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Constant tingling down there


Midwestgal

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hello - new to forums, new to herpes. I guess I am just looking for feedback that is from real people with real experiences and not my dr. For four weeks I have been experiencing tingling but no actual lesions etc. confirmed hsv 2. has anyone else had this happen and will an actual outbreak happen or could this be the extent?

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What you are experiencing isn't uncommon. An outbreak can be as little as tingles or this could be prodrome signaling an outbreak is about to pop up. However, prodrome typically doesn't last this long and you would have seen blisters by now if it was prodrome.

If this is your first outbreak and you don't have blisters, then going forward your outbreaks probably never will have blisters. For almost everyone their first outbreak is the worst and any subsequent outbreak you have won't last as long. Initial outbreaks can last as little as a couple of days and as long as a couple of months. It all depends on your immune system.

Good luck!

JB

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hello - new to forums, new to herpes. I guess I am just looking for feedback that is from real people with real experiences and not my dr. For four weeks I have been experiencing tingling but no actual lesions etc. confirmed hsv 2. has anyone else had this happen and will an actual outbreak happen or could this be the extent?

hi Midwestgal,

sorry you're experiencing this, and i can totally relate. my outbreaks are basically all tingles all the time--and it makes me totally crazy. last week my doc gave me some lidocaine to try to numb it a little so i could maybe obsess over this a little less. as i'm sure you know, it's tough to forget about herpes when you constantly have "the tingles," as i call it. anyway, the lidocaine doesn't make a huge difference for me but maybe helps a little. i also posted on here about this issue a while ago and someone suggested some diluted tea tree oil--so you could try that (i haven't yet cause i keep forgetting to buy it). anyway, good luck! hope you feel better soon.

sugaree

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Thank you for the info and support. This has been a "trying" time to put it mildly. It's embarrassing to discuss and even worse to call and have to ask follow up questions because, let's face it, I didn't expect this and probably wasn't in any condition to focus when the dr gave me the results. Thanks so much for the support and going back through posts has been helpful - I know I am not alone in this!

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