifs. Cette médiatisation s’inscrit dans une approche abolitionniste aux effets néfastes, ceux-ci incluant une surveillance accrue, des arrestations plus fréquentes et des risques de déportation plus élevés pour les travailleuse(-eur)s du sexe.
Marcus and David have been dating for three years. Marcus is HIV-positive and David is HIV-negative. David was worried when he told his parents that his new partner was HIV-positive, but after they saw how happy Marcus makes him, they have welcomed Marcus into their lives. At the same time, they still worry that their son may become infected.
Faith is living with HIV, and her partner, Scott, is HIV-negative. Faith often finds herself having to educate Scott on what she has to do to manage her condition and Scott has had difficulty understanding because information changes quickly. They fight more often — about sex, about health —and about where they see their relationship going.
These are hypothetical examples of two different types of relationships that involve HIV, yet many other couples have their own, unique experiences. So it is hard to know what kinds of experiences are the most common for people in these relationships.
The CATIE Blog is written for people and organizations working and volunteering in Canada’s response to HIV and hepatitis C and hosts the views and opinions of frontline service providers.