Skip to main content

Still ranting

I'm lying here at 5.30am unable to sleep. I have been awake all night. All bloody night. The irony is that the bay is near silent tonight. No snorers, no machines beeping, no nurses disturbing me at 2am to do a blood test so I really have no idea why I'm wide awake. 

It seems as good an opportunity to continue my rant from one of my last posts because yesterday it got even worse. 

Bearing in mind that the last visitor of the old lady in the bed next to me left about 11pm on Sunday night I was astonished to see them all descend again yesterday morning at 8.45am. Not one. Not two. But four. Four visitors coming in over 2 hours before visiting was due to start. 

I had totally had enough by this point so in the absence of the ward sisters I took myself off to see Matron. Matron Ummi is a middle aged Asian lady whose waist is so tiny I could probably get my hands around it. But her eyes and tone show that she's formidable and she runs the St Marks wards with a mixture of fear, respect but also warmth to the staff and patients. 

I explained what had happened on Sunday and that there were visitors there already including a man. She agreed that it was out of order and that it was especially bad in the morning when we are all getting washed and dressed etc. She gave me 5 minutes to get back to my bed then she came in.  

She told them only 2 visitors at the bed, that visiting was 11-8 (which is super generous anyway compared to most hospitals) and that under no circumstances was a man to be in the bay at this time of the morning. 

Off they slunk to the dayroom until 10 minutes later they snuck back in. Fed up I went back to see Matron and told her I was going for a shower and could she please sort it out? She assured me she would. 

I had my shower (and you know how much I enjoyed that!) and went back to my bed. Feeling invigorated I decided to get my body lotion out and slather up. So you can imagine how shocked I was when the man walked back into the bay while I'm sitting on my bed in my bra and knickers basting myself like you would a turkey on Christmas Day. 

As soon as the lotion had sunk in I was dressed and back to matrons office. This was getting ridiculous. She came back and kicked them out again. She agreed that they could have 3 at the bedside and that they could have visiting until 8.30pm but of course if you give an inch...

At various points of the day there were up to 10 around the bed and did they leave at 8.30pm last night? Did they hell. Try 10pm. 

I'm supposed to be moving to the Intestinal Failure Unit tomorrow now that I don't need to be on the surgical ward and I tell you, I can't wait to go. This is all doing my head in. 

I just want to point out that whilst my lovely bed neighbour is elderly she is neither dying or gravely ill. If she were I would have no problem with the family being there at all. She is having a colitis flare. Like half the people in St Marks. Like I've spent years having. 

Even at my sickest after having major, life saving, complicated surgeries Hubby has always had to observe the visiting rules and on the occasions he was so worried about whether I would last the night he's spent the night sleeping on a bench in the cafeteria or some other part of the hospital to be close to me. It would seem there's one rule for most and then those who just don't care and do what they bloody like. And if you kick up no doubt they would accuse you of being racist. 

But on another very serious matter I have nearly used all of my January allowance of 3G! So that means that Vodafone will now start charging me a million pounds a minute or gigabyte or whatever to use the Internet. Super. 

The doctors have said that I'm going to be in at least for the rest of the week so this could be a problem. I will have to limit my Facebook, Twitter, Instagram, Email, eBay time and not check them every 10 minutes like I do at the moment!  I suppose I will just have to get my book out and read. 

The doctors have said that I'm not strong enough to go home yet. I'm still not able to tolerate enough food or drink to keep me adequately nourished. They seem to have took my appetite away along with the Stoma! And because I've spent the last 6 months on a very severe fluid restriction I've trained myself to over-ride the thirsty feelings and can go through the whole day on less than one cup of water. 

Knowing that unless I get more food and drink into me I won't be going home I've set alarms on my phone every two hours to remind me to eat and drink. 

One thing I'm enjoying is a bit of mash and gravy. The picture makes it look gross but trust me it really is a little plate of heaven to me!



I got my veggie gravy brought in from home and can make it up in my mug from the hot water thing in the dayroom- what are they called, the things on the wall plumbed into the water that has boiling water constantly? i just can't think of the word probably due to lack of sleep. 

On Sunday I had one scoop of mash and half a mug of my veggie gravy and yesterday I had 2 scoops and a whole mug full. Half way through I was starting to feel full and a bit sick but it was like an episode of 'man versus food' and I was not to be outdone by the extra mash. There was a lot of huffing and puffing and heaving but I am proud to say I won. In your face extra scoop of mash!

I have a good friend coming to visit me this afternoon and she's bringing some snacks in the hope that it will kick start my desire to eat. I'm not sure it will but I will force them down because I want to get home to my family. 

NB x




Comments

  1. 'In your face extra scoop of mash! Haha You go girl!!
    Try not to worry too much about others around you. Yes I'm sure it is super annoying to watch them flaunt the rules, but you should be 'resting' and taking it easy. Put your feet up, stick your head in a good book and try to switch everyone else off. Take some 'you' time. Hope you are feeling better super soon x
    colitisandme.blogspot.co.uk

    ReplyDelete

Post a Comment

Popular posts from this blog

Light at the end of tunnel

I’m sat writing this blog post in St Marks, the specialist bowel hospital in London. So much has happened in the last few weeks; it’s all been a bit of a whirlwind. But I finally feel like there is some hope at the end of the tunnel. Let me tell you why.  At the beginning of June I was admitted yet again to QMC in Nottingham with huge amounts of pain, my bowels not working properly and just feeling generally unwell. I had only been home a couple of weeks since the admission in May but I had been feeling so rubbish most of my time had been spent in bed. I had tried everything I could to stay at home but the pain had become so bad I was barely able to stand or take a few steps on my own.  I had expected to maybe be in for a week or two to get stronger pain meds and get back on my feet but I ended up being in for almost a month. They put me on morphine injections and ketamine but then stopped them when my heart rate dropped to 30 beats per minute and my breathing to 7 breaths a minute. Th

The light at the end of the tunnel is a train

Last week was a busy and pretty crappy week for me health wise. I had to go and have blood tests done with the nutrition nurses and I had two hospital appointments; one with the gallbladder surgeon in Nottingham and the other with colorectal surgeon at St Marks. I was hoping to have at least one surgery date to write in the diary following these appointments but I came home empty handed on both occasions. Here’s what happened.  I began noticing over the last few weeks that I’ve started feeling really crappy. I’m feel lucky to have been at home for the last 6 months and I have been the most well I have been for years but it felt like things had shifted slightly recently but I couldn’t quite put my finger on it. But years of being sick means I know my body and I can tell when something isn’t right. I have been feeling permanently exhausted and having way more bad days than good. I’ve gone back to spending 2, 3 or more consecutive days in bed, unable to do anything but watch tv and sleep.

The wrong size line

I’m on the M1 heading back to Nottingham after a road trip to St Marks to get my line repaired. But this is me, and as usual it wasn’t a smooth ride. More like a bloody shit show. So what happened? Let me tell you… After being admitted to QMC in Nottingham on Sunday with a broken Hickman line I was taken down to Interventional Radiology on Monday afternoon to get my line repaired. Firstly, I couldn’t believe it was happening so quickly and secondly I didn’t want to get too excited because, well it’s me, and usually things don’t go according to plan. And sadly I right to rein in the excitement.  When the doctor came to consent me for the procedure it was for a replacement, not a repair. I assumed he had made a mistake so I told him I was there to get my line repaired and was definitely not there for a new one. He looked at me and said “I hate to be the bearer of bad news…” and that’s a sentence that never bodes well. He then went on to say that they didn’t have any repair kits and that