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Thanks to everyone who can help with this topic.
Yes I have had HSV 2 for at least 27+ years. I had no symptoms for approx 10 years and then I had as far as I know my first outbreak. My doctor who so far is still my doctor diagnosed it visually and so he gave me only Zovirax ointment (which is a useless treatment) and advised me to use that to heal the herpes sores when I had a problem and to avoid sex when I had an ob. I told my wife and it was not an issue. So for approx 17 years that is all I used. I found that as years went by after intercourse I would get an outbreak that would last approx 1 week it would heal and then after about a week a would get something different which I am not sure if it is herpes related but I would get an uncomfortable feeling and I had to go to the bathroom a lot. That would last about a week and then I would be fine until I had intercourse again and the cycle would start all over again. I am married and have been faithful to my wife all this time and I got this before I got married. Any how I finally found the WebMD site (Aug 2007) and when I was looking around the site I found the Living Day to Day GH Board and while lurking in the background reading post I realized there was a blood test for herpes. So November of 2007 I asked my Doc to test me for herpes and he would not do it nor would he give me a Rx for Valtrex either. In the beginning of 2008 I had to go to a walk in clinic to get tested and found out I was negative for HSV 1 and positive for HSV 2. I again told my wife of the status that was now confirmed and she has been very understanding. The walk in clinic Doc had given me a Rx for Valtrex and what a difference it made. I started taking Valtrex in April 2008 and I have not had an outbreak since. I feel a lot better in the gential area. I would estimate that I would normally have 6 or more outbreaks in a year so you can see that I have been dealing with this for all these years till just April 2008 when I got the Valtrex. In regards to severity they were not to bad but a bother and always stayed in the same general area which is a blessing. If you are not on suppressive therapy and decide you would like to and cannot afford Valtrex or one of the new antivirals then you can always take Acyclovir as it is a lot less expensive and is now a generic drug. The only drawback is that you have to take it twice a day for the same type of result. I understand that there is no stats on it as to its effectiveness to decrease shedding as there was never a study done on it and now that it is a generic most likely there will not be a study done. Of others who have been on it for years though they seem to believe it to be as quite effective.
From what I have read the herpes type specific IgG blood test for HSV 1 and HSV 2 has been around for about 20 years
In the last year since I have been on Valtrex and Valacyclovir which is available where I live but not in the US till Dec 2009 as a generic of Valtrex I have not had a full blown ob. I have had approx 3 times when I have had to increase the dosage to suppress the virus but not a full scale ob.
Yes I am stiill married and faithful to my wife for 28 years.
Cheer up. God Bless you.
Hey y'all. Haven't checked in on ya in a while. I was reading several of the latest posts from those of you who just received your diagnosis. Just an fyi--I am HSV-1 positive. I started having problems October 7, 2007 and received my official diagnosis October 11, 2007.
When I think about that period of my life, it was one thing after another. My grandfather was getting worse with Alzheimer's and other health problems, I was homesick, my boyfriend at the time and I were on the rocks, my parents and I were on the rocks, I was doing poorly in school/student teaching, etc. I was spiraling. After a breakup with my boyfriend and then a fight with him, I broke school policy twice. I snuck up to the guys floor after hours and I broke our integrity policy. I went to a friends house, got very drunk, and slept with two of my so-called friends back to back. That was 5 days before my diagnosis. I still cannot pinpoint who I contracted HSV from because of the fact that I was with multiple partners in such a short time.
After I was kicked out of school, my boyfriend and I got back together. It only lasted two weeks however before he left me again. My parents were trying to deal with the fact that their daughter was kicked out of school, had an STD, and were too busy trying to cope with their end of my problems to be able to fully help me with mine. As the month of November went on, I moved in with my grandparents. Because of my grandfather's condition, he still doesn't know about my situation but my grandmother did and she was amazing! I couldn't tell you how many nights she and I sat up discussing my situation and our living situation. My grandmother struggled immensely with my grandfather's care.
December came and on the 2nd I found myself starting a relationship with an amazing man. On the 3rd, I was busy taking care of my grandparents, baking, cleaning, and doing laundry. Justin showed up on our front steps. He met my grandparents, my brother, my uncle, and my dog (very important ). He and I talked for 3 hours. It was perhaps the best three hours I have spent with him yet. It was the nervous, weight-shifting, interrupted type of conversation that happens when you first start off with someone. But it didn't matter. I knew he was special in some way yet to be discovered and my grandmother loved him!
December 6, 2007--I told him my secret. I revealed to this man that I had HSV. He asked a few questions about how and then decided that he was better off not knowing how some man/men hurt me. He didn't care. He apologized that someone hurt me before he could show me how I deserved to be treated. He said that he loved me for who I am and not what I have. I was floored! After being rejected and ridiculed by so many, this man choose me despite my imperfections and mistakes.
It is 2 days shy of our seven month anniversary and we are happier than ever. We have had our fights but we work through them and never go to bed mad at each other. We have discussed children. We both want them. We have discussed suppressive therapy. We don't want me to have to go on it. Openness and honesty are so important in our relationship. If I think I'm having even the slightest problem, everything is off limits. He helps me too though because I regularly keep an eye on what's going on down there. If I cannot see a particular area that itches, burns, or feels bumpy, he will check it out for me. He is so understanding about the whole thing and knows that we both want the best for each other. Thankfully he has not had any problems so far. I am coming up on another marker as well though this one is much different. As of July 7, 2008 it will be nine months since I began having symptoms.
I won't lie to you, I didn't date many people after my diagnosis. I went back to my ex-boyfriend after I found out but he cheated on me two weeks later. Then I was friends with benefits with another man for a very short time. Then I reconnected with a guy that I had met over the summer (we've been together almost 8 months now!). It's so cheesy but he and I honestly had an instant connection. I was still reeling from a lot of heartbreak from the cheating episode and a lot of bad decisions that I had made so things were slow. BUT they went forward.
Four days into our relationship I told him about my "secret". He didn't care! He said that he wanted to be with me for me and the HSV didn't matter. I have type 1 so I don't necessarily have to be on anti-virals but before we had sex, I asked him what he wanted me to do. I explained the numbers, the risks, everything and then I left the decision up to him. He told me that I didn't have to go on them (with the exception of a pregnancy). He said that they were unnecessary. Justin often forgets about the HSV. It is not a factor to him.
He realizes that our children could be affected or that he could be affected but he's willing to risk it. I was very fortunate but I also was very careful. I didn't sleep with Justin before I told him (although I have made that mistake). That helped him in his understanding. I waited until the right moment for both of us. He knew I had to discuss something very serious and I had to prepare myself. I am also very cautious about the friends/family that I tell. If I think that by telling them, they will be comforting and still love me no matter what...I may tell them if it comes to that. BUT if I think that my life will simply be made more difficult but them having that knowledge, I won't bother.
I don't bring my private matters into the work place. Only 2 of the people that I have worked with since my diagnosis know what is going on. One is my boss because I have spoken in public about what happened and I don't want it to go through the grapevine and cause problems. The other is a good friend that went with for moral support when I spoke in public the first time. You don't have to keep it a secret but you do have to be cautious who you tell.
From my own personal experience, I know that I get a little frisky when I drink. So...I limit myself. I don't drink 1/10 of what I did immediately after my diagnosis. If I do, I make sure that I'm with friends who know to keep me in check. That of course was before I started dating Justin. Now that Justin and I are together, I direct my attention towards him.
When telling someone for the first time, Betsy has amazing advice! Read her posts about how to tell a partner. She has had HSV for 22 years so she's had her fair share of experiences. Give them facts and give them time. Let them do some research on their own so they can fully grasp what's being said to them. Most of all, remember to relax. Your life is not over. You can go on. You can have a relationship. You can have children. You do not have to be a hermit. You can live your life to the fullest if only you will put on a smile and have an optimistic outlook. It will be tough but it will be more than worth it in the end.
Ok. So there you go. Remember those are old posts from...Last July? Something like that. But they still hold true. Later that month, I got engaged to my honey bunny. He is amazing. He is very understanding. When he sees me typing on the computer, he asks me if I'm on my boards. He knows that you guys are all very special to me and that it helps me to help you. I hope this all helps.
Have a wonderful day. You guys are all special people in this world and if someone can't see that, they're not worth your time.
*******
and the statistics aren't as bad as most people think (as far as chance of transmission from partner to partner). Good luck to you!The hardest part is just getting the words out.
It was obvious I was nervous about something because he could feel my heart just about beating out of my chest and asked me what was going on. As calmly as I could, I told him I had genital herpes. I asked if he was familiar with it. He told me he had it in his mouth and had a prescription for Valtrex for when he got cold sores. I then went into my speech about the facts and told him where he could go if he wanted more information. We discussed always having to use condoms and that was it. I think we discussed it one more time after that and it was never brought up again. Now I rarely even think about it. We have been dating about five months. I consider myself very lucky to have had such a successful first experience. It's scary to be starting over dating at 37, let along dating with herpes.
I love the how do you have sex question! It would have been even funnier if you left off the without infecting your partner part. We just do. We have decided (He decided) that we aren't going to use condoms and I am not going to be on suppressive therapy. I have type 1 and haven't had an ob since my initial ob.
At the last time that he was tested (before we started dating), he was negative still. He hasn't had any problems since we've been together (over a year).
BUT this is all what we decided was best for us. Other people use all of the precautions (condoms, meds, boxers, blah blah blah).
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