Tuesday 7 March 2017

Lymphoedema Awareness Week ~ Ruth

Be the first to comment!

Read Ruth's story in the first of our #ResilienceInLymphoedema series to mark Lymphoedema Awareness Week:

I'm Ruth and I was diagnosed with breast cancer in 2004 and again in 2008, with two lots of surgery, chemo and radiotherapy on my left side.

I didn't develop lymphoedema until 5 years later. It started very gradually - the first sign was when I noticed my left arm looked bigger. I was referred to the lymphoedema clinic where I was diagnosed with mild LD and given an arm sleeve.

All remained stable for about 15 months when quite suddenly (and frighteningly) on Christmas Eve of 2014 it started swelling quite badly and aching too. I got an emergency appointment with the LD nurse on 2nd January and entered a period of trying to get it under control. At this point I was very, very miserable - it felt like a deformity and I just wanted to hide! Various treatments were tried including taping and lymphatic drainage massage (which I paid for privately).

Since then it has been up and down. I found that working at the computer made it worse (and probably triggered the sudden worsening) so I try to take regular breaks and stretch my arm. Ready-wrap is wonderful when it flares badly but bulky, so I now rely mainly on my compression sleeve and a morning self-massage routine.

The support group L-W-O has been extremely helpful to me. I have now largely come to terms with it and it is just part of who I am and a small price to pay for still being here. I try to always look after my arm - no lifting and always keeping it well moisturised.

One of the things that I found difficult was other people's reactions to my arm sleeve. I often get asked what I've done to my arm. My answer varies from "don't ask!" to "it's holding my arm on!". I find the black arm sleeve easier to wear (in terms of my vanity) than the beige.

The photos are of me wearing my sleeve (my LD is currently fairly stable). I am lucky that at present my hand is unaffected.


To anyone just starting out on this journey I'd like to say that whilst LD is unlikely to "get better" it is liveable with and can improve.


Monday 6 March 2017

Lymphoedema Awareness Week ~ World Lymphoedema Awareness Day ~ 6 March 2017

Be the first to comment!
Over the next week we'll be sharing the experiences of some amazing women living with lymphoedema, but what exactly is lymphoedema?

Lymphoedema, pronounced lim-fo-dee-ma, is a chronic (long-term) condition that causes swelling and leads to pain and a loss of mobility. It usually affects the arms or legs, although, following breast cancer can affect the breast and trunk.

About 2 out of 10 people (20%) with breast cancer develop lymphoedema: http://www.cancerresearchuk.org/about-cancer/type/breast-cancer/treatment/lymphoedema-after-breast-cancer-treatment

 This is because one function of the lymphatic system is to drain excess fluid from tissues and if the lymphatic system is disrupted or damaged as a result of surgery and/or radiotherapy, it can lose this ability and the excess fluid will cause the tissue to swell.

Swelling is a natural part of the healing process following surgery and usually settles down as you recover. Lymphoedema can develop soon after surgery or radiotherapy. But it can be triggered many years after treatment - the risk of developing lymphoedema is life-long where the lymph nodes have been removed or damaged.

There is no cure for lymphoedema, but symptoms can be controlled using a combination of different techniques, usually massage and compression garments but also taping. There are also things you can do to help prevent the condition getting worse, such as specially designed exercises, good skin care to avoid infection and having a healthy diet and lifestyle.


Tuesday 28 February 2017

Weekly Discussion Summary ~ Finding the New Me

Be the first to comment!
In this week's discussion we explored the ‘positives’ and ‘negatives’ of living with cancer and its effects and the challenges of understanding the ‘new’ me.

Naz began by asking some challenging questions:
Should the cancer have changed me? For the worse AND better? 
What should my ‘profile’ look like? Stronger? Weaker? Both? 
If both, then how can weak and strong live together in harmony?

Naz explained the huge role working memory plays in our everyday lives and how our responses to cancer can lead to cognitive interference as our working memory is dominated by our vigilance. She believes we need to build resilience. This allows us to develop cognitive flexibility by finding a lightness within our fear and sadness. Bringing together the 'good' and the 'bad' can lead to a new normal which can be special and complete. 

Our responses were diverse: some spoke of physical challenges, and our points of view were partly shaped by whether we were recently diagnosed, living with 'no evidence of disease' or whether we had a secondary diagnosis. We agreed that whether we like it or not, we are not the same, we have changed bodies and feel different. Some of us described feeling comfortable with our new selves. Some of us feel anxiety and fear, a sense of loss and grief for the person we once were. Many of us described seeking new opportunities and discovering a new zest for life, even while experiencing sadness and loss. 

While we could acknowledge that we are different, accepting our new selves is another matter. Many of us experience fatigue, but are reluctant to admit our physical struggles as we don’t want to appear weak, especially at work. The fear of recurrence is strong, but can also be a driver for positive change leading us to adopt a 'can do’ attitude. Many harness this to make life changes, and others say they’ve stopped planning for retirement, preferring to live life now, spending more freely to enjoy the experience of being alive and taking more pleasure in the everyday. 

Some of us look back and cannot relate to who they were before cancer, we are perhaps more emotional, sensitive and empathetic now. Some days we find ourselves grieving for our old selves, we feel lost and want to hide away. Some days we feel strong, we can take on the world. The challenge of being on this rollercoaster is to bring these extremes into balance. 

We learn from cancer that we need to live now. As one member put it: ’The old me was worried about getting old, the new me is scared she won’t get to.’ 

Our overall discussion concluded we are undoubtedly changed. We are weak, AND we are strong. We are darkness AND we are light. We are sad AND we are joyful. 

If you are a woman with a diagnosis of breast cancer and you would like to join our closed private group, please message us on our public page:
https://www.facebook.com/resilienceinbreastcancer/?ref=aymt_homepage_panel

#ResilienceDiscussion



A big thank you to Jo for allowing us to share this beautiful image of bluebells.

Thursday 23 February 2017

Guilt

Be the first to comment!



Naz introduced guilt (and shame) as self-conscious, negative emotions that are directed at the self, which involve being critical, ashamed, and self-depreciating. Often, the anger is self-directed. In the context of trauma, guilt and shame have been extensively studied in relation to childhood abuse as well as more recently in the context of ‘survivor’s guilt’ post trauma, for example accidents, war, casualties, and cancer. A link below takes you to a paper that reviews research on guilt and shame quite nicely.

Naz found little research carried out on guilt in the context of cancer, but because guilt and shame are known to be risk markers for depression, they have been studied implicitly in depression. With the exception of a couple of studies, there is hardly any evidence related to 'guilt' in breast cancer – she found an interesting, which is not research based, and a link to that is also provided below.

Our common experience of feeling guilty manifested itself in myriad ways - from that first diagnosis when we ask why me? And - what did I do wrong? Our long list of guilty feelings poured out: why didn’t I find my cancer earlier? How awful we had found it to share the burden of our illness with our loved ones, causing them anguish and worry. Then for those of us who have come out the other side of treatment, there’s survivor’s guilt – why am I doing ok when another didn’t make it? Those of us with secondary breast cancer feel a sense of guilt about the impact of our illness on our children, including the painful knowledge that we might not be able to support and guide them into adulthood. Those of us with faulty genes shared our guilt about finding out, the worry that relatives may have the gene too and whether we’ve passed the fault on to our children.

Catholic guilt was mentioned and a deeply ingrained sense of responsibility for getting cancer. Then, of course there’s our work – we feel we let down our employers, our colleagues. We are continually apologising to everyone around us for having cancer. Our guilt spreads to the everyday stuff - that we don’t feel well enough to get everything done that we used to do, that we have to ask for help, that others have to care for our children, that we can’t exercise as much as we used to, that we can’t eat as well as we’d like to, because we don’t have the energy to cook, that we can’t engage fully with all the social events going on around us, that we have to pace ourselves, rest and relax (we are lazy, is how we unhelpfully see it.) The list goes on and on.......

But as our list grew, some of us began counteracting with questions, suggesting to one another that we had no need to take on so much guilt, and with this came the realisation that we are full of good advice for others, but reluctant - or find it difficult - to listen to ourselves.

And then came the voice of reason: ‘Why is guilt an acceptable emotion and others not?... I think that guilt is a harsh emotion to inflict on yourself just to make others feel better. Other people's emotions are their responsibility - don't make them yours.’ This point made a real impact on many of us, and brought us back to the negative futility of the guilt. Some of us shared that we don’t feel guilty, we know that getting cancer isn’t our fault, we didn’t do anything to deserve it, it’s just the hand we’ve been dealt with in life.

Naz questioned whether guilt serves a purpose, whether it can have a useful function in some cases? Our discussion came up with no easy answers, and our conclusions perhaps were more around how we can be resilient about our feelings in general – our anger, our sadness, our frustration, our sense of unfairness, our regret. We wondered whether embracing these emotions night allow us to be more truly be in touch with ourselves and to reframe our guilt. We often talk about self-compassion in our group, and this discussion highlighted once again how hard we can be on ourselves and that if we are kinder to ourselves, perhaps we can stop wasting so much of our precious energy on feeling guilty. Our discussion concluded with a powerful reminder that we are strong, powerful, vibrant, passionate women with rich and full lives.

This week our discussion explored our guilt and the sense of responsibility we feel for the worry and pain our loved ones experience as a result of our diagnosis with primary, or secondary, breast cancer.

Guilt can be one of the strongest emotions we experience - we feel guilty for bringing this disease into the lives of our families and its impact on our husbands, our partners, our parents, our colleagues, our employers. We feel guilty for exposing our families and friends to worry, fear and uncertainty. Those of us who are mothers are haunted by our sense of having allowed an unspeakable horror into our children’s lives; those of us who want to be mothers feel guilty that we may be unable to give our partners a family.

 

Some of us described feeling as though we had failed our loved ones in some way. Rationally, we know we are not to ‘blame’ but we can’t help but wonder what it was we did, or did not do, that might have caused us to develop breast cancer. We find ourselves questioning our life-style choices, our experiences and asking whether they could have contributed to our diagnoses. The questions that follow us are: why me? why not me? where did I go wrong? did I bring this on myself? Is this a punishment? We find ourselves taking on responsibility for developing primary breast cancer, for facing side-effects and complications, and if our cancer returns, for developing secondary breast cancer.

 

Naz explained that we are not as well-equipped to cope with guilt as other emotions. This is because guilt carries with it a strong emotional and cognitive component that justifies this emotion. Usually, our cognitive brain systems regulate or down play emotions that run high, but with guilt, our cognitive systems often serve to re-affirm our guilty feelings. This is one of the main reasons that feelings of guilt can last for a long time - for years post trauma.

 

Unwittingly, the expectations and reactions of others can re-affirm our guilty feelings. We are advised to - ‘stay strong’, ‘be positive’, ‘your family needs you’, ‘you need to keep going because of them.’ But often we don’t feel positive or strong and these 'sympathetic' comments increase our guilty feelings, we feel we shouldn’t complain, we are supposed to feel ‘lucky’ - because we have a ‘good cancer’, because we didn’t need chemotherapy, or radiotherapy, or haven’t had a mastectomy.

 

The media, we decided, plays a role in exaggerating these unrealistic expectations: are you strong enough? Brave enough? Tough enough? to ‘battle cancer.’ Women with secondary breast cancer described their emotional anguish as a result of the unspoken, offensive subtext that accompanies these messages - that they were somehow not strong enough or brave enough to stop their cancer coming back. The reality is that our power in influencing cancer outcomes and recurrence is very limited. So we feel doomed to failure. Yet we suffer in silence, unable to talk openly about the realities of secondary breast cancer.

 

Those of who have finished active treatment described how we want to meet the high expectations that we and others hold of ourselves. But we are exhausted, thrown into an ocean of uncertainty, trying to find a safe harbour to shelter from the storm of cancer which can be a long and turbulent. We want others to understand, to empathise, but we find ourselves mute and numb, unable to communicate how we feel and what we are going through. Some of us described feeling ‘survivors’ guilt’ when we have lost friends as a result of breast cancer.

 

So can guilt ever be made to disappear?

 

We can try to prioritise our own needs. We can share our vulnerability so that others see our interior experience as well as the tough image that we project outwardly. We can remind ourselves that we have very little control in the development of this disease. We can forgive ourselves.







Saturday 18 February 2017

Weekly Discussion Summary ~ Diet and Breast Cancer

Be the first to comment!
The subject of our weekly discussion was 'Diet and Breast Cancer.'

Diet can be contentious issue and there are diverse and varying views on the role of diet, both in the prevention, and treatment of cancer.

We considered the reasons why diet is such a popular topic in discussion, not only in relation to breast cancer, but 'cancer' as a whole:

Naz suggested that firstly, we can control what we eat and this is very important because cancer and its treatment completely undermines our sense of control over our bodies and lives, in particular the little control we have over breast cancer occurrence and recurrence. Yet, we can choose what foods to eat and what to avoid and this allows us to exert a sense of control, empowering us at a time when we feel extremely vulnerable. 

Secondly, our diet interacts with our physical and psychological well-being, influences hormones, cognitive function, and most of our organs, including the brain. So, it is perfectly reasonable to think that diet can have a direct effect on cancer diagnosis and progression. 

However, Naz told us it has been very difficult to substantiate a direct and causal influence of diet on cancer diagnosis and/or cure because the way in which diet affects individuals so differently, depending on our genetic make-up and environment. At a molecular level it is easy to substantiate with much certainty the effects of certain foods on physical well-being, but, when it comes to epidemiological research, it is hard to derive conclusive results because of history, natural variation in physical make-up as well as environmental experiences and influences. 

This mixed approach leaves us in a confusing position. Most of us would like to believe that good nutrition will help us, however, there is often a lack of clarity and agreement over what constitutes 'good' nutrition.

There was an extremely wide wide variation in our views as a group - some of us follow a vegan diet, others, a ketogenic diet, others avoided dairy products or foods associated with oestrogen. Individual members reported significant improvements in their health and well-being, including a reduction in tumour size as a result of changes made to diet, even though different diets were followed. Weight gain - and loss - as well as fatigue due to treatment was a consideration, impacting on our confidence and self-esteem and we also talked about our views on alcohol. However, our over-riding concern was how we could support our health and well-being while enjoying a quality of life, given the challenges we face, impacted by our unique experiences and perspectives.

We considered that irrespective of cancer, the 'food industry' is loaded with media claims advertising foods, including both specialised diets and therapies. Naz explained that while there is no substantiated evidence to back up the use of specialized or alternative diets, there are anomalies in traditional medicine, even though this is the predominant and scientifically accepted approach. Naz suggested that the absence of evidence does not mean evidence of absence. 

As a group, we were able to respect each other’s diverse views. We considered that given that as we currently do not know the effect of diet on cancer prevention and cure, it seems reasonable that we support one another to have the confidence to act on our own informed views about what each of us considers the best way we can support our physical and psychological well-being.

If you are a woman living in the UK with a breast cancer diagnosis, and you would like to join our private members group, please message us on our public page: https://www.facebook.com/resilienceinbreastcancer/?ref=aymt_homepage_panel


#ResilienceDiscussion




Wednesday 8 February 2017

Weekly Discussion Summary ~ Self-Compassion

Be the first to comment!
This week our discussion focussed on the concept of self-compassion and its effects on our well-being.

Naz explained that self-compassion, like post traumatic growth, is a relatively new concept, but one that has been researched in relation to its protective effects against anxiety and depression. Engaging in activities that promote self-compassion have been shown to correlate negatively with depressive and anxiety related symptomatology - this means that the more self-compassionate we are, the less likely we are to experience anxiety and depression.

Naz told us that the definition of self-compassion used in research identifies the following three elements:
i) “self-kindness (versus self-judgement);
ii) mindful awareness of one’s emotions (versus over-identiļ¬cation), and; 
iii) understanding the universality of human suffering (versus isolation of self)”.

As a group, we intuitively understood self-compassion as being kind to ourselves, putting ourselves first and doing things that make us feel good (point i). Almost all of us were able to share examples of the way we were practicing greater self-compassion, for instance putting our own needs first, doing things that made us happy and consciously choosing to 'treat' ourselves. For some of us, being kind to ourselves meant forgiving ourselves for if we needed to cancel plans at short notice (when perhaps we had been brought up to prioritise social obligations), giving up our previous strivings to be 'perfect', accepting our limitations, as well as accepting that we might never understand why we had developed breast cancer.

Points ii) and iii) above bring a more fruitful meaning to self-compassion, allowing us to be in tune with our emotions and to understand human suffering in others. Some of the group shared their learning with us, whether this was through counselling, taking part in a mindfulness course, or using the Headspace app. Some of us shared that we found it incredibly hard to feel self-compassionate, and that our experience of breast cancer fed painfully into our low self-esteem, sometimes, but not always linked to our previous experiences. However, we all felt that we could consciously practice self-compassion, perhaps through positive self-affirmation. Those of us who found mindfulness helpful described having learned to be able to stand back from their thoughts and feelings, recognising that they are just thoughts, and not our reality.

Naz told us about recent research showing that self-compassion can reduce feelings of distress in women with a breast cancer diagnosis and women who practiced self-compassion were less distressed and felt more confident about their body image. While the research predominantly looked at how self-compassion relates to negative feelings about body image, it does talk about how self-compassion can act as a buffer against distress and help boost self-confidence.

Several members recommended 'The compassionate approach to recovering from trauma using compassion focussed therapy' - Deborah Lee and 'The mindful path to compassion' - Christopher Germer, as well as this website:

Our a private psycho-educational group offers women with a breast cancer diagnosis a safe space to share their feelings. If you would like to join, please message us on our public Centre for Building Resilience in Breast Cancer

#ResilienceDiscussion



Many thanks to Anita for allowing us to use this beautiful image, calling to mind summer days and sunshine!


Saturday 4 February 2017

Celebrating Unity, Embracing Diversity on World Cancer Day 2017 ~ Naz

Be the first to comment!
Celebrating Unity, Embracing Diversity

The Centre for Building Resilience in Breast Cancer is almost 15 months old. Born in October 2015, we are proud to be celebrating our second World Cancer Day. Last year, on this day, we launched our blog, Panning for Gold, showcasing the colourful experiences of trauma and resilience of numerous women living with breast cancer and its effects; the roller coasters of joy and sadness, of elation and despair, of uncertainty and living with fear, of learning to be courageous and flexible.

Only 15 months old, the centre is rapidly expanding with over 2000 followers already. Our private psycho-educational support group, inclusive of just under 600 members, expands on a daily basis.
Our aims are translational and educational: to understand the complex roots of anxiety and depressive vulnerability in breast cancer and promote resilience using newly developed scientific research.

As a cognitive and affective neuroscientist working on emotional vulnerability and resilience for nearly 20 years, and having suffered breast cancer myself, I remain more determined than ever to bring new insights into the emotional and psychological needs of women living with breast cancer and its effects, promoting mental well-being and psychological flexibility in a population most need of being empowered through resilience.

Up to 80% of women with a breast cancer diagnosis continue to experience post traumatic stress symptoms for years post diagnosis, with depression and anxiety impacting health and well-being significantly. The statistics show that around 60,000 women are diagnosed yearly with breast cancer in the UK alone, with increasing rates in younger women noted and around 30% of us go on to develop secondary breast cancer. Addressing the unique needs of women with breast cancer is a both an individual and societal necessity.

What is the unique feature of the centre?
At its forefront, our aim is that the centre will unite the many diversities and segregations seen in breast cancer research and practice. We see primary and secondary breast cancer, not as separate entities, but on a continuum where the understanding of both the common and specialised needs of each can inform the other. Secondary breast cancer receives little attention for funding, but these women continue to live rich and fruitful lives, contributing to their families and society and it is imperative that their psychological needs are met and their voices heard. My aim is that the centre provides a public platform to educate through research the ways by which we can manage the cancer-related emotional vulnerability that we take forward with us, and practice resilience, given our limitations.

Our educational support group provides a unique and integrative platform for women of all ages and at all stages of the continuum. Our Sunday discussions are guided, referring to research and theory, mixed with the sharing of emotions and experiences that are both common and unique sensitivities.

Promoting resilience is at the forefront of our mission. Research shows that psychological flexibility towards resilience can be achieved through talking about and embracing our anxieties, fears and sadness. Attending to the ‘negative’ can facilitate our experiences of ‘positive’. We research the ways by which we can manage our fears and worries, and not simply hide away from them. Our women promote the practice of gratitude, grit and solidarity.

Today, we are about holding hands, embracing our diversity and celebrating our unity.

Thank you to all our amazing members and followers for your support.

Nazanin Derakshan