Diagnosed with Breast Cancer at 41

Breast Cancer Stage 2A diagnosed at 41

I thought I would write down my experience with breast cancer because when I was first diagnosed at 41 I used to spend hours on the computer trying to find other people with similar situations as myself and I wanted to see what their story was and how they coped with it all.

So I’m hoping, in some small way, you might feel better after reading this or have someone in your life who you are supporting and this will make you feel more confident about what is going to happen with them.

DISCLAIMER: This is very important, I AM NOT A MEDICAL DOCTOR AND I HAVE NO MEDICAL TRAINING, please refer to a professional medical consultant for medical advice. This is merely my experience of cancer and my own choices and does not attempt to influence you in any way when it comes to your own decisions.

My Breast Cancer Stats

  • 41 years old at diagnosis
  • Stage IIA
  • Node Negative
  • 2.4 cm tumor
  • ER + (A LOT!) and PR + (but then was – on the oncotype analysis)
  • Grade 2
  • Oncotype Score 26

Worrying About Getting Cancer

Let’s go back a bit. True confession, I had always worried I would get cancer.

Which I know sounds a little strange but this is what I used to worry about.

We had immigrated to the US when my kids were quite young and my main concern would be that I would not be able to take care of my children because my husband worked long hours. I also worried endlessly about the costs.

However, I used to remind myself that I had breast fed my children for 3 years in total, I had no history of breast cancer and my Dr had once remarked that I would never get it.

Well that turned out to be very much NOT TRUE!!!!

Finding My Lump

One day I was in the bath and my hand brushed against a “lump” that felt hard, but smooth. My heart sank and I instantly “knew” it wasn’t good. My immediate thought, was great, I knew it!

As if somehow being right was a good thing, cue eye roll.

I made an appointment to go to the Dr, but to be honest, it was not straight away. I think I was hoping that it might just go away, like a cyst. Eventually after a few weeks I went to the Dr and he examined my breasts and he too thought it was a cyst and that if it was still there after I came back from my trip to Africa, I should go and get a mammogram.

Which in hindsight, was wrong. I should have gone and gotten it checked out straightaway. When I got back it was still there and so I went and had a mammogram.

I had a big “X” marks the spot on my breast and yet, still, they only called me back 48 hours later, to the point that I was like, oh well, this is clearly not an emergency. My thought (and it is merely my thought process) is that it was actually difficult to find because I had very dense breasts.

The Nurse from the Drs office called me and said I needed to go in for an ultrasound. She sounded terrible when she called and I had done some interim research and so I asked her what the Bi-Rads score was (this is a score from 1 to 5 that is assigned by the radiologist, 5 being cancer) and she said it was a 5 but that it still needed to be confirmed. But it was the highest Bi-Rads score you can get so in my heart I knew.

That is truly the hardest part, when you know in your heart you have cancer and you don’t know the severity of it. I was such a mess, I could not think straight but I didn’t want to alarm my kids who were 9 and 7 at the time.

So I tried my hardest to be brave and focus on just getting through every day. I used to sit in my closet and cry!

And that’s when I used to google and google ALL the stats and all the stories, desperate to find out something about what I would be experiencing.

So that’s why, 6 years on I have written a summary of what went on and show a pic of my scar (because that was the one thing I wanted to see when I was googling!)

At the ultrasound you could clearly see a spiky mass in my breast (most benign tumors are round and smooth shaped). I didn’t even have to wait as I knew already what was on the cards.

A punch needle biopsy confirmed it all. It was cancer.

And this is where you have to trust whatever it is you do, your own intuition, your spirituality, the Universe, whatever it is that you hold on to in really desperate times, this is when you get a grip on it.


Now, one of the things during this whole process, was the fact that I kept on getting “signs”.

Which is so “woo-woo” right?!

However, I believe we choose to see “signs” and I want to encourage you to look out for them too. I wrote an article about “Looking for the Beauty in Life” which explains this a little more.

Sign No.1

I was given a list of Drs to call. I could not get through to the first Dr but managed to connect with the next Surgeon on the list.

She was my saving grace. She not only managed to be quite blase about it all (you’ll be fine she kept on telling me) but she also told me which Oncologist to see and she turned out to be the most wonderful person.

She lived in my neighborhood, her kids were at the same school as mine, she was the same age as me and her husband had recently been treated for cancer.

Sign No.1 was getting the right people in my life.

Tip: Embrace all the amazing medical professionals around you, feel blessed by their knowledge and commitment to saving your life.

Sign No.2

I picked up my Bible, closed my eyes and prayed for a verse that would help me. I can’t remember which one it was exactly but it was about God being there as you went up the mountain and in that moment, I felt surreally calm.

Tip: Find your peace, search for it and when you find it,  hold fast to it.

Sign No.3

The other thing, and this is very difficult to write and will probably be difficult to read, is that I became very calm about my children. It suddenly occurred to me that possibly my greatest gift in life was to be able to give birth to them.

That they would make their way in the world and I was being selfish by thinking that I was the only person that would influence them or encourage them, or even love them.

Does that make sense? The fact that I could give them life was my role and that I didn’t necessarily have to feel guilty or even angry that I might not be able to see it through.

Tip: Let go of your guilt, it isn’t your fault that you have cancer, you are not letting anyone down.

Sign No.4

I called my sister-in-law to tell her that I had been diagnosed and she said “I know”! What??!! She had had a dream the night before about feeling a lump and having it removed, intact, like a pea.

That’s what I wanted to hear, just like a pea, removed intact.

I literally visualized that before I went into surgery.

Tip: Visualize yourself with no cancer, either through surgery or through treatment. 

Sign No.5

The final sign, my dearest friend who I had grown up with in South Africa, was diagnosed a month before me and she spent time Skyping with me going over what it all felt like, what to expect and so many useful tips.

She even showed me her head without hair and so I felt so prepared and she looked healthy and well and again, I visualized myself looking like her.

Tip: Know that there are SO, SO many of us in the same situation, you are not alone in any shape or form. You are going to be amazed at how many people have been on the same journey as you.


Again, please note, these are my personal treatment options and they are not to be perceved as medical advice

My surgeon started to discuss options for surgery. It was quite interesting in that it wasn’t this immediate, get into surgery NOW type of thing, I actually was only scheduled a few weeks out, no-one was rushing.

One of the things the surgeon suggested was to have a more detailed look at my breasts, via a mammogram with radiation to see if it was in both breasts.

If it was and also if I was a carrier of the BRACA gene then I would opt for a mastectomy otherwise she suggested a lumpectomy.

When I went to have the mammogram the lady doing it said, ‘I am a 10 year survivor, would you like to see my scar’? OF COURSE I BLOODY WELL DID!!!

The thing is, whatever your “scar” looks like, whatever procedure you end up doing, it’s all really, really beautiful, because you are.

Scars are merely road maps to life. We should share them like badges of honor.

Please ignore my old lady hands, sigh……

Lumpectomy Scar Stage 2A Breast Cancer

I also opted for an Oncotype test and my results came back as a 26 which was quite high and it was suggested I had chemo as an “insurance” policy.

I was totally fine with that and had a port inserted. It’s super easy, quick day surgery and then they don’t have to try and find your veins, it’s nice for drawing blood too.

Since I was BRACA Neg and there was no other evidence of cancer in my other breast I went in and had surgery on the 1st March and my surgeon came in and said she had “got it all” which was all I needed to hear in that moment.

And I hung on to that, so fiercely and visualized her cutting out the lump and it being gone (as per my sis-in-laws dream).

I also had a Sentinel Node biopsy and she ended up taking out 4 nodes as they were matted together.

So in my head, and it is still in my head every day, is that it is gone and was gone on that day.

I went home in the afternoon.


Yes, I did actually just embrace the fact that I had to have chemo. I guess it was because I saw my friend handling it so well that I knew that I could too.

The first chemo session is so odd because you feel so healthy and well and not ill at all. I went in and was pleasantly surprised at how “festive” it can be and how friendly everyone was. I had my husband and a really good friend with me and she had bought blankets and food which is ESSENTIAL, note to self, it’s freezing and you will be so hungry.

I did have a reaction to one of the drugs, which is not the greatest feeling, but they just dripped it in slower and I was fine. You watch movies or sleep, it’s kind of relaxing (bearing in mind I had little kids so this was like enforced relaxation time!)

I was working part time, so I did feel in the last two rounds (I had four in total) that it took me longer to recover from them. I would take a week off and then work for two weeks.

The worst part is your tastebuds change so much. I developed a craving for beer which I have always hated! Nothing really tastes that good, popsicles are useful to have around.


It happens, shave it off, get a wig and it will start to grow back before the end of your last chemo. I thought it would be the worst thing in the world, IT WAS NOT AT ALL!

I had a wig called “Barbara”, my kids named it. I didn’t actually wear it that often, I preferred scarves and buffs (which are amazing).

One of the beautiful things that came out of wearing a headscarf was having other women come up to me ALL THE TIME and say, “oh that was me 10 years ago” etc. There were so many lovely stories.

There was also someone that said “do you wear head coverings because you can’t be bothered to do your hair”. Oh it was so hilarious when I said “No, I’m having treatment for cancer”, her face, priceless!


People will ask you how they can help.

It is such a difficult question to answer because you don’t always know what help you will need.

But accept it all, it’s truly such a gift and it will make other people feel so good about themselves too.

I accepted meal trains (best thing ever!). I had help with my kids, they loved all the extra attention, I appreciated every kind word and note.

Even though I’ve just said “accept all the help”, one of the hardest decisions I made was to send my parents home before my chemo started. They had come out to stay for a few weeks whilst I prepared.

The main reason I did that was that I didn’t want to look “sick” in front of the kids, because in reality I wasn’t actually “ill”.

It was so tough because my Mom is the most amazing “Nurse” but I’m glad I did that because I made myself get up every morning and see them off to school and made sure I was up in the afternoon to see them too.

However, that was my decision and if you need extra help, take it all!!

You’ve Got This!

You’ve got this. I am 6 years out. My Aunt is 30 years out, my cousin is 20+ years out, my friend is 6 years out, Kylie Minogue is at least 10 years out. (I used to google lists of long term survivors)

I can’t say the worry gets any less but then I worried so much BEFORE I got cancer that it really doesn’t make any difference in my life.

The best thing though, is that I faced my worst fears and came out the other side. My attitude towards life is so different now!

I’m still a pretty anxious person but that is just who I am, but I certainly don’t tolerate people and situations that I don’t feel like are enhancing my life.

I honestly see this as a “blip” in my life. Was it great, nope, not particularly. Was it the worst thing ever, no.

It was a “tunnel moment” when you are in the dark for while and then you emerge.

Into the light, into the future, armed with power, and fortitude and a blazingly strong spirit.

I hope in some small way, this might make you feel better if you are going through this, or if you are supporting someone else you have a better idea of what to expect.

Please contact me if you have any questions (non-medical related) and I will be happy to answer them if I can.

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Diagnosed with Breast Cancer at 41


  1. Gill
    / 5:25 pm

    You are an inspiration to others going through the same thing. Can’t believe 6 years have passed since your diagnosis. Well done for keeping it together for the kids. Think this too makes you stronger. Sometimes it is too easy to give up and let self pity take over. Not an easy time of your life, but you got through and come out the other end shining.

    • Jen
      / 11:39 pm

      Thank you so much for your beautiful comments. I am so grateful for your love and support in all aspects of my life. xx

  2. Gina
    / 5:23 am

    Loved your story! I’m 37 and recently diagnosed. I’m going on treatment number 2 this week and needed to read this as I just shaved my head and it really isn’t as bad as I thought! You’re so positive about your situation and its a breath of fresh air. It’s easy to get down and out when going through this all and I am trying to stay away those stories and blogs as I don’t want that in my life. This really does change a person! Thanks for sharing your story and I wish you all the best

    • Jen
      / 9:35 pm

      You have completely made my day! Thank you for your wonderful comments and welcome to the positive cancer club! The beauty of it is that you now realize what a strong person you are and that is going to have the most incredible impact on the rest of your (very long and successful) life. All the best too and I would love it if you stayed in touch. Jen xx

  3. Marcella
    / 1:27 am

    Thank you! Reading this has been very helpful. I was diagnosed in March. Shocked to say the least. My Radiologist and surgeon are great. Both have said that my yearly mammograms were the key to finding this one. It’s the only way it would have been found! No finding a lump or anything else unusual. I had surgery in April and began radiation late May through June. My skin is recovering, the fatigue is terrible, but I never stopped , life continues. My family, friends and my faith have been a saving grace. I am a survivor in many ways. 17 years ago, I suffered a perforated colon due to Ulcerative colitis , a duodenal ulcer bleed out and kept me hospitalized for 3 months. Several more surgeries over the following 13 months, all the while, my 3 children growing up without me. They thrived and are all living very happy lives . Shortly after all this, I was diagnosed with Rheumatoid arthritis. So, my life medical journey continues. I will continue to smile and get through this journey with faith and grace and plenty of support like your story and so many others. I do wear my scars with honor! Thank you!

    • Jen
      / 10:06 pm

      Wow! You are an incredible woman! Your story is so inspiring, thank you so much for sharing. The more we tell our stories of how we get through things, the stronger this community becomes, you are the light xx

  4. Terri Van Dusen
    / 7:02 pm

    Our stories are very similar, but I’m 55 so I have 2 adult children and one 16year old son at home. I agree that sharing our journey is important. I want to encourage others. The unknown is the worst. Thank you for sharing your story. I had chemo, then surgery in January of 2019 and radiation that ended in April. I feel I’m getting stronger every day, and I want to get started on an exercise routine. I’m going to start with some yoga and would like to walk. We have a gorgeous well know Bidwell Park here in Chico, CA. I’ve been struggling with the lingering effects mostly from radiation and Lymphedema in my breast. I’ve been going through PT trying to overcome the pain so I can get started on exercising and living a healthier lifestyle. You encourage me. Thank you.

    • Jen
      / 4:56 pm

      Thank you for being part of the GwG community and I am so incredibly glad you feel encouraged. You are brave and strong and I am 100% supporting your new healthy lifestyle, we are all in this together. Much love x

  5. Nicole
    / 1:06 am

    Beautiful tips! I will keep them in mind, diagnosed Dec 11, 2019 at 31 years old invasive ductal carcinoma, estrogen and progesterone positive, brca2 positive, awaiting bilateral mastectomy with diep reconstruction. I know I have a long haul ahead of me but so many lovely blogs and real life survivors to look to for advice! Thank you!

    • Jen
      / 1:39 pm

      Nicole you are amazing! Thank you for sharing your story with the GwG community. I’m sure you’ve already had your first surgery and are well on your way to recovery. Thinking of you my fellow warrior and know you are in the best hands. Jen xx

  6. Judith
    / 2:33 am

    Wow, thank you. I needed to read something like this. I am 62 and still work, still going strong, so I thought. I was just diagnosed with birad4 8mm size cancerous tumour in my left breast. Having my surgery December 15, 2020. Honestly have been going along fine. Not freaking myself out, however time closing in now and yes, I am afraid to hear it moved to my lymph nodes. I pray not. I do not know yet what the plans will be after the surgery , chemo, radiation or both. Reading your story has inspired me to stay positive and fight. Thank you.

    • Jen
      / 7:59 pm

      Hi Judith, thank you so much for your lovely comment, I’m so glad you felt inspired by reading my story. I am just checking in with you, I hope your surgery went well, I would love to know how you are doing. And Happy New Year, it can only be better I think. Much love xx

  7. Stefani
    / 2:24 pm

    I am 41 and I’m in the waiting for a biopsy stage. I’ve never been so anxious in my life. My first mammogram showed a mass and upon further ultrasound I was given a bi rad score of 4c. No family history. Lymph nodes clear. Less than 1cm. I see those all as positive signs, but my mind has gone down the rabbit hole. This has given me some peace and hope. Thank you!

    • Jen
      / 8:08 pm

      I remember that feeling like it was yesterday. But it wasn’t and in 8 years time you will be chatting to someone going through the same thing and you will say that too, I remember it so well. The waiting stage is honestly the worst, when you are googling everything and trying to find stats etc (bear in mind the stats are created over many years and don’t always factor in the vast array of new treatments that are developed). I know it’s not easy but try and keep as busy as possible, you will only know when you know. And from that point onwards it’s all action and every day of “action” be it surgery etc is a step towards healing. And then you will be on the other side, trust me it really goes by so quickly. I would love to know how you are getting on, please don’t hesitate to reach out to me if you ever wanted to chat. I know you’ve got this. Much love xx

  8. Lisa
    / 5:25 pm

    Thank you so much for sharing your experience. I turned 40 and went in for my first mammogram. Well, stage 2 invasive ductile carcinoma was hiding out so good thing I actually followed the recommended screening starting at 40. The MRI shows it being about 2.5 cm at the largest point. I’m negative for all the nasty fast growing proteins but haven’t received my genetics info back yet. As far as I know, breast cancer does not run in my family, but we are a small family so not much data to base it off of. I go in for a lumpectomy tomorrow and while I’ve felt very strong emotionally for the last couple of weeks, today I suddenly felt very sad and scared. Reading others experiences(yours and the comments) has been so encouraging. I keep telling myself that this is just a blip in my life. A difficult time that I’ll get through. Your experience just reiterated that. Once again, thank you for sharing. I’m going to quit googling now.

  9. / 12:49 am

    Thank you for sharing your story. I recognized so many of the feelings you described. I just had bilateral lumpectomies a few days ago. The small malignant tumor in my right breast was found through my annual mammogram and I am so thankful it was caught early. I never even felt it. The subsequent MRI found some “atypical” cells in my left breast, but thankfully a biopsy result determined the left side is not malignant. They still recommended removing those cells. I start radiation next month, after I recover from surgery. I’m nervous about that but thankful it was caught early. My mother is currently fighting Stage 4 BC and doing so well. My dad was diagnosed with Stage 1 BC seven years ago. He’s been cancer free for 6 years. We have all tested negative for BRCA or any other genes associated with BC, so it’s a mystery how we all have it. I draw strength from them and from the stories of so many strong women (and men) who have fought this and come out strong!
    Thank you