In the beginning, I thought like that, too. My disease was my enemy. My medications were weapons. In learning more about my illness, I was
arming myself for the future. Sometimes
I was advancing; others, retreating.
Every day I made tactical decisions in my fight to overcome these obstacles. I was a soldier, drafted into a conflict I
didn’t want to fight, but doing it nonetheless.
But this isn’t a war.
This is my body. It tries to kill
me, but it also allows me to walk at night, balance in Crow pose, drink coffee. It is sick, and it is damaged, but it is the
only body I’ll ever have. There is no
known instance of a person with no mast cells surviving. They heal my wounds, thin my blood and
protect me from infection. It pains me
to admit it, but I need my mast cells.
It’s harder to envision this as a war when you know you will
never win. I will never be able to kill
off all my mast cells; I have to live with this faceless horde. I can only appease them and mitigate my
damage. When you think about this every day,
it begins to change you. You might still
see your body as an adversary, but you grudgingly find ways to work
together. And not often, but sometimes, you
find that by doing this there are things you can do that couldn’t before. In some ways, you can learn to play your
disease to get everything out of your body that you possibly can.
My disease has caused me to accept my body. It is scarred and misshapen and swollen, but
it is still here. Looking in the mirror
is like visiting a monument to the resistance.
We’re outmatched, but we try anyway.
Sometimes it is better to work with your enemy than to fight them on
principle. There is a kind of quiet
honor in that.
Some days it is still a battle. But most of the time, it is just my life,
living in this body, trying to work with it.
Another excellent one, Lisa. Thanks.
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