I was seven metres from our main bathroom. I had overdosed on laxatives trying to counter the large amount of analgesic medication I am currently taking. My fellow lounge dwellers watched in horror as I tried to clench my way to the toilet. Two metres from the bowl it was clear this was not going to end well. I have no butt fat or muscle left to clench. It was like the scene from Bridesmaids where she sinks into the middle of the intersection in the largest wedding dress, in tears, knowing the biggest meringue now has a chocolate filling.

I landed on the toilet in a spiral of shame and my clothing completely pasted to me on all sides. My husband offered help (bless him). He would do anything. But it was my mum who I ended up calling on. And she fixed me up and hugged me like I was still her baby.

I tell this story not for a laugh although I think it might make a few of you laugh. But because I have been dreading this day since my diagnosis and have since learned how many of you have shit yourselves in the funniest places, awkward moments and most public of events. And I would love the brave of you to share your story in the comments. It would be the perfect Christmas gift. 

An update for you all. So I am sitting in our lounge room looking at the most magnificent Christmas tree which is as tall as the ceiling and smells of the sweetest pine and it is bliss. I lie back in my new recliner to make adjustments for my very distended and hard tummy. I look out at a beautiful garden and know that my family will visit soon as they have been since I entered my new phase of home based care. I am in a very peaceful place and space and whilst I go through periods of pain and discomfort, we are learning how to manage those things with priority. 

I have left Alan, Karen and all those names I gave my cancer behind. I have left cancer behind. I am no longer in a treatment/intervention pattern and this feels extremely relieving for me. I am living my most precious life right here with my people. I know that on the downside, I can’t include all of my people in that experience with me. So many of you have reached out and want to visit and talk with me but I need to hold space for my own emotions. It’s a lot. 

I also want to enjoy time with Magro where he is not my carer. I need quite a bit of help with personal care and mobility but our experience of what marriage offers shouldn’t only be limited to the most fabulous of weddings followed by a slow and steady progression to him wiping my arse. 

But I want you to know that from my perspective, you and I have no unfinished business between us. If you read this blog, if you have supported me in friendship over the years, if you have shown care or empathy to my friends and family, then we have love between us. Whilst it is a true honour to read about the impact I’ve had on your lives, it makes me proud of the person I am. You have had an impact on me too. I believe the authentic connections between people, alive or dead, never truly end. We carry each other through our lives and beyond. 

I have been processing that I am dying for a long time and some of you are just getting your heads around it now. Please know that I am not scared. I feel at peace with the process, very well looked after by the team and my family and in a space that makes me feel loved. It’s also my favourite time of year. Full disclosure: I never started writing Christmas cards and sending them and this is a decision I have never regretted – it’s a trap and a never-ending cycle of guilt and demand!  But bless those of you who do it. My friend Bev must write more than 300.