Up, Up and Awaaaaaaaaaaay :)


so excited

This is me right now 😀
(Actually that’s a lie..me right now is sat in leggings, a baggy top and a hoody in my room at my desk, procrastinating doing one of the many essays piling up infront of me…but you know what I mean 😛 )

I am having such a good, CROHNS FREE time at the moment, and I just cant get enough of it! I have been on my easter holidays back at home for about 10 days now (time flies!!) and have been having such a nice time 🙂 I have been working quite a lot on university work, which isn’t fun; but balancing out with plenty of other activities! I have been working quite a lot for my mum and auntie – who own their own business – because my mum hasn’t been well recently; and although the extra shifts were unplanned for and therefore impeding on my uni work time, they have given me the perfect opportunity to earn that little bit extra money, just what I needed! Aside from that I have been seeing a lot of my friends, we played some tennis and badminton, chatting, a cheeky McDonalds McFlurry run here and there!
This weekend I went into London with a few friends and we went on the Shoreditch pub crawl – which was hilarious and such a nice fun night out 🙂 We then stayed at his flat in London – which was gorrrrgeous! Although I ended up with literally the worlds biggest blisters on my feet, had to limp home and get mum to pop them for me (gross I know). Next week I am going away with my dad, stepmum, brother and half brother and sister for a week down on the south coast- which I am really looking forward to 🙂 Unfortunately taking work with me but there we go!

I am sorry that I have nothing that much of interest to share with you – no dramatic stories, no horrible tales; but I hope that for some of you who have been reading for a while, it will be nice to know that there is no more of that at the moment! As of right now, I am just revelling in my freedom and my ability to do what I want Crohns free! I worry about this blog -about boring people, about writing too much or too litte, about posting too often…but I am just going with what feels right- I still CANT BELIEVE how many of you out there read these warbles, and it truly warms my heart! Thank you, thank you, and thank you a few times more. You will never know how lovely it is 🙂

H x

“clap along if you feel like a room without a roof…”


This song is just a feel-good song, I mean, you have to be having a REALLY bad day for this not to put a smile on your face!

I am sat here, at my window doing some work and watching the rain hammer down, and later am due to go swim some lengths with my friend at the uni gym- you know what that means? It means my scar is going to be out for everyone to see for the first time since the operation. Now that IS scary. That means that I wont be “introducing it” there will be no “yes, look here is my scar” it will just be me, walking in in a public place, in my bikini, and my scar will be there. People will see it, strangers who have no idea of the battle behind that scar, or of what it means to me, and trust me I am terrified. But, I don’t have a choice, I am not never going to wear a bikini again – and, as my friend said to me, if you can do it now when its at its most obvious, then it wont be an issue ever again. Wise words. She also promised to violently dunk someone if they dared stare for too long – which may have helped more than the wise words… 😉 But regardless, a day of facing fears. Wish me luck!

H x

Recovery Time


Turns out having surgery to remove part of your insides and getting stitched back together again is something you don’t bounce back from all that quickly..

From all the talk before hand about needing weeks to recover back to 100%, and having to miss my university exams in January and the deadlines for coursework that I have – I never really appreciated just how much it would affect my everyday life, I know, stupid, I had buried my head in the proverbial sand in an attempt to ignore the changes that were approaching in my life. After the operation I was in a very weak state, only what was to be expected in retrospect. As I described in my last post, https://livingmylifewithcrohns.wordpress.com/2013/12/30/the-operation-with-a-capital-o/, when I woke up I was hooked up to several different tubes running off into some scary looking machines; but at the time I was in too much of a morphine induced haze to care. I think in summary of the entire procedure I would say im surprised at how little the actual wound hurt me, but shocked at other issues (such as a sharp pain in my shoulders, that was apparently caused by the air pumped into me during the keyhole surgery which had not yet escaped) and how they affected me. In all honesty it was a little bit terrifying, I cannot remember having so little control over myself – an inability to even sit up and hold my own cup of water for the first day or so. Not something I want to repeat. I was lucky enough to have my parents stoically by my side doing everything from holding my hand constantly for the 5 hours they stayed, to sponging my mouth with water when I couldn’t drink, and sitting in a silent room bored watching TV whilst I slept – I don’t think I will ever have enough words to say thank you.

Anyway, this is due to be a general post about my recovery and the related activities- I am pleased to report that as of today (tomorrow will be two weeks since the surgery, and one week of being at home) I am feeling a lot more like a human being! I am managing to wear nice normal clothes again (a new dress from Christmas yay, with tights rolled right down so as not to press on my stomach) and managed to get driven into town to hobble to a coffee shop to chat with my friends; all of whom are sadly going back to university this week. Its official, I missed pretty much my entire Christmas break being dependent on my parents or in hospital and unable to leave the house, I am truly not impressed. Aside from that the eating is going really well, and feeling a lot more independent and happy that I may actually get my life back – something which seems a long way off on Christmas morning in a hospital bed! The day after I was discharged I was advised to have a bath to help remove the dressings and as a relax, which I duly did (do love a good bath!) and the wound started to bleed- HELP! It was only droplets at a time, but pretty steady and after no sign of it stopping we were advised to go to A and E. It turns out that they reassured me it was nothing but some “healthy bleeding” as the muscles etc had been cut through, and it wasn’t infected. They were all busy admiring my wound and saying what a beautiful scar it will turn out to be- I think you have to be a nurse to see it, I hate it! Aside from that, and 5 days on it is still bleeding a little bit, I have to have a foam plaster/ dressing on it all the time to stop it leaking onto my clothes, but I am hoping it is part of the healing process.

I think, and I rarely speak about myself like this, but I think a bit of self-congratulating is in order, both mentaly and physically. Well done body, you have taken less than 14 days (yes with some medicinal help) to get back into a semi-working order, something that has allowed me to be a person again not just a bundle of clothes unable to do anything for themselves. I am impressed and proud with how well I can walk – when I went to A and E when I got back, about the bleeding, they couldn’t believe how well I moved and that was nearly 6 days ago! yes, its slow walking, yes I cant walk far or for long, but I CAN walk. One week ago my biggest achievement was making it shuffling round the ward to the lift and down into the main entrance of the hospital, and now I am managing to function normally enough to get into town without attracting too much attention and to get around my three storied house all okay. GO BODY. Aside from that, I really don’t think I moaned too much about it all – I did let it get to me, and I am feeling the emotional strain from the operation and everything I missed; but I think that I coped well and have accepted what is happening as a force of nature and something this has to happen, no point crying about it. In the spirit of this paragraph I have to be honest, in the dark depths of my worst night in hospital (I think the Monday night?) I texted my parents asking them in the most ratinoal way possible to break into the hospital give me painkillers and smuggle me home because I was dying alone in the hospital and I had never been so miserable. Potentially a bit cruel on my parents, as I knew at the time they would have to say no, and then I got angry at their lack of care – how dare they not break me out?! Aside from that blip, I think I coped well and I got on with it, and still am so now. Even as all my friends head back to uni, and the partying, and the socialising, I am stuck here at home – but I am determined to make the most of it, enjoy the home cooked food and the family support.

I don’t feel the need to go into the details of all of my recovery – it would read as a boring and elongated medical diary to everyone out there; and I am hoping that more people will follow the blog, rather than bore people senseless! I had the catheter in for about 4 days, and when it was removed it was pretty scary – I suddenly felt like I wouldn’t be able to cope with controlling my own bladder; and although I was fine it reminded me just how fragile everything was, and how much I used to take basic bodily functions for granted. I had the cannulas switched to just one in my other hand as they became very sore, and slowly as the morphine usage reduced I had that removed too – I think on the Tuesday? I struggled quite a lot with sickness, but slowly that decreased as my water intake upped and I began to eat. It took me about 3 days of just on yoghurts, jellies and soups before I mangaged to eat without being sick – and I am talking about 3 or 4 mouthfuls as a meal, nothing really. On Christmas day my big meal and treat was a chocolate mousse, of which I managed to eat half – wild child! I had to keep forcing myself to eat little and often, and to go on walks around the ward which I tried to do at least twice a day, going further each time. By the point of leaving the hospital I managed to be able to walk for a reasonable distance, and could eat small mouthfuls of “normal” food without feeling sick. As of today I am pleased to report that (touch wood) the progress is constantly upwards, slowly but surely and I am determined to build myself back up as soon as I can.

I am sorry for the long and rambling posts. When I started this blog it was a way for me to track the physical and emotional challenges I am facing; in an attempt to increase awareness about Crohns and to come in contact with others in similar situations. Never did I expect that within the month so much would happen to me, and so many changes would occur, or that I would lose 15cm of my insides! Please, comment below or message me, I would love to have some feedback on the blog or on anything you guys are interested in; or general interest in terms of others experiences.

Keep Smiling, and a happy new year to you all!

H x