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So I made it to month four without a visible sign of an outbreak. I had a really bad outbreak in the ending of April and was diagnosed with GHSV1. My initial outbreak took about a month to heal and left scars (a lighter pigmentation from my overall complexion on my genitals). Sadly I have been ridiculously paranoid to the point I have taken two 7 day treatments of Valtrex. More than likely it was probably just yeast infections (I get them way more than I should, even before getting hsv). I also take lysine twice a day and three times a day when I feel like an outbreak is coming on. I’ve been applying tea tree to my genitals everyday since getting diagnosed to dry out any potential outbreaks that are present that I possibly mistake for an ingrown hair. When does the worrying stop? How often have anyone on this forum with GHSV1 get outbreaks? What’s are some good tips and tricks?
June 3rd I may of been exposed to Herpes.
Performed oral and vaginal sex with a one night stand. A few days later, "felt off" and got tested on the 7th (negative for all stds, but not tested for herpes)
Took a round of Doxycycline the following week around the 14th for a few days as I was feeling extremely Hot and urinating frequently. It seemed to help for an instant, however still feeling off.
Tested again n the 28th - Negative for all stds including HSV igg however positive for HSV igm with an index of 1.14 (Positive being anything greater than 1.1) *approximately 26 days after suspected exposure
Dr. prescribed Valacyclovir 2x day. Started taking medication July 2nd.
Pain and discomfort in the penis continuing. With sensations in the pelvic area and kidneys.
Tested again on July 20th - Negative for all stds and HSV igg/igm.
Tested again August 6th - Negative for all stds and HSV igg/igm.
I have been taking valacyclovir since July 2nd 2x daily.
I have felt just not right since the possible exposure date (or shortly after).
My penis has gone through feelings of tingling sensations, heat, pain but not to touch, pain in my pelvis. Things seemed to of started with a burning sensation in the inner thigh.
I feel as I am having shooting sensation in my legs and occasionally have an itchy/tingle around where my pubic hair is from time to time. Hell, today and maybe yesterday I've noticed tingling in my scalp.
I tried again today to not take the valacyclovir and lasted until about 11:30 am after waking up around 8 am. My lips and the skin around my face starts to burn and the tingling around the pubic hair area of my genitals increase in its sensations. It's almost as a sleeping demon is waking up when I don't take the meds. When I take it, it takes about a day or so for things to get back in control.
My penis/genitals have also not smelled the same since. It seems my scent has changed.
Today is day 68 - is this how it's going to be forever?
I am worried I have this all over my face as the burning is in the corners of my mouth and down my chin, as well as my nose.
I have not shown any sores however I do feel my penis and scrotum has felt hot and sometimes red, typically on the head of the penis at the urethra. Multiple dr's say it looks normal to them.
I am so lost and feel like I am falling apart physically, mentally and emotionally. I guess I just wait until week 12 (in a few more weeks) to maybe test positive... but then what?
I’m still trying to process this but I am a gay male in my late 20’s that was recently diagnosed with HSV-2 in October 2018. I haven’t been sexually active since 2015 and have only engaged in sexual activity with four people in my life. I’m feeling a lot of emotions because of this; sad, angry, confused, violated, ect. Thoughts like who would’ve thought someone like little ole me, compared to all of the VERY promiscuous people in the world, would end up with Genital Herpes ESPECIALLY when I’ve been abstinent and just focusing on myself for years. That was a gunshot to my soul. It’s crazy that I’ve ALWAYS done regular STD testing, thinking I was negative for everything only to find out that Herpes was never included in my testing because I never knew you had to literally ask for that until this year. The CDC and medical industry is so fucked up and wrong for that. I’ve always used protection, except with my first boyfriend but that was back in 2009-2010 and a condom broke with a sexual encounter I had back in 2011 and I remember immediately putting a new one on him. Unfortunately, all of the men I’ve dealt with sexually are questionable. Half of me wants to know who gave this to me but the other half is like what’s the point. I only have access to contact three of them (I don’t know where the other guy is) but I haven’t spoken to two of them in years, one of them in a whole decade and it would be pretty awkward for me years later to write them a message about herpes. My first boyfriend and I are cordial but he’s still immature so it would be very awkward with him. Anyways, as I’ve been thinking and backtracking my life, I would think I caught this back in 2011 because I remember my anus itching so badly but I thought it was just my hair growing back because I do recall shaving before having sex so I guess that was my first outbreak. Other times I would just get a minor itch in and on my buttocks but I never would’ve thought herpes. I’ve never got outbreaks on my penile area. This is all still confusing and baffling to me. I’m still sad and feeling like my future love life was taken from me. I feel like part of my confidence was taken from me. I don’t even feel comfortable flirting and finding people attractive right now. I’m just releasing my thoughts about my situation but I do have questions. My results also came back saying I had extremely low Vitamin D deficiency; does HSV-2 have something to do with that? Is there a test I could take to tell me exactly when I contracted this virus? This question may be TMI but I masturbate and I notice that a lot of sperm doesn’t cum out sometimes, does HSV-2 have something to do with that?
Since May I have been taking Valtrex. At first it was 500mg once a day then it increased to 1000mg once a day in June after frequent outbreaks persisted. I've had a total of 9 outbreaks since May and was diagnosed with hsv2 in March of this year. The past three weeks I've had severe dizziness, especially when lying down and getting up in the mornings. Today my doctor suggested taking acyclovir 400mg twice a day. Has anyone switched from acyclovir to valtrex and experienced better results/less breakouts?
Hello people well let me start by saying I've suspected that I've had HSV for years now me and my wife. But I've been to afraid to come to her with it. She's had fever blisters as she calls them and she gets huge painful bumps and clusters of blisters at the top of her butt crack and she has major irritation down there often. Which makes me believe we have it. I dont usually get anything but itching and as of lately I have irritation inside my penis and on the head but never had an outbreak.
Well I had an encounter with a sex worker I used a condom but for some reason she decided to put lotion on the condom I only received oral from her no sex. After doing some research I found out that can damage condoms. But it didn't tear. But I've been feeling very irritated down there like I described earlier.
Is it possible to be re-infected with a different type of HSV or do you guys think that it is something else going on?
I've been so depressed lately and having major anxiety. I want to get checked so bad but I'm afraid she will accuse me of infecting her. Also I just want relief I've bought acyclovir online and have been taking them for a day now hoping to make the irritation go away. My friends says it's all in my head. I've been tested for most STDs and all negative.