health

A Life Of Peace – Scan Results

This cancer ‘journey’ can be full of twists and turns and highs and lows.

Most of all, it can be full of surprises.

Recently I had the surprising news that my abdominal tumours had resolved and it ‘appeared’ that the only remaining tumours were two in my right lung. This opened up the potential for unexpected treatment options including lung surgery or SABR radiotherapy. It was exciting and terrifying and, to be honest, I wasn’t overly keen on either….I mean, my previous experience of cancer surgery was hardly ‘simple’.

However, before these treatment options could be confirmed as viable I had to have a PET scan.

Previously I had only ever had CT scans. During these you are injected with a contrast dye that is great at showing abnormalities in the body (such as tumours), but they don’t always show up everything and they also don’t show how ‘active’ the abnormalities are.

PET scans, however, work in a different way. For a PET scan you are injected with a radioactive glucose mixture. Beforehand you fast for 6 hours so that your ‘normal’ cells are forced to use other energy sources such as your fat. Cancer cells aren’t able to use other energy sources (they need glucose) and so when the mixture is injected it goes straight to any active cancer cells in the body. The radioactive part of the mixture then makes these cells ‘glow’ on the scan. It’s amazing eh?! This was helpfully explained to me by the radiographer doing the scan.

So I had my first PET scan a couple of weeks ago and then I waited, not so patiently.

Today I got the results.

I must admit, as soon as I was told I was getting the results I knew they were not going to be good news. I had this deep sinking feeling in my stomach that I’ve never had before.

‘You just want to get straight to the results don’t you?’ My oncologist asked, knowing me so well after 3.5 years of caring for me. I should highlight, again, that she is incredible. I mean I have never met another consultant so focused on person-centred care. She really is a joy and I feel so lucky. I know this isn’t the case for every cancer patient in the world.

Sorry…’just get to the point’…I’m sure you are muttering.

So the scan confirmed that yes the two lesions in my right lung are very active and growing…nothing surprising about that.

It also showed that the lesion above my heart that had been visible on the previous two CT scans is in fact active and not ‘dead’ as we had hoped. This means no lung surgery for me as it would be far too risky.

Also, it showed some activity in my lymph nodes including one under my right armpit and one in my upper abdomen. This is not good. Everyone with cancer knows that it being in your lymphatic system is more than a little shite.

And yet, still, I find myself oddly calm and at peace and here’s why…

Stay with me, things might get a little ‘woohoo’ for some…

When I bought my 1996 VW T4 Campervan recently (if you missed that news flash I have no idea how as I have posted a billion photos!…well at leats 4 or 5 haha) I wanted to give it a name.

While Ewan and I were on our test drive the name Alfonzo came to me. It sounded kinda cool and I thought to myself ‘OK, this is what the van wants to be called‘. Then, when I got home I looked up the meaning of Alfonzo and was surprised to discover that it means ‘ready for battle’.

Even better,’ I thought, ‘The perfect name for a warrior’s van.’

But then something weird happened when I was driving the van yesterday.

As you may already know I am training to be a shaman. This means that I work with the spirit of things, energy and intuition (amongst other ‘stuff’ I’ll save for a future post).

So, it wasn’t unusual for me that when I drove the van to hospital for my treatment yesterday that I got a sense that the van wanted to be called Winifred, not Alfonzo. Yes, you read that right, the van wanted it.

‘Winifred doesn’t sound anywhere near as cool as Alfonzo‘ I thought, ‘So that’s not happening.’

Well, when I left hospital the van wouldn’t start for me. I sat in that car park for over an hour trying to start it, only to have Ewan rescue me and it start first time.

OK, maybe you can be called Winifred‘ I thought.

So, here’s where it gets freaky – yes that wasn’t the freaky stuff.

When I looked up the meaning of ‘Winifred’ I was amazed to discover that it means ‘joy, peace and reconciliation’ – the exact opposite of what Alfonzo means! Crazy eh?!

Now, here’s the thing. I now think this was some kind of crazy, insight, instinct, message from the universe (call it what you will) that I just need to let go, slow down, be at peace and reconcile any pain, trauma or grief that I’ve been carrying around with me.

And that, my dear lovelies, is exactly what I’m going to do, because firstly, what is the alternative? I wallow and mope and waste the fact that, right now, I still feel surprisingly well (compared to most other stage four cancer patients, not compared to healthy people I hasten to add) and secondly, my precious instinct has served me well up until this point so who am I to ignore her wisdom now.

As I move forward through the uncertainty of living (yes LIVING) with stage four cancer, I will not fight it, I will not desperately look for ‘the magic cure’, I will not read book after book in search for the answer that may have been missed elsewhere and I will not be angry that this is happening to me (most of the time – sometimes I will shout ‘f*ck this‘ at whoever happens to be listening or in earshot).

No, instead I will use it as a catalyst to live my life, and what a beautiful life it is, filled with love and joy and adventure!…and now I will work at bringing peace and reconciliation into my life too…because it’s needed, boy o boy, is it needed!

Above all I will strive to live like I am dying, to practice what I preach and to find the good and the gratitude in each and every day because isn’t that all any of us can do in our pursuit of happiness and fulfilment; to live a life to it’s fullest and to focus on what we have rather on what we have lost?

My cancer may never my cured, but it is certainly the tool through which I am healing my life. And that feels pretty good to be honest. It’s certainly better than living the life I lived before, filled with drama, anger, stress and unfulfilment. No thank you! Life is too short for that nonsense!

Now, on a much more serious note, what on Earth am I going to name my campervan?

With love in my heart for you all for reading my words and sharing my story.

Thank you, Fi xx

Read more in my books

Visit me at one of my workshops.

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Stay on one of my retreats.

—–

Fi is Currently:

Loving my precious life.

Feeling grateful to still be alive.

Sitting on our sofa wrapped in a blanket after a lovely afternoon on the beach with Ozzy.

 Waiting for Ewan to come home with a takeaway because who would cook on scan result day?

Uncategorized

First Day of Chemo…

“Every journey begins with a small step, every race has a starting line, keep on reaching out for your goal, don’t give up, just give it time.”

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Well today I start chemo…just 16 days after I received the news I have ovarian cancer and I’m feeling great about starting my journey to being me again ๐Ÿ’–๐Ÿ’–๐Ÿ’–

However, whilst I’m always positive about my cancer diagnosis – because really there is no other way to be in life – cancer is not an easy journey and so today I’d like to share the darker side that I usually hide because I think it’s really important that people talk about what cancer does to patients physically and give it the awareness it deserves….
….so here goes.

This is not a moan…I feel as positive as ever…but this is a journey that not everyone can take so positivity and that sadly thousands go through every single day xxxx

I’m told every day that I ‘look so well’…this is thanks to firstly an expensive skin and makeup regime!
Secondly it’s thanks to three different anti-sickness drugs that allow me to manage small mouthfuls of food (but never a full meal) without throwing them up.
Thirdly it’s thanks to two kinds of morphine – a tablet I take twice a day and a fast acting liquid I take when I just can’t take the pain….which is most days.

  • I can’t walk more than 5-10 minutes without needing to sit down – over the weekend
  • I had to go to hospital because I fainted trying to walk around the block.
  • I can’t get through a day without sleeping.
  • I’ve had over 35 blood tests in the last two weeks – I stopped counting at 35!
  • I had a drip 10 days ago when I couldn’t eat or drink anything at all and got too dehydrated.
  • That week I also had fluid drained from one of my lungs without any pain relief – holy cow I thought I would collapse from the pain!
  • Last week I had 4.5 ltrs of cancerous fluid drained from my abdomen (this was following 5ltrs one week before my diagnosis).
  • The next day I had a very painful tumour biopsy taken from my abdomen – I had to be sedated (although awake) because the pain was too much. My tummy still feels like it has a knife in it.
  • In the last 8 hours I have taken 20 steroid tablets in preparation for chemo today – 10 at midnight last night and 10 at 7am this morning.
  • I’ve lost 1.5 stone in fat and muscle in the last 6 weeks due to an inability to eat properly.

This is just a brief insight into ‘the medical side’ of my first two weeks with cancer.
I feel that whilst every day has to be full of medication, pain, tests, Drs and nurses I can get through it by understanding that I choose what else it is filled with . And I choose love, hope, positivity, family, friends and laughter.

So my first two weeks have also been filled with some of the best experiences and making some of the best decisions of my life! ๐Ÿ’– for instance – I never would have donated my hair before but I’d do it again in a heartbeat! I’d never realised how loved Ewan and I are – but we we must be the richest couple in the world because we are surrounded by love and hope and every day we receive over a hundred messages offering support for every step of our journey ๐Ÿ’–

Without this I don’t think I’d find the strength I need – so thank you all a million times for your love and support xxxxx

12644866_10208073645057206_3951477712065967210_n.jpgCancer is a painful journey and it is a challenge every single day but by taking it a day at a time it is an achievable challenge. I promised I would do a marathon one day and I guess this is my version of an epic marathon.

love and light,ย Fiย xx