A lot of you have been asking why I was in Hospital recently so I thought I’d post you a bit of an update. It feels weird to be writing this now but I wanted to wait until I was out of the woods to write about it because I tend to see the positives a little better after some time has passed.
If you’re following me on Twitter you’ll have seen that a few weeks back I was trying my best to get in with my Consultant or GP because I knew things weren’t going well. I ended up making a visit to our local out of hours service after Mum, Matt and I decided it couldn’t wait any longer.
They decided pretty quickly that I needed to be admitted and I probably should have been sooner. Things had gotten worse, I wasn’t keeping food down, I wasn’t keeping water down and I wasn’t managing to walk around on my own. It wasn’t a routine stay.
We spent a couple of hours in a bay of a&e whilst they got things ready for me to be moved to a ward. After a bit of poking they managed to get a cannula in me and started some IV rehydration. The lovely male nurse had never heard of my condition and the Doctor was in the same boat. It was pretty blatant that I was severely dehydrated, I’d known that was coming, but they also noticed that the Ph of my blood was far too acidic – I had Metabolic Acidosis. That was a new one for me!
I actually can’t remember some of my stay, I don’t remember how I got to the first ward from a&e, all that tells me is that things were probably a bit worse than I realised but after a game of musical beds I ended up on Oncology. They use the same drugs I take so it was the logical move. It also came with the hidden bonus of staying in a relatively new area of the Hospital with single rooms, all with ensuites and lovely comfy beds. Matt had fun in the remote controlled chair and I was pleased to see some art on the walls. It might have still been a Hospital but I wouldn’t complain if my Hotel room looked like this!
Oncology are also very lucky to have a higher nurses to patients ratio than most other wards in the Hospital. That means they have a little more time, and makes it an all round nicer place to stay – you can really see the impact just a few more nurses makes. They really went above and beyond their duty.
One of the nurses was so interested in my condition that she did some research. She got in touch with a Doctor at Great Ormond Street that treats a child with the same disease and arranged for him to speak to my Consultant. Hurrah! My GI Consultant was happy to have found someone that has some experience of EGIDs and is now in the process of arranging for me to go down to Great Ormond Street to meet this other Doctor. See what nurses can do when staffing isn’t stretched to breaking point? (Take note politicians).
My Consultant wanted to take some more biopsies of my stomach whilst I was in, a pretty routine procedure but things got a little hairy because my blood pressure dropped below 70/40. That’s far too low. More bags of things were added to my IV pole, a second cannula was stuck in me and poor Matt was left worrying. He was told I’d be out in 30-40mins but he didn’t hear anything for a good 2 hours. I honestly don’t know how I got him but he’s pretty amazing!
After that, things were on the up. I’d had some lovely vistors and some equally lovely drugs so I started my petition for discharge at the start of day 3. My Consultant wasn’t over the moon at the idea but I’d finished any drugs I needed on IV and he saw my point – why keep me in if it’s just for things I can do at home?
As far as Hospital stays go, this has been my nicest to date. We popped back with a huge box of Malteasers to thank the Nurses. It’s was reassuring to have had such a positive experience especially with all the negative journalism surrounding FGH at the moment.
So what have I been up to since? Last Saturday, I got to spend a few of hours with my girls. It felt so good to get dressed up after weeks in PJs. It knocked me back but it was worth it.
Right now I’m still trying to get as much rest as I can and build myself up again. You’ll find me curled up on the sofa with a cup of tea in my lovely new mug from Utterly Personal. They have lots of lovely gifts to customise and I was over the moon with how cute this mug is, I just love the quote on the back:
gleepface says
That actually does sound like a lovely stay, if there is such a thing! So nice to hear that you’re getting to meet somebody who knows about your condition, sounds like really great progress!
http://www.gleepface.com
Vicki Higham says
It’s a bit annoying that it has taken 5 years to get to this point but my Consultant is so busy and the nurses are always over run with things to do. Just shows what a bit of spare time does! x
Carly x says
aww lovely blog post 🙂 Glad to hear you’re on the mend x
Charlotte Stewart says
So glad to hear you’re home and also great that maybe some progress is being made in terms of you going to gosh. Hoping and praying for lots more positive things for you over the coming year 🙂 xxx
Beeta says
I hope the rest is doing you some good and glad to hear that you are out of hospital. That little quotation on the mug is very sweet – not seen it before which is unusual with things like that these days!
Ellie Hill says
Thank you Vicky on behalf of all the hard working nurses that people don’t see working behind the scenes. I hope that you get to see the other consultant very soon so your illness can be managed better. You are such an inspiring young woman I’m so proud to have as a friend. x
Jade Culbert says
Aw I’m so pleased your getting to see a specialist!! And how amazingly nice of that nurse, angel in disguise!! Hope your feeling better now xx
Beth says
Poor you, hope you feel better soon and keep getting the help and advice you need x
http://www.beths1986.blogspot.co.uk
Glampire Victoria McEwan says
I hope you feel better soon *hug*. That little mug is adorable.
xx