Skip to main content

Going home

After 4 weeks in hospital the doctors have told me I can go home tomorrow. I text a few family and friends earlier to tell them and they're so excited. So why aren't I?

It's not that I don't want to go home. I do. Desperately. I want to wake up in the mornings next to my husband. I want to put my kids to bed at night and watch them sleep, looking like angels. I want to go to Tesco and do laundry and all the other boring stuff that makes up life. 

But it wasn't supposed to be like this. 


In my head I was going to come into hospital, have the operation and come home 'fixed'. Maybe I'd told the kids that simplified version so many times that I had started to believe that it really was that simple. 

According to the pre-op letter I was only supposed to be in 4 nights, but we told the kids 2 weeks just to be on the safe side. I never imagined that I would be in for double that. I should have known really that this is me we're talking about and nothing ever goes to plan. 

I certainly didn't expect to be coming home still needing TPN (feed). I was hoping that I would be able to clear all the medical equipment out of the house so that it no longer resembled a community hospital but it seems the drip stand and that bloody rucksack will be with me for some time yet. 

As it stands I'm on liquids only at the moment so will need 'topping up' until I'm eating and drinking properly. That could be weeks. It could be months. No-one knows. 

I also didn't expect there to be this much pain. I knew I would have pain immediately after the surgery but I expected it to die down and then go away. Maybe I wasn't being realistic. Maybe I was hoping that was how it would be. 

I thought that that they would take the Stoma away and everything would be fine. I would be 'normal' again. But I'm still left with insides jumbled up, full of adhesions and scar tissue. My stomach still resembles an AA road map and I'm still going to need medication to keep everything ticking over, at least for now. 

What I have to try and remember is that the operation was successful, I didn't need that second emergency operation and there's nothing majorly wrong with my bowels other than them being stubborn and refusing to work quite as they should. I have bowels with attitude...would you expect anything less from me?

Writing this has made me realise I have a lot to be thankful for. I'm sure my kids won't care if I'm having to 'hook up' to feed at home, because I will be at home. And that's the important thing. It doesn't matter if I can only drink ensures and eat mash and gravy at home, because I will be at home. It doesn't matter that it wasn't supposed to like this. Because I will be at home. 

Actually, I'm quite excited now about going home. I'm still a bit scared and I know there's still a long road ahead of me. But I'm going home! 
I'M GOING HOME! 
I'M ACTUALLY GOING HOME! 

NB x

Comments

Popular posts from this blog

Caravan wankers

Over the last few years when I was stuck in hospital for long periods of time Hubby and I would talk about what we would do if I ever got ‘better’. During some of those times when I was so, so poorly the idea of just being at home for more than a few weeks at a time seemed like a far fetched dream. But I’m currently living that dream! And obviously I know I will never ‘get better’ but for these purposes ‘getting better’ meant being well enough to be at home, not in pain 24/7 and not in bed all day, every day. Not too much to ask now is it??  So in our talks, once I was at home and was well enough to do the real basic things like watch Big Fella play football, Big Girl play netball, go to Tesco, play with the dog, go to the cinema etc one thing kept cropping up. We would love to have a motor home and tour round the country. We talked about the places we would like to visit, how much Buddy the dog would love it and how it would give us a chance to reconnect with each other.  But...

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 sl...

Now I’m panicking

This morning I saw my consultant on the ward round. I was excited to find out the plan to get me home later this week but it looks like the plan is a little bit different to what I thought… The gastro consultant had spoken to the microbiology consultant who said I need two weeks of antibiotics from the first date I had them. Depending on which antibiotic we are counting from (as I’m currently on three different types) that takes me up to either the 18th or 19th December. So far this was what I was expecting and so in my head I was thinking that I would probably be home for the weekend, just in time for the annual tradition of Christmas bowling with Bestie and her kids on Saturday 21st December.  But then he told me that we need to leave it 24-48 hours with no antibiotics and then do another blood culture from my Hickman line. After taking the blood culture we then need to wait 2 days (minimum) to make sure no bugs grow on the culture and only when they are satisfied that the line i...