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Timmy
"My face is too sexy for you." - TehSlapHappy

Age 38, Male

Philadelphia, PA

Joined on 1/12/05

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So frightening.

My beard eats girls like you WHOLE D:

*GASP* Not your beard!!

ITS TRUE

That wasn't on the agenda!

Om Nom Nom

Ohshi- You forgot the beanie! It just doesn't look like you without the beanie!

FFFFFFFFFFFF

HI! MY NAMES TIMMY!!! TIMMY TIMMY TIMMY TIMMY TIMMY THE MODERATOR!!! AAAAAAAAAAAAAAAAAAAAAAHAHAAHAHAHAHAHA HAHHAAHAHA

You got me good

Are you keeping the beard for the meet, or does he have something scheduled for that day (ie. fucking black chicks, saving the world, etc.)?

I wasn't going to - but now I might keep it.

Maybe I'll shave AT the meet :O

Going to Wizard Con this year?

If it occurs and NG has a booth, I'll be there.

can i have a beard like yours some day? :D

Only if you feed and water it twice a day! :D

Herpes has been known for at least 2,000 years. It is said that Emperor Tiberius banned kissing in Rome for a time due to so many people having cold sores. In the 16th century Romeo and Juliet, it is mentioned that there are blisters "o'er ladies' lips." In 18th century it was so common among prostitutes that it was called "a vocational disease of women."[89]

Herpes was not found to be a virus until the 1940s.[89]

Herpes antiviral therapy began in the early 1960s with the experimental use of medication that interfered with viral replication called deoxyribonucleic acid (DNA) inhibitors. The original use was against normally fatal or disabilitating illness such as adult encephalitis,[90] keratitis,[91] in immunocompromised (transplant) patients,[92] or disseminated herpes zoster.[93] The original compounds used were 5-iodo-2'-deoxyuridine, AKA idoxuridine, IUdR, or(IDU) and 1-%u03B2-D-arabinofuranosylcytosine or ara-C,[94] later marketed under the name cytosar or cytorabine. The usage expanded to include topical treatment of herpes simplex,[95] zoster, and varicella.[96] Some trials combined different antivirals with differing results.[90] The introduction of 9-%u03B2-D-arabinofuranosyladenine, AKA ara-A or vidarabine, considerably less toxic than Ara-C, in the mid 1970s, heralded the way for the beginning of regular neonatal antiviral treatment. Vidarabine was the first systemically administered antiviral medication with activity against HSV for which therapeutic efficacy outweighed toxicity for the management of life-threatening HSV disease. Intravenous vidarabine was licensed for use by the U.S. Food and Drug Administration (FDA) in 1977. Other experimental antivirals of that period included: Heparin [97], trifluorothymidine (TFT)[98], Ribivarin,[99] interferon,[100] Virazole,[101] and 5-methoxymethyl-2'-deoxyuridine (MMUdR).[102] The introduction of 9-(2-hydroxyethoxymethyl)guanine, AKA acyclovir, in the late 1970s[103] raised antiviral treatment another notch and led to vidarabine vs. acyclovir trials in the late 1980s.[104] The lower toxicity and ease of administration over vidarabine has led to acyclovir becoming the drug of choice for herpes treatment after it was licensed by the FDA in 1998.[105] Another advantage in the treatment of neonatal herpes included greater reductions in mortality and morbidity with increased dosages, something that did not occur when compared with increased dosages of vidarabine.[105] On the other side of the equation, acyclovir seems to inhibit antibody response and newborns on acyclovir antiviral treatment experienced a slower rise in antibody titer than those on vidarabine.[105]

Erm...good to know?