A message of hope after breast cancer

On the 27th of November 2024 l was diagnosed with breast cancer, two in my left breast and one lymph node. The two tumours in my breast were small and early, which meant l could have a lumpectomy and would only need radiotherapy. It feels quite strange writing this now, as although it never leaves you, it seems so long ago you sometimes wonder if it really happened.

I’d set myself up for a speedy recovery, as it was early, the tumours were small and l was really fit – the fittest and healthiest l’d been in several years. My recovery took a lot longer than l’d anticipated though. Surgery took place on the 10th of January 2025 and within a week l’d developed two unpleasant conditions – cording and a seroma. The seroma (it’s like a bag of fluid, which collects in the space where surgery took place) caused a lot of discomfort and delayed my radiotherapy. It did go eventually, but has caused scar tissue formation and firmness to the breast. It’s improved by massage, but will always be there to some extent.

Then in early March my boob turned a very bright pink …. on a Sunday morning, of course, which meant a trip to A&E. I was then admitted with a condition called cellulitis and was put on IV antibiotics.

Slowly, as the year went on things did improve, although the fatigue was something else. I didn’t expect to feel so tired all the time. I’d signed up to do a walk on Bannau Brycheiniog (the Brecon Beacons) for Cancer Research UK in July, but sadly that didn’t happen, I now realise how overly ambitious l was in thinking l’d be back to normal in a few months. To be honest, l was very lucky with the cancer in my breast, but the surgery and recovery for the lymph node involvement was debilitating. They took 18 lymph nodes in total. Only one had cancer cells in it, but it does always give you that sinking feeling of has it gone anywhere else? I’m now on letrozole for the next five years, which comes with its own set of ‘fun’ (not fun!) side effects, but it reduces the chance of recurrence, so l’ll stick with it,

I managed to start my Bounce class again in July – although l now only go once a week instead of the three classes l used to do. I’m hoping to go twice a week this year, but will see how things go week by week.

Other positives are l have joined a choir – which l LOVE; l now go to yoga which is amazingly calming and grounding; l’m back volunteering at a lunch club for the elderly on Wednesdays; l meet up regularly with three other volunteers at the lunch club and we go out for coffee, or the theatre; and l meet up monthly for coffee with my Macmillan ‘Hope’ group and Breast Friends group for lunch, or coffee.

Would l have done these things if l hadn’t oot breast cancer? ……. Probably not. So although 2025 could be the year to forget, as cancer is a terrifying, life changing event, for many, many reasons it is the year to remember. I am still here, l am feeling (nearly) like my old self again and l’ve met so many lovely people that l wouldn’t otherwise have met.

I guess what l’m trying to say is be kind to yourself and those around you. Whilst you are the one who has had cancer it affects all those around you who love you and want to care for you. There may be set backs along the way and you may have to manage your expectations and to pace yourself. Yes, sometimes there may be disappointments when you desperately want life to be exactly as it was before, but live in the now and try to make the most of every day. It’s taken getting breast cancer to make me realise this, being the world’s biggest worrier, but some things are out of our control and worrying about them won’t change things.

This time last year l’d just been taken down to surgery for my lumpectomy. In 4 hours time l will have been cancer free for a whole year. I’m feeling really emotional today, but l’m also reflecting on where l am now. lt was a longer journey, to feeling more like myself again, than l was expecting, but l’m getting there now.

So wherever you are in your treatment journey, be it newly diagnosed, waiting for results, having surgery, getting through radiotherapy, or chemotherapy – stay as strong and positive as you can.

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Thank you so much for your honest and encouraging words they really have helped. The future is never more unknown than during cancer therapy. It puts all my past worries well and truly in a very different light. I am determined at the end of this journey, I will come out a more resilient and much happier person. Exactly as you have.
Happy one year cancer free :heart::heart::heart:

Thank you foxgem, this is a journey none of us wanted to be on, but now we are, we need to try and look forward and enjoy each and every day, as best we can. Sending you love and positive energy and thoughts :heart:

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Hi @cat2025

I too was diagnosed with cancer in my left breast in November 2024. The week before you. Ironically, like you, today is another anniversary. Not surgery, but it’s the day I was told it was in my right breast too.

2025 was focussed on getting through treatment. Chemo, targeted therapy then surgery. I have started Letrozole and Zolendronic acid infusions. I’ve two more doses of trastuzumab left. I’ll slope out of the chemo suite when the last dose is given next month.

Like you it seemed insurmountable 14 months ago, but my body which had let me down then got me through it. When I reflect on that time the only part that I have strong memories of are in the diagnostic phase of the process. I suppose because it was shocking and life changing. Once treatment began life took a different rhythm and the only certainty I had were the cancer related appointments. Any other plans were loose in case I had to cancel them. I went where the flow took me, head down, determined, quiet and with as little fuss as possible. Living life slowly was nice. I valued the simplicity and quiet. I can honestly say that the year was not as bad as I had imagined it might be. Unkind at times but doable. Those before me and those on this forum led the way plus I walked the well trodden pathway made by breast cancer experts.

The 17th of January will mark a year since I started treatment and ten years since my lovely Mum died. I will honour the day as it needs marking. I will remember how fortunate I was to have her for 46 years and how grateful I am to be here. x

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Hi Mrs Jelly

Good luck with your last two doses of trastuzumab - you’re nearly there! I think this time of year is always a contemplative one. Everything seems so cold and bleak, but if you look more closely at nature you’ll start to see signs of growth and renewal, as the bulbs begin to push through the soil and the birds begin to collect moss to line their nests. You’re so right about taking things slowly. I’ll be thinking of you on the 17th. Take care xx

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This is such a good post. I have chemo starting February 26 early TNBC, and posts like these really help me step back and stay calm!

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Hello barley1 I’m so glad what l wrote has helped you feel a little calmer. I’ve found talking to others going through cancer diagnoses and treatments so helpful. They truly understand what you’re going through, as they’ve had the same concerns and fears. I wish you the very best for your upcoming chemo and recovery beyond. Stay strong xx

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I hope you had a special day yesterday remembering your mum and how far you’ve come since your treatment started and as you’ve said celebrating that you’re still here xx

Thank you @cat2025

Didn’t meet up with my sister in the end.

The day was alright. I can only smile when I think of my Mum now. She was a very kind and loving soul. Was dealt a really rotten hand when it came to her health. She used to say she must have been really wicked in a previous life! She would have been heartbroken to know what I’ve been dealing with. Like her I found humour in the dark times and have just got on with it as she did because it’s the only way forward.

It’s the 9th anniversary of our Dads death on 5th March. Just 8 months after Mum died he was diagnosed with stage 4 liver cancer. He too had the ‘get on with it’ attitude too and I suspect in his grief he ignored his symptoms. The outcome wouldn’t have changed so I guess he protected us from a longer period of preemptive grief. As a family we spent three consecutive Christmas’s with them at the hospice.

Mum wanted to live till their golden wedding anniversary but missed it by 19 days. Given the date is between their anniversary’s, I’ve suggested to my sister that we go something on that day instead. More fitting and joyous than thinking about them when they left us. This will be their 60th wedding anniversary so I’m planning two days of niceties with my big sister to honour them and us. x

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Thank you @cat2025 I need to read this today. Recovering from surgery to clear margins from my December therapeutic mammoplasty and coming to terms with the consultants brisk comment of my oconotype score meaning oncologist referral post surgery and probably chemo. My “journey to health” as we keep calling it just keeps being extended atm it seems. But one day at a time. Today is a good day.

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Thank you for sharing. It is a difficult and individual road we travel.
I think I’ll always feel a bit different abo to my diagnosis due to what was already happening or happened in my life at the time, and then continued to do so after.
Which doesn’t mean I took my diagnosis lightly. It just felt with everything else that had been before I shrugged my shoulders and went ‘is that it’ right what do we do so I can move on. Then with my brothers death a week after my surgery. All my grief is mixed together. However I continue to find good moments, and an so thankful for the many ways we can be treated individually which is hopeful of the best outcome we can receive.

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Hi thank you! Sorry for the late response! I had the pre assessments today and start Ec on Tuesday. Feeling calm now and just crossing everything it goes ok :slight_smile:

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It’s a shame that everyone at the hospitals are always so busy, that they often forget to show a little more empathy and give a little more time to explain the process. The mental health effects of what you’re going through is often given so little time. I know, at the moment, things are really rubbish for you, but they will get better and although your news wasn’t delivered with much compassion, the good thing is, that your results are constantly being monitored to make sure you get the best treatment plan possible for you. Stay strong. Sending hugs xx

You’re so right hen - you’re clearly a very strong person and have taken a really pragmatic approach to what you’ve been through. It must have been devastating to lose you’re brother so soon after your surgery and dealing with your grief, whilst also coping with your own recovery. I admire your positivity. And yes, we should all be thankful for the approach that is taken to look at our breast cancers individually, to make sure we have the best plan possible for us to beat it xx

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