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Does cancer affect us all equally? Events

Does cancer affect us all equally ?

Mavis and Sasha re-opened the conversation about cancer in March 2021. This time the event was opened by Dr Rose Thompson, Chief Executive and Founder of BME Cancer Communities and Chief Executive and Co-Founder, Sistas Against Cancer. She shared her outstanding contribution and wealth of knowledge around the care and experience of diverse communities affected by cancer.  This was followed by a lively panel discussion around cancer and cancer genetics to help us think about the question ‘does cancer affect us all equally?’

Introduction by Dr Rose Thompson, Chief Executive and Founder of BME Cancer Communities and Chief Executive and Co-Founder, Sistas Against Cancer. Shares her outstanding contribution and wealth of knowledge around the care and experience of diverse communities affected by cancer. (music: Unconditional Bae, Sauti Sol, we do not own the rights to this music).
Panel discussion for the Genetics Engage event ‘does cancer affect us all equally’ with Sasha Henriques, Principal Genetic Counsellor,  Dr Bianca DeSousa, Consultant Cancer Geneticist  and Suresh Rambaran, Specialist Nurse, Founding member, Cancer Equality. (music: Unconditional Bae, Sauti Sol, we do not own the rights to this music)
Panel discussion for the Genetics Engage event ‘does cancer affect us all equally’ with Dr Rose Thompson Chief Executive and Founder of BME Cancer Communities and Chief Executive and Co-Founder, Sistas Against Cancer,  Sasha Henriques, Principal Genetic Counsellor,  Dr Bianca DeSousa, Consultant Cancer Geneticist  and Suresh Rambaran, Specialist Nurse, Founding member, Cancer Equality. (music: Unconditional Bae, Sauti Sol, we do not own the rights to this music)
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Events Research Showcase

Research Showcase

For our first research showcase Mavis spoke to some remarkable women about their work. There are exciting projects using genetics and genomics knowledge to answer many questions around health and disease. Yet each new application of the technology also produces and magnifies dilemmas around ethics and resource allocation. Sasha and Mavis learnt a lot through these conversation about the dilemmas and the complexity of diversity in genetics research.

Mavis and Sasha introduce the research showcase and the conversations Mavis had about inclusivity in genetics this week. Make sure you watch the interviews below ! Sam Cooke, Wonderful World – We do not own the rights to this music
Genetics Engage: What research is happening in genomics? Interview with Vivienne Parry, Head of Engagement at Genomics England. Sam Cooke, Wonderful World, we do not own the rights to this music
Genetics Engage: What research teaches us about diversity in genomics? Interview with Dr Roz Williams , Wellcome Trust Research Fellow – Talking about stem cell research and the complex meaning of race/ethnicity. Sam Cooke, Wonderful world – we do not own the rights to this music
Genetics Engage: Inclusivity in cardiac genetics research, Mavis meets ….Tootie Bueser, Cardiac Nurse – HEE/NIHR Clinical Doctoral Research Fellow; Talking about cardiomyopathy research and the role of research and diverse populations in providing better clinical services , Sam Cooke, Wonderful World – we do not own the rights to this music
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Events

The UK Story of Sickle Cell and Thalassaemia.

This month Sasha and Mavis enjoyed hearing about the story of Sickle Cell and Thalassaemia. The event was introduced by Prof Dame Elizabeth Anionwu the first sickle cell specialist nurse in the UK. It was an enlightening afternoon spent reflecting on the experience of the Sickle Cell and Thalassaemia community and what that could teach us all about improving inclusion in genetics.

Introduction with Prof Dame Elizabeth Anionwu to the Genetics Engage event ‘The UK Story of Sickle Cell and Thalassaemia’
Interview with Prof Kark Atkin about his 20 year experience of research and service development for Sickle Cell and Thalassaemia.
The UK Story of Sickle Cell and Thalassaemia : What can in teach us about inclusion in genetics? Sasha and Mavis talk to friends from the Sickle Cell Society, The UK Thalassaemia Society, The Sound of Sickle and Those involved in the care of Sickle Cell and Thalassaemia Society.

The Sickle Cell Society https://www.sicklecellsociety.org/

The UKTS https://ukts.org/

The Sound of Sickle https://www.instagram.com/tssuk_/

Our Journey, Our Story: History and Memory of Sickle Cell Anaemia in Britain 1950 – 2020 is available online at:

http:// www.bcaexhibits.org/exhibits/our-journey/  

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Blogs

Race, masculinity and genetic counselling.

During my conversation with Suresh Rambaran about Black men and prostate cancer I surprised myself by stating that I had never seen a Black man in a genetic cancer clinic, in the UK, in nearly 10 years of working in genetics counselling.

While it may be expected that less men seek genetic counselling for conditions which increase the risk of breast and ovarian cancer, there are genetic conditions that increase the chance of cancer for both men and women. Conditions like Lynch syndrome and familial adenomatous polyposis (FAP) syndrome that increase the risks of bowel cancer for example. I work in a diverse part of the country so even accounting for the expected differences, it remains both noticeable and curious to me that I cannot recall seeing a Black man for genetic counselling for any cancer condition. It is important to note that I have seen patients for a range of other non-cancer genetic conditions and although the numbers are often smaller than expected, I have seen Black men in these clinics.

Low numbers of men presenting in healthcare is well recognised. Men appear less likely to recognise symptoms, report them early or to adhere to screening. The health seeking behaviour of men with hereditary conditions that primarily affect women show similar trends though additional factors like being less likely to receive information or having lower risks of cancer can contribute to the differences observed.

For me, these issues raise questions about how personal and social perceptions of masculinity drive health seeking behaviour and even how they contribute to what genetic information is shared with men. The intersectionality of race and masculinity on health seeking behaviour has been considered for years. Studies have looked at the cultural norms, values and expectations that impact how men seek services. From the individuals we have spoken to through Genetics Engage we have heard that difficulties accessing services can be due to who professionals refer to specialist services like genetic counselling. Perhaps professionals may worry that patients might react negatively to referrals or at worst they may hold assumptions that they just would not benefit or be interested.

Reflecting on a month like Movember certainly makes me think about ways in which conversations can be had to better support men to engage in genetic services. Specific and tailored interventions just will not be possible without talking to Black men about what they want and need to offer services that improve their health.

Sasha