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  1. Not a cure - but making strides https://www.newscientist.com/article/2217255-herpes-vaccine-to-be-tested-in-humans-after-best-result-yet-in-animals/
  2. Really bummed to see that excision bio delayed all their phase 1 clinical trials especially the HSV1/2 - they had initially been set to start in 2021 now delayed til 2023. I figured with the amazing news surrounding their HIV research that it would have sped up the process, not delay it. Thoughts/opinions on why they may have done this? https://excisionbio.com/pipeline/
  3. Does anybody have any suggestions on how you deal with pain at work or when you are out? I have hsv2 I am in the beginning of a break out this one is bad. I can’t really afford to call in so if anybody has any tips I would greatly appreciate it! Thanks.
  4. Hi guys, this is my first post but honestly i´ve been lurking around for a while (lol ikr) Lets get to it. I had unprotected sex with a friend, she claims she´s clean and two months later i noticed this in my pubic area. No itching, no pain, no flu simptoms just these lil fuckers (sorry for coursing) I went to the doctor and he claims thats not HSV2 but i live in south america and honestly i dont trust doctors, i made another appointment with another doctow this week. Also i had blood test done and it came out negative, but im waiting to the 13 week to be sure. Im extremely paranoid and anxious about STD´s so u can imagine im dying over here. Its been around 5 days that hey appeared and havent changed, like i mean they havent became ulcers or crust. Sorry if my English is kind of sloppy its not my native language. I really would love to have an idea of what this is or could be, and what to expect if its HSV2. Im currently dating a girl and i told her about this so were not having sex until im sure i dont have anything, honetly im getting really paranoid. PHOTOS: https://imgur.com/gKS2D0r https://imgbbb.com/image/pAZKc
  5. SeeB89

    Hsv2 on butt?

    I was diagnosed in 2013 with hsv2. back in March, after I went to a public place & used the bathroom, I got a small bump on my butt. (May of been a coincidence but I remember it) Figured it wasn’t my hsv outbreak but still took my meds to suppress it, if it was. Now here we are, 5 months later & it’s gotten worse. More bumps & are on both buttocks. Could this just be hsv showing up in my butt/lower back region? Should I get tested again? Any oral ointment I can take? I take my acyclovir but it only suppresses for my mouth. Doesn’t even seem help for my lower body regions.
  6. Hi. We all know that in theory it usually takes 12-16 weeks (sometimes up to 24 weeks) to get positive IGG blood test for HSV2. What are your personal experiences of testing positive for HSV2, i.e. time since exposure? And IGG score? Can you also state if you had HSV1 (oral or genital) and took any Antivirals prior to IGG testing? TQ
  7. Hi everyone . I’m just here to ask a question since I can’t seem to find an answer anywhere. I had unprotected sex with someone who has herpes2 . She stopped me after maybe 20 seconds of me being in her and told me I shouldn’t freak out but she has hsv 2 . So naturally now I’m freaking out. She seemed really confident telling me not to worry and that she hadn’t had an outbreak in years and that she’s had the virus since 16 years ago etc. basically she said I shouldn’t worry but than called me next day to apologize saying sorry I messed up. My question is how likely is it that I cough it from her, she says she was with someone 5 years and didn’t pass to him. But I think she’s dishonest . Also I read here people who have been with someone with hsv2 for years and never got it from their wives. How worried should I be? Thank you for any feed back. Also she takes meds as needed apparently.
  8. I was diagnosed with HSV2 in the form of whitlow on the palm of my hand over a year ago. Since then I have had breakouts almost every single month, sometimes more. I take valcyclovir 1000mg daily and had been ob free for a couple of months. I missed one day of medication and am now struggling with a terrible outbreak. My anxiety is through the roof- especially with the fear of viral shedding when I don’t have an ob. When I have an ob I am EXTREMELY fatigued and can barely function. Does anyone else get run down this easily? I know it’s only supposed to happen with the first outbreak but I’m going on 15+ in the last year with terrible side effects. Will I need to wear a bandaid for the rest of my life- even when not experiencing an ob?? I get massages regularly and am always paranoid when they massage my hand that I might spread it to them through viral shedding. The bandaids irritate my skin- does anyone have a better solution to keep my Palm covered all the time? TIA
  9. I’m a woman with HSV-2 in my vaginal area. I’ve never had symptoms orally & was diagnosed from swabs from my vaginal area. i gave the woman I’ve been dating for the past 3 weeks oral sex a few days ago, and had “the talk” with her after. She was ok and said we could figure out how to protect her from getting it. Now she’s having cold symptoms that are getting progressively worse, similar to what I had when I had my first outbreak. I’m very afraid now that I may have HSV2 orally & I just didn’t know I had it & gave it to her. What should I do?? She’s going to feel like I lied to them. 😩
  10. Alwayssmile_

    Hsv 2 oral/face

    Has anyone experienced hsv2 on the face/lip/cheek? I know everyone is different but does it look the same as hsv1?
  11. alsalam aliykom sisters and brothers im looking for 7alal inshaAllah .. i have been diagnosed hsv2 since 5 years ago .. my ex wife passed it to me .. i was 32 years old virgin man .. she was my first but ..alhamdulillah i believe that every thing happens for reason .. anyway im here seeking 7alal so we can complete and love each other .. may Allah make it easy for us to find our ways E mail: mohammed_tempe@hotmail.com
  12. 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
  13. Kappa69

    HSV-2

    So I was recently just diagnosed with HSV- 2 , 26 years of age, no signs of symptoms till a week ago. Taking VALTRAX, sores are slowly but surely healing and going away. My question is how have you handled this with your partner? I’ve been completely honest w/ her throughout this entire process, and she seems to be taking it in more roughly than I am. I’ve had the same partner for 2 1/2 years and no signs or symptoms have had ever occurred till now. My doctor said it could have been distress or poor immune system to trigger my flare up. Sexually, what are tips that have helped you prevent these flare ups. New to this so, any advice would be great. Home remedies for further prevention?
  14. Hi there, Long time lurker, first time poster, and I'll keep it simple and condensed. I've only signed up because I realize the depths of suffering some people are in, trying all sorts of desperate treatments, and I've basically been sitting on something that has taken me to near 0 outbreaks (hsv1 genital). When I first got infected some years back, I had an atypical presentation--no pain or itching, but permanently there. Bumps going up and down within the same day even, but pretty much permanently covering the head of my penis. Doctor swabbed it--came back hsv 1; he said it looked like it to him too. Now to the meat of it--rubbing alcohol. Its simple, and I'm pretty surprised that I've only seen it mentioned once here--a woman was talking about it, so I assume it works for girls too. I apply once daily, to once every 3 days, and that keeps me pretty much permanently outbreak free. It quite literally went from every day broken out for me to just about nothing. Anyway, to the what and where of it all... I use 99% isopropyl. 70% seems good too. I now have a spray bottle, but used to just dump it on the head and roll my foreskin up over it for like 20ish seconds--whatever process is actually happening, I like to think I'm facilitating absorption into the soft tissue by doing this and wreaking havoc on the virus. Obviously, you may have to do it a bit differently, genital depending. I've been doing this treatment for a few years now, so it has staying power. I read once that herpes is shreded by alcohol, so if true, I guess that explains it? However, iterupting regular treatment seems to have anecdotally, but not with great surety, made the herpes a bit less suceptible to the alcohol upon resumption. Yes, it burns terribly at first. Over time it gets better. Some days it still really burns, and in those cases I advise listening to your body and cutting the countdown short. Other than that, it feels really damn good to basically tell herpes to eff off. I don't know what kind of health risks there are. Or whether using a high % grain (drinking) alcohol would work / be healthier. I advise asking your doctor--afterall, alchohol is implicated in throat cancer. Who knows if 20-30 seconds daily on your junk can do something too. But for those who struggle constantly, I truly hope this can help someone other than just me. I also hope that this finds its way to the right forum. I wanted it in a place where casual, straight from Google, viewers would see it when they came here, and I'm hoping--and asking, please--that if I didn't get it in the right place, a moderator can instead. And, should it help as I suggest, perhaps even stickying it one day. I'm sorry in advance, I'm not a big forum person and don't come here crazy often. It just felt like something I should do for everyone else's sake. Hopefully you can excuse me if I'm an absentee topic starter. Thanks for reading, - Taylor Edit: I forgot to add in any negative effects I've experienced. Sometimes, if its burning more than usual and I leave it too long, it does make the skin pinker than it should be, and sore. The big question, what about loss of sensitivity? I worried that may happen, and its possible actually that I've lost some amount. But if I have, it wasn't even enough to remember when posting this originally, hahaha. Still every body is different, so I can only speak for me. But yes, for me, my sensitivity down there is still in great shape. Over the last few years I've on average had less stiff erections, and dysfunction, which I never had before. However, I've also been less physically healthy, I've been mentally disengaged and highly anxious around sex and sexuality (and when I'm not anxious, it often improves quite a bit), I read once that herpes itself can actually cause forms of ED, and I'm also now out of my 20's, so... Possibly related? But also very possibly unrelated to the alcohol. I'm biased though, both in mentality and my words here. So, perhaps consult a doctor if you're concerned. Cheers!
  15. So about 2 months ago, I started having unprotected and protected sex with a new person. During this time, I was experiencing a lot of itchiness and some burning. When realizing this, I decided to go to my gynecologist who tested me for all vaginal bacterial infections and all stds. The results came out negative even though I have been having this constant itching and burning on my labia. I have also learned that when I have sex, the itching and burning gets more intense and sometimes my whole vulva would be inflamed for a day or two. My sexual partner also got tested for stds and he was negative as well. I don't know what to do to make this itching and burning stop. I stopped having sex for more than a month now and the problem still hasn't gone away. I keep thinking its herpes even though I got a blood test and never had any kind of sores and my partner has never experienced any kind of symptoms for it. What can I do?
  16. 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)
  17. Hi everyone. I never thought I'd see the day that I would be posting in an online forum, let alone for this topic. I also never thought in a million years that I would get this. Im not really sure what to say on here, I just needed to say something. I was recently diagnosed positive for GHSV2... like "4 hours ago" newly diagnosed. I am still just in complete shock. It hasn't settled with me yet that I will be dealing with this for the rest of my life. I already picked up my medication, Valtrex, and it took me a solid 3 minutes to even bring myself to swallow the pill, cause I had this deep sinking feeling, like "once I do this, it's for real... this is actually happening... this is actually my life now.. this isnt some terrible nightmare that Im going to wake up from." Ive already called my (new) boyfriend and broke the news to him. He was much more understanding than I had expected and is actually going tonight to get himself tested, so we can decide where to go from there. So I had my doctors appointment yesterday with a new gyno who upon immediately examining me came to the conclusion that what I had was herpes. I didnt want to accept it and continuously reassured her that it couldn't be that because I had just gotten tested in June and those results came back NEGATIVE. Or so I had thought... Apparently, my results in June did NOT come back negative, and in fact came back positive for HSV2, yet NO ONE called me to review these results or follow up with a care plan for me. I don't remember much from that time, but considering the fact that I have been living for almost 5 months now, unknowingly with this virus, tells me that IF/WHEN I had spoken to someone at that particular doctors office, than they must have told me that I showed negative for everything, because I went on living my life like I had nothing. Im not sure what the protocol is in different states, but for VA (where I live) the doctor usually calls you and states that "they received your results and then they proceed to read off said results for each test" over the phone. I know for a FACT, that I would have remembered being told that I was positive for ANYTHING back in June.. especially considering I usually get myself tested often at and take testing very seriously, since I always dreaded the thought of ever catching something. And now.... look where I am left!!! I feel incredibly hurt and angry that this office failed to discuss these results with me! I never received a paper copy of my results, no email, nothing. The only thing I ever received from that visit was a bill stating the amount of money I had left to pay after insurance, and what tests the charges were for. Had I known that I tested positive back in June, I would have NEVER exposed my boyfriend who I very much care about and saw a new future with. I will feel incredibly guilty if his results come back positive and come to find out that I AM the reason for his diagnosis. Im sorry this is so long, I just have so much inside me that I need to let out. Clearly, you can see I am incredibly angry at this. I feel immensely isolated. I feel dirty. I feel like no one will ever love me again. I feel like even if I find a new partner, how can someone willingly choose to be with a person who has herpes, when they are not infected themselves? Why would they subject themselves to that exposure when there are plenty of other people they can be with who aren't exposed? I have always had a poor self image, I'm incredibly self-conscious. I consistently, on a daily basis struggle with self esteem issues and self-worth... and now, to have this psychological trauma and burden to add on top of all of that?! I don't know how to live with myself and I feel like my world is falling apart and I would be better off dead, than have to deal with a lifetime of loneliness and misery that comes from this psychological pain I am going through. I know I keep reading that "this isn't the end of the world", and "things will get better", etc etc. but being as this is DAY ONE for me.... and I feel like this... I can't imagine having to feel this way EVERY DAY, for who knows how long... until I just feel completely numb from it. I guess when that day finally comes, it'll also be the day that I start getting over it and dealing with this. But from this point A until that point B... the thought of that time in between just feels like so MUCH to deal with. So much pain, and hurt, and sorrow, that I just don't want to feel. not right now, not for a few months, not ever. I can't be the only one who has felt this way. I am trying to be positive and divert my energy into researching this illness and finding support groups and forums like this, but I just need to know that I am not alone in this. I know for right now, that in my physical, every day life, the relationships/friendships I deal with in-person on a daily basis, I will be alone for the time being... but I really just need to know that I can, at least, find some support online... from others who understand me or have felt similar to what I am feeling right now.
  18. Missingmynormal

    New and trying to understand

    All I have been doing is research over the past three weeks and I still don’t even know where to begin this post because it’s still so shocking. This post might be long but I hope someone will read it and help me. I feel like the doctors don’t really truly know about this topic in depth and I have no one to learn from and I’m so so scared. My first outbreak was 10 months ago. I had just had sex with a new person and started my period. The doctor said it was BV and a yeast infection. I knew that it couldn’t just be that. My labia was terribly swollen and cut up that it was so painful to go to the bathroom. Got better but then was cut up again about 2 weeks later and I think after antibiotics really had a yeast infection too. About 3 weeks ago I felt really itchy one day and the next day I had a cut on my inner labia and started my period that same day. After closely inspecting it I realized that maybe it could be a blister. I got the doctor to swab it and they confirmed it was hsv2. From the time the doc saw it my labia did get a little more raw but def not as bad as what happened 10 months ago. Of course at that point my stress levels are high and I went back to the doctor a week later to get tested for everything else to make sure I was ok. So of course high stress again. Once my initial cut was healed I shaved and ended up with what I think was another outbreak but this time next to my outer labia. I went back and forth if it was from shaving but I feel like there were two spots and they had itched and were painful. Those spots are not fully healed but no longer hurt. This morning and for most of the day I felt a sunburn type feeling on my right butt. When I’m looking at it now I swear that I can see these small bump patches that might look like little blisters ... I don’t think they look like regular little butt bumps. They are so small and it’s hard to see but it does feel tender. So this makes it seem like the 3rd little outbreak within 3 weeks. I have always had very dry sensitive skin and I have been very super aware of every little thing since this diagnosis. I’m supposed to start my period next week and I’m terrified that with it will come a 4th little outbreak. This is not as painful as that first outbreak but it’s more upsetting cause it feels like it’s lasting longer. 1. Does any of what I’m describing sound normal. Can you get it in 3 different spots within 3 weeks like this? Why does it keep restarting and it didn’t last time. Is it ever going to end!? 2. How can I figure out what this is going to be like for me if every single circumstance has had different symptoms. 3. I thought it was mostly supposed to be in the same place so why does this seem like 3 different places? Also, the spot on my butt if it’s hsv2 is this just a place where it can show up or did I spread it there? 4. If this is a spot on my butt does this mean that I can shed there? I’m so terrified of spreading this to my family. The spot on my butt is in a place that could be potentially touched by someone as it’s on the top and wouldn’t maybe be covered by s bathing suit. If I’m holding my niece on my hips and her legs happen to rub against that part of my butt and I’m shedding could I pass it to her. 5. I went 10 months between these outbreaks and I’m hoping that I won’t have to deal with this often but I’m not understanding why all of the sudden for 3 weeks I’m having something new pop up each week. I’m so scared that this is going to be my new normal. I just want to feel like me again and comfortable in my own skin and for the last three weeks all I’ve felt is uncomfortable in my skin. I’d appreciate any help that someone who has been through this can help. I feel hopeless I’ve been taking everyday a. Probiotic b. Vitamin c c. Vitamin d have periodically used coconut oil, lavender, rosemary, and have taken lysine a handful of times.
  19. Hey guys, new here as of today. I’m currently 27 weeks pregnant and I’ve been having more days with outbreaks (single lesion, same spot) than not. I’m praying for a vaginal delivery but obviously want to do what’s best for My Baby but the thoughts of not being able to bring baby into the world vaginally wrecks me... At 20 weeks I was diagnosed with HSV2 after requesting testing because I had known for probably 3 years but was too ashamed and was in denial to go to a dr and get the actual diagnosis but wanted to take all precautions for my baby... Anyway, the DR put me on Valacyclovir 3x a day for 7 days and then 2x a day. I noticed absolutely no change. It was like that one lesion would heal for 2 days and then come back for a week. Today I asked her to switch medications and she told me to just keep taking the Valacyclovir for suppression. I guess my question(s) are #1) how long did it take some of you to see suppression? 2) How many of you had to have a c-section because of active lesions and 3) did anyone’s dr miss a lesion during delivery and was your baby ok? I’m so torn because I don’t want my family to know and what am I suppose to tell them in the event of a c-section when they’ll all be there at the time? 😭— Thank you for any and all comments in advance. I’m so hoping I can find some peace of mind within this forum. PS: Recently I found that Tree Tea Oil keeps the lesion away longer than the medication did and the dr gave me the ok to continue. Anyone else?
  20. I'm really desperated, I've been visiting three different doctors and they didn't help me at all. Here is my story. I'm a 30 years old male in good physical and medical condition. Healthy and sporty lifestyle. - April 2018 : One-month holiday trip, including a lot of protected and unprotected sex with stranger girls. - May 2018 : Back home. I'm noticing redness on the glans and the foreskin of my penis, a few spots under the corona, and my glans looking wrinkled, very dry, and the foreskin looking like "sticky" when retracting the foreskin. I've been thinking about a fungal balanitis, so I've been applying Econazole, without any amelioration. Decided to get tested for HIV, IST, and HSV 1/2. Everything came negative, except HSV1 IgG Positive (IgM 0.70) - so pretty much an old infection. Showed my glans to Generalist Practician who said it looks normal, advises to avoid any chemical, soap, or whatever. I feel pretty much tired all the time, coffee won't help - but I don't feel pain. Tiredness could be related to pollen allergy - I've been tested with a very high IgE. - June 2018 : Things didn't improve. Exactly the same. Very intense redness after sex, that last up to a week. Decided to go to a dermatologist - even if I showed photos where the redness and the spots are really noticeable, she says she doesn't know, but it doesn't look like herpes to her. She told me to do nothing, avoid chemical and treatments, things should come back in order as nothing has been diagnosed by blood test. - November 2018 : After another rash/redness episode, went to an urologist. He said my glans and foreskin look normal. The reaction of these 3 doctors to my problem is absolutely incredible. My penis looks completely sick, I told them it has never been like this, and they say it look normal - I don't understand anything. I tried Fusidic Acid cream (antibiotic) without success. Then, I tried antifugal cream again, no result. Foreskin still stick when retracting. I'm beggining thinking about a rare genital HSV1, which outbreaks could be caused by rough sex. Here are some pictures of how my penis was looking at that time. - December 2018 : Had another blood test. HSV1 still positive, HSV2 still negative, HSV1/2 IgM now in gray zone. - January 2019 : Since a few days I have the most impressive outbreak I've never had. My glans and foreskin are now covered with red spots. I still don't feel pain - at most a little itchy - but my eyes are blood shot/pink. I don't really feel tired. Yesterday I ran to the pharmacy to buy Valaciclovir - I'm taking 500mg in the morning, 500mg in the evening. It's been now 8 months I'm dealing with that, and I still don't know what I'm fighting against. As you can guess, it's very hard for me, psychologically. I'm avoiding having sex and when I do, of course I use protection. Since this last outbreak that really looks terrible, I wouldn't even dare have sex. I'm ashamed, feeling guilty, and it seems like doctors won't help me. My only hope is this forum. What is your opinion ? Do you think it looks like an HSV1 outbreak ? If not, what could it be ? Thanks in advance.
  21. Hello I live in the DMV/Baltimore area and was diagnosed a little over a year ago. I only have like two penpals but no one really here in area. A couple of people I've met are still on the downside of the news. I'm more so coming to terms with it and accepting it as one of my truths. This has made me happier. So... Now I'm more so looking for positive 'positives' who still enjoy life and see how they date and manage normal life changes (marriage, child-bearing, prevention and suppression). I also feel like I have a calling for outreach, so also feel free to chat with me:) Peace
  22. Has anyone tried Longdanxiegan (LDXGFG) as a treatment? There seems to be scientific evidence of great results in animal trials. This is the link to the study https://www.sciencedirect.com/science/article/pii/S1028455916000322. It is a Traditional Chinese Medicine formula that now has won some scientific attention. I have previous experience using Traditional Chinese Medicine for improving symptoms of another rare diseases I suffer and, seeing this has been backed by some research, I am considering giving it a try. Thanks to all contributors to this forum for all the valuable information shared.
  23. Hi I'm losing more hair than usual and not on any suppressive meds. Was wondering if anyone else experienced this hsv2 diagnosis or even hsv1 diagnoses If so how did you solve the problem? Thank you.
  24. I disclosed my HSV2 diagnosis right from the start and only because we had this GREAT connection. He said he did his research and we would just be careful. Well, after dating for 2 months, he decided that he didn’t want to date anymore and “I’m sorry for how shallow that seems”. I was crushed. I think I’m living on false hope that he may change his mind if he does even more research (not one hour online). Just wondering if anyone has ever reconnected with somebody after being rejected by them.
  25. 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
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