education
im gonna educate yall real quick and i hope this reaches a lot of people, cause there is just too much excessive negativity and ignorance in this sub. please take the time to read through this.
there is way too little positive productive acknowledgment and education on this virus, and way too much stigma and naive perspectives. that is ultimately what leads people to getting it, and also finding it hard to live with, so these are some things i wish i knew. lets think critically and realistically here.
firstly, the stigma about this is a stereotype. the suffering this comes with is mostly psychological conditioning. yall are arguing over whos worth more cause of which strain you have. ITS A VIRUS. stereotypes and generalizations are never reasonable or realistic in any context, neither are people’s egos or pride. realistically, whether anyone wants to admit it or not, and this goes for literally everything, we are all equally human and impressionable, trying to figure out this life. herpes is a common physical human condition you can get by chance just like any other contagious condition, its not a personality trait. a lot of people are just in pursuit of human connection when they get it, which is normal! life is more complicated than most people wanna admit. people like to dumb things down to black and white to make it easier and more validating for themselves, but everything is case by case. we cannot know how to navigate everything, thats the whole point of trial and error, which is inevitable for EVERYONE. a common, easily contracted virus you cannot control does not automatically define a person. i am 23(f), im a musician, i have many hobbies, i love and care for people very deeply and ive only ever slept with 5 people, all but one were long term relationships. i contracted oral and genital through S/A and abuse. i currently have an amazing, smart, talented boyfriend who has a lot in common with me and loves me unconditionally. i am not a “dirty gross unlikable person”, i was abused and betrayed and now i get bumps on my skin sometimes. my father also has HSV2 from being cheated on by his ex wife! not his fault and doesnt define him! my mother still loves him unconditionally and theyve been together my whole life! guess what? i went through the processing of the abuse and blaming myself and regret and grief, thats what got me here! i am more enlightened and ive learned to not take anything for granted and to love even deeper than i already did!
secondly, this virus doesnt present itself exactly how its portrayed online. SHINGLES from chickenpox is a form of herpes virus. it can occur in your eyes, your fingers/hands, and in extremely rare cases causes a brain infections. this sounds scary but literally any infection can be serious in immunocompromised people. this virus is not serious, it just causes bumps on your skin and can seriously mess with your ego. most people dont know they have any kind of herpes cause it usually is dormant due to your immune system keeping it at bay. a lot of people genuinely dont understand that HSV1 and HSV2 can occur both orally and genitally and both are medically the same virus, they just thrive better in different parts of the body. and having it on your genitals doesnt make you lesser of a person!! you were in pursuit of human connection!
it is not always a cluster of blisters, it can just be one or a few bumps that can look like a pimple. it can also present on your thighs, buttocks, and even sometimes your lower legs. generally anywhere in the “boxer region” or where your nerves in that area extend. it is easier to transmit to women cause they have more mucosal surface area, and women usually have more symptoms mostly due to more fluctuating hormones, which can occur around a menstrual period.
sometimes “prodromal symptoms” can happen such as intense tingling or itching, without actual sores forming. it can shed and be contagious even when there are no or little symptoms, and literally anyone you know could possibly have it!! but that shouldn’t automatically be something scary! you should not look at someone you wouldnt suspect to have it as someone different or scary. things genuinely just happen and you never know what someones been through or has just by looking at them.
guys, at the end of the day, ITS A VIRUS, not a personality trait!!!! we dont define people by their disabilities or illnesses or skin conditions or anything else! this is not actually as scary as its portrayed. people who live with this should not be conditioned to feel compelled to end their lives or live in grief over bumps on their skin and neuropathy that can be easily managed. stress is the main cause of symptoms with this so why are we making it harder on people than it needs to be? where is everyones critical thinking and empathy and humanity!