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  1. Hello world! I had my first HSV2 outbreak 8 years ago. The first one is the worst -- the actual outbreak hurts like hell. The outbreak itself was very tiny and localized in a small genital area. However It came with side effects I didn't expect like an acute and intense tingling sensation in my lower back, buttocks, and spread down to my feet/toes. Fast forward years. I rarely get actual outbreaks if ever. But I do experience that intense nerve pain I remember that comes before an outbreak manifests as a skin lesion. So now the outbreaks don't happen, but the prodrome pre-tingles happen often. Except now those piercing sharp tingles aren't just perceptible in the aforementioned areas. I feel it all over my body intermittently - neck, shoulders, arm, yes leg and lower back, foot, etc.. To emphasize, I never experienced any chronic pain remotely similar to "herpes tingles" pre- first HSV 2 outbreak. Several Questions: Does this pain sound familiar to you? Has it migrated outside of where it was when you first had an outbreak? When I bring this up to multiple doctors, I'm baffled that they have no idea what I'm talking about. Or don't see the connection between the nerve(?) /lymph node (?) pain / neuralgia/ paresthesia and HSV. Every time I see a "Lyrica" commercial for fibromyalgia I think to myself, "well this is fucking it. this is what I'm feeling/experiencing in my body." Is there a link between fibromyalgia and herpes? I wonder how many patients diagnosed with fibromyalgia have either HSV 1/ HSV 2/ shingles/ varicella-zoster viruses or something related? It seems to me there is a there there. But I also feel I'm being gas lit by the world and that in general researchers / HCPs are too "embarrassed" to even commit to research around the "not talked about" symptoms of HSV; or even HSV in general. How can herpes be so "common" and yet not a single medical professional is conversant in the totality of the disease or specializing in it? >_< Not related, but where can I purchase acyclovir cream? That stuff is like contraband in the USA lol. ugh this country sucks in this arena.
  2. 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?
  3. I was dating this guy who has genital hsv2 like me. He thinks that he got hsv2 on his nose from going down on me. It got really bad and had a lot of puzz. The docotr said that they could not be sure that it was herpes because more than 48 hours had passed after he got the outbreaks and swab tests would be unreliable(Never heard that before) I started doing my research based on his symptoms and found out that it can be a staph resistant to antibiotics infection too. I wounder if anyone has had this experience before? How often can you find staph and herpes at the same time?
  4. Hi all I had an unprotected exposure 14 months ago after 4 months after the encounter i saw a wart on my glans penis my doctor said its HPV and removed the wart with RF. He also said i have candida blantitis and asked to apply antibiotic cream for it ..After this i start getting some small red dots on my glan penis along with painful urination and tingling pain inside my urethra my doctor said i have NGU and asked me to get HSV IGG,IGM sero done ..The results were HSV 1&2 IGG 0.18<, he said its not herpes ..This was after 5 months after exposure ..These red dots used to appear on the glans penis and tip of urethra and disappear after few days ..In septmber 2017 again i had sex with someone using protection before having sex i had these small red spots on the glans and after sex next day they urethra become raw and reddish and when i touched it with tissue it was bleeding and my doctor said to do HSV1&2 again this was almost 12 months after last unprotected exposure this time the result came negative but with higher range 0.64 HSV1 IGG and 0.62 HSV2 IGG My doctor said it is not herpes but we don t have swab options in my country its only the blood test ..Now its been two months since the last test the red dots are appearing all around the glans penis in more numbers plus i also have very bad urethritis burning sensation on urination and sometimes tingling pain ..i am attaching the pictures here can someone tell me is it herpes or something else ..As i am totaly confused is it herpes or something related to the HPV i already have and if its herpes i just don t want to delay my treatment and i will restrain from having sex with anyone as i cannot take the guilty of giving this to anyone ..I don t even wish my enemy get this Herpes ..It just destroys your inner peace of mind ..Can someone here really help me looking at these pictures .. plzzzzz
  5. Hello. I am diagnosed Hsv2 positive, never had same kind of spots I had on glans since first ob, but a lot of side manifestations, mild itch, sensitive glans with lot of tiny bumps... Now about 10 days ago got this on boxer area external side leg, is this a typical hsv2 related? Doesn't itch
  6. AiCuris and Pritelivir have been mentioned in a few threads. Read it all or skip to the last paragraph for the relevance to hsv. https://labiotech.eu/hcmv-antiviral-fda-approved-aicuris/
  7. Hey i have been using something for a while now and I'm convinced it works. I don't want to be greedy so I'll share my recipe and I'd be interested to know how u get on. Can be used as a daily ointment on the area effected or 3 x a day when u sense an outbreak coming on applied with cotton wool. 25 ml fractioned coconut oil 25 ml virgin olive oil 12 drops Tea Tree oil 20 drops origano oil 8 drops propolis liquid Mix well before use and if any irritation increase olive/coconut oils Good luck I also want to keep u up to date with my progress. I use the above to treat/stop an outbreak and have recently started the following to work on ridding myself of the virus altogether. Morning and evening 5 drops of an oregano oil mixed with unrefined olive oil under the tongue. Mix 8-10 drops of oregano oil to every ounce of olive oil. Shake well before use. I will rub 4 drops of oregano oil mixed with pure coconut oil at the base of my spine. Only recently added dmso to this. Well it's been 3 weeks so far and no hint of an ob. Ill keep u posted
  8. Has anyone found a way of stopping menstrual-triggered outbreaks/viral activity? This is the main trigger for me now after three years of having hsv2 but I don't know if there is anything that can be done without having a hysterectomy or using a contraceptive that stops it. Not keen on this or taking antivirals during my period so, are there any non medicinal solutions?
  9. I apologize, this maybe a duplicate of my other question. But I'm really concerned on what is happening. Since my first ob that consisted in tiny widespread blisters on glans and (not sure if herpes sores but) two behind leg and two on arm, I feel like my glans never returned to its original skin. What I can see (sometimes most visible on erection) are tiny skin bumps. It feels like I'm always on outbreak, is this even possible? They look like these (pics are not mine, just found them on internet searching "herpes glans" and they describe how my glans looks right now). Could herpes give status of constant tiny bumps in people with low body defence? And since I have them, means I'm constantly shedding? Thanks for your opinions! https://goo.gl/images/v5MXKh https://goo.gl/images/iPv3sW (I am tested HSV2 positive with value 1, three months after exposure)
  10. Herpetic nosodes, homeopathy, micro/energetic-vaccination, decreasing your outbreaks/symptoms.... ok, so what if all the dollars on research to make a therapeutic vaccine were really inappropriate and there's already something out there that can help on a similar level? What is this product? It is essentially a way to homeopathically vaccinate yourself to some herpes viruses (1&2 and others), thereby giving your body insight as to what HSV looks like, enhancing your body's ability to identify, tag and destroy it. What are nosodes. Nosodes are a homeopathic (very minute concentration) dilutions of an energetic impression of a pathogen. So with herpetic nosodes, it'd be energetic impressions of some herpes viruses. Please, I know, I really don't like explaining homeopathic medicine because the more one read or hears about it and the more I explain it, the less I feel others are convinced and the more confusing it is. -But for $16, this is worth a try... So I'll tell about my personal experience. In the beginning of my herpetic initiation, I found a homeopathic nosodes remedy for 23 pills at $40. It helped when prodrome happened but it wasn't incredibly powerful. That company discontinued their product but, by then, I had build up an immunity and things were better. I still experience symptoms of tingling on/around my genitals, sacrum, perineum/crotch and low-level sores on my lips. I'll take SJW for a day and will feel liberated for 3 days then things will steadily creep back. Depending on other symptoms, I have other things I take to address them... But the prodrome will return and the cycle continues.... So I just received my Herpetic Nosodes tincture yesterday in the mail and I tried it. I tried too much of it. I think it says 10 drops and I put half a dropper under my tongue. It was wild, the tingling and whatnot got slightly worse for a minute and then subsided. I felt my spleen organ (to the left in the rib cage) get tense. Usually when an organ is tonified, it will become literally "toned". The spleen is the major lymphatic organ that is in charge of, among many other things, adaptive/learned immunity. So taking this herpetic nosodes shows my body what the virus looks like, just like a vaccination, and my body learns and makes smarter antibodies to identify, tag and destroy the virus. $16. If you have frequent outbreaks, give it a try. you really don't have anything to lose, except $16, which is nothing. Here's a site of the product that I got. https://www.pureformulas.com/herpetic-nosode-2-oz-by-professional-formulas.html I don't know how the long-term effect is. I just got this and started using it 3 days ago and have been amazed. Just thought I'd share my latest find/exploration.
  11. Hey all, I am just so tired of being constantly anxious. I had a vaginal birth with no transmission and my child is now almost two but every time I even see the smallest spot (wether bug bite or allergic reaction etc.) on their skin I go into full intense and shaking panic mode. I just don’t know how to calm down and it’s doing nothing for my stress levels and eating habits. Almost every month I have complete breakdowns in fear of transmission. But logically, there’s no chance my child could contract it. I’m always covered, washing hands throughly after washroom use, no skin to skin contact with my effected areas ever and only one outbreak this year. Any advice or words of support would be awfully nice right now. Thank-you.
  12. SillyGirlMel

    Getting a Labbox??

    Should I send a link to the labbox testing for the guy I hooked up with? I told him I have HSV2 after the deed was done and of course promised to pay for any expenses for testing. I found the link to labbox through honey, but I’m worried if I send him the link the horrific description about hsv2 beneath the merchandise will give him a heart-attack. What should I do? I messed up and I’m trying to help without making it worse.
  13. Dopa.lene

    Viral load??

    So ive tested negative for most std's but my doctor never gives me the viral load count?... Is this because im testing negative??.. How can i contract something if its undetectable?? Does that mean it's gone??
  14. Hey everyone! I've seen a various posts across various forums regarding disclosing (or not) and have seen a bit of a trend in people thinking that it's 'hard to pass' with one encounter (lol) condoms make it impossible to pass, blah blah blah. So let's just try to compile some short & sweet answers to some basic H transmissions stories and questions...Could be helpful in many ways to lots of people! 1. Did your giver: show symptoms / asymptomatic / disclose H to you? 2. Protected or unprotected? Oral/vaginal/anal? 3. How many encountrs with giver? (time frame of encounters ie. one weekend of several months?) 4. How were you diagnosed? (swab or blood test) 5. Are you a symptomatic carrier (showed signs ie. outbreak) or asymptomatic (never showed signs, diagnosed by blood work) 6. How long from sexual exposure did you start to show symptoms? 7. How long did your primary outbreak last? How frequent have your recurrences been? (ie. one a month/year?) 8. How long have you been H+? 9. Are you on antivirals only during outbreak or suppressive therapy? Or have you gone the natural route? 10. Words or wisdom/support for newbies? ********** I'll go first... 1. No visible signs of H. Asymptomatic carrier not diagnosed with at the time so no disclosure. 2. Unprotected vaginal/oral. 3. 2x in a weekend (Friday night and Sunday morning) 4. Positive swab test during terrify primary outbreak. 5. Symptomatic HSV2+ 6. Friday/Sunday sex; initial first symptoms started Tuesday and quickly got aggressive. (in hospital by next Sunday) 7. OB lasted a few weeks. Cleared up, then I had a couple minor recurrences due to alcohol in following weeks but MINOR in comparison (just more annoying not excruciatingly painful) still working through this ATM. 8. I was infected Mar9/18 - diagnosed with Mar23/18. 9. Antivirals during primary OB; lots of supplements and vitamins every day now and have changed my diet. 10. It does get better. Not back to normal better, but better. Take care of yourself and do whatever it needs for you to heal physically and emotionally. Find a good friend/family member/counsellor to confide in to help lessen the burden you are carrying. Get wine drunk with a friend and cry all night. Go to the top of a mountain and scream at the top of your lungs. Amazon shop till you max out your credit card buying things that make you happy. Hope this can help some peope! Love & light everyone! x
  15. So, I found some one who was willing to have sex with me .( He doesn't have HSV2 or 1. ) I hadn' t had sex for over 7 months. I am really disappointed. It did not go well. The condoms didn't make it any safer. They kept falling off or slipping down, Its just not safe sex at all. Plus, He couldn't stay erect. He couldn't feel anything. I couldn't feel anything... Maybe from the lubrication I had to use so I wasn't rubbed raw to cause an outbreak. So we had to stop every time. We tried for 4 days. It just wouldn't work. The last day he thought it was Ok to have anal unprotected and just did it. I didn't stop him. I thought he knew it wasn't safe but didn't care. ( so that was the only good sex we had) The next day he said he thought it was safe and I had to tell him it wasn't. There is no point to have sex anymore if I can't get oral either. I tried a barrier over and it was pointless and I felt nothing. And the whole 4 days I was obsessing and checking my vagina to make sure I didn't have any Obs to infect this guy, And everyday , even while taking AVS, i still "felt" sensations or something that is herpes-like, like I do every day. I had what turned out to be an ingrown hair that I wasn't sure about either .So 2 of the days I had to explain to him I wasn't quite sure and I handed him latex gloves. Total disaster. Pointless. pointless to risk his health for unfulfilling half-real sex He was a good sport though. He didn't get so scared. He was willing to try at least. He trusted me to know. But honestly, I don't see how I can be sure and know. I don't know when I am getting an oB- cuz everyday I have some issue that makes me think I am getting one. every. damn. day. Fuck this shit. I just want to cry and die. I want my old life back before this disease. I know the sex would have been awesome this past weekend if not for HSV.
  16. HSV. Everyone's favorite topic! If you read my other piece, you know about my struggle with Viral Meningitis. But now I get to share with you (because it was just shared with me) how I got it. As if I wasn’t already depressed, hurt, and confused, here comes the nurse from the hospital calling to tell me that one of the possible causes of Viral Meningitis is the Herpes Simplex Virus and they tested me for it when I was there. Surprise! I have the Herpes Simplex Virus type 2, or as I like to put it, Genital Herpes. I cried almost as loud as I did the day I got the severe headache from the Meningitis. I immediately thought, I am 21 years old and my life is over. I thought about all the cons, no more dating, the difficulties having children without infecting them, dating rejection, my friends judging me, having to worry about infecting people around me, every possible negative thought came rushing at me all at once. I can not believe this is happening to me. I had to mourn the death of the person I once was for a few days of course, but after coming to, I realized that although it is not curable, this is not a death sentence. I thought let me learn a little more about this before I just shut out the world and everyone in it. I found that 1 out of 6 people have HSV. So if you know more than 6 people, one of them most likely has some form of HSV. Some people know, some people don't, but they do. So yeah that is A LOT of the population. Some people get symptoms like itching, burning, and bumps on their genitals sometimes and some people can go years without having one single outbreak. There are Antiviral medications and even suppressive treatments to help lessen the outbreaks. To prevent the spread of the infection you can: Use condoms getting regular STI tests and ensuring sexual partners also get tested regularly reducing the number of sexual partners being in a long-term monogamous relationship with an uninfected person avoiding sexual activity during outbreaks of the herpes virus using anti-herpes medication daily if one partner has the herpes virus abstaining from sexual activity Source: WEBMD.com The best thing to do if you find out you have HSV is to contact your doctor so they can answer all of your questions and help you find the best option for treating the infection. On another note, I felt like although I could treat it to minimize outbreaks, dating is going to be a nightmare from now on. I thought, who would want to be with someone with Herpes, one of the scariest STIs out there. I immediately thought ok, well what if I find someone with herpes like me to date, I could possibly find a guy that way. I mean, who could turn away someone with the same condition as them? This notion, I soon found out was a problem. I signed up for a HSV dating site and I realized that I was scared to share too many details about myself and even post a picture of myself. I noticed that I was scared to reveal that I had herpes even on a HSV dating site. Odd, I know. I was struggling accepting my truth. I went on to search for forums, discussion boards, etc (as I did when I found out I had Meningitis). I was searching for people my age with HSV who were struggling in the LOVE department. I found them. I could not help but fully relate to every single person on the discussion board. It was the best thing I could have ever done for myself. One blogger expressed how she would never sign up for a HSV dating site, as it can influence people who carry the virus to conform to only talking to or being with others who have it which is crazy. She opened my eyes to understand that we are all people and should not live under the stigma that Herpes is this big scary monster thing and we have to alienate ourselves from the rest of society. After all HSV is really just a few outbreaks of uncomfortable bumps and itching. It's not to say you shouldn't be careful with your health, it is just that the stigma behind Herpes is that it's a death sentence and its not. The posts made me laugh and informed me of so much. People my age, in college just like me, everywhere, going through the same exact thing. One girl and guy on the board went on to say don't be afraid to disclose that you have the virus to people. The girl told about 50 guys and had only been rejected by about 5 of them or so. She had been in 7 relationships post HSV. A guy said the girl he met had it and he didn't really care and slept with her. All of this was good news to me, not because I just HAVE to be in a relationship or have sex, but to know that I don't have to restrict myself to find love or be ashamed of myself for my condition. I also learned to ditch the stigma because its not as bad as anyone thinks and is easily contracted. Anyone can get it and not even know it. I don't know if I am quite as ready as these folks to be as open as they are with HSV, but I can say that I had a huge sigh of relief that I can be if I choose to. Tip of the day is to not be afraid of rejection. Not everyone will reject you.Take a chance, try it, disclose to someone and be positive about it, because you won't know the outcome until you try! These are the two websites I went to to research: The first is the forum from the people’s stories that I used in my entry. The other is an article. I hope you find these as helpful as I did. https://herpeslife.com/herpes-forum/discussion/8423/dealing-with-herpes-in-college The Overblown Stigma of Genital Herpes - The Atlantic
  17. cracked

    Neuralgia

    Hey everyone. I’ve read a lot of posts and have talked to some people from the forums who suffer in various ways from this virus. I’ve also heard the term ‘neuralgia’ being thrown around in posts, but have yet to figure out what kind of pain and its origin is for all the people that said they experience it. Please do me a favor and comment below about your experience with it and where it causes you problems and what kind of pain is it exactly? This might help some other newer members also understand. Thanks.
  18. Marley91

    Help :( so lost and stressed

    Going on 11 weeks of back to back obs. I was diagnosed with HSV2 but it is on the palm of my hand. I just now started taking daily antivirals. Im nervous about taking the meds and any side effects I could get from taking them daily, also wondering if my body will become immune to them? Is it normal to have so many outbreaks? I’ve never had an ob on my genitals but I feel like I would know if I ever had right? I’m scared because my dr told me I didn’t need to tell my sexual partners and didn’t need to worry about using condoms because the ob is on my hand and I always keep it covered. Last night I started freaking out about the possibility of having it on my Genitals and wondering if I have passed it to my current partner and I’m freaking out about having to tell him. Can anyone help? I have a doctors appointment next week so I’m stuck waiting and stressing until then. Im avoiding caffeine and I’m taking lysine plus a million other vitamins. What are common triggers that you all deal with? I’m staring to think I’m having so many long lasting ob’s because I’m in the sun all the time? How does that even trigger the ob?
  19. Hi! There is lots of info on the web about how HSV2 can be transmitted. There's so much, but it isn't all very specific so it's been very hard to determine with my particular case. I was diagnosed 7 years ago. Had it, took meds, was gone in a few days. My doc even told me I wouldn't have to worry about it again. And I haven't, totally in the back of my mind. Then a few months ago, my immune system was compromised due to a kidney infection and I started seeing something downstairs that I didn't recognize. Here it was again!!!! Seven years later!!! I had honestly forgotten about it. I'm here because I wanted to know if anyone has any info/experience with breakouts as infrequent as mine have been (so far, at least). I'm Female, and had to disclose this to a Male partner. He did not take it well. We have never been intimate anywhere near the time of either my outbreaks (last time was Feb, and I didn't know him my initial OB). And we had unprotected sex once last Fall. I disclosed to him this week because we were going to become sexual again and with my OB this April, I wanted him to know. Lots of info says there is a 4% chance of it being spread F to M with barrier and no meds, but I just don't know how much that relates to someone who has had two outbreaks in 7 years. Please help with any advice or links!!!!
  20. Jayday

    OUTBREAK OR NOT?

    What’s up community! Ive had HSV 2 via IGG blood test for about 7 months now and only had one minor outbreak (2 small lesions that did not hurt at all). My question is I don’t have lesions or blisters but do have some discomfort in the urethra but it doesn’t hurt when I urinate, I don’t have any tingling sensations but that discomfort in the urethra. Is that considered having an outbreak??? Please let me know thank you!!
  21. Trial and potential vaccine sale information Click on the link below for the full article Rational Vaccines: A case study in pharma deregulation. As the debate picks up steam in Washington, Rational Vaccines is fast-tracking its live attenuated vaccine for the herpes simplex virus (HSV) to the market — wherever that may be. Enrollment will soon begin for trials in Mexico and the Caribbean, following a single Phase 1 study of 20 patients in the Federation of St. Kitts & Nevis. “Mexico has about a four-to-five year window for sales if the trials go as we think they’ll go,” Fernandez said in a recent phone interview. “We’re doing trials in the Caribbean as well and we’ve been approved for sale in a couple of jurisdictions in the Caribbean.” The move is less about rebelling against the FDA and more about getting to patients as soon as possible, Fernandez said. The U.S. won’t be ignored, but it’s a much longer path-to-market. http://medcitynews.com/2017/03/rational-vaccines-pharma-deregulation/
  22. I just had what seems like a good idea in my head. Billboards are expensive, a march for HSV is hard to organize, and most other methods are difficult to make happen because people don't want their identities to be exposed. I'm sure most of you have seen vehicles such as cars or trucks with ads on them, right? What about raising money to have a message or slogan placed on trucks and other vehicles which would be willing to be paid for that? Those vehicles travel long distances and more people would see the message every day without us having to do anything extra and they wouldn't be stationary like a billboard, right? I'm not sure how much this would cost per vehicle, but I think it would be negotiable and not as much as a billboard? If we raised enough money on a crowdfunding website for this, would anyone be interested in donating or willing to ask in your area how much it would cost? I think this is one of the best ways to remain anonymous while still doing something that allows us to get the message in front of people. We could include the stats for how many people have HSV, how people should get tested, or anything else that's short but to the point. You can message me if you'd like if you don't want to post here. Thanks.
  23. Dear all, I have created a group on Facebook called Theravax HSV1 & 2 as a platform for people to share their experiences from the Theravax Trails. This is a closed group. Please avoid any negativity as we already have enough of that in the outside world and we don't need it here on this group. You can share your experiences on the consultation, pre and post travel as well so that it helps every one make better decisions. Members of this group can also help each other to travel together to get the vaccine (Not necessarily by means of funds) but just support as it's not always easy to go to a new country for an objective as strong as this. This group is for support. We are with you. <3 I urge the aspiring participants and the people who have been selected for the trails to join the Group and share their experience. I uger
  24. WildFlowers92

    My Outbreak Story

    Hello, So I finally bit the bullet and decided to make an account. Since I'm a newby who's been dealing with HSV2 for about 10months I thought sharing my story would be a good ice breaker. So I was celibate for 1 1/2yr and I was minding my business at the DMV waiting in line to take my driver's test. When this guy came up to me and asked me how I did ( I failed!!!!). Instead of making me feel like a loser he encouraged me and we had a few laughs in then he asked for my number. While texting I quickly learned we're both scorpios and the sexual tension flourished quickly... After a few dates it happened and it was everything I thought it would be. Well not everything... fast forward a month later I was getting ready for my cruise and i decided to see him a few nights before I left. So I hopped in the shower and shaved my life away and accidentally nicked the tip of my cliterious. (If you're wondering yesss it hurt like hell). But after sitting in the shower for 15mins I mustard up the courage to still go and that it only felt a lil irritable. (BIG MISTAKE) Now I'm in Miami boarding my cruise and felt horrible. All I wanted to do was sleep my life away. I was also cramping b/c SharkWk was in full motion. My lympnoids swelled and became painfully infected, I had a burning sensation when I used the bathroom, and began having flu like symptoms. Finally I decided to get a mirrior and look at my lady bits and seen a lesion on my cliterious and left side lip. I thought it was just infected by my razor. Ignored his texts for the rest of my vacay b/c I didn't know what to think. I waited until my Gyno visit where by 1st sight she already determined it was Gential Herpes. I laughed and told her no way these have to be infected razor bumps. But my Gyno gave me a blank stare and that's when fear seeped in. She swabbed me and 1wk later it came back positive... I told him and he was pretty shocked. I ask if hes been tested and he said yeah but not for HSV2. He felt horrible and wanted to see me that same day but I couldn't. I was too upset at myself, at him, and at life. I thought my world was crumbling and felt like things were unfare. I'm still unsure on who gave it to who. In the beginning I was having 2 break outs per month which lasted 3-4days . Then I've researched my life away and looked into taking natural supplements. So far I've taken Oil Oregano, Spirilina, and Black Seed Oil. I'm only taking Black Seed now and it's making my. OB almost nonexistent. I'm just trying to find ways of making things easier and staying positive along the way no pun intended.
  25. Hi everyone, I haven't slept with anyone since the man who gave me HSV-2 I'd love to hear everyone's tactics and best things to say when disclosing that they have genital herpes, tips, and word-for-words, please!
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