Skip to main content

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 is infection free they will need to test the line out by giving me feed through it. So doing a quick addition of all of those days realistically that’s looking like a Christmas Eve discharge. And that’s so long as everything goes to plan. Not really the news I wanted to hear. 

In all my years of being unwell I’ve managed to avoid being in hospital on Christmas Day. I’ve been discharged on Christmas Eve before and admitted on the 27th but never actually woken up on Christmas morning in hospital. And I know the kids are big now but Christmas is something I’ve always managed to be at home for. We’ve celebrated countless birthdays, anniversaries and other special events in a hospital day room but I just don’t think I can do Christmas. And if I am stuck in here I think it will break Hubby. I’m trying to think positive thoughts but inside I’m panicking and I feel sick. 

Because I was expecting to be home this weekend I thought I would have a couple of days to do last minute present buying, gift wrapping and food shopping but now that looks unlikely. Luckily I bought the vast majority of the kids presents over the Black Friday sales but there’s still little bits I wanted to pick up and other people in the family that I haven’t even begun to think about. And because I’m literally hooked up to a drip 24/7 while they try to replace everything I would normally get in my feed it’s not like I can even get home leave and pop out for a couple of hours one afternoon.

Hubby is under huge pressure at work at the minute and now I have to add more on to his to do list because I’m stuck in here. I’ve looked at getting an online food delivery but of course all the Christmas slots sold out weeks ago. And in terms of present buying I’m pretty much limited to ordering stuff from Amazon as they’re the only place that I know will get the deliveries out to me in time for Christmas. 

Deep down I know that the most important thing is that we are all together on Christmas Day, whether that’s at home or in hospital. I know that people will understand if their gifts are late or missing. I know that the doctors will do everything in their power to get me home for Christmas. But I also know that right now I need a good old cry. I’m sad and angry because yet again my illness is ruining things. Because yet again my kids are counting down to Christmas, but not in the same way as their friends. They’re counting down the days and wondering as the number gets smaller if their Mum will be home in time for Christmas.

The only good thing about being stuck in hospital is that I’ve had time to watch all the old episodes of Gavin and Stacey ready for the final episode on Christmas Day. Although having said that the new episode is on at 9pm by which time I will probably be fast asleep so I reckon I will be watching it on Boxing Day!! 




Comments

Popular posts from this blog

New car smell

After everything that’s happened over the last 5 weeks not many days have been good days but today was. I will write a blog post about everything that happened but that’s for another day!  Today I went to pick up my new motability car and got to breathe in that new car smell. I am now the proud lease holder of this lovely Volvo XC40.  To be honest, part of me wasn’t sure whether to write a blog post about getting the new car with everything that’s been going on with the disability benefit reforms. There’s been so much written about motability cars on social media but a lot of it is misinformation and hate and that made me nervous to write this post. But I figured that most people reading it are friends and family and understand my need for the car. But for those that don’t let me explain a bit about how the motability scheme works.  I am lucky enough (or unlucky enough depending on how you look at it) to claim PIP- personal independence payment. This benefit is designed t...

The germs have got me 🦠

Being on azathioprine, influximab and prednisone is helping to control this recent Crohns flare up. But unfortunately they work by wiping out my immune system making me more susceptible to all the bugs doing the rounds. I refuse to stay at home and be held hostage by these meds though- for me they are there to give me my life back, not to make me a prisoner in my own house, so the inevitable has happened and I’ve got a cold.  ‘It’s only a cold’ you might think, but with no immune system to fight it off this cold has made me pretty poorly. Yesterday I couldn’t get out of bed and felt so, so ill. I was coughing and struggling to breathe so I’m pretty sure I’ve got a chest infection too. But I can’t confirm that because apparently even being immunocompromised with a suspected chest infection is not enough to see a GP these days!  I spoke to the receptionist at the GP surgery this morning who told me that all the urgent appointments for today were gone (and this was at 8.25am, aft...

Disability benefits cuts

So in Rachel Reeves spring statement earlier this week it was confirmed that there will be massive changes to the benefits system including the way that PIP is assessed and changes to the health element of Universal credit.  As someone who is receipt of both PIP and ESA disability benefits I find this whole situation…  🔲 terrifying  🔲 baffling  🔲 rage inducing  🔲 disgusting  🔲 [all of the above] I honestly cannot believe that a LABOUR government is looking to balance the books of the country by taking money from some of the poorest and most vulnerable in our society. This is the sort of thing I would have expected the Tories to do but when I voted Labour I honestly thought that not only would they look after and protect the neediest but they would actually make things in our society better and fairer. How wrong I was. Looks like I’m going to have to get some ‘Fuck Labour’ merch to go along with my ‘Fuck the Tories’ stuff I already own!  Now I do b...