ELIZABETH VAN DEN BRINK

Derek van den Brink - Family & Friends

Fundraising for Neuroendocrine Tumor Research Foundation
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In memory of Derek van den Brink

Story

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Derek was diagnosed with High Grade Neuroendocrine carcinoma in March 2016. His early symptoms were what we'd think as not 'out of the ordinary' - tired, indigestion, bit of acid reflux - something peptobismol and sleeping should resolve. As the symptoms persisted, went to GP (who didn't think much of it either). Blood tests identified liver function levels were abnormal. Ultrasound tests later confirmed his liver was 'full of lesions' and further tests were performed. The whole process took 5 months before diagnosis. The treatment options were limited for his type of cancer, as his was identified as more rare within the umbrella of 'Rare Cancers' - his was 1 in 20,000 of cancer cases. 

He faced his disease with a stubborn determination, he'd say constantly to himself and everyone around him - "don't worry, I'll be fine". After 4 rounds of chemo that only 'stabilizied disease' but didn't reduce tumors, he received 4 treatments of Peptide Receptor Radiotargeted Therapy (PRRT), which helped in stabilizing disease further, and reduced some of the tumors. He was stable for ~5 months. And then cancer got 'smarter' again, and came back with a vengance, a different type of chemo helped again for ~5 months, but that too stopped working earlier this year. And so the disease progressed until his body could not fight it anymore. 

He died in his sleep, without pain or suffering, and was incredibly well looked after by his specialist oncoligist and the NET team. He was supported by all his family, friends and colleagues - and was always appreciative for it. 

We miss him everyday, but he will continue to live in our hearts and memories until we meet again. How lucky we were to have known him, loved him and we are thankful for he affected our lives during his time amongst us. 

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£4,721.05
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