Showing posts with label bad. Show all posts
Showing posts with label bad. Show all posts

Monday, 5 May 2014

Terrified

Im home...thats the main thing. By this though im home in body, not in mind. Two weeks ago, my other half went out for a walk with Dixie. About half an hour later it started to happen. I was so scared. I had no idea how long she would be and I couldny get through to her as she had no signal. So I sat there waiting. Nebbing. Worrying. When my lovely lady returned she was worried. She called an ambulance straight away. Because of how long I was sat there on my own nebbing, by the time the ambulance crew came my chest was silent. Honestly though I was only sat there for roughly 45 minutes and then we were waiting about 10 minutes for tge ambulance crew so not really that long considering how I used to leave things whilst living in the city. Being rushed into resus I knew what was coming...shit loads of blood gases and boy wasnt I fight. The nurse that was assigned to me was initially nice...and then found out I was gay. She gave my partner the most filfiest look ever, then chucked a peak flow meter at me, then yanked the neb mask off my face half way through a neb and told me I need to stop panicking. By this point I was telling my other half, one more bit of nasty treatment and I was leaving and taking myself to plymouth. The doctot that was assigned to me initially didnt want me to have any drugs either. I told her what treatment I needed but she said I wasnt poorly enough. Off she sends me for another xray as the first wasnt all that clear and then come back to me and says "I would like to do another blood gas as the first two shows signs off deterioration. If this one does also ill put up some magnesium and we will have to get ITU to take a look at you". Funnily enough because treatment hadnt been started, my third blood gas was worse again. After one lot of IV antibiotics, my cannula tissued and my arm blew up. I told the doctor but they didnt believe me so left it 3 hours for my arm to shrink before running the magnesium through it. And guess what, my arm blew up again and they had to recanulate. By this point of course I had been moved to the medical admissions unit to be closely monitored. I think it was around 5 am (though not entirly sure as I was asleep) and I got woken by the lady doctor again asking if I was ok as my observations were going off the chart. She listen to my chest and the next thing I know shes running away from me. Then I heard it, she was on the phone to ITU. 4 more blood gases later, 15liters of oxygen on a rebreathe mask and finally the magnesium, oh and of course an ITU doctor. Thankfully though at this point the remained wanting to keep an eye on me. By the time alk this had happened it was now morning (officially in hospital world) and I had the day med reg come to see me who thankfully was a respiratory reg. She was not impressed with how I had been treated and demanded I needed IV aminophylinne immediatly. Once this was up and running, and I had all the oxygen running through for roughly 12 hours I started to feel a little better. The lovely resp reg came back to see me at 8pm to make sure I was ok before going home. We had a good old chat and she told me that she spoke to my team at derriford and new abit more about my asthma which was going to help her treat me. Unfortunatly though the next day she was in clinic and wasnt able to review me herself. Once all the aminophylinne had run through, my partner took me in my wheelchair out to the corridor on my oxygen to see my friend. She wasnt allowed on the ward because she has an 8 month old son which is fair enough. Whilst out in the corridor, the resp doc saw me and asked how I was. I told her the truth. I was starting to feel shit again since the drip had been down. By 9pm, I had 4 doctirs at my bed. The resp reg couldnt make it herself to see me but she sent a team of docs into review me. Suprise suprise my chest was back to being silent...AGAIN. Another dose of magnesium and more aminophylinne and we were going through it all again...and ITU looki g after me on the ward because there were no beds up in ITU. (This following bit I cant actually remember, its what my partners told me) The next day, I was very very sleeepy. After lunch I got up for a wee and then I remember no more. Aparently I was very sleepy and not really responding. I had more magnesium and of course the aminophylinne was still running. My partner got asked whether she wanted my mum to drive down because I was really poorly. The next thing I know, my mum and step dad, my mother in law, plus 3 docs, 2 nurses an ITU reg and an ITU consultant was at my bed...and I was off to intensive care. The next 24 hours was all a bit of a blur and I hated it. Thankfully though the ITU team were fantastic, though left me bruised from foot to wrist...literally as they started using my feet to get blood and give me drugs. It turns out that the whole of the lower half my lungs were fully of infection. The nasty thing is, because the Infection was irritating my lungs so much I had now started coughing up blood. I had physios and doctors all working with me to help me get better. A week later I felt better. I was no where near safe but I couldnt cope being on ITU so I asked to go home if there was no beds on the resp ward. My pf was still only 150 but I agreed to stay in bed and not move...and ive stuck to my word. The thi g that got me the most in ITU was a CODP man got rushed in 2 days after me. He started iff breathing on his own. It then mived to NIV. And then it moved to him being tubed. Everything I could hear was exactly like when I was tubed. I didnt sleep at all since that man arrived. Each time I closed my eyes I got flash backs and was terrified. So on the wednesday the docs agreed for my mental health It would be safe for me to go home. I have my partner here looking after me and ITU arranged for the early intervention team to pay me a few visits to make sure I was still going in the right direction. Now that im home though, im still not sleeping well. Im napping on and off throughoit the afternoon. Then I fall asleep at mindnight for an hour and then im awake again till 0630. I think sleep for roughly another 1 - 2 and then im awake again. I hate it. I just want to sleep and recover. Thankfully though, I have a great friend who stayed with me through facebook when my attack started two weeks ago and this same friend has allowed me to use her netflix account so that I can watch films through out the night on my kindle whilst my other half and pooch are asleep besides me. One bonus about being awake at 5am is that you get to hear the birds waking up as everything else is silent. Its actually very peacful. TTFN XXXX

Monday, 3 March 2014

Not My Day At All!!

I woke up at 3am, initially with massive pains in my joints. I thought nothing of it, went for a wee and then went back to bed. When I woke at 0730 I have never felt so poorly in all my life. My temperature was 39.2, I had a splitting migrane, was sweating out and had those horrendous joint pains still. Along with this, I just felt detatched from my body, my co ordination was shot, and I just didnt feel right at all. Im annoying stuck in bed as its to dangerous for me on the stairs, ive had to strip right doen, open my window and eat paracetamol just to try and sort out my temperature, which currently is remaining high. I havnt a clue whats causing it, I dont feel drastically bad with my lungs, but I cant think where else the infection could be...if its that, thats causing it. My other half has yet again been a gem, shes cancelled her volunteering for the day to look after me. Although this makes me feel bad, in a way im glad shes here, and thankfully shes rearranged things for thursday. Im a little bit ticked off though, as about an hour ago I decided I actually wanted to eat something do the other half went and made me some toast. When she got downstairs, yet again her mum started having ago at her because she hadnt done the dishes whilst they were out shopping. My girlfriend tried telling her mum that shes been looking after me and making sure im ok. According to her mum though, she doesnt have to stay upstairs with me just because im poorly, and also that she needs to start pulling her weight more. I feel so sorry for her, she wanted to stay with me coz one I feel like shit and can hardly move, and two, why should I be left up here on my own just because my body doesnt want to work. Its completly unfair, and this shit for not pulling her weight, my other half cooks all three meals a day for both of us, she does the washing, she washes the dishes, she does shopping. Sge tidies up and she helps out with all our pets, I dont see what more she can do, especially as shes a full time carer for me also. Its a lot for her to take on. Her mum seems to be having ago at everyone, but she doesnt see it, and she thinks that shes doing nothing wrong, yet most days and evenings now shes left in the living room on her own as the rest of us cant stand being in her company, I mean, doesnt that show you in itself that theres clearly something not right with the attitude and atmospher!? Clearly not!! Well, im feeling crap again and starting to nod off, I hope this nastiness starts to fade pretty darn soon!! TTFN XXXX

Wednesday, 19 February 2014

Dentist Disapointment

I final managed to get to a NHS dentist after 4 months of being on the waiting list. Horray...or not so it seems. When they rang me to tell of the surgery that will have me, I rexplained that I am disabled and not very good on stairs, they said this was ok and sent me the details to make an appointment. The only perfect thing about this surgery is that it is very local. The rest goes down hill. To get into my surgery you have to go up two flights of stairs (er what happened to disabled friendly). My actual dentist funnily enough has ubber bad breath which is really off putting when your led there breathing through your nose sucking in his aroma and the last bad thing is. The dentist doesnt seem to have heard about asthma, strange one I thought. As suspected though, it was about time for my steroids and nebisers to start effecting my teeth, and in two weeks I now need to have treatment. Im really not looking forward to it as the last NHS dentist I saw in Bristol butchered my mouth and has put me iff ever since. On good notes though, my oral hygiene is good!! Ill let you know how it goes in two weeks!! TTFN XXXX