So I found out that I had HIV in January of this year, even today its hard to believe that its me. Currently I am not on any meds, because my viral levels are still low and my Immune system is still fighting. I contracted Hiv from my ex boyfriend who never told me anything. I found out 6 months after we broke up and I moved away. It pisses me off that he lied to me for so long and that he didnt do anything to protect me. I have alot of support from my friends and family but I still feel confused…I need answers from him that I will never get.I have came to realize that HIV is no longer a death sentence, like it was back in the 80's but its the fact of feeling tainted. Im terrified to date because what happens if I tell the person my status and then be rejected I dont need to be hurt anymore. What makes the HIV real is when I do my bloodwork, I tend to get anxious and freaked out, especially because I hate needles. Im worried that when its time to begin meds that my mood will get worse because then it will really be real. right now its just monitoring but what happens with the meds? is it trial and error until they find the right combination? Will my depression worsen, or my anger get more intense. I feel like a part of myself died and I have lost the person I used to be. There is alot of shoulda, coulda and would have but whats done is done. The worst relationship I have ever been in is going to haunt me for the rest of my life. I wish there wasa cure or a shot that could just take this away from me. But I know currently there is no chance. So i continue to keep my head up and believe that everything will be okay, its just going to be a bumpy ride. Until next time over and out!
My opinion on being HIV+
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There You Are
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None
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Womans HIV Healing Retreat
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It doesn't hurt me.You wanna feel how it feels?You wanna know, know that it doesn't hurt me?You wanna hear...
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Compassion
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Let's utilize our rights
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I have been a resident of New York State most of my adult life, and have seen much...



Hello Chrissy, Welcome to the tribe, and rest assure that you are in good hands here. Lots of great people willing to help and lend a shoulder. I was diagnosed in 1991 at 22 years old, and I was a lot like like you. Unfortunately, I stayed in denial of the disease for about 18 years and hid in my shell. But I am doing well, and didn't even start meds until 19 years in. I am doing well and surrounded by friends. I am living life and enjoying it. Anything you need to ask, there is a wealth of information on this site with some great members. Hang in there, you will be okay…… Tracy
just want to thank you guys for the comments and reassurance, good to know I got people to turn to and understand what I am going through. thank you again 🙂