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One Good turn - Why Clodagh Dunleavy is taking part

My name is Clodagh, and I am part of the Social Impact team here in Deloitte.

This is my first-time taking part in OGT, I have signed up for the 7.5km run and I am excited to be part of it!

I am getting involved this year as the charities that Deloitte are supporting are very close to my heart. Unfortunately, most families across the country are affected by cancer in some way and mine is no different.  In 2021, about two months after having my third baby, I was diagnosed with breast cancer.

I had been attending the family risk clinic in St. James hospital for about 15 years owing to the fact that my sister lost her life to breast cancer at a very young age and there was a suspicion that it may be genetic.

Shortly after beginning my cancer treatment, I also found out that I tested positive for the BRCA2 gene mutation which means that my chances of getting a number of different types of cancer are significantly increased. Other members of my immediate family subsequently tested positive for this mutation. (You have a 50:50 chance of inheriting it once a parent has the defective gene).

Until I got my diagnosis, I really underestimated the importance & significance of each of these 4 organisations that are being supported through OGT. The support they give patients & their families is truly immeasurable & the research they are undertaking is saving lives. 

I faced into a summer of chemotherapy and subsequent multiple surgeries but although a daunting diagnosis, armed with this genetic information meant I could give myself the best possible outcome in terms of my treatment plan. Most importantly it gave me the knowledge and awareness about being extra vigilant about any changes in my health and body.

I am grateful for all the treatment and care given by the oncology team in St James and support from Arc Cancer Support that I have received. I feel lucky that vital research and genetic testing has advanced since my sister’s early diagnosis which meant that I was able to receive this genetic information.

Until I got my diagnosis, I really underestimated the importance and significance of each of these four organisations that are being supported through OGT. The support they give patients, and their families is truly immeasurable and the research they are undertaking is saving lives.

Getting involved with OGT also presents an opportunity to improve my fitness and wellbeing and meet some of the other fantastic people who have put their hands up to get involved for such a worthy cause. I am grateful to be able to be part of it.

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