Emma

Selfie photo of Someone Like Me volunteer Emma. She has long brown hair, is wearing a scarf, and is smiling.
Bio
Emma was shocked when she was diagnosed with DCIS at the age of 41 and needed a mastectomy. Emma found making the decision about what type of reconstruction to have impossible. With the support from someone who had had the same diagnosis, Emma chose to have an immediate implant reconstruction. Now feeling more like herself again, Emma wants to support other by sharing her experience.
Treatments:
  • Mastectomy and reconstruction
Experiences:
  • Children under 10 when diagnosed
  • Younger woman

Hi, I’m Emma. I was 41 when I was diagnosed with DCIS in 2022. I was working full time, juggling 2 young children aged 3 and 6, with a career in Buying. It had been a challenging few months for various reasons, and it felt like our world was imploding. I’d never had any health concerns, and my first thought was “how will I tell the kids that mummy has cancer?”

My diagnosis came as a huge shock. I was at the GP for something totally unrelated and mentioned I thought I had a blocked milk duct. The thought it might have been serious didn’t even cross my mind. The doctor examined me and as a precaution sent me for a routine check up at the Breast Clinic. A week or so later I was told I had DCIS and the only treatment was having a mastectomy.

It took some time to get my head around things – it really was an emotional rollercoaster. I didn’t feel like I met anyone that was like me, and at times I felt isolated and alone. It felt incredibly unfair – I had a non-invasive, low risk cancer, which had been discovered early, yet I had to lose my entire breast. I was tormented by what type of reconstruction to have. The doctors were informative, but reluctant to give their views on what was right for my body.

Finally, I spoke with a friend of a friend who’d had the same diagnosis whilst having young children. She was the first person that I felt really understood. She was pivotal in helping to decide what was the best reconstruction option for me, and gave me confidence that I was not alone, and that everything “would be ok”. She inspired me to volunteer for Someone Like Me.

I had a skin saving left mastectomy with immediate implant reconstruction in October 22, followed by a nipple tattoo a year later. It has taken me a while to feel like myself again, but I got there. I really want to share my own experiences so that others can be as prepared as possible for the journey ahead – you are not alone. Please get in touch emma@breastcancernow.org

“I really want to share my own experiences so that others can be as prepared as possible for the journey ahead”