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We know that having cancer at a young age can be isolating and lonely - and we’re working to change that. We provide support and activities both online and in person.

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Information and Resources

Information on topics that we know are important to young adults living with a cancer diagnosis. We also share some of our favourite organisations. 

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All about Shine

Shine is working to create a community of young adults with cancer. All of our work is designed to bring people closer together and ensure that they get the support the need. 

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  • Our vision is that every adult in the UK living with cancer in their 20s, 30s or 40s can access the help and support that they need in a way that suits their lifestyle, and that they are a part of a confident, supportive and empowered community of young adults living with cancer.
  • Our mission is to provide tailored information and peer support for anyone in their 20s, 30s or 40s diagnosed with any cancer. We do this through a range of activities including lunches and drinks evenings, beach walks, multi-day getaways, workshops, online networking, and mentoring.

Find out more about Shine on our about page

 

Events in your area
Want to meet up with other younger adults facing cancer?

Our Networks are not typical support groups: we don’t meet in hospitals, there is no set agenda, and we never sit around in a circle ‘sharing’! Our Shine Networks meet up on a regular basis for drinks, dinner, beach walks, bowling and more. And as a bonus, Shine always buys the first round!

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We are really grateful to all of these organisations who support Shine in a variety of ways. From funding to staff time and specialist advice, we couldn't do what we do without them!

Raelene Salter, uterine stromal sarcoma

 

When were you diagnosed and what with?

In April 2005 at 23 I was diagnosed with a uterine stromal sarcoma. Nearly ten years later, in October 2014 I had another tumour of exactly the same type of cancer in my abdominal muscle.

How did you find out you had cancer?

The first time after surgery to remove what my doctor had hoped was a fibroid. The second time I felt the tumour under my skin in my abdomen and after surgery testing confirmed that it was cancer.

What did you think and feel when you were diagnosed?

The first time: shocked and fearful. I was only 23 and really healthy with no history of cancer in my family. I was the third and youngest woman in South Africa to be diagnosed with this type of cancer. Looking back, I think I also felt targeted, by whom who knows, but I felt it. The second time: shocked and fearful! I was planning on having a “10 years cancer-free” party! I spent so long focused on being well that I didn’t allow the possibility of the cancer coming back to enter my mind. Then BOOM! I actually had a panic attack when my consultant told me that he thought that the growth was highly likely to be cancerous and that I needed surgery.

How did the people around you react?

The first time: my family and my boyfriend (now my husband) were incredibly supportive and kind. Friends were a real mixed bag: some were great but most were awful – they either avoided me or pretended nothing had happened. I think that at that age most people just don’t have the life skills to deal with this kind of trauma.

The second time: my husband was amazing. Friends were supportive and lovely – I’d learnt my lesson about who you let into your life. My family were great but it was entirely different because they were all in South Africa and we were in the UK. I think I managed them and their fears much more than the first time!

What treatment did you have?

The first time I had a hysterectomy. The second time was surgery to remove the tumour and a chunk of muscle around it.

How did you feel through treatment?

The surgery was very quick and I recovered quickly both times. In both cases I was relieved to have the tumours out of my body!

What happened after treatment finished?

The physical healing after surgery was the easy part – the emotional and mental recovery has been a lot longer! Considering that my physical recovery was so quick most people around me thought that I was, or should be, “back to normal” which also made it difficult. It was tough dealing with the consequences of not being able to carry a baby and the effect of that on my relationships with my husband, parents, siblings, in-laws and friends. Even strangers have an opinion on my ability to procreate! I’ve had to learn to deal with anxiety and panic attacks because suddenly anything out of the ordinary felt like it could be something killer – e.g. I truly thought that I was having a heart attack when it was indigestion.  Suddenly all things bad and unlikely were possible. My husband and I lost a lot of friends. I had just started working at a large audit firm in Johannesburg and it was incredibly isolating being in a group of my peers who I no longer felt I had anything in common with as my whole life perspective had changed.

How did you get involved with Shine?

After the second tumour and I had DVT scare and I went to the Mulberry Centre at West Middlesex hospital and a lovely woman there gave me a Shine pamphlet so I went along to a drinks evening.

What difference has Shine made to you?

Shine has changed my life. I have met so many wonderful people and have made incredible friends. I am much more confident now – previously I was always weary of talking about my health and cancer experience to avoid judgement… But now I truly don’t care what other people think about me. I love myself as I am.

How do you feel now about your experiences?

They will always be tough experiences. But I am content to be where I am now.

If you could give one piece of advice to yourself before what would it be?

Comparison is the thief of joy.