The Big C and Me.

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The Big C and Me. Diagnosed with a Rare Anal Canal Cancer 21/11/2023
Stage 2 Warrior
Let's talk openly about The Big C. Tears, humour, information - it's all welcome here!

03/04/2025

All my one year scans and results have just come in

NO new tumours and no metastatic disease!!! 👏

No cancer here baby!!

🙌🏻

21/03/2025
My one year post-treatment sigmoidoscopy went well ☺️ here’s my nervous before shot and my groggy post-anaesthetic shot ...
19/03/2025

My one year post-treatment sigmoidoscopy went well ☺️ here’s my nervous before shot and my groggy post-anaesthetic shot 🤣

No sign of new tumour growth 👏 👏
My proctitis and inflammation is still the same, and I’ve been having a lot of pain and bleeding again lately so that will need to be dealt with but I’m hoping it will improve a little now I’ve had my first lot of hyperbaric treatment.

Now I have my MRI and PET/CT scans to go to check for any metastases- keeping our fingers crossed!

I’m off for a lil noddy now, the anaesthetic wiped me out this morning.

Happy with the news so far and looking forward to getting good news from the scans 🩷☺️

A month just for us butt cancer peeps - how special 😆And timely because March is my one year post treatment scans and si...
13/03/2025

A month just for us butt cancer peeps - how special 😆

And timely because March is my one year post treatment scans and sigmoidscope! Next week is a big one 😮‍💨 🤞🏽

March is A**l Cancer Awareness Month! This month and every month, we support the a**l cancer community on this journey. Join in the support by resharing this post to raise awareness of a**l cancer.



Read more about how we’re educating people on a**l cancer at A**lCancer.com. **lCancerAwareness **lCancerEducation **lCancerACtion

22/02/2025
40 sessions over 11 weeks - hyperbaric oxygen therapy - DONE!It’s been a huge commitment and exhausting, but worth it. I...
22/02/2025

40 sessions over 11 weeks - hyperbaric oxygen therapy - DONE!

It’s been a huge commitment and exhausting, but worth it. I’m going to miss my little HBOT family - the other patients I came to know so well, the gorgeous nurses who took care of us, the technicians who did our dives everyday, the wonderful doctors.

Let’s hope it did its job and my body keeps healing from the radiation and chemo effects. 🙏🏽

Hi everyone, wow I can see it's been a long time between updates indeed. I hope that you are all doing well, and had a n...
05/02/2025

Hi everyone, wow I can see it's been a long time between updates indeed. I hope that you are all doing well, and had a nice break over the summer holidays.

I managed to have some nice times in the break, spending a lot of time at the beach, and resting, seeing friends and family when I could.

The hyperbaric therapy has taken up most of my time though. It's been a long.. and exhausting... process. I'm very grateful it's an option here in Australia, and covered by my health insurance (and fully covered by Medicare btw, if you don't have private health). The nurses are lovely and I've grown very fond of the other patients I'm in the dive chamber with each day.

But the process itself has been so tiring, 5 days a week, and I've had troubles with my sinuses and ears at times, resulting in a bruised eardrum and an increasing sense of claustrophobia in the chamber, especially with my oxygen helmet on. I think the treatment is having a positive impact - my head is feeling less foggy from the chemo, and there is definitely internal healing going on. It just leaves me feeling so exhausted every day, which is hard when I've got kids to run around after, and a household to look after.

But - I've done 33 sessions and have 7 to go! It's taken almost 11 weeks because when your ears aren't popping properly I can't go in, so I've had a number of days off for that, or public holidays. I'm almost at the finish line and I can't wait!

I've recently had some heart scans as well, because I was getting very dizzy when exercising. I'm happy to report my heart looks really good, and it's a blood pressure issue from the chemoradiation. I've got low blood pressure now and when I exercise it dips too low. So I'm on electrolytes every day and that should make me feel much better :-)

My big one-year post treatment scans are coming up in March - I'll be having a MRI, PET, and CT scan, and doing my usual scope up the backside! I'm nervous, the 1 year post-treatment scans usually do fill people with 'scan'xiety, and I am certainly not immune. But I'm staying positive and hoping that the treatment did the trick, and this HBOT that I'm having now is helping me heal nicely.

I've been processing an enormous amount of grief lately, of all different kinds. I have been to 6 funerals in the last 15 months, and that is finally hitting me right now. I've been feeling very sad, and trying to come to terms with all of these losses, and how they've impacted not only me, but all the people around me. I've also had people very dear to me, have signficant struggles of their own, including many with their own cancer journeys, and a few weeks ago my Dad had a sudden stroke, which was very distressing.

I'm also grieving the life I had - I was on this steep trajectory with my career, my paramedic degree, my volunteer ambulance work, and now life looks very different at the moment. I've had to make huge sacrifices for my health, which I'm 100% committed to and grateful I can actually do, but it's been a lot to process too.

It's honestly been one of the most challenging times of my life to date. It's felt too overwhelming to even manage at times - yet I do.

I have such amazing support around me, it enables me to be resilient even when I think I'm reaching my limit. Somehow I keep getting up and moving forward, and for that I thank each of you.

I've been quiet on here, and also in my own life. But I think of you all often, and always feel grateful when you reach out. 🧚‍♂️

p.s. - I'm in the back right corner, this was us just before Christmas. I really love all of my chamber buddies, and we do have lots of laughs!

3 sessions of hyperbaric oxygen done, 37 to go 😮‍💨 I’m getting used to it, and the staff and patients are really lovely,...
11/12/2024

3 sessions of hyperbaric oxygen done, 37 to go 😮‍💨

I’m getting used to it, and the staff and patients are really lovely, but boy does it WRECK me! I am shattered by the afternoon. Apart from tiredness I’ve had few side effects - headache, tummy ache, and feeling a bit dizzy with sore lungs. But these are mild. I’ve added some photos so you get an idea of what the set up is like. We go in at 10.15, get changed into cotton scrubs from the hospital, take our book or crossword puzzle into the chamber. They lock us in, attach our space helmets by putting a tight ring around our necks and then fitting a clear plastic helmet to it, so it covers our whole head. They attach an oxygen tube to it, and a tube to collect our expired air. Then they compress the chamber over 10 minutes, to 14 metres below sea level. Once we reach that level, they pipe 💯 oxygen through our tubes, and we breathe that in through our space helmets for 2 hours. A nurse checks us all constantly and a doctor outside of the chamber monitors our vital signs and the atmosphere in the chamber. At the end they slowly bring us up to sea level and then we get dressed and go!

We get to sit in recliner chairs, it’s quite relaxing except for the big awkward space helmets on your head.

The patients I’m in with are lovely, three men with damage from radiation, and a lovely woman who gets transferred from another Hospital every day, with complications from APR surgery after her a**l cancer diagnosis. We were both so surprised to meet another person with a**l cancer - it’s so rare! And she was diagnosed in November just like me, but she had to have the Abdominal Perineal Resection and Colostomy after her chemoradiation 😢 it is very sobering for me to talk to her, about what can happen with a recurrence 😢 and made me all the more determined to finish the whole 8 weeks of this hyperbaric oxygen therapy and do my best to keep my body healthy and free from metastases.

Hi everyone 👋 I hope you’re all well and looking after yourselves as we head into a hectic season.I had my 9 month post-...
29/11/2024

Hi everyone 👋 I hope you’re all well and looking after yourselves as we head into a hectic season.

I had my 9 month post-treatment sigmoidscope on Wednesday and I’m happy to say that there continues to be no sign of recurrence at the primary tumor site ☺️😮‍💨 My radiation proctitis has also improved, which was an added bonus.

My next lot of PET / MRI scans will be in 3 months, and another scope of course. The all important 1 year post treatment scans 🤞🏽

I saw the excellent doctors and nurses at the hyperbaric oxygen unit at Royal Adelaide 2 weeks ago, I’ll be starting treatment on December 9th. It will be 5 days a week for 8 weeks, and each session is 2 hours. So - a big commitment, but I’ve had some good reports from other cancer buddies that it’s helped them a lot, and I’m ready to give it a go 💪🏽

This is all really great news and I feel very grateful right now. It is also incredibly bittersweet for me. Last Thursday I posted on my personal page that I had reached my one year anniversary of being diagnosed. I thanked a man very very special to me - Russell Conley - my a**l cancer mentor and an incredible human being. Russell was introduced to me by Rare Cancers Australia, they offer a mentor to you when you’re diagnosed with a rare cancer, and Russell became mine.

He was diagnosed with the same cancer 15 months before me, and we became instant friends, forming a wonderful friendship that has been so precious to me this past 12 months. Russell was CEO of a Gastrointestinal Cancer Institute in Australia, and immediately introduced me to his oncology colleagues that gave me advice and suggestions to build an excellent oncology team that also valued research.

Russell and I have had such an incredible 12 months of getting to know each other. Through many phone calls, text messages, photos, videos, and gifts. We have gotten to know all about each others lives and families, while supporting each other through cancer. Russell’s cancer metastasised this year, and it’s been a true privilege for me to return the abundance of support he’s given me.

I haven’t even known how to write this, or even face this yet - but my beautiful friend and mentor peacefully passed away at home last week. I am heartbroken, and I miss him terribly. I can’t even bring myself to write anymore right now, but in time I will because I want as many people as possible, to know what an incredible man he was and all that he did to help others.

Vale Sweet Russell.

Karen xx

Hi everyone 👋🏼 Thank you for all the lovely messages and calls this last month - I know I haven’t responded to a lot of ...
29/10/2024

Hi everyone 👋🏼 Thank you for all the lovely messages and calls this last month - I know I haven’t responded to a lot of them but I’m starting to emerge from my cave now, and am slowly but surely getting back to people.

It’s been a REALLY tough time - a lot of grief and shock to work through. I’ve been in great hands with my oncology psychologist and cancer community, and I’m starting to venture out into the world again.

I saw my surgical oncologist 2 weeks ago, he’s referred me to the Royal Adelaide Hospital for Hyperbaric Oxygen Treatment - to heal all the damage from radiation. I’m not sure when I’ll see them for an assessment but I’ve heard good reports from other anorectal cancer patients about the benefits of the treatment. I’ve posted a link to how it works ☺️

I’ve got my next scope in November, fingers crossed all is still looking good. I’m definitely getting stronger now, my rehab sessions are paying off! I still struggle with fatigue and foggy brain a lot, and my veins are totally crap which is making it more and more difficult to get bloods and cannulas in.

For my next scope we are trialling no anaesthetic.. as it took longer to get a cannula in than it did the actual procedure. I’m nervous about this! But they’re going to try using penthrox instead - otherwise known as the green whistle you have in an ambulance 😃 I’ve been known to say some funny things on penthrox so this should be interesting! 😂

Much love to you all 🌺💕

21/09/2024

A short update and to say thank you to all of you for supporting me and my family, for always reaching out to find out how I’m doing, I appreciate it so very much 🫶

I know I’ve been very quiet here and not contacting people the last few weeks.

The reasons why are multiple, so incredibly difficult and deeply sad, not related to my cancer, and that’s all I’d like to say here right now 🤍 Thank you for your patience and understanding.

I’m still showing a good response to treatment, and working closely with my oncologist and medical team for surveillance and treatment for radiation and chemo damage to my body. I see my oncologist in October for a review and then November will be more checks, bloods, scans etc.

I’m going to rehab 2-3 times a week, and getting stronger each time. I have recently been released from care by the palliative care team - this means I no longer require complex pain management which is amazing.

I 🫶 you all and think of you often.

Karen ###

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