Julia_dances
03-23-2005, 07:53 PM
First of all, so glad to find this wonderful support forum. I feel good about posting my queries here!
I contracted herpes in November from my boyfriend, who had a cold sore and gave me oral sex. I believe my doctor said I have Type 1. My outbreak was the hardest thing I have experienced in my life. Within 24 hours, I went from zero syptoms, to itchy red bumps all over the outside of my vagina, to painful blisters and sores on the outside AND inside of my vagina. I am sure I spread them horribly by itching, simply thinking I had an itch! On top of all the other side effects, I was in so much pain that I was unable to walk OR go to the bathroom. I am a young teacher, and had to have a supply teacher work for me for half a week, because I could only urinate while sitting in a warm bath. I didn't want to eat or consume liquids, because going to the bathroom without the aid of a bath became impossible. It was the worst time of my life, to be immobile for a week under "strange circumstances" to all who knew me, but my boyfriend and best friend. I have never experienced such pain.
Obviously, I have feared my second outbreak with every bone in my body, knowing the complete shut-down of my professional and personal life and the unbearable pain and coping techniques that accompanied my outbreak.
Obviously now it is March, and yesterday, I had my second outbreak. I was devastated. I didn't notice any tingling or warning signs, just as I didn't before. Immediately, I prepared for the worst and begin brainstorming the "lies" that could help me cope again privately and opt out of life like I was forced to last time in order to survive. I prayed that my internet research was true - that after a primary outbreak, symptoms, pain and duration decrease.
Surprisingly, I feel I am still waiting for the worst - and don't know what this means. Last time I had horrible blisters - they looked like "cauliflower heads" and I couldn't even have clothing touch them, much less anything else touch them, or even walk. I have flesh-coloured raised, hard bumps - almost like little bug-bites, and they are surrounding the vaginal lips. I know I have a few on the inside, but I have worked so hard not to spread them. Peeing hurts a wee bit, but nothing like before.
I refilled my Valtrex prescription (I get 6 pills per outbreak) and began taking that half a day after I knew I had the bumps/slight peeing pain. I also purchased Lipactin for cold sores, and applied it to the external bumps.
Are these going to blister like last time? They haven't yet... although there seems to be a bit more and they seem a bit bigger than yesterday. They are itchy. Am I stalling the process by applying Lipactin... like, do they NEED to go full course without a topical agent, and am I just delaying that process by applying Lipactin?
I didn't call for a supply teacher, because if the third day (tomorrow) is like today, I can handle the side-effects and urinating, unlike last time. Also, it's Easter weekend... that buys me some recovery time. However, if it is going to get bad again in any way - I am fearful of my family obligations, and I can't run a bath every time I need to pee, or wear huge pajama pants to events!
Basically, I don't know what to expect in the future, and my life was in shambles after what happened to me the first time around. What advice do you have? I would truly welcome any, to help me know both what to expect, and how outbreaks that aren't primary, run their course.
So many people here say that after multiple outbreaks, you figure out how to manage. This is the kind of thing I came here for, to find some sanity and hope about the situation!
Thanks for reading,
Julia.
I contracted herpes in November from my boyfriend, who had a cold sore and gave me oral sex. I believe my doctor said I have Type 1. My outbreak was the hardest thing I have experienced in my life. Within 24 hours, I went from zero syptoms, to itchy red bumps all over the outside of my vagina, to painful blisters and sores on the outside AND inside of my vagina. I am sure I spread them horribly by itching, simply thinking I had an itch! On top of all the other side effects, I was in so much pain that I was unable to walk OR go to the bathroom. I am a young teacher, and had to have a supply teacher work for me for half a week, because I could only urinate while sitting in a warm bath. I didn't want to eat or consume liquids, because going to the bathroom without the aid of a bath became impossible. It was the worst time of my life, to be immobile for a week under "strange circumstances" to all who knew me, but my boyfriend and best friend. I have never experienced such pain.
Obviously, I have feared my second outbreak with every bone in my body, knowing the complete shut-down of my professional and personal life and the unbearable pain and coping techniques that accompanied my outbreak.
Obviously now it is March, and yesterday, I had my second outbreak. I was devastated. I didn't notice any tingling or warning signs, just as I didn't before. Immediately, I prepared for the worst and begin brainstorming the "lies" that could help me cope again privately and opt out of life like I was forced to last time in order to survive. I prayed that my internet research was true - that after a primary outbreak, symptoms, pain and duration decrease.
Surprisingly, I feel I am still waiting for the worst - and don't know what this means. Last time I had horrible blisters - they looked like "cauliflower heads" and I couldn't even have clothing touch them, much less anything else touch them, or even walk. I have flesh-coloured raised, hard bumps - almost like little bug-bites, and they are surrounding the vaginal lips. I know I have a few on the inside, but I have worked so hard not to spread them. Peeing hurts a wee bit, but nothing like before.
I refilled my Valtrex prescription (I get 6 pills per outbreak) and began taking that half a day after I knew I had the bumps/slight peeing pain. I also purchased Lipactin for cold sores, and applied it to the external bumps.
Are these going to blister like last time? They haven't yet... although there seems to be a bit more and they seem a bit bigger than yesterday. They are itchy. Am I stalling the process by applying Lipactin... like, do they NEED to go full course without a topical agent, and am I just delaying that process by applying Lipactin?
I didn't call for a supply teacher, because if the third day (tomorrow) is like today, I can handle the side-effects and urinating, unlike last time. Also, it's Easter weekend... that buys me some recovery time. However, if it is going to get bad again in any way - I am fearful of my family obligations, and I can't run a bath every time I need to pee, or wear huge pajama pants to events!
Basically, I don't know what to expect in the future, and my life was in shambles after what happened to me the first time around. What advice do you have? I would truly welcome any, to help me know both what to expect, and how outbreaks that aren't primary, run their course.
So many people here say that after multiple outbreaks, you figure out how to manage. This is the kind of thing I came here for, to find some sanity and hope about the situation!
Thanks for reading,
Julia.

