ELLA'S STORY

ELLA'S STORY

I am a 34 year-old wife, mum of one and cancer sufferer.

Two years ago I had been happily juggling my busy role in investor relations at Infracapital with motherhood, when a trip to my GP with a minor cough resulted in a diagnosis of an advanced form of a rare and complex cancer, Adenoid Cystic Carcinoma (ACC) and changed our lives forever. The week of scans, biopsies and consultant appointments that led to my diagnosis was utterly terrifying and heart breaking – it is difficult to describe the depths of despair, and the sheer strength required not to fall into the deep dark precipice that comes with facing such a diagnosis.

With no other symptoms, and being a young, fit and healthy non-smoker, it was a huge and horrid shock to us all. The cancer had taken over my right lung and surrounding areas, and within 2 weeks, I underwent a 9-hour operation to have my entire right lung removed, as well as areas of my diaphragm and surrounding tissue. I was in intensive care for 10 days following complications, and finally returned home bruised, battered and breathless, to my amazing husband James and beloved one-year old daughter Olivia a week after that. What followed was a relentless battle to overcome the excruciating pain, physical limitations and draining anxiety, whilst doing my best to be mum to Olivia and shield her from it all.

The challenge with ACC is that it does not respond to chemotherapy and there is no known cure for the disease. We were advised that the cancer would likely return, but there was no way of telling when or where that would be.  In November 2017 following further rounds of terrifying scans we were dealt the devastating news that I had already suffered a relapse and I had a tumour pushing up against my spine, which was treated with radiotherapy. Shortly after this, we received our heaviest blow to date, the ACC had spread further and I now have many tumours growing in my remaining left lung. I have since had lung brachytherapy in the US, immunotherapy and further radiation to my spine.

Given what is known about ACC to date, we are in the difficult situation of searching for treatment options which we hope will hold off the progression of cancer for as long as possible. One of the hardest aspects of our journey has been the lack of knowledge around treatment options. The continuous contradictions in opinion from the few leading ACC specialists about my treatment plan has been both daunting and demoralising at times. Together with our families, we have worked tirelessly over the last two years to research and assess all the treatment options available. It has been incredibly difficult and immensely stressful to be tasked with making such enormous treatment decisions, and finding the right team of experts to work with.

Through our research, we met with Medical Oncologist and Clinician Scientist Dr Rob Metcalf, who is the UK’s lead researcher into ACC.

WHAT IS ACC?

Adenoid cystic carcinoma

Often abbreviated to ACC, it is a rare and frequently lethal type of cancer. It typically originates in the salivary glands but can also start in other types of gland in the body such as those in the lung, breast and skin. The two defining features of this disease are a high chance of spreading from the primary tumour site and resistance to current drug therapies. These features combined mean this is the most lethal of salivary gland cancers and a cure is not currently achieved for most patients. Being a rare type of cancer, ACC is not in the public spotlight and does not benefit from the substantial government grants and fund-raising efforts that more common cancer types benefit from. There is an urgent need to develop new and better treatments.