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After two and a half years or false negative IgGs and random single bumps I took the western blot and found out I have GHSV-1. While Iā€™m relieved to find out after so long Iā€™m more or less curious to figure out a few things.
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So long story short I had an outbreak back in early 2020. Ever since then I would get a single bump every several months. It was never painful but I have experienced tingles and what not.

I think the most confusing and annoying part of this ā€œjourneyā€ was people telling me I donā€™t have it and to stop worrying. I know this isnā€™t a big deal in the grand scheme of things but I also know my body. I know when I see a pattern something is up. I also know how to do my own research.

I also know that if someone I plan to date isnā€™t cool with me having something (especially if that something is almost 90 percent of people having) then thatā€™s on them.

What I do know about GHSV-1 is that:

  • itā€™s less contagious or sheds less than GHSV-2
  • I probably got it from some blowjob
  • literally most people have this strain
  • the one negative thing Iā€™ve read about the 1 strain is it causes meningitis or Alzheimerā€™s?

My next and really only step is to maybe start taking a supplement like L-Lysine to suppress. What do you think? I donā€™t like the idea of taking a big ass Valtrex pill everyday but I would if I was in a relationship.

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2 years ago