There is something few of you will ever know, and I pray you
never feel it yourself. It is when
something about you so bothers another person, that when the look at you, they
are afraid for their life.
There is a look of fear that I’ve inspired within others
since I found out I had HepC. It’s not a pleasant look, and it’s nothing I can
control. Some people have it, and others do not. The first time I really came
across it was when I was a senior in high school. It was where I’d least
expected, in a hospital room, a newer nurse drawing my blood, looked at me with
fear in her eyes as she spoke as few words as possible.
I’ve rarely come across the look, and when I do, I explain and
educate, but sometimes it is knowledge that’s the problem. At the end of the
day, I pose a risk, by choosing to be near me, you risk exposure you otherwise
would avoid. While I know, and live with the idea and fear that I may unknowingly
infect someone else, albeit transference isn’t exactly easy, it hurts to be
actively reminded of this fact.
While I’m aware it’s unintentional, and I know it’s not me
they’re afraid of, but rather the virus and the danger it poses. At the end of
the day, until I’m through this treatment, it’s a part of me. I take it
personally, when I see that look in someone’s eyes, when I hear the ignorance
and fear in their words.
I have many acquaintances, whom I’m sure would be good friends
if not for the virus. But I’m glad the barrier exists, because at the end of
the day I’m left with friends who care no matter the risks.
This post is in a way dedicated to my friends, without whom
this treatment would be impossible. I long for the day I can have a drink with
all of you, for all that it means.
I am so sorry you not only have to and have had tolive with this illness but have had to witness the rude, ignorance of certain people first hand. You are a good person Ric and its just terrible how people can be sometimes.
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