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admin 12.12.2015

I’ve had Herpes Type 2 (Genital Herpes) for nearly 4 years and I felt really ashamed and if you can imagine I didn’t have a boyfriend for a while … well, a really long time.
I want to keep this short and simple so I won’t be going into details about everything with my life (maybe I will write about it in another post).
As you may know, I couldn’t talk to my friends about it, because of the shame – I kept it as a secret all this time – I know I should not, but I did because I felt ashamed. As you consider the benefits of owning this book, you might like to think of how easier your life will get. But to be honest – this isn’t for everybody. In fact, the CDC reports a quarter of a million people get infected with herpes every year.
Herpes Protocol is a new product that is supposedly an all-natural, safe and effective way to treat herpes. I decided that I wanted to give this new product a try for myself and see if it would actually stand up to its claims. I thought maybe it was just a fluke and that the herpes would come back and attack in the coming days. Needless to say, the fast results made me a believer in Herpes Protocol and I’ve suggested it to two of my friends since. After researching and looking through hundreds of herpes prevention products, I chose Herpes Protocol as the preferred pick.
For a limited time only through this online offer, Herpes Protocol is allowing customers to try the product for a discounted price after the special herpes awareness day! Overall, I had a very positive experience with Herpes Protocol, which was very surprising to me. Genital herpes is passed between partners through intimate, skin-to-skin contact, such as contact during vaginal sex, oral sex, anal sex, or just genital to genital rubbing. Sometimes people are concerned that all sexual activities could lead to a herpes infection. If you contract herpes through oral sex, you most likely contracted the strain the causes cold sores, or HSV-1. You can reduce the likelihood of transferring herpes to your uninfected partner if you use condoms, use antiviral suppressive medications, and refuse to have sex when you have an active herpes outbreak, or if you take Gene-Eden-VIR. Contrary to popular belief and reports herpes is actually treatable to a point where the virus is removed from the body. There are blood antibody tests available now that can determine if you are infected with the herpes virus even if you never had any symptoms.
The authors of this article are responsible for its contents, including any clinical or treatment recommendations. To assist the USPSTF, the Oregon Evidence-based Practice Center, under contract to the Agency for Healthcare Research and Quality (AHRQ), performed a targeted review of the literature published on this topic from 1994 to 2002. Herpes simplex virus (HSV) is a DNA virus with 2 subtypes: herpes simplex virus 1 (HSV-1) and herpes simplex virus 2 (HSV-2). In a primary infection, the patient has an initial exposure to HSV and no type-specific antibodies to either HSV-1 or HSV-2 exist at the time of the infection. A non-primary first-episode infection is the first genital HSV infection in an individual who has heterologous HSV antibodies. Asymptomatic viral shedding occurs with intermittent viral reactivation without associated clinical symptoms.
HSV can be vertically transmitted to the infant during the antenatal, intranatal, or postnatal periods. The clinical presentation is nonspecific and includes lethargy, fever, irritability and failure to feed at 1 week of age. Viral culture is the gold standard for diagnosis of HSV infection, and has a sensitivity of 50 percent and a specificity of nearly 100 percent.
Serological tests are used to detect previous infection with HSV-1 and HSV-2 in asymptomatic patients, or to diagnose infection in a symptomatic patient when culture is not feasible or the clinical syndrome is unclear. Antiviral medications (acyclovir, famciclovir, and valacyclovir) are approved for treatment of genital HSV.
The goals of educating infected individuals and their sexual partners are to assist them in coping with recurrent symptoms and to prevent sexual and perinatal transmission.
Routine screening for genital HSV infection in asymptomatic persons using culture, serology, or other tests, is not recommended (D Recommendation). Routine screening for genital HSV in asymptomatic pregnant women by surveillance, cultures, or serology, is also not recommended (D Recommendation). Clinicians should consider asking all pregnant women at the first prenatal visit whether they or their sex partner(s) have had genital herpetic lesions. There is also insufficient evidence to recommend for or against the examination of all pregnant women for signs of active genital HSV lesions during labor and the performance of cesarean delivery on those with lesions (C Recommendation).
There is not yet sufficient evidence to recommend for or against routine use of systemic acyclovir in pregnant women with recurrent herpes to prevent reactivations near term (C Recommendation). One hundred and twenty-seven abstracts and titles were identified from our MEDLINE® search.
No studies were identified that directly evaluated whether screening asymptomatic individuals for genital HSV reduces symptomatic recurrences and transmission of disease.
No studies were identified that directly evaluated whether screening asymptomatic pregnant women for genital HSV reduces neonatal HSV and complications. No studies were identified that defined a set of risk factors and used them to guide selective serological screening for HSV-1 or HSV-2. Four studies estimated the incidence and prevalence of HSV-1 and HSV-2 and examined associated factors for HSV infection.
Seroprevalence rates based on HSV-2 results do not include the contribution of sexually acquired HSV-1.
New technologies include polymerase chain reaction (PCR) and glycoprotein G based, type-specific HSV serological tests.
A comparison of viral cell culture, direct antigen detection by HSV enzyme immunoassay (EIA), and PCR for diagnosis and typing of genital HSV was conducted in symptomatic adults. The FDA approved (1999-2000) the new glycoprotein G based, type-specific HSV serological tests for use in adults. Short term, emotional responses that included surprise, denial, confusion, distress, sadness, disappointment, and relief to know.
Short-term, psychological responses that included fear of telling sex partners, anger at the source partner, guilt about acquiring or transmitting, and concern about transmitting to a child.
Participants exhibited strong emotional and psychological responses to their serological diagnoses of HSV-2. Couples were randomly assigned to receive either 500 mg of valacyclovir once daily or placebo for 8 months.
After counseling, 37 percent of the couples reported at each monthly visit that they never used condoms for vaginal or anal intercourse during the study. Vaccines to prevent genital HSV have not been approved by the FDA, and vaccine trials are ongoing. Limited evidence exists on the use of antiviral therapy to reduce viral shedding and therefore reduce transmission of HSV to neonates.
Results of observational studies of surgical effectiveness do not always predict the results of controlled trials, and no controlled trials of cesarean section to prevent neonatal HSV transmission have been conducted. Cesarean section and vaginal delivery were used for different patient subgroups in the cohort.
At this time, no professional health organizations recommend routine screening for genital HSV in asymptomatic adolescents and adults. Herpes will cause sores to form and those sores will often break and leave painful ulcers that can take a few weeks to heal. People who suffer from one outbreak should expect to have four or five more of them within a year. To diagnose herpes, your doctor can inspect an outbreak, take a sample from a sore and get it tested, or give you a blood test. I even lied to cute boys and handsome men that I have a boyfriend already and we shouldn’t date. It’s called The Ultimate Herpes Protocol and they’re selling their method for $37. I was VERY skeptical about this product, but I realized that they offered a money back guarantee if I was unhappy with their product and I didn’t have anything else to lose. Not only did it provided me with a possible way to cure Herpes forever, but also I could date who I wanted and when I wanted, plus, I got provided with tonnes of useful information. It is a viral infection that’s usually treated with aggressive anti-virals that can have serious side effects. At first I thought it was just an allergic reaction, but then in a couple days it grew and became a really imposing looking sore! Most people get prescribed strong antiviral medications, but those can have their own long term negative health effects and can severely affect your body.
Their company says that the protocol they use was researched in the 90ies and was proven to be just as effective as BIG pharma’s solutions, and it also has no long term negative health effects and is very easy to use.
Herpes Protocol is currently only sold online, so I visited their website and to my surprise they were offering 100%, 60 day no questions asked money back guarantee! It was written in clear English without any fluff and with simple to follow step by step instructions. Not only was it the simplest to use, but it had the most studies conducted and research showing that it really works.
What once seemed impossible has now turned into a reality, and I’m recommending all my friends order discounted Herpes Protocol in order to prevent herpes from becoming a hassle in their life! Herpes Protocol has agreed to keep the discounted price active for our readers for a short while longer. There is no way to contract a herpes infection from touching a toilet seat, sharing a pair of clothing, etc.


A genital infection with HSV-1 is usually lighter with less frequent outbreaks than with the more common genital herpes virus (HSV-2). In fact, WebMD says that a poll showed that the stigma of having a genital herpes infection ranked second only to HIV.
You always risk transmitting herpes to your partner (unless your partner already has herpes). The current medical text books say that herpes causes painful, burning sores that can last up to two weeks but the virus does not cause cancer. These treatment options are not being promoted by pharmaceutical companies because they make more money selling remedies which mask the symptoms and offer only temporary relief. One out of five Americans is infected with the genital herpes virus, and many infected people have children. Comparison of Commercial HSV Type-Specific Antibody Tests with Each Other and the Gold Standard, Western Blot AssayTable 2.
No statement in this article should be construed as an official position of the Agency for Healthcare Research and Quality or the U.S.
Lesions may appear 2 to 14 days after exposure and, without antiviral therapy, may persist for an average of 20 days. The rationale for screening would be to identify asymptomatic infected individuals capable of unknowingly transmitting HSV to partners and neonates. The analytic framework and key questions guiding the literature searches are described in the Figure (13 KB). References cited in the 2002 report and references suggested by expert reviewers were also included.
Does Screening for HSV in Asymptomatic Adolescents and Adults Reduce Symptomatic Recurrences and Transmission of Disease? Screening pregnant women and their partners resulted in more tests for the same benefit than screening only pregnant women (about 24,000 tests per case averted).
Other independent predictors of HSV-2 infection included less education (defined by last year of education completed), poverty, cocaine use, and a greater lifetime number of sexual partners. Of the 821 isolates from individuals with first episode HSV infection, 20 percent had HSV-1. Of 194 patients, HSV was detected in 93 (48 percent) by viral cell culture, 76 (39 percent) by HSV EIA, and 115 (59 percent) by PCR. Overall, HSV was isolated in 3 percent of samples and HSV DNA was detected in 12.1 percent of samples. Participants were recruited from clinical settings (STD, maternal and infant care, family medicine, and research clinics) over a 10-month period and completed an in-depth interview on their responses to receiving a HSV-2 diagnosis. Themes included how physicians prepared families for screening and treatment, managed stigma, and perceived parental reactions. How Effective Are Interventions in Reducing Symptomatic Recurrences and Transmission in Adolescents and Adults?
Median time to recurrence was 222 to 336 days for famciclovir groups compared with 47 days for the placebo group. The source partner was aged 18 or older, had recurrent HSV-2 with fewer than 10 episodes per year, and did not use daily antiviral therapy. The susceptible partner was evaluated monthly for clinical signs and symptoms of genital HSV, and the source partner was followed for recurrence of genital HSV. Covariate analyses, accounting for reported use of condoms during the study, indicated that once-daily valacyclovir use continued to be associated with reduced rates of transmission.
Condom use was low throughout the study; only 61 percent of the couples reported ever using condoms and only 8 percent reported condom use for each sexual act, despite counseling at each clinic followup visit. The study was conducted from 36 weeks' gestation to delivery, and HSV cultures were obtained at delivery. The P-value was calculated by Fishers exact test, while the confidence interval for the odds ratio was calculated by logistic regression.
In the study sub-analysis of 177 women who had HSV antibody tests, as well as positive cultures at term, 56 of the 68 cesareans were done in subgroups of women who had no cases of neonatal transmission regardless of delivery method.
Findings from the acyclovir registry did not show an increase in the number of birth defects when compared with the general population.
Using these data, the average obstetrical cost per patient not treated with acyclovir was estimated as $7,625.
No test result is 100% reliable however but a blood test that is positive for HSV 2 most likely means that you have genital herpes.
You can also prevent the virus by being in a long-term monogamous relationship with someone who has tested negative for it.
It may be no more harmful to your health than the common cold but it has the potential to severely affect your personal life. Only your healthcare provider should diagnose your healthcare problems and prescribe treatment. The doctors told me it’s very unlikely that I will find a Herpes cure, but I decided to search for one anyways so at the very least, I will be more informed about Herpes. One of the things you are going to love about this natural cure for Herpes is how easy it is to get rid of the Herpes.
There has been thousands of people who have gotten rid of their Herpes through the methods described in this book. Needless to say, I was surprised because I had a steady girlfriend at that time and didn’t understand how could I get an infection. Finally, a new innovative all natural treatment as discovered and people are saying it’s given them stunning results.
Of course the main problem as far as big pharma is concerned is that this ancient treatment can’t be patented. I knew I had nothing to lose because I could always request my money back if it didn’t work for me. I tested out this new innovative treatment and found that it immediately got rid of that nasty herpes problem for good. You should be aware that refusing to tell your partner about your herpes infection is illegal in some states, and can wind up in legal trouble if you pass herpes to your partner without their knowledge. Because of the partial protection of the preexisting antibodies, symptoms may be fewer and of shorter duration; however, this varies.
Lesions from recurrent infections are present for approximately 7 days with viral shedding for 4 days.
Sixty-one percent of patients with a previous history of genital herpes and 68 percent of patients without known genital herpes had asymptomatic shedding.
Infants with encephalitis have a 15-percent increase in mortality, and those with disseminated disease have a 57-percent increase in mortality compared with infants with SEM disease only. Women who were HSV-2 seropositive but had no reported or recognized recurrences were followed.
Identification could occur by serological testing or by education followed by diagnostic testing of newly recognized lesions. Asymptomatic HSV shedding was detected in late pregnancy and during delivery in 0.43 percent. In both groups, HSV-2 antibody was strongly associated with female gender, years of sexual activity, number of lifetime sexual partners, and past infection with STDs. The investigators reported a linear relationship between the ability to isolate viruses in the culture and the log number of copies of HSV DNA in the sample.
The HerpeSelect® showed sensitivities of 80 percent for HSV-1 and 88 percent for HSV-2, and specificities of 97 percent for HSV-1 and 100 percent for HSV-2. Techniques for fostering good communication included being direct and honest and ensuring that the time and place for discussion were appropriate.
No significant differences were reported in the frequency and severity of clinical adverse experiences between the famciclovir and placebo groups.
After the treatment period, 69 percent of the patients who received valacyclovir were recurrence free compared with 9.5 percent of the patients assigned to placebo. The lowest observed rates of transmission were among couples who reported almost always using condoms during intercourse, and the source partner was taking once-daily valacyclovir. Patients received vaccine or control injections at 0, 1, and 6 months, and were then followed for 19 months.
The frequency of recurrences was reduced in the vaccinated women patients at both 3- and 6-months followup. However, the monthly rate of recurrences was not significantly improved in the vaccine group. None of the published studies had adequate power to address the effect of prophylactic acyclovir on neonatal HSV, and no neonatal HSV infections were reported. Vaginal delivery was permitted if no clinical recurrence was present; otherwise, a cesarean delivery was performed.
Group 3 (n = 201) comprised women who were not given prophylaxis, had a history of genital herpes, and had no active episodes during pregnancy.
Of these, 40,023 had HSV cultures obtained from the cervix and external genitalia, and 31,663 had serum samples tested for HSV twice. Fifty cesareans were done in women who had reactivation of previous HSV-2 infection (a group that had no neonatal transmission regardless of delivery method). The average obstetrical cost per patient treated with acyclovir during the last weeks of pregnancy was estimated as $7,442.
A potential 82 percent decrease in neonatal herpes incidence would be possible with screening and suppressive therapy, but would cost $363,000 per case prevented. Herpes can also help the spread of HIV by making people more susceptible to contracting HIV and making HIV-infected people more infectious. There is no cure for this virus but by taking antiviral medications, you can shorten outbreaks and prevent them from returning.


In order to stay safe and protect yourself remain abstinent, practice safe sex always, or stay in a mutually monogamous relationship. When I found this out, I was jumping around like a little happy puppy having his very first bone – or if you translate this into human – a boyfriend – finally! My Herpes disappeared within 2 weeks! Really awesome feeling, you deserve to experience it!
The least I can say is that this book will provide you with a TONNE of useful information about how to properly treat Herpes – much better advice than ANY doctor can give you. HSV-2 is mostly genital herpes whereas HSV-1 usually presents itself on the lower lip or your face. I recommend that you use Herpes Protocol if you are infected with herpes and stop it off once and for all!
The USPSTF determined that a brief update was needed to assist in updating its 1996 recommendations on screening for genital herpes. Additional symptoms associated with primary infections may include intense pain, dysuria, itching, lymphadenopathy, fever, headache, nausea, malaise, and myalgia. The duration of lesions in a non-primary first-episode averages 15 days, and shedding lasts for approximately 7 days. Sensitivity is 80 to 90 percent for specimens obtained from lesions, although sensitivity and specificity vary by laboratory. Two type-specific glycoprotein G serological tests are commercially available in the United States. After education and counseling regarding genital HSV, 45 percent of women who were HSV-2 positive but did not report recurrences were able to precisely report symptomatic reactivations of genital HSV.
Sixteen percent of seropositive women reported a first episode of clinical genital HSV during their pregnancy, demonstrating that education can assist asymptomatic, seropositive women in recognizing lesions. Forty-five percent of those with HSV-2 antibody reported having symptoms suggestive of HSV infection, and only 27.4 percent had a previous diagnosis of HSV. Importantly, this relationship persisted with men and women in HIV negative and HIV positive participant samples and on days when lesions were present or absent. The study did not provide age specific information regarding accuracy of HSV serological testing. Strategies for managing stigma associated with screening included placing the diagnosis in epidemiological context and discussing the potential severity of the disease. There was no reported difference in efficacy between the treatment regimens or between men and women.
The adverse experiences reported were similar for each of the 4 valacyclovir groups, the acyclovir group, and the placebo group. The endpoints of the studies were occurrence of genital HSV disease in the patients in study 1 and in seronegative women patients in study 2. Overall recurrence reduction for both men and women after 6 months did not reach statistical difference. The proportion of women undergoing cesarean delivery for recurrent HSV at delivery was 19 percent (n = 12). No specific instructions were set up for obstetrical management except for cesarean delivery in case of suspected herpes lesions at the time of labor. Among the 202 women HSV positive at the time of labor, 10 (5 percent) had neonates with HSV infection (OR, 346; 95% CI, 125-956 for neonatal herpes when HSV was isolated vs not isolated).
Conversely, there were only 3 cesarean sections among the 15 HSV-1 infected women (a group that accounted for half of the cases of neonatal herpes). Amniotic fluid samples were obtained during labor, and simultaneous umbilical cord and maternal plasma samples were collected at delivery.
However, data from reported cases do not represent a sufficient sample size for reaching reliable and definitive conclusions regarding the risk for acyclovir to pregnant women and their developing fetuses.
Without prophylactic acyclovir, an estimated 1,082 cesarean deliveries would be performed to prevent 2.8 cases of neonatal HSV in a cohort of 10,000 women.
You can also take medication as a daily suppressive therapy of symptoms, which will lessen the likelihood of transmitting the virus to partners. When lesions and other symptoms are present, people should abstain from having sex because they are more infectious. I can feel the pain of guys with the Herpes also – except the need for intimacy is 10x stronger and so is the shame. So the sooner you start reading the book, the sooner and better are chances you will ever get rid of the Herpes. Untreated herpes can cause psychological stress, anxiety, tension, risk of having it spread to other parts of your body, risk of infecting other people and more. This is because the baby could be infected with the herpes virus while going through the birth canal. The clinical presentation of a primary infection cannot be reliably distinguished from a non-primary first-episode infection. Results of this study indicate that HSV-2 seropositive adults are capable of transmitting genital HSV-2 whether or not they had prior symptoms. These drugs relieve discomfort caused by HSV lesions, speed healing in uncomplicated primary and recurrent genital HSV infections, and reduce viral shedding. The higher rate of asymptomatic infection in men may be a factor in the higher rate of male to female HSV-2 transmission. Famciclovir was well tolerated in all treatment groups with an adverse experience profile comparable to the placebo group.
Intention-to-treat analysis indicated efficacy of 38 percent (95% CI, 18 percent to 68 percent) in study 1 and 42 percent (95% CI, 31 percent to 74 percent) for women patients in study 2. The vaccine induced high levels of HSV-2 specific antibodies in vaccinated persons who did and did not develop genital HSV. No patient in either group experienced asymptomatic viral shedding, and no infant in either group had clinical or virological evidence of HSV infection. In 82 patients (85 percent) adherent with therapy, only 1 percent had clinical HSV recurrences at delivery. The authors attributed the high rate of transmission in HSV-1 infected women to the fact that cesarean section was not frequently used. Laboratory studies were performed to screen for evidence of toxicity in mothers and infants.
Similarly, the data for prenatal exposure to valacyclovir were too limited to provide useful information on pregnancy outcomes. Costs include $1,319,457 per case of neonatal HSV prevented, and $3,012,459 per death or disability prevented.
They are used as a short course during recurrent episodes or for chronic daily suppressive therapy. Trials of antiviral therapy were rated for quality by 2 independent reviewers using USPSTF criteria (Appendix 2). Further, a systematic review of antenatal HSV screening in the United Kingdom was reviewed. In the post-hoc subgroup analysis, the vaccine provided higher levels of protection in women but not in men.
Six percent of the women in the study had persistent detection of HSV by PCR more than 20 percent of the days, despite reporting taking 90 percent to100 percent of the acyclovir doses. No adverse experiences related to acyclovir treatment in neonates were reported at 1-month followup.
In an intention-to-treat analysis of the entire cohort, 4 percent had clinical recurrences (compared with 18 percent to 37 percent in historical controls). Seventy-five percent of cesarean deliveries in group 2 and 10 percent in group 3 were done because of genital HSV.
While this interpretation may be correct, the study does not provide direct data to support it.
There was no significant difference in drug elimination half-life or in time to peak concentration between valacyclovir and acyclovir recipients at either sampling interval. Using prophylactic acyclovir, the rate of cesarean deliveries would be reduced to 216 per 10,000 women, preventing 5.5 neonatal HSV infections.
Viral shedding lasts an average of 12 days and ceases before complete resolution of lesions, if present.
Neonatal outcomes were similar between groups, and the study did not examine neonatal safety.
Costs include $493,641 per case prevented, and $1,127,034 per death or disability prevented.
The rates of symptomatic genital HSV-1 infection and oropharyngeal HSV-1 infection were the same (0.5 case per 100 person-years).
Drugs were well tolerated, and no significant laboratory or clinical evidence of toxicity was detected. Prophylactic acyclovir and followup of infants exposed to HSV at delivery without performing cesarean deliveries would prevent 5 cases of neonatal HSV infections at a cost of $400,382 per case prevented, and $914,114 per death or disability prevented. Unlike protective antibodies to other viruses, antibodies to HSV do not prevent local recurrences.
The vaccine was not efficacious in women who were seropositive for HSV-1 and seronegative for HSV-2 at baseline or in men regardless of their HSV serological status. Maternal valacyclovir therapy resulted in higher plasma levels, with significantly higher peak concentrations, and daily area under the curve values than acyclovir therapy.
The majority of doses of vaccine were followed by soreness at site of injection, and most symptoms reported were mild to moderate.



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    Congressional action, can compromise?your herpes simplex virus type 1 (HSV-1) is known to trigger.