Breast cancer is a disease usually associated with women aged over 50. But alarming new figures show cases are rising among younger women ā the number of diagnoses in those under 50 increased by 1.4 per cent a year between 2012 and 2022, compared to 1 per cent for older women, according to the Breast Cancer Research Foundation ā and itās not clear why.
Here three mothers, whoāve not had the disease, and their daughters, all recently diagnosed, talk frankly about their life-changing experience and its effect on their relationshipā¦
Sue Hall, 68, a former primary school teacher, lives near Leeds, with husband David, 76, a retired chartered surveyor. They have a son and a daughter, Becky, 34, who was diagnosed with incurable breast cancer last year
When Becky and Mark [her husband] said they needed to talk to us, I thought she was going to announce she was pregnant. It never occurred to me that she was going to say she had breast cancer.
Much as I wanted to break down at the news, I couldnāt: my daughter needed us both to be strong.
Until that point, weād led a rather charmed life. Two wonderful children, private education, lovely holidays, no major health worries. And then, crash: and you realise money means nothing.
We bought a lot of books on cancer but David took it upon himself to do the reading as I couldnāt face it.
Becky insisted that David and I go on our planned holiday to France a few weeks later. But it was there that we got the devastating news the cancer had actually spread to her bones.
We didnāt know what this meant at first ā that it was incurable. Learning this put a totally different perspective on things. Suddenly, David and I werenāt thinking: āWeāll get through the next year and everything will be fineā ā it was: āThis is forever. We donāt know how long we have left with her.ā
We found our different ways to cope. David is good at research and Mark, who sheās been with for 14 years [married for four] helps practically, attending appointments and cooking all Beckyās meals from scratch.
The best thing I can do for Becky (and myself) is to distract her: there are often times where Iāll say: āCome on, letās go for a coffeeā to keep her occupied.
I have a lot of guilt about her diagnosis. Iāve lain awake at night wondering if itās something genetic in me or David thatās caused this.
My maternal grandmother died of breast cancer and my paternal grandmother had breast cancer in her 70s, but died years later of another cancer.
Davidās mother also had breast cancer, but any genetic test for Becky has come back negative. I also find myself wondering ā did I give her a healthy enough diet as a child?
Both David and Iāve said that if we could have the cancer for her, we would. I think any parent would. Even my 92-year-old mum has said the same. It breaks my heart that Becky now canāt give birth to a baby. Her cancer is driven by oestrogen and her treatment means sheās going through menopause.
Surrogacy is a possibility but sheās at that stage of life where lots of friends are having children and that must be very difficult for her.
Iām lucky because I have people I can confide in when Iām feeling a little tearful. My mum lived through the war so sheās so stoic. My girlfriends also give me perspective ā no oneās life is perfect, we all have things going on in the background.
So even though I wake up every day and the first thing to hit me is this nightmare, Iām able to get on with the day. And we all take our strength from Becky, whose attitude has been remarkable.
She is pro-active, sticking to a healthy diet and exercise and keeping on top of new research, treatments and trials.
Sheās now on a variety of drugs including injections that shut off her ovaries and another drug ā an oral CDK4/6 inhibitor that helps stop cancer cells multiplying.
Itās a lot for her to cope with but she doesnāt complain ā she just gets on with it.
Becky and I have always been close but weāre closer than ever now. But living with the uncertainty is the hardest ā life isnāt normal, itās always there at the back of all of our minds.
One hope we all live with is that a new ground-breaking trial will be offered and as long as we have hope, we donāt dwell too much on what lies ahead.
Becky Craven, 34, a teacher, lives in Horsforth, West Yorkshire, with husband Mark, 34, an IT developer
We were trying for a baby when I found a lump in my right breast ā I thought it might be something to do with pregnancy hormones.
The GP referred me for scans and when I was having an ultrasound I felt the āvibeā in the room shift ā and I was told later that day they were 90 per cent sure it was cancer.
I couldnāt believe it: I remember saying: āSo what do I do with that?ā
Mark came to meet me and telling him was so sad. I rang my best friend ā a doctor ā and had a bit of a cry.
But I had a wedding to go to the next afternoon and decided I wouldnāt tell my parents until after that, to give them the news in person ā I thought there would be some big emotional breakdown, but Mum and Dad were stronger than I anticipated.
I had a mastectomy a month after finding the lump and then the following month, I underwent egg collection because one day weād like to have kids.
We ended up with nine embryos, which was a good amount.
But on the same day, I got a call to say the cancer was in my bones. I had no idea what this meant but thoughts such as recording my own eulogy were popping into my head.
If anything, I felt grateful that if ābad newsā was going to hit our family then it was my bad news rather than something awful happening to one of them.
I only discovered that cancer in the bones is incurable when looking at a leaflet in a waiting room. I remember then asking a really silly question ā do I have 80 years left to live? ā which would make me over 110 when I died.
The doctor pulled a face and asked if I wanted a prognosis. I said no. I know that the average is two years on the treatment Iām now on, but Iām hoping for at least five and then I can go on to a new treatment and hope to have ten or more years after that.
Telling my parents that my cancer was incurable was really difficult ā I was saying things like there was no chemo that could treat my cancer and it took my parents a while to understand and it taught me that the more I try to hide scarier things, the more difficult it is.
Mum and I have always been close and Iām seeing her more than ever now that Iāve stopped working ā every few days.
My dad is super positive and really into all the clinical detail, which allows me to leave all the research to him and my brother.
Iām aware Mum feels guilty, and she shouldnāt. Itās a funny one, because Iām constantly trying to manage my own feelings but at the same time, Iām aware my loved ones are also going through their own cancer journey.
For now, weāre all moving forward optimistically.
Sonia Jacomb, 72, a retired admin assistant, lives in Woodbridge, Suffolk. She has three sons and a daughter, Jo, 43, who was diagnosed with breast cancer in 2022
Until the day Jo told me she had cancer, Iād had no experience of it ā no one had had it in our family, nor any of my friends.
I knew Jo was going for some kind of breast screening and afterwards, she rang and said: āItās cancer.ā Shock hits you first. Then incomprehension. She was only 41. Iād heard that younger women were being diagnosed but I couldnāt understand why her ā sheās a fit and healthy young woman.
She had a lumpectomy to remove the fairly small lump from her left breast, then chemo: two months into treatment, she split up with her partner ā he hadnāt been coping with her illness ā and I knew sheād need me even more.
While Iād say weāre close, sheās quite private and I understood that she wouldnāt want me to talk too much about it unless she wanted to talk herself.
When Joās ill, she doesnāt want people around her ā sheās always been like that ā so although sheād been living with me (along with one of her brothers and the dog), I knew she needed somewhere quiet to isolate after treatment so I found an Airbnb nearby.
I accompanied her to chemo ā it was very difficult seeing her suffering with the side-effects.
But probably the most difficult part for me was seeing her after she made the decision to shave off her hair.
I understood it, but seeing her bald for the first time was a shock.
While we didnāt really speak much about her actual illness, there were times when I sobbed my heart out in private.
She kept her emotions hidden, too, although just occasionally she would have a cry. During one very difficult time towards the end of her treatment I remember her saying she felt she couldnāt go on. That was really hard to hear.
I did my best to find some counselling for her, but the charity I spoke to was useless. But she came and stayed with me, talked a little and she got through it.
Jo finished her treatment last year, but of course Iām fearful that the cancer might come back.
Every time her annual check comes round, I have a feeling of dread.
I donāt see her as often now ā sheās building a new life for herself with her new partner and Iām really pleased for her. But although sheās moved away, I think weāre closer. Whenever I see her and we say goodbye, I always give her a hug now. Something we rarely did before.
Jo Tooke, 43, a civil servant, lives in Suffolk with partner Martyn, 49, who works in shipping. She has a daughter, 23, and two granddaughters, aged four and five
Around my 41st birthday I started experiencing pain in my left breast when I went cold-water swimming ā something I did regularly.
After a few weeks I went to my GP, who thought the area was more dense and that it could be an infected gland ā but sent me for a mammogram and ultrasound.
This showed what they thought was a cyst, however when they inserted the needle to take a biopsy I could tell the lump was hard. And Iād been a student nurse so knew this could be cancer. A week later it was confirmed as oestrogen-positive cancer.
Psychologically Iād prepared myself but it was still a shock. Thankfully they had caught it early and I hoped I could simply have a lumpectomy and get on with my life, protecting those I loved ā my daughter and my mum ā from finding out, because I knew theyād be distressed.
But the surgery was just before Christmas and as it would affect our plans, I had to tell them. Naturally, my daughter was upset and shocked. I donāt actually recall how I told Mum or how she reacted, itās all a blur.
I didnāt want to confide emotionally in her because we donāt have that kind of relationship ā weāre close and sheās very supportive but sheās emotional: I knew sheād get upset and frustrated and that would make my life difficult.
However, she was brilliant at organising things practically, such as helping me to find somewhere to recover away from everyone else. Iāve spoken to other breast cancer patients who moved in with their mums while going through treatment, but I hated the thought of being nursed by anyone.
I needed to protect Mum and my daughter from seeing me during the worst stages of chemo ā it was also a form of self-protection: I wanted to deal with this on my own so, when it was all over, I could forget about it.
Today, weāre still close but in a different way: Iāve always either lived with Mum or very close by, but Iāve just bought a house about 30 minutesā drive away.
I feel itās good for both of us. I know sheād be there for me no matter what, but itās time for us both to build our lives more independently so we can all move on from the cancer.
Julie Baxter, 60, who works in the care sector, lives in south-east London, with her partner Darren, 56, who works in the food industry. She has two daughters, Natalia, 38 and Becky, 32. Natalia was diagnosed with breast cancer in June 2023
No one needed to say the actual words when I found out Natalia had breast cancer. Sheād told me sheād had a biopsy and that the specialist had mentioned āirregular edgesā of the lump ā when Iād Googled it, I had a sinking feeling.
When Darren returned home from work early on the day of Nataliaās results I immediately suspected something was wrong.
Natalia had clearly wanted him to break the news to me gently. But when I saw his face I knew without him saying a word. He opened his arms out, but I ran underneath them, up the road and to my parentsā house. You never know how youāre going to react when youāre in shock and I needed my own mum in that moment.
My mum, who is nearly 80, was incredibly upset too. Natalia was so young, we felt if anyone was going to get it, it should have been one of the older generation ā she didnāt drink, smoke, sheās just so healthy and thereās no breast cancer in the family.
I have so much mum guilt. I keep remembering a time when I left her out in the garden as a baby and she got sunburnt. Or what about the talcum powder I used on her? My daughters tell me to stop blaming myself, but thatās what mums do.
Itās been horrible watching Natalia go through so many procedures ā a double mastectomy, a reconstruction and then another operation to correct her reconstruction five weeks ago. Sheās had radiotherapy too and been so brave.
I have helped out in practical ways ā looking after her children, cleaning the house, making the beds.
Iām there all the time now, much more so than before. But I donāt bring up the subject of her illness unless she wants to talk about it.
At the beginning, even saying: āCan I do anything to help?ā made her burst into tears so I learned quickly to just get on with things and if she wanted to confide in me, I was always there.
Sometimes itās hard for me ā sheās so independent and wonāt open up more to me ā but she doesnāt like people seeing her get emotional.
Now, coming out of the other side, I can see a worry in her that wasnāt there before. Sheās still a happy-go-lucky person, but I sense that the thought of her cancer is playing at the back of her mind all the time ā itās there for me, too.
Natalia Leyser, 38, is a co-director of a family company, with husband James, 39, and lives in south-east London with their children, aged eight and four
In the summer of 2023 I discovered a lump just below my armpit ā the GP wasnāt too worried as I had no family history but she referred me to a consultant, who also wasnāt too worried given my age.
A mammogram didnāt pick anything up, so I had an ultrasound scan and a biopsy. A week later, I found out I had Grade 2 oestrogen-positive breast cancer. The first reaction was panic and thoughts of death. Fleetingly, I remember thinking I wanted people to wear white at my funeral.
My main priority is to be around for as long as possible for my children, so when a mastectomy was mentioned I said I wanted both breasts removed.
When Mum found out, she went into panic mode: she kept asking why not her, why me, and saying silly things like it was her fault.
My mother-in-law Sara is less emotional and so she would come to appointments with me ā and take everything in when I was overwhelmed.
But Mumās been a brilliant help with the children and around the house ā she knows how much I love having clean sheets on the bed.
After the surgery I needed radiotherapy and felt very flat emotionally ā but that finished in November 2023 (though Iām now taking tamoxifen).
Mum, my sister and I have always been close but I confide in Becky more now, to protect Mum and myself from too much emotion. But Mumās been amazing.
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