The day my life changed forever

Originally written and posted 19th February 2019

After a somewhat rocky start to 2018, I remember sitting in the room with the senior consultant. The monitor was on, and I remember feeling sick as he said, “When we did your MRI this morning, we found this…”.

You didn’t need to be a neurosurgeon to know that the white, golf ball sized blob at the side of my brain shouldn’t have been there. I didn’t know what it was, whether it was benign it not, what would happen next. I had to wait whilst the consultant spoke with the DVLA to check I could still drive.

He told me it was a Vestibular Schwannoma, sometimes referred to as an Acoustic Neuroma. It was growing on my hearing and balance nerve and untypically it was growing inwards, compressing my brainstem rather than out towards my ear canal. This explained why I felt unbalanced. I discovered at a later appointment, that the tumour was cystic and causing some compression of my brainstem. I attribute this to the reason why within a few weeks of my diagnosis, I had forgotten how to write, had high blood pressure, and a resting pulse that was no longer in the healthy range of 50-60bpm, but now a minimum of 108, an extremely heightened sense of smell and incredible fatigue, as my body struggled to do “business as usual”.

After suffering a haemorrhage 3 weeks before surgery, I ‘forgot’ how to write.

My life, as I knew it, was flipped upside in an instant. Of all the things I suspected could’ve been wrong with me those last few months, shingles, Lyme disease, Lupus, MS – I had been told I had a vitamin D deficiency – a brain tumour wasn’t anywhere on the list. I think he was trying to bring me a little comfort when he said that there was nothing I could have done to prevent getting this.

The usual advice he would give patients to eat healthily, lose weight, stop smoking and drinking, exercise more, well none of that applied. Later, I would wonder why I bothered looking after myself, it clearly hadn’t done me any good. But as a military friend had pointed out, I should think again. I later began to realise that whilst it hadn’t prevented this from happening, my fitness – and mindset – would be instrumental in my recovery.

Neil (my husband and best friend) arrived minutes later, and after a chat with another consultant he drove me home. We were both stunned, worried and upset. I was angry this had happened to me, and ashamed that I was about to ruin things for everyone when I told them. I didn’t want to tell them, and what would I tell them? How do you tell them…? In the days that followed, I googled myself to death several times. I was 1 in 100,000. Why me?

I’m currently trying to get more writing projects off the ground, so if you enjoy what you’ve read so far, for just the cost of a coffee, you can support me here.

Published by Sara C

It's hugely important to raise more awareness of brain tumours and the implications they can have on patients' lives. I aim to help to create wider understanding of the effects brain surgery and a diagnosis can have on an individual and their families on a emotive level through my own experience.

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