Suzie, NSW

53-year-old Suzie, became intimately acquainted with the challenges of neuroendocrine cancer when diagnosed nearly six years ago.

For two years before diagnosis Suzie experienced lower right pain. Eventually, the pain intensified, prompting a visit to the GP, who wisely suggested a CT scan. The results revealed a distressing possibility of metastases, echoing memories of losing her father to cancer years prior.

Suzie’s sister, Jennifer has played a crucial role in this tumultuous journey. Together, they have navigated the shock of cancer and the subsequent quest for information.

“If she’s in it, then I’m in it.”

Both were deeply affected by their father’s previous cancer battle and turned to the internet for answers when the diagnosis was first received. Jen stumbled upon the Unicorn Foundation (now NeuroEndocrine Cancer Australia – NECA) and the NET nurse helpline.

“They’ve been a lifesaver.” 

Inspired by Suzie’s diagnosis, Jennifer has become a NECA volunteer, driven by a mission to raise awareness about neuroendocrine cancer, particularly among some healthcare professionals.

“People need to know what neuroendocrine cancer is.”

Jen’s devotion to her sister throughout Suzie’s NET diagnosis has been unwavering. From accompanying her during PET scans to demonstrating solidarity by staying in the room despite radiation concerns, Jen’s commitment is resolute.

“If she’s having the scan, I’m having the scan.”