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Testing positive for HIV often leaves a person overwhelmed with questions and concerns. Remember there is support available to help you come to terms with a recent diagnosis and along your journey. Check out this page for people, tools, counselling and other support that you can access. People living with HIV have the same human rights as everyone else, including the right to health, privacy, non-interference from the state and non-discrimination. No one can refuse you a job, housing, medical services or dental services because of your HIV diagnosis. This right to non-discrimination extends to your partners, family, friends, colleagues and other people associated with you. No one can treat people unfairly because of their relationship with you.
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I thought it would last six months or a year,” he recalls. Burton was first diagnosed in the s, when much of America was still treating HIV and AIDS like a problem that didn’t matter much because it supposedly only killed gay people and White House officials laughed about the problem. He describes those early years as living in “survival mode. But by the mid-’90s, as the first protease inhibitors were integrated into healthcare and HIV-positive people started getting a little less sick , it became clear there was still a life left to lead.
But survivors still had to cope with the social stigma. You told your family about it and they were gone. The Internet was a gold nugget we found because we could socialize with other positive people all over the country. To me, that was a life-saver. More than 15 years later, HIVNet is still going strong, with some members dating back to the original founding of the site. Its membership is restricted to people who are actively living with the virus—a point of pride for Burton—but it’s far from the only site of its kind on the Internet.
There’s Hope , which bills itself as “the best free herpes dating site and App for singles with herpes and other STDs to find love and support. The interface of these services are not unlike what you might find on Tinder or OKCupid.
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New Zealand H Friends is a social and support group for those with genital herpes living throughout Aotearoa. We offer advice and empathy – and good company in a safe, relaxed environment. The newly diagnosed are particularly welcome – we fully understand how difficult this time can be for you. Current membership spans all age ranges, with a great wealth of experience for newbies to draw upon.
We are fully inclusive and non-judgmental — all are welcome. Although Meetups are largely Auckland based currently, we also have organisers in Wellington and Christchurch. Those from other areas wishing to organise Meetups locally are encouraged to approach us to discuss. We will do everything we can to support you through the process.
This is a private group.
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You can find almost anything on the internet these days, especially if you’re browsing for love. Or, at the very least, a shag with a random stranger thank you Grindr, Blendr, et al. But here’s a new one; dating sites for those with sexually transmitted diseases.
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The New Zealand Herpes Foundation: Herpes and Relationships – This is a resource for people preparing to have “the talk” with their partner.
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By Stacy Liberatore For Dailymail. Sexually explicit pictures, audio recordings and private conversations shared in dating apps, such as SugarD and Herpes Dating, have been exposed online. Sexual explicit pictures, audio recordings and private conversations belonging to users of dating apps, such as SugarD and Herpes Dating, have been exposed online.
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Heather Haskins was on her way to celebrate her birthday in Virginia Beach in the US about four years ago when she got a phone call from her doctor with some news: Haskins had tested positive for genital herpes. She was diagnosed with herpes simplex virus type 2, which affects more than 1 in 8 Americans. And even though Haskins had never had an outbreak, she was petrified by the idea of disclosing the virus, terrified that she would face rejection.
She fell into a deep depression and even contemplated suicide. For years, Haskins searched for a support group for people with the virus. She found empowering communities on Instagram and groups based in other cities, but struggled to find one in the District of Columbia in the US, a place where seemingly “everyone knows everyone” in the dating scene, Haskins said.
Such spaces only existed in secretive groups on Facebook, Haskins said, mostly disseminated by word of mouth, and often requiring a password to join. So Haskins, 32, decided to start a support group of her own. Last month, she launched HSV in the City, a gender-inclusive teleconference support group for people in the Washington area to meet twice a month to talk about living with herpes. In each session so far, a group of two to six people have called in for hour-long conversations about how to feel comfortable dating, how to disclose to potential partners, how to cope with being “ghosted” after telling a date about herpes.
Try dating with a sexually transmitted infection that you can’t get rid of,” Haskins said. There has been a growing willingness among younger generations to start publicly sharing their experiences with herpes on social media, much as they have with other issues such as sexual assault and abortion, said Jenelle Marie Pierce, executive director of the STD Project and the founder of a herpes activists network.