Brief summary-
should a stage 4 cancer patient with actue ischemic colitis have to wait over 72 hours for a bed on a ward and have not seen a Dr since Friday morning? Much longer version below…..
Hi, I’m just looking for some guidance on what is normal for A&E or if we should be pushing for more for my parent.
A bit of background my parent has stage 4 cancer (pancreatic) and their chemotherapy regime is brutal and this cycle’s side effects have caused awful diarrhoea leading to awful cramps which needed a trip to A&E in an ambulance at 2am Friday morning. They were quickly given a CT scan and told it’s ischemic colitis (can become very serious!!) and that they would not be able to leave the hospital until the cause is found and treated- this all happened before midday on Friday. Initially they were in resus before their bed was moved the corridor and finally to a side room after we complained that they were severely immunocompromised because of the chemo and outside a toilet in the corridor was not the best place.
Since Friday lunchtime they’ve not seen a doctor, just had obs done by various nurses and when asked when they’ll be moved to a ward or seen by a doctor have been told there are no doctors or beds available as it’s the weekend.
The whole thing is complicated by the fact I live 300 miles away in England and they are in Wales so I can’t support by being there all the time ( i need to keep time off for when things get more serious 😓). I drove down on Friday evening and stayed until last night and during that time I had to ask for pain relief and also if they could have anti-diarrhoea medication as the pain and trips to the toilet were becoming really concerning.
I know the NHS is stretched but their experience during this stay is a million times worse than my elderly in-laws have experienced recently (not in. Wales). Is this normal and to be expected?!?! Even as a stage 4 cancer patient?
This is all new to us as my parent was a healthy fit (as far as we knew!) 64-year-old last spring, then was fobbed off for 5 months as having heartburn/ anxiety/ muscle aches, followed by a CT scan that no-one looked at for 3 months despite it showing a pancreatic mass. When the diagnosis was finally made at the end of December it had spread to the liver which meant there was no chance of the tumour being removed. I’m not sure if the delay in diagnosis is clouding my expectations of how they should be treated in A&E or if what is happening now is just to be expected in some healthcare trusts?
Sorry, if that was a massive waffle, my head is all over the place and I don’t know what to do to help.