J.L2018

So when you’re pregnant they will only put you on them from 36 weeks to prevent an outbreak during delivery !i actually had an outbreak a week before still but was still able to have baby naturally 😊 acyclovir etc does pass through the placenta but it’s not known to cause any harm to the baby and both of mine have come out at full term and healthy 😊 before I met my partner I was on daily suppressive acyclovir for 2 years and I was worried about long term but my partner didn’t want me taking them so apart from when I’ve been pregnant i have stopped taking them ! X

awh I’m so glad it helped ! 💖 & thank you so much ❤️

Heyy me and my partner of 4 years haven’t used protection for the majority of our relationship. I told him my status from when we started dating and said I’d take acyclovir and he was absolutely fine with that. I actually stopped acyclovir after a few weeks as he said he didn’t want me having to take tablets for something with such a low risk. We’ve just had our second baby and he still hasn’t ever tested positive or had an outbreak! We’ve even had sex when I’ve just started with an outbreak and still nothing. I know obviously everyone is different and it can be transmitted at any time but I just wanted to tell you my experience to hopefully make you feel better about the chances. If he’s happy to be with you he’s accepted the risk that could come. Don’t feel guilty you’ve been upfront with him !

It’s always scary but just know the people who are worth your time will accept you and your diagnosis ! It really does filter out the time wasters ! I was on suppressive antivirals but then my partner said he’s rather me come off it because he didn’t like me taking them 3x a day everyday so for about a year and a half I’ve not been and we don’t use anything as we were trying for a baby. I just avoid anything if I feel a sore coming. Hope this helps

Hey ! So I’ve had GHSV-2 for about 3 years now. At first I really let it ruin my life, I was single, it was from a very short term relationship with someone who ended up ghosting me , I felt absolutely worthless and I was convinced no one would give me a chance and my dreams of having a family were over. I felt this way for around 2 years and herpes was all I could think about , not a day went by I didn’t let it bother me. however now I really don’t even give it a second thought ! I’ve met my soulmate who loves me so much he didn’t even bat an eyelid when I told him about it ! He doesn’t have it after 2 years of us in a relationship and unprotected he is still negative so that’s a bonus! But I literally am in the best relationship of my life and I now have a gorgeous 7 week old baby ! I wish I never got so depressed about my diagnosis because the right person won’t judge you and will love you ! I also thought I had outbreaks all the time so that made me worse but actually it was just other things eg thrush or even just my pants rubbing, instead of being rational I associated every tingle, pain etc to HSV when it actually wasn’t most of the time! during pregnancy I had about 3 outbreaks but i went on acyclovir for the last 6 weeks and everything was great ! I had a normal vaginal delivery and gave birth to the most perfect girl. I hope anyone who’s struggling reads this and realised that this diagnosis doesn’t define you and won’t ruin your future ! Life goes on!

I breast feed my baby& have Ghsv2 ! She’s 7 weeks and thriving ! If you have genital herpes then it’s only transmittable from the genitals!

That’s a very bold statement for someone who doesn’t know my situation! You don’t know who I am , so I don’t get how you can even assume that ! I’ve had a massive struggle and I’ve been to the lowest points where I thought it was the end , I still struggle with this but I’ve learnt that with a positive attitude it isn’t the end of the world! I’m also not saying what she did is ok , because it’s not, but expecting to get revenge and feeling better as a result isn’t going to happen, what I’m saying is to let all the resentment and hate go, it isn’t going to change anything , apart from harbour stress which will cause more outbreaks ! Take it how you want but by getting revenge you’re just lowering yourself to that level and people will see that as bullying if you post it on social media, so if you want to do that just know that you are accepting any of the repercussions that come from it ! I got this in pretty much the same way and situation , once I let go of the hate, resentment and what ifs it honestly took away the power HSV held over me and I was able to develop a more positive attitude, I can’t emphasise this enough ! I’m definitely not arguing, but I just want you to really understand the potential consequences this advice could have on everyone involved. This situation happens very frequently in people who have HSV and people who don’t and it always feels horrific, so to acquire HSV under these circumstances I can fully relate and understand the impact this does have! In order to find peace though you need to understand what it is , how you can try and reduce the impact it has on your life and the importance of accepting this isn’t going anywhere, so don’t live in the past of regret and sadness because this will cause more and more outbreaks and symptoms ( it’s a vicious cycle that you need to get out of ) revenge isn’t the answer to finding peace , acceptance and a positive outlook is! Start looking at healthy foods, foods to potentially avoid, vitamin supplements, medication if that’s the route you want to go down etc , doing this worked for me as it allowed me to feel like I had a bit more control over it.

I’m sorry but this is a very bad way to deal with it! It’s bad that she didn’t tell him till it was too late but having HSV of any kind isn’t the end of the world, outing her to all her family and friends out of spite and bad blood, could be the end of hers. People talk, it’ll get into the wrong hands, so if you want to take revenge and out her to everyone that she knows just makes you equally as disgusting as you believe she is, whilst also creating a bad stigma towards having HSV! Please think about the real consequences theses actions could have before promoting this response !! Also getting revenge won’t make you feel better, because once it’s all said and done, it doesn’t change the fact that you have this ! Instead of focusing on the revenge, focus on accepting what you have and keeping healthy and stress free to combat the symptom and live a happier healthier life ! That’s the best option, be the bigger person and focus on your health and happiness, without sabotaging someone else's.

Thank you so much for the response ! I’m In the Uk also, I wonder why I’ve been give only 400 daily, but yeah it’s working fine so I’ll stick at it 😌

Hello, I’m currently taking 2x 200 mg of acyclovir daily as prescribed by my doctor, it seems to to working fine but I’ve read on here that to be able to suppress it and cut the chances of transmission you need 500-800mg daily is this correct ? I’m debating if to ask for a higher dosage or start taking 4 of my tablets daily if that’s the case .. but don’t want to do that if it what I’m on is already enough Thank you 😊

That’s brilliant!! Thank you

Hello, quick question as I’m starting to worry, so I have hsv2, I’ve had it for nearly a year and I don’t have many outbreaks as I’m on Acyclovir however I’ve just booked to go to Mexico for 2 weeks and I’m just wondering if I’m actually aloud to take the tablets in my luggage ? Or would it be best to just leave them at home and hope for the best ? And will the sun and sea make outbreaks more likely and frequent ? I know the sun can trigger cold sores but I wasn’t sure if it was the same concept down there as obviously that area won’t be as exposed 🙄😂 Thanks in advance 😌

Hello I’m a 23 year old female from the uk with HSV-2 , I’ve been diagnosed for about 6 months now and although I do have a lot of good days where I try not to think about it, I’d love to be able to talk to people in the same situation or similar situation 😌 to provide and receive support, advice etc , no gender or age preferences.

Hello 😌 I also had something similar on my first outbreak, I couldn’t wee without being in excruciating pain for about 2 weeks and I’d try and put myself of going in fear of the pain, the Drs wouldn’t swab me for herpes so I was given antibiotics which actually made everything a whole lot worse ( my body doesn’t react well with antibiotics) which extended it to about 3 weeks of having to wee in a freezing cold bath pretty much under the cold water tap, I literally cried every day until I went to the specialist Sexual health clinic and was given some acyclovir .. 6 months later I’ve had about 2 proper outbreaks and I can assure you that they won’t even come close to being as bad as what you’re currently going through & that itself makes them a lot less stressful and a lot more bearable ! You will be able to wee without pain soon and it will be the best feeling ! Keep up with the supliments and don’t stress ! I know in this situation it’s hard , I was a little ball of stress,however that maybe what’s prolonging the outbreak, so keep positive, know it will go soon & remember it isn’t likely to ever be this bad again ! Hope it clears up for you soon.

@MarieH thank you I will try that 😌