In this week's discussion,
we explored the impact of breast cancer on our families.
Breast cancer impacts on
our children, partners, parents, siblings and wider family relationships.
At a time we most need
support, our families are under enormous stress and we heard about the
different ways people cope and express their feelings; that sometimes families
gather together to face our diagnosis with us, but that for others it seems too
much to bear and they remove themselves or don't talk to us about our cancer.
We heard that there is love and laughter and inevitably there is tension and
stress. We heard that some people and relationships crumble, but others are
strengthened and renewed.
A universal concern in the
group was the potential impact of breast cancer on our children, particularly
young children, those with vulnerabilities and at transition points. We heard
about the different ways younger and older children expressed their feelings -
some, but not all asked questions, or talked about their fears, sometimes
behaviour was challenging; some struggled with school or academic work; some
support and care for us.
Those of us with partners
were aware of the impact of our cancer diagnosis on them, we worried that
no-one was looking out for them, that they didn't share their feelings and
fears with us, that they were under pressure to be strong. We heard about the
amazing variation in the way that partners supported us, practically and emotionally,
whereas others simply could not.
Whether we have primary
breast cancer, a recurrence, or secondary breast cancer was important - some
individuals and families had coped well during one bout of cancer, but then
struggled further on. Other factors included - whether we were single parents,
had caring responsibilities ourselves, for very young children and elderly
parents, and some of us felt a strong sense of responsibility to protect them
from the burden of our illness.
Naz only found a few pieces
of research on this subject, these argued that that children struggled
emotionally and were rated as less competent by their parents, compared with
children from families with no breast cancer. However, she considered these
results carried biased perceptions from parents and that objective measures of
well-being, as well as reports directly from children should be collected over
time. A good study, looking at the long-term effects of breast cancer on
physical and emotional outcomes, is lacking.
When we previously
discussed emotional vulnerability in spouses and partners, we learned that
psychosocial support is missing; that partners of those with recurrent breast
cancer suffered from high levels of anxiety; that male partners are especially
at risk of high vulnerability as they tend not to be open to emotional
expression and, as some of us experienced in our group, silently suffer, become
unresponsive or can’t find the words.
Not all relationships
survive the crisis of breast cancer. Yet, at the heart of our vulnerabilities
lay stories of resilience, of women coming through the dark days to meet new
partners, of children stronger, more empathic and confident, even though the
hidden fears remain. It is clear that our families face our diagnosis with us,
it affects them, and this in turn, affects us. https://www.researchgate.net/publication/40760311_Women_with_advanced_breast_cancer_and_their_spouses_Diversity_of_support_and_psychological_distress
If you are a woman living in the
UK with a diagnosis of breast cancer and you would like to join our private
group, please leave your name in the comments.
#ResilienceDiscussion
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