I have just received an appointment letter that mentions having a neuroendocrine tumour. Me being me, and far from the bravest of people, I’m scared. I’m trying not to show my daughter I’m scared.
The intellectual part of me is trying to rationalise things. The tumour was found by a polyp removed in March. In the UK there is the 28 day pathway.
Copilot says: > The 28-day pathway is part of the Faster Diagnosis Standard by NHS England. Here’s a brief overview:
Key Points of the 28-Day Pathway:
- Purpose: To ensure patients referred urgently by their GP for suspected cancer receive a diagnosis or have cancer ruled out within 28 days.
- Benefits: Reduces anxiety for patients, allows quicker treatment initiation if cancer is diagnosed, and provides peace of mind if cancer is ruled out
I’m not sure if I’m still on it. What I do know is that the last endoscopy was done before the appointment to discuss removing my teeth. That took place late June. So it’s about 5 months at the very least since the last endoscopy. The intellectual/rational part of me says they’d have contacted me ages ago if there was something bad, re the 28 day pathway. I have pain but that’s re my legs. The left side where I fractured my femur . The right side probably due to RA.
Yes I have various health problems, but I haven’t experienced a noticeable decline in my all round physical health over the last few months. My daughter even thought I’d put on weight recently. My appetite hasn’t lessened.
Then there’s the severely mentally ill prone to anxiety(health and social) and paranoia ‘me’. The one that has read so many articles as to how those with SMI get inferior treatment of their physical health problems. That they’ve deliberately kept the truth from me.