I posted here last week, I didn't include a picture so here it is. Also my previous post if no one saw it. Does it look like herpes to you?
Hey guys and girls. Anyone any advice for me? I feel at a loss. I haven't been properly diagnosed, only a visual diagnosis. On Friday night I was with my fella, we've been seeing each other for 5 months and always used a condom. Everything was fine, then Saturday I felt a little nippy down below. Sunday came and I decided to have a look down there. I was horrified at what I saw. In the entrance of my vagina was a rather large white patch,it looked like a hole, filled with white stuff. After that it got really painful to pee, very painful to walk and even sit down. I told him it looks like herpes, as I googled it.
So that night I took a bath, and had another look after my bath. The white stuff had gone, and honest to God all i could see was a bright red looking hole. So this morning I went to my local clinic, and had a nurse take a look. she said it does look like herpes, it could be herpes, but it may not be. She tried to take a swab but the pain was that bad that everytime she touched it you had to peal me off the ceiling so she had to give up, gave me anti viral medication and an ointment to apply and I've to go back next week. I've had my suspicions for a while now as my ex had coldsores, and after a night with him I started to feel funny down there. This was a year and a half ago. Eventually I got diagnosed with vulvodynia, which I'm now thinking it may have been herpes all along.
I don't know what to do. Feel disgusting. My boyfriend says if we'd never break up over it, but I'm an over thinker and I'm thinking the worst. I only done 2 things different last week, I used a hair removal cream, and used a different condom to the ones we had been using. Racking my brain trying to think of what else it could be, but honestly I do believe it's genital herpes and I'm gutted. It's the worse physical pain I've ever been in, peeing is the worst.
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.
Hey guys for those who struggle with daily nerves pain with doctor saying its not related to Herpes, please have a look on "Elsberg Syndrom" on Google.
It describes exactly what we have, there are few study of it.
It's important that doctors are aware of it, changing the vision they have of herpes, which is not just a "skin condition" for some of us
Approximately 5 years ago a girl gave me a peck on the lips, I wiped my lips off.
The next morning I woke up with a painful rash all over my top lip that dried up and resulted in chapped lips, where the skin died and regenerated. No pus or obvious cold sore.
I have had this same outbreak approximately once a year in the same place except for this year where I have had it almost continuously, I have been very stressed.
I went to the doctor who says it isn't cold sores (I have to wait 2 weeks for a blood test), however I have found someone ( To those with oral HSV2 only by Penumbra,) who tested positive for HSV2 by blood test with my EXACT symptoms.
Before an outbreak, my lip/nose area is tingling a lot and I feel a strong twitching in my lip.
Is it possible that I have mild cold sores?
I would greatly appreciate any help
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.
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.