Kate Drummond, a 25-year-old woman from Devon described by her sister as “fit and healthy,” tragically passed away after a cancer diagnosis was initially missed and mistaken for sciatica. The family's story highlights the challenges of recognising rare cancers that present with common symptoms.
Kate first experienced severe back pain in 2020, which she attributed to poor posture or overtraining following changes in her exercise routine. After consulting her GP, she was prescribed painkillers, but her condition worsened when the pain spread to her hip, accompanied by warmth and slight swelling. In May 2021, Kate sought emergency care at a local hospital in Devon, where blood tests and an X-ray led doctors to diagnose her with probable sciatica—a nerve condition causing pain from irritation or compression of the sciatic nerve. According to her sister Kelly Drummond, medics noted that Kate was one of the youngest patients they had seen with sciatica.
As her pain intensified and her mobility declined, Kate decided to privately undergo an MRI scan after a spinal physiotherapist expressed concern about her symptoms. On 7 July 2021, the scan revealed a “grapefruit-sized” tumour in her pelvic region, along with numerous deposits on her spine. A biopsy conducted at Birmingham Hospital confirmed the diagnosis of Ewing sarcoma, a rare cancer affecting bones or soft tissue, on 3 August 2021.
Within weeks, the cancer spread aggressively to multiple organs, including her lungs, liver, skull, jaw, and other bones. Kelly described the diagnosis as life-altering for the whole family, saying: “I felt shock and disbelief, but also a bit of guilt, as well as you think ‘could I have done more to push her to seek help sooner?’ It all felt really unreal, and it shouldn’t happen to someone so young, especially someone so fit and healthy.”
Kate underwent emergency radiotherapy and chemotherapy over several months, during which she showed signs of improvement. Kelly praised her sister’s strength and positivity, stating: “She remained so strong and so positive the whole time, it was beyond us and we will never understand it.” However, from January 2022, Kate’s health rapidly deteriorated as her liver and kidneys began to fail due to the disease. Her condition declined swiftly, leading to her passing on 17 March 2022.
Kelly revealed that Kate was never given a terminal prognosis until the final weeks, underscoring how suddenly the situation worsened. Reflecting on her sister’s character, Kelly shared: “Kate was the most kind and considerate person, and people were just generally drawn to her; she was really warm. She had really good wit, and she was just hilarious – she had this amazingly infectious laugh. We all say her laugh is what we miss most about her.”
In sharing Kate’s story for the first time, Kelly aims to encourage others to “listen to your body” and “advocate for yourself” in seeking medical advice. She believes earlier diagnosis might have changed the outcome, pointing out that the tumour was sizeable by the time it was found, and doctors suggested Kate’s cancer may have been developing for up to two years. She commented: “What started as some lower back pain turned into cancer within a matter of days, which then turned into multiple cancerous tumours in almost every part of her body – the rapid progression was shocking. Kate’s story shows just how unpredictable cancer is, and clearly, early diagnosis has been shown time and time again to save lives.”
The Drummond family continue to honour Kate’s memory by embracing the values she lived by, including living in the moment and cherishing laughter. April marks Teenage and Young Adult Cancer Awareness Month for the Bone Cancer Research Trust, the UK’s leading primary bone cancer charity, which aims to raise awareness of conditions like Ewing sarcoma.
The Mirror is reporting on this poignant account to highlight the complexities of cancer diagnosis in young adults and the potentially fatal consequences of misdiagnosis.
Source: Noah Wire Services