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Seven months after Ella Dawson says she was diagnosed with genital herpes, she remembers a young man at a college party offering her a sip of his beer. Dawson, 22, was just learning to shed the shame that came with her infection, which affects one in six Americans. She could already tell this sense of isolation was worse than any outbreak.
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NZ Herpes Support. likes. NZ H Friends is a support and social group for those with genital herpes living throughout Aotearoa. See ‘About’ section.
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.
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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.
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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.
Project Accept, an advocacy group, asserts on its Web site: “[Herpes] was Dawson said she plans to keep blogging about dating with genital.
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