Hey any help would be great. I’ve been losing my mind of this and I’ve been procrastinating on going to get tested because I’m scared of the results and also I have no insurance or anything to consult with a doctor.
so I got tested may of 2018 and I was positive for hsv1 which I feel like I may have gotten as a kid not sure, but since that test I’ve received unprotected oral sex twice and every since I’ve slowly been growing bumps on the meatus. I’m uncircumcised as well. Could this be herpes, warts, chlamydia? My girlfriend (I cheated on her and don’t know how to explain to her I might’ve caught something) has had a bit of blood discharge on her underwear in between periods. I work a lot and wear sort of tight clothing and I get smegma under the head as well. Smells bad too. Help!!! I’ve had this for months.
I have noticed that I now have chronic constipation after my primary outbreak. Scientists have found a link to it. Has anyone else had this issue? Treatments?
I was recently diagnosed with HSV 1 a week ago and the emotional strain has been horrible. I’m the type of person who hates the unknown, so I’m trying to figure out if I have it genitally or orally. I had sex with someone who has been tested for herpes, but he doesn’t remember which strain he has. He hasn’t had an outbreak in years and has taken medicine, so my doctor initially said the chance was extremely low that he gave it to me (especially because it was only for about 1 min and that was it.) I get mouth ulcers regularly and I also get what I believe is a cold sore right in the corner of my mouth (which I’ve read isn’t a real cold sore?) so I’m wondering if that’s why I tested positive. We had sex a month and a half ago, and the symptoms started about a week and a half ago. Burning while peeing, and the occasional itching. When my doctor looked (she also did a Pap smear) she said she saw no lesions which I took as a good sign. I’ve been taking Valtrex for 5 days now but my symptoms haven’t improved at all. I just need people to talk to who know how I’m feeling. Thank you all
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.
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