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    • Jesusislove777
      By Jesusislove777
      Hello, 
      I was diagnosed with hsv1&2 earlier this year. I was prescribed 1g of valtrex (valacyclovir) a day for suppressive therapy.  Valtrex helps greatly with my symtoms, but I recently had to leave my job for health reasons and will no longer have health insurance to get prescribed valtrex. 
      Does anyone know where I can purchase valtrex (valacyclovir) online without a prescription?
    • RSL888
      By RSL888
      I've had HSV2 for 4 years now. Recently had an unrelated minor spinal injury that caused some severe neuropathy. So instead of taking narcotics for months, my doctor just had me try my first round of Immunoglobulin IVIG treatments (4 days getting the intravenous blood infusion) labeling my symptoms as something called CIPD (google it). (IVIG treatments give you a boost to your immune system).  Also note, I can't take steroids long term also because it spikes my sugar and I have Type 2 diabetes. 
      I wonder if anyone else here has tried IVIG? I have read that some people have taken it to suppress HSV. Love to hear from others. It's too early for me to know if this works - I'll report back in several months. Just so you know my background - I had OBs in the first year about every 8 weeks, which consisted of neuropathy and maybe some small bumps. Then the second year I only got those same symptoms every 4 months or so, then i only get these now about once or twice a year, and it's mostly just some tingling and nerve pain. So we'll see how this works out. There are articles out there too. 
      @WilsoInAus
      Edited to add this link... 
      https://pubmed.ncbi.nlm.nih.gov/7759773/#:~:text=Since intravenous immunoglobulins (IVIG) proved,%2FKg every fourth week).
    • HSV2sucks
      By HSV2sucks
      I am experiencing a lot of nerve pain, numbness, shooting pain, back pain, leg pain, pain in my butt cheeks... and I found some studies on nerve pain & HSV... 
      https://jamanetwork.com/journals/jamaneurology/fullarticle/795486
    • Freefalling87
      By Freefalling87
      I contracted the virus anally 2 years ago without a primary outbreak, just the fever like symtpoms. Only had my first visible outbreak 4 months later and took valtrex for a few days. Only afyerni was done with the meds, that's when the nerve pain started. Ever since then, I never used any meds again and only have a small red dot outbreaks in my inner left and right thighs near my dick. 
      However, the nerve pain is constant on my left inner thigh in the crease and it sometimes moves to the head and shaft (nerve tingly pain). This pain has been constant for 2 years. Just wondering if I'm the only one with this problem, but are there any guys who have constant nerve pain from hsv2? 
    • Theairplanelanded
      By Theairplanelanded
      I started talking to a girl and we had sex. Two days later I find these spots on my penis and I’m starting to stress. I have jagged off without lotion so it can be that but still can you guys help me ? Does it look like herpes ..?
      https://ibb.co/5hf1F11
      https://ibb.co/56qctQ6
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    • CHT
      1.11 on the IgG test is still really low and could easily be a cross-reaction with the antibodies you have for HSV1..... based on all your data, it sure does not seem as though you have HSV2.... I'd relax and go with that....
    • CHT
      Hey Willily..... what would make you think you have HSV2?  Have you been tested?  Results?  The idea of getting it in the kidneys is unheard of (at least in my non-medical opinion)..... HSV2 tends to stay in the urogential area of the body and to a lesser degree can also be transmitted to the lips/mouth but, inside of an internal organ?  No.  
    • CHT
      Hey Lucy.... well, I guess getting much the same answer from the gyno specialist sort of puts the whole issue back into the category of "it's not likely HSV" you're dealing with down there..... and stick to the 1 gram of valacylovir (which I think is good advice).... did she pull any blood samples or did you bring the data you already have with you?  If I recall, your HSV2 antibodies level were very low, almost "borderline" thus giving more doubt that you may actually have HSV2.  Not sure why she would lean toward HSV2 and not HSV1 based solely on your IgG results..... So she thinks you have seborrheic dermatitis down there?  I've never heard of that but, that means nothing.... hopefully with the new medication, that will be under control in a few weeks or couple of months..... then it will be interesting to see if you have any sign of problems in that zone.... particularly if you stay with the valacylovir.    BTW, the full nude body exam must have come as a surprise!  LOL.  But, she was being extremely thorough I suppose.... better than rushing you in/out.   Oh, and to answer an earlier question, so far, it's been about 3 or 4 weeks back on 1 g/day of valacylovir.... and so far all clear!  It's not a record for me but, I am encouraged.  Also interesting to note that I've been dealing with a whopper of a stomach virus for last 5 days (fever, chills, aches, etc).... I thought for sure this would put too much pressure on my immune system and allow my HSV2 to reactivate but, fortunately, all clear, not even any prodrome.... but, I won't get too excited just yet, it can all change in a second!  
    • Fernie
      I’ve been diagnosed with hsv1 and have had some cold sores on the inside of my lips.  I’ve been diagnosed for some time with that. But around July 2020 I went in for an std panel and to my surprise my hsv2 IGG levels were equivocal.  My doctor at the time told me that I indefinitely had hsv2 although I’ve never had any symptoms.  This began a whole craze. I switched doctors and ordered another hsv2 test that also came back equivocal and was told that what the first doctor said was correct, that I do in fact have hsv2. The fact that I wasn’t testing positive and none of my past sexual partners tested positive led me to think I should keep getting tested to confirm whether I do or don’t have it.  So I went for the third test and it was .72 IGG which would be a negative. (Around July 2020 as well) I was still a little confused so I went for another a couple months later in October 2020, this hsv2 test was .89 IGG which is right under equivocal but still negative.  So armed with this data I went to a private doctor that I paid out of pocket for because I began to think that the Medicaid doctors might be wrong and maybe underpaid or whatever I dunno it just didn’t make sense. So I went to the private doctor and at the time I had what seemed to be like a small ingrown hair and I showed them and showed them my data. They said based off the ingrown hair that it was just an ingrown hair, and that the lab results were correct and that I had no hsv2 and that the prior doctors were wrong. The doctor said I should’ve never been tested because I never had any symptoms prior to that small ingrown hair.  So this made me happy but also made me lose faith in our healthcare system.  But just recently I went back for my 10 panel and on 6/9/2021 my hsv2 results were 1.11 IGG which indicates I am positive. This is driving me crazy and on a side note I noticed that my hsv1 IGG levels were both gradually going up as the hsv2 was creeping up. I dunno if there’s any correlation there but it’s just something I went back to look at out of curiosity because I do know I’m hsv1 positive.  At this point I just want to know if I am in fact hsv2 positive, what should I do? I want to get the western blot test because it’s supposedly the golden standard.   here are copies of my tests  https://ibb.co/Wskdtqs https://ibb.co/fGgjJxd https://ibb.co/HryKn8g
    • ohno35
      I'm sorry you're struggling to find answers; I feel like I'm in a similar place.  When I stopped worrying about the symptoms, they eventually went away completely after almost two years. Then, I did not experience any symptoms AT ALL for 2.5 years. In April I started worrying about the symptoms again, and they came back and are pretty much constant, as they were before. I know that it looks like it's *just* anxiety. But my gut is telling me there might be something else going on. I'm getting the WB done so I can finally rule out herpes completely.  I've been diagnosed with somatic symptom disorder, and I've wondered if it's not just anxiety about symptoms but hyperfocus on certain parts of my body that makes the nerves more sensitive and causes neurological-like issues. I've always struggled with hyperfocus and I've found I fit into the diagnostic criteria for Autism, ADHD, and OCD, but do not have enough of any of the symptoms to qualify for a diagnosis (though I have been misdiagnosed with 2/3 multiple times). The concept of Vulvodynia seems interesting because my understanding of it is that it results from hypersensitive nerves from a variety of initial causes. I wonder if hyperfocus on my vagina, vulva, and mouth is causing certain symptoms.  I definitely had extreme anxiety about herpes before my symptoms started, but I did have an outbreak on my mouth of something that seemed too long-lasting and blistery to just be a pimple, so I wonder if herpes or another related virus is involved too. I know I'm anxious, but I still know my body and I've never had anything on my mouth like that before, as far back as I can remember. I still have the scar from the huge blister almost five years later!!!!! Otherwise I would have been effectively gaslit by my doctors that it was a pimple and I was overreacting. It's possible though that I have had HSV-1 since childhood and had a rare herpes outbreak, but all the other symptoms are largely unrelated. I was hospitalized at age 4 for an extreme reaction to mono and possibly HSV-1, so I'll have to see if I can locate those hospital records. If I can confirm I was positive for HSV 1 at age 4 and also come up positive on the WB, I could still probably rule out my current symptoms being caused by herpes.  If my herpes WB is negative, I do wonder if another virus could be the culprit. I'm not sure if other things can cause blisters on the mouth, or if the oral blister and my other symptoms are unrelated. I know CMV is not out of the question. I know that hand, foot, and mouth disease was epidemic at my University at the time, so it could have caused the oral sore and maybe been an instigator for chronic pain? I've been reading about how certain infections can be catalysts for nerve pain, reactive arthritis, and so on for people with certain genes, autoimmune issues, high levels of stress, and/or other pre-existing risks. I've always had weird reactions to things despite being seemingly healthy, so that would not be out of the question.  We seem to have very similar symptoms, so I'll keep you updated on what I find! I'm getting blood drawn for the WB next week, and then I'll see what happens after that. 
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