Showing posts with label Cancer. Show all posts
Showing posts with label Cancer. Show all posts

Friday, 22 September 2017

It felt great to be able to share my story on national radio and discuss body image issues and cancer - Lydia Greenwood

Lydia Greenwood

Lydia Greenwood
Body image and cancer are difficult things to talk about at the best of times. In a way, talking about them can make you feel vulnerable and you could even say there is a stigma, especially with body image. Although that is not necessarily what I believe.

So you might be reading this wondering why I agreed to go on national radio with BBC Radio 5 live earlier this summer to talk about my experiences, along with two other young women and a member of staff from The Christie.

I think I did it because since being treated for cancer at The Christie I feel like a different person now, in a good way. I feel stronger, more willing to do adventurous things and I’m more confident in my own body.

There are so many people who helped me on this journey both within The Christie and amongst my friends and family to feel confident in my body, its strength to fight this disease and my changing appearance. From the many doctors and nurses to the body image group run by Anna at The Christie as well as those who helped me with confidence and strategies to cope with the relentless cannulas.

In fact, I was astonished when a magician magically showed up just after an awful experience with a cannula to cheer me up! And one close friend even cut her hair short in solidarity with me as I lost mine. Others supported me through messages of encouragement on Facebook, long phone calls and even hundreds of people praying for me from different church circles that my parents knew. It all gave me the strength to fight my battle.

It was a weird experience to be back in hospital in the Palatine ward, as it felt like my time there had been a lifetime ago.

When I was speaking on the radio, at first, I was a bit nervous. But then it felt great to be able to share my story with potentially millions of people and possibly help others with issues they have about their body image. And it was great to listen to the two other young women taking part, Chelsea and Seren. We were all at different stages of our treatment, and able to give encouragement to each other, and also share some advice we’d learnt along the way!

If you’d like to know more about my story please read on.

I was diagnosed with Acute Lymphoblastic Leukaemia in October 2015. I was 16, had finished high school, and was ready to have a fresh start at a new college.

Before my diagnosis, I was a pretty average teenager with the kind of body image issues that I think a lot of teenagers have.

I was self-conscious about my size and didn’t feel confident to walk around in tight clothing, usually sticking to baggy clothes. I would see girls who were ‘thin’ and wished I could be like them. However, these feelings did improve after I started feeling more comfortable in college.

I’d only managed about a month of college when I started getting weird symptoms, such as extreme fatigue and being breathless when doing hardly anything. I began thinking this wasn’t normal for a teenage girl. I’d also started getting tinnitus (ringing in the ears), half-hour-long nosebleeds and my appetite was depleting.
At one point I wondered if I had cancer. Then told myself not to be stupid because people my age don’t get cancer! When I look back on it now, I think I was only trying to convince myself of that.

I hardly knew anyone, young or old, who’d had cancer. I’d heard of Talia Castellano, a brave young blogger who had fought cancer for six years, but I’d never made the connection that it could happen to me.

Finally, on 23rd October, my mum took me to A&E. We were supposed to visit my family that day, but I was too tired to get up and it took all the energy I had. My skin was also paler than usual. A few days before, my grandma had noticed how tired I looked and suggested it could be anaemia as it runs in the family. We went to the hospital expecting to get iron tablets but left with a cancer diagnosis.

Within 24 hours of my diagnosis, after getting transferred to Oldham hospital for the night, I was transferred to The Christie’s Teenage and Young Adult Unit. It may sound strange, but I was actually glad to be there. It wasn’t like the average hospital. The unit always had stuff going on, from crafts one day to a movie and pizza night the next. For me, it was a break from all the painful experiences with cannulas and the chemo brain.

One thing that stood out to me in the more than seven weeks I spent in hospital was the body image group facilitated by one of the members of staff, Anna. She had invited a small group of young women to come and share our experiences. We sat and talked a lot about cancer diagnosis, how it’s affected everyone and how our body image had been affected. As I looked around the room, I saw hope. There were women who had either completely finished chemotherapy or were outpatients, and that helped give me the strength and perseverance to know that if they can do it, so can I.

In hospital, I didn’t really pay much attention to my body’s state; I was too busy dealing with the intense chemotherapy to notice that I had started to lose a lot of weight due to the effects of treatment and being unable to eat enough. By the end of my time in hospital, I was around 52kg (about eight stone) and could barely walk because of how weak I was.

I found this quite upsetting and unsettling at the time. About three months before, I had wanted to lose weight. But now that I had, I realised it wasn’t all that it seemed and the truth was I looked extremely frail and not how I imagined looking. Ever since then, I’ve promised myself that I would never get to that state again. There’s nothing wrong with having fat and our bodies fight to keep us alive every day so our bodies are ideal just the way they are and not how the media tells us they should be.

In reality, some of the hardest things to do with body image during my treatment haven’t been visible to those around me, and that was the extreme fatigue and chemo brain that I’ve felt throughout treatment. What people see and what you experience are two completely different things. Only you as a person knows how you are feeling and it can be hard for people to empathise with patients who are having treatment.

A patient’s image of what they would like their body to be able to do is often different from the reality. Understanding this can be a great support to someone on this cancer journey.

I want to thank BBC Radio 5 live and The Christie for giving me the opportunity to share this story and to discuss a really important issue facing young women and men who get cancer. I want to thank the many people that have helped and supported me. Lastly, I want to thank anyone who has read this blog!


You can listen to Lydia, Chelsea, Seren and Anna discussing cancer and body image at www.youtube.com/watch?v=Zu3dbQS2oHs

Monday, 11 July 2016

The Big C & Me - Sarah Burton

Sarah Burton, Christie fundraiser

Sarah with husband Shane
Did you watch the recent documentary about cancer on the BBC? It was called ‘The Big C & Me’ and it followed the lives of a number of difference patient with cancer at hospitals throughout the country, including The Christie.

I watched the three programmes with great interest because my husband Shane is a patient at The Christie. 

Just like all the other people featured in The Big C and Me, we had the shock of finding out that Shane had cancer. We really didn’t know what to expect on our first visit and we really didn’t expect to see so many people being treated for cancer. 

Before you go to The Christie you have no idea what to expect. You imagine that it must be a sad and morbid place. If you watched the programme you realise that this is not the case at all. 

The people receiving their chemotherapy, shown having a gossip and supporting each other is very typical of what goes on throughout the hospital. The programme really did show how people diagnosed with cancer just want to be treated normally without people feeling sorry for them.

My husband Shane and I are so grateful for what The Christie have done that we recently set up a fundraising group for The Christie, called the FlatCaps. We’re from Yorkshire - hence the name.


Members of Flatcaps
We are working hard to inspire the members of the group and are doing everything possible to explain how The Christie is such a supportive and caring place. We have asked friends to come with us when Shane has had appointments. This is because it doesn’t matter how much you try to convey how special The Christie is, nobody can really understand or believe it until they have experienced it for themselves. 

So one of the great things about The Big C & Me is that it showed how good The Christie is and it also showed how difficult it is for the family of someone who has cancer. It showed all the emotions that people experience on the cancer rollercoaster. It showed the difficult decisions that have to be made. But most of all it showed people getting on and trying to make the most of life, which is very inspiring.

Having cancer is a bit like being part of an army where everyone is fighting something inside them. Everyone’s battle is different. Everyone is wanting everyone to keep going or win. None of them thinking or believing that they are brave. 

Thank you to the patients who were featured on The Big C & Me and to The Christie and the other hospitals for allowing this programme to be filmed. An especially big thank you to the brave families of Sally and Mark who sadly lost their lives. We need more programmes like The Big C & Me to help quash the taboo that surrounds cancer.  

You can watch the final episode of The Big C & Me and clips from the whole series on BBC iplayer at www.bbc.co.uk/programmes/b07f2gwd.

Monday, 2 November 2015

Helping you to help yourself – our new web project will provide patients with an aid to managing their life with cancer - Dr Michael Leahy

Dr Michael Leahy - Consultant Medical Oncologist

Dr Mike Leahy
I'm delighted to announce the launch of a new project at The Christie which will provide patients who are living with advanced cancer access to a self-guided care plan to run alongside any medical treatment for their cancer.

The inspiration for this project came from the number of patients who kept asking consultants like me if there was anything else they could do to help themselves live with cancer.   

Alongside the modern up-to-date medical therapies being provided at The Christie, many people are interested in what else they can do to help themselves through diet, exercise, complementary therapies, talking therapies, mind and spirit and other activities.

A little research among patients attending one of our clinics demonstrated that many patients are already seeking out information on self-care for themselves, with many trying out something that they feel will be of benefit - from dietary changes to counselling or aromatherapy. However, our patients have told us that they feel there is more we could do in terms of giving advice and helping them make wise choices amidst the many therapies or products on offer that make claims of benefit.

It may surprise readers to know that there is increasing research showing that a well-rounded health and wellbeing programme focussing on improving and enhancing general health can have a significant impact, not only on quality of life, but also on survival. It seemed to us that there were things that people were missing out on that they could do to help themselves and we decided that, as their oncology team, we ought to be giving this more attention.

We applied for funding from the Manchester Cancer and Macmillan Innovation Fund for a one year project to develop a programme for patients with advanced stage cancer.  We were successful in our application and our project manager Liz Islam, started work in September.  We now have a year to construct a pilot programme, develop an interactive website and evaluate it with a group of patients. The working title for this project is PlanBe

The reason behind the name is that getting cancer is no-one's Plan A, but this programme is much more than a second thought - it is about being as well as you can for as long as you can; about being more in control of what is happening to you; about being more in the moment; about the idea of being responsible for your wellbeing.

We are really interested in people's comments and suggestions to help us in this project. What other activities do you participate in besides your cancer treatment? What have you found that has been really helpful, or not so helpful?  And, if you are living with advanced cancer, what help and advice about your PlanBe would you find useful? We'd love to hear from you about this project and what you think, so please email the project team at PlanBe@christie.nhs.uk