The C(F)loak of Invisibility

The C(F)loak of Invisibility

the F is silent

let me set the scene…

It was the night of my 24th birthday, and we were celebrating. We were at the bar with a shot of tequila in the air cheering to any excuse to let go and dance the night away. We had the usual gang, our boys who were still talking about last weeks football, and the girls, feeling ourselves in our best sparkly little dresses, one was already chatting up the bartender and the other was defying the advances of someone else. On top of that we had two newbies… Friends of a friend, I didn’t know them, but they were sweet and both joined in the birthday cheers.

sadly my temper flipped just a few seconds later…

One of the two newbies then came up to me and handed me a drink. I’m not going to pretend that I remember what exactly lead to his foot being jammed in his throat and it is irrelevant to why I got angry. The anger that came up was already bottled up inside from my past. Which meant this wasn’t his fault. We had all been drinking and the music was loud, confusion and intoxication coloured the conversations around. So, let’s just say that he did not know anything about me before he said, “well it seems like you have a lovely and easy life.”

sometimes I do question my own psychological response to anger, because on the moment all I did was stay quiet, nod and smile when in actual fact, I was raging on the inside

In all honesty, I was hurt. So, I ended up yelling at him, walking away and simply getting on with my evening. My friend wasn’t surprised by my actions, knowing me, but she didn’t understand why I was offended by someone not seeing my illness.

I don’t think I even knew why I was so hurt in the moment…

so, I unpacked it…

I was born with an illness that is incurable, degenerative and painful, but none of this is visible to the naked eye. All of my dysfunctions are internal. Yet, the damage is extreme, especially over a lifetime of forcing our bodies to continue pretending to be normal. One of my most problematic areas is my lungs, they have been collapsing day by day, and recurring serious infections have eaten whole sections of my lungs over the years. Breathing capacity I never got back.

I don’t know how to explain how it feels to not be able to breathe in life, but the only thing I can compare it to is trying to breathe through a wet cloth

it is difficult

and it is frightening

What threatens me is within my body. It is simply not capable of functioning on its own, medicine helps, but it will never be independent or free. And all of this is invisible.

In a way, I felt like it was real only for me.

I once thought this was a blessing.

It meant that I could keep it away from my friends. Kids growing up didn’t know how to handle it and it either turned into something that was taboo or something I was bullied for. So, as a teen, I started to choose who I shared it with. And when I moved out the country at 18 I tried leaving it behind but the secrets just threatened my new friendships. It was pointless anyway because they always ended up finding it out in the end.

I thought it would free me to hide it, but the secrecy was just a different type of shackle

As an adult, I avoided bringing it into conversations because it changed how my friends acted around me. I saw partners turn into nurses and sign the death sentence of our relationship. I had friends who simply didn’t know what to say after I had told them, forcing both of us to sit in silence across french toast during brunch. The reaction I hated the most was when I saw pity in my friend’s eyes. I was proud of who I was despite my illness, being defined by it was my worst nightmare.

And losing my identity to CF after I admitted what I had, felt like the worse punishment possible.

What I realised hurt me now on my 24th birthday, was that I had erased, from my own history, the battle that had made me into the adult I was. I had removed it from my image and my identity. All this time, I thought I was hiding my biggest weakness, when in actual fact I was ignoring what had made me strong. Projecting a curated image of who I was had just been an extra safety blanket to help me feel normal growing up.

in a way it was only denial

So, yes, I had been lucky to not be defined by my illness at first glance, but it also made me feel very alone. Dividing my own life in these two separate worlds made me feel detached from myself. It’s also why I was such a terrible patient; I hated stepping foot in my CF nightmare, and often I lost control of my own emotions and rage when I was confronted by the realities of my illness. I had separated myself from it so much that I felt insulted to be categorised by mutation.

And that is how I unconsciously hid a massive part of myself from my own reality.

talk soon

Ballistic xx

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