Skip to main content

Going Home!

Tuesday 27th March 2018

So they reduced my Prograf level and I felt so much better really quickly! Prograf is one of my anti rejection drugs and its extremely toxic, it works by effecting the production and function of your T cells which are your cells that fight infection (essential part of your immune system). The levels need to be between 8 and 10 and mine were 14.5 when I went back onto the ward, so it's no wonder I didn't feel well!

Before going home I spoke to the occupational therapist and went through things at home, the main thing we talked about conserving energy when I go home. She explained that I'll be way more tired at home than in the hospital because I'll be doing so much more, so I need to sit down when cooking and she suggested a bench for the shower as well. I also spoke to the dietician about food safety, so I am more likely to get food poisining but also if I get food poisining it's very dangerous for me to be sick because I wouldn't absorb my medication. I don't eat meat, seafood or cheese so I don't eat most dangerous foods but I have to be careful when I eat out. Also, I can't eat buffet food because it's been sat out and becomes germy and when I eat out I need to check the hygiene rating of places.

I had my second biopsy Monday 26th and all was good, no rejection, which I was really worried about because I'd been so sick a few days before! When I go home I don't need to have another biopsy for 2 weeks, but I need to come in in a week to have my bloods done. They're still checking my bloods for my kidneys, white cell count, infection markers, prograf level etc.

Tuesday morning my doc said I can go home! I knew it would take a while because it always does when you're discharged from hospital! The pharmacist came and made sure I had all my medications to go home with. So on the ward I was taking:

IV: Paracetemol, ondansetron (antisickness), antibiotic
Oral: Prograf, MMF, Prednisilone, Aciclivir, Sildenifil, Co-trimoxazole, Fluconazole, Lanzoprozole, Cyprofloxacin, Pravastatin and Metronidazole. I was also on Bumetanide (diuretic) but I came off that only a couple of days after being on the ward. I was also prescribed 2 laxatives but I never took those on the ward, I think they're prescribed in case I had issues from codeine.



MMF, Prograf and Prednisilone are my three anti rejections, which I'll go into in more detail in another post, and the rest are to prevent issues from the antirejections such as antibiotics, antifungals, antivirals, stomach protector etc.

So I finally went home at about 4pm on Tuesday evening, my mum helped me pack up all my things and drove me home. I got dressed, even put on a sports bra and knickers which was weird as its the first time I'd worn underwear in over a month! Haha. I put on a bit of makeup too for the first time, and it made me feel more like myself! I was quite sad to leave all the wonderful nurses on Jim quick and the safety of the hospital but I was very excited to get home!




The one thing I'd been craving in hospital was chinese noodles with tofu, possibly because it's the last meal I had at home or just because it's full of veg and tastes so good! So Ciaran made noodles for dinner and ran me a bath! It was soooo nice to have a bath! And the warm water really helped my chest pain as well. I got quite emotional while I was in the bath, I am so blessed to have recieved my transplant and to be home and be so well! And to have such a wonderful family and boyfriend that have supported me throughout it and taken care of me.







Comments

Popular posts from this blog

5 years of being a heart transplant recipient

I wrote this post 3 years ago and it just sat here as my blog wasn't live, but I wrote it to process my feelings around hitting such a huge milestone, it's obviously now out of date but I decided to just post it as is! The blog is back. It might be a one off, I might stay consistent, who knows. As I often say 'life has a plan but we'll never know what it is'. I'm not quite 5 years post transplant, my anniversary is 27th Feb 2023 but the countdown to this anniversary has been going on for months now. Every year feels like a big deal but this anniversary feels like a huge deal and I'm not fully sure why. A lot has happened since I was 21 and put on that transplant waiting list, in fact, looking back is like watching a film about a girl I kind of know but not very well. I have a scar down the centre of my chest to remind me of what I've been through, but even that has faded to a point where I don't even notice it.  So my emotions have been quite mixed r...

Still not listed!

Friday 5th Jan 2017 I spoke to Ruth on the phone this afternoon to find out if I'm being listed and I have to wait until I've switched to Warfarin! So currently I take Apixaban (anticoagulant) because I had a blood clot in my heart, and I still take it to prevent getting another one and possibly having a stroke. Apixiban is a newer version of anticoagulant so it's a fixed dose whereas Warfarin you have to have the INR in your blood monitored and they adjust your dose and it can also be affected by certain foods. Warfarin works by blocking Vitamin K which is what clots your blood, so if you ever had an emergency operation they would give you Vitamin K to reverse the effect of Warfarin. However, there is no reversing agent for Apixaban so because I know I'll be having an operation at some point they will put be on Warfarin to ensure there's a reverse agent. This is annoying because I already knew I needed to switch to Warfarin and I could have done it weeks ago h...

6 Month Checkup at Liverpool

November 17th 2017 Today I was at Liverpool Heart and Chest Hospital for my 6 month follow up. I had an ECG, an Echocardiogram, and then I went to see Dr Todd. My ECG today shows that my ventricles are starting to struggle more and can't get as much oxygen around. A CT scan that I had done while I was admitted in August shows that I have enlarged lymph nodes in my chest. I've done a bit of googling and there are a few things that can cause enlarged lymph nodes in the chest including sarcoidosis and an infection. The doctors had a discussion and they think I should have them biopsied to check they're nothing scary. They're pretty confident that they're only swollen because of my heart but they have to tell the transplant team about it in case they want to investigate.  I had my DNA tested a while ago (it takes about 4 months to come back) so today I saw the genetics lady at Liverpool, Dr Mckay. She said they've found a faulty gene in me, so my mum and dad ne...