Lying awake at 4 am squeezing Grant’s hand praying for the pain to stop, waiting for the pain killers to work. This is the side of cancer we often do not see or want to think about. It is these moments that make us question everything, cause while that pain is not permanent while it lasts it feels like ages.
The pain has been manageable until about the last 3 months where the intensity crept in. It surprises you as it comes and goes, I can however say it is more frequent than before. My side hurts, my shoulder hurts due to the liver being connected to a nerve in your shoulder, my tummy aches or I am exhausted, sometime these pains are isolated sometimes I experience them all together it varies.
This is the reality of cancer, apart from all the treatments and the side effects they bring the cancer itself also brings pain. The only solution in my situation is to manage it with pain killers, lots and lots of painkillers. I have my own medicine tub and thanks to my very diligent personal pharmacist (aka Grant), he makes sure I take the right tablets and everything on time as is needed.
Beginning of 2024 as the pain was worsening my oncologist advised it is the liver lesions referring the pain to other parts of my body like my shoulder and back etc. We did a new base line scan in January and the results were positive, no new brain lesions, and all liver, lung and breast lesions had not grown. Yet for me the pain was increasing.
Late February one evening the pain became so excruciating Grant took me to the emergency room. The Dr on call was thankfully extremely thorough and insisted on a sonar. Low and behold she discovered I have gall stones, which can only be seen on an ultrasound. Honestly to anyone who has ever had gall stones I give you the biggest respect, the pain is unbearable. The sad reality is other than give you pain meds there is not much that can be done and in all honesty the pain meds for some reason do not take that gall pain away, my other pain was dampened but that gall pain stays constant. If the gall pain does not subside or keeps reoccurring your only other option is to get your gall bladder removed.
This is where I ended up 12 March, in hospital having my gall bladder removed. I am sure I not alone in the world, but I am not a fan of surgery. I will admit though the relief and the reduction of pain the surgery bought, was worth with it, I still feel pain but nowhere near as excruciating as it was. The sad outcome is that the surgeon doing the surgery confirmed that he saw lesions on my abdomen wall, another difficult thing for CT scans to see. We are not sure how long the lesions have been there, but they are there. Following the surgery, I am still experiencing liver, back and shoulder pain but nowhere as intense as it was, so we continue adjusting my meds to manage the pain.
In December we did Gama Knife radiation on the 5 lesions that were visible in the MRI, the Radiation Oncologist is positive that as we caught them early, when they are still tiny, this procedure will have the best results in eradicating the lesions. The Gama Knife radiation is targeted only to the lesions and the side effects should be minimal. Even though the experience was very unusual, and I felt like I was part of a horror movie, thankfully the treatment did not stop us from going on our planned UK and Paris Christmas and New Years trip.
Since the surgery of my gall bladder removal, my headaches have unfortunately not reduced but increased. So, bring on yet another MRI scan on the 22nd of March and yip you guessed it, new lesions have appeared on my brain. 10 tiny new buggers and some possible hidden ones that we can’t yet see.
The new lesions are a lot more spread; this means on Wednesday the 3rd of April we start 10 treatments of Hippocampus sparing whole brain radiation. Unlike the gamma knife radiation, I had in December, for the first tiny lesions we saw, this is not targeted on the individual lesions but going to apply the radiation across my whole brain except the Hippocampus. The hope is that this radiation will put all lesions seen and unseen in a stateless condition preventing them from growing or spreading. The sparing of the Hippocampus is to avoid effecting cognitive and mental functions.
Due to this treatment, I will however once again lose all my hair, but this is not as scary 2nd time round.
My life with cancer keeps going, the hits keep coming, the cancer keeps spreading but I keep fighting. As per the words of my surgeon, “There is nothing we can do, we know the inevitable outcome, but your body is coping, your spirit is strong, keep doing what you are doing. “
You must be asking by now when is enough, enough. The reality is I have accepted death, I am not happy about it but I have accepted it, it doesn’t scare me anymore and it is out of my control. I have been blessed with a great life I had a great work career, married the best husband, got to be a mother to 2 beautiful smart, happy girls and surrounded by amazing family and friends. I am comfortable in my belief that I have had an impact on people I have met and know and do not’ feel like I have missed doing something or have unfinished goals.
My girls are my beautiful legacy to this world, and I know they will make it a better place. My only bucket list is to experience and create as many moments as I can with the ones I love. So, when is enough, enough, I suppose the answer is when I can no longer be part of great moments and become a burden. Until then I will continue as best I can and appreciate each moment I get.
A few pics from our amazing holiday in the UK & Paris:
London Markets, Harry Potter Studios, Madame Tussauds, Disneyland Paris, Paris Segway Tour, The Louvre (amazing place) & of course New Years eve on The Champs Elysée & Eiffel Tower





























11 Responses
I still continue praying for you and your family xxx Keep being as strong as you are – I know ow it’s hard and the pain is extremely unpleasant but keep pushing through.
Thank you for the prayers xxx
Oh my friend, I applaud your honesty and your bravery. You continue to fight, remaining positive and a light to all those around you. I am so grateful I have gotten to know you in the last little while and I look forward to a good few more laughs and moments together❤️
Thanks Cathy, really have appreciated our friendship and you support over the last couple of months. Definitely looking forward to creating some more happy moments together.
There are no words to describe your tenacity and grit. You are a warrior.
@michelle you meant to say I have left an English teacher lost for words 🙂
Thank you for all the love and support, it too can’t be explained, but know it is priceless xxx
My beautiful friend, this is such a hard read. The tears flow. Yet what stands out for me is your incredible ability to remain positive and strong. You just keep fighting no matter what. You are such a special person and I am so glad you my friend. Here’s to more memories- love you, your beautiful girls and hubby always here and still praying everyday for you my friend.
The tears are tears of happiness and us knowing we still have many more moments to create together.
Love all the support and willingness to be there when we need no matter what.
Thank You for your friendship xxx
Your fight is that of a true warrior! Your positivity is inspirational. Love you Dee ❤️
I was part of your life for a short time but my goodness, how I treasure those memories. You’re incredibly brave Dee. ❤️
Rest with the angels Dee.
You fought so hard.
No more pain, no more suffering 🎗️