Wednesday, 24 September 2008
half way through iv's, yeay!
Monday, 22 September 2008
My secret drugs stash let me down
Thursday, 18 September 2008
Feeling sh*tty
Yesterday I got my pjs on at about 3 in the afternoon and I slept on the sofa, I brought in the sleeping bag as I was cold. I couldnt be bothered getting the duvet as it had loads of my clothes on and I hate putting my clothes on the floor and I couldnt be doing with sorting them out!
Today I got up to do my drugs at 7 then fell back asleep until 10.30, i only woke up because Alfie wanted to go outside for a wee. I then sat around for 2 hours doing nothing really, I did call the hotel to pay our deposit for our wedding reception. We are now officially getting married on the 11th September next year. No terrorists allowed.....!
I then got ready at about quarter to 1, I had a bath because when i'm on my ivs I find it easier than a shower. I dont like getting my port wet because the dressing peels off, its already peeling off near my armpit after only 1 day! Then when it peels off i'm scared of getting the needle wet, cant be very hygienic. Therefore getting a bath is easier plus when your tired its difficult mustering up the energy to stand in a shower, trying not to get your port wet whilst probably coughing......
I then decided Alfie deserved a walk and also decided if I actually did something I might feel better. This was not the case, I was walking with my eyes shut some of the time and felt quite dizzy. I was quite rude to people walking past me smiling at Alfie and going 'aw' etc, I basically ignored them. I'm just a horrible person... I took my jacket off so people could see my needle and then I thought they might leave me alone or excuse my bad manners, that was my theory anyway. I like to imagine what people think my needle is when they walk past me and wonder what is wrong with me.
So after that I came home put my trackies on (yep if the trackies come out its pretty bad) and curled up on the sofa again with my sleeping bag and watched a french film called Amelie which was a very strange film indeed. Yes thats right I can speak french, no just kidding, it had subtitles. The only problem with subtitled films is a) they are usually weird, not your average hollywood blockbuster b) you look away for a second and you miss whats going on, you have to watch the tv all the time. You most definitely cannot eat whilst watching it.
So now i'm just on the laptop a cup of hot chocolate, think I might have pie and chips for tea. Nice and easy, just shove them in the oven. Pete is at some work thing (or maybe having an affair!) so i'm by myself all night. Fun times.....!!
Wednesday, 17 September 2008
Starting IVs
So heres what happens when I start my ivs. I arrived at the ward after i was very lucky and found a parking space right outside in a disabled spot (this does not usually happen!). As soon as I arrive I am told what room to go into. The ward has a few treatment rooms for outpatients starting ivs and emergency visits and then about 12 rooms for inpatients all with their own bathrooms, tvs, fridge etc. In the treatment room there is a bed, computer and trolley full of things like needles etc. I tend to lay on the bed rather than sit on a chair because then I can chill out! I stay in the room the whole time and they bring everything to me including a cup of coffee if I would like one. This is to prevent patients bumping into one another and causing cross infection, they even shut the door which is abit harsh as I like to nosey at the people walking past! They do the following to me
a) they take my temperature, blood pressure, sats which were 97% and my blood sugars levels which were apparently abit low at 3.7 but they did not seem concerned. They also take my weight which was 57kg today.
b) the physio comes to test my lung function. This is a portable machine that I blow into. I do a slow long blow for as long as I can and then one as fast as I can. Today it would appear my fev1 has improved to 41%, maybe I didnt try very hard on monday. I also give the physio a sputum sample for her to send off to see what is growing on my chest etc. I also gave her another sample which is going to be involved in some experiment, I hope it is not to grow a big psuedomonas bug that will eat people! I also asked her about my physio as now I am doing it twice a day I would like to do other things than patting as when I do it myself it hurts my hand. She is going to order me an acapella, apparently it vibrates as you breathe out. Sounds interesting...! She is also ordering me a new chamber for my ineb for my tobi as I told her it keeps leaking.
c) the dietitian comes to see me, asks me about my poos etc. Its always a pleasant conversation. She told me my weight was fine and to keep up the good work
d) the nurse comes and sticks the needle in my port, whilst she is preparing everything I sit and bite my nails because I hate having my port touched. The nurse today had never flushed my port before so I was very, very nervous, people have missed my port before and it hurts! She got me to lay down whilst she did it and she did it fine. She had to find me my special dressing I have as im allergic to nearly everything, the one I have is called supasorb. Im allergic to tagoderm, dermafilm, iv3000, opsite and a few others. My port bled back, yeay! I dont know what they do with the blood they take form me, I think they are making a clone of me somewhere.... She then connected up my first drug as the first lot has to be administered at the hospital (even though I bring them in from my stock at home) to make sure I dont have an allergic reaction. Im on colomycin and aztreonam again and I change them over myself, I freaked out as she gave me the heprin for at the end and put it on the bed!!! I was like 'erm thats not very hygienic, can you put it on the trolley?', these medical people are useless!! Its so much safer doing ivs at home!
e) doctor comes and sees me, I dont know why because its already been decided what is happening. He was one of these doctors that just goes through the questions, he took forever typing stuff up, god know whats he was writing!
When my drugs have finished going through i am free to escape once I have collected all my extras such as extra dressings for my port, prescription for tablets for my thrush (I always get it when on my ivs) and my epipens for incase I have an allergic reaction (it is a pen that shoots out a big needle and gives you adrenaline, the needle is so big I would have to be literally dying to have the guts to use it...). And thats it im home and I feel tired already from my first dose! xxxx
Monday, 15 September 2008
Hello my names Gemma and i'm a binge drinker
Dunno who this guy is, but my friends must have liked his tattoo...!
Can you believe Pete proposed to someone else? Unbelievable! Luckily he said no to Pete, phew!
So anyway today I decided i've had enough of my cough and my large volumes of sputum I am coughing up. On friday morning I had a really bad pain in the bottom of my chest so did some physio and coughed up a big, hard piece of sputum. It was like a rock and about the size of a 5p coin. It hurt my throat coming up cos it was so hard. Ive been doing my physio loads and I swear the sputum never stops coming up, I could keep doing my physio forever and it would keep coming. I also getting really breathless and wheezy. So I called the hospital today and went in this afternoon to pay them a visit. My fev1 is down to 37% and my fvc is 58%, so its not down loads but my lung function doesnt change alot, only by a few %'s if i'm ill. I had to have an x-ray done which may I add was done very quickly and efficiently, I was impressed! Although, when did they stop giving you a thing to hold over your bum to protect it from radiation when you have the xray done? Hopefully the rays may have zapped abit of the fat off my arse.....hehe.
My weight is now 58kg so it is clearly not affecting my weight! I also peeked at my notes (they are all the computer now, its very fancy) and I found out my gene types are both df508. This is the most common types to have if you have cf, im such a commoner!!
Anyway i'm going on ivs on wednesday (sigh), I think I made just about 2 months without having any. The doctor says if I dont improve they will think about giving me voriconazole and steroids for my aspergillus, but they are very reluctant and want to use it as a last resort as they are quite toxic, so want to rule out infection first. She says my psuedomonas levels are quite high 100+ (whatever that means). Im slightly annoyed im having to have ivs again so soon, I dnt actually mind been on ivs, but been on them every 2-3 months isnt a good sign is it?! I feel like its just a sign my health is getting worse.
Thursday, 11 September 2008
straight hair
Wednesday, 10 September 2008
feeling useless
In the evening Petes parents took us out for a meal which was nice and I had some wine which woke me up abit.... Pete asked if was drunk on the way home (which I was not) because I was 'chatty' and this made me miserable again. I always interpret things he says to mean something else, see I interpreted this as meaning i'm not usually chatty because i'm boring because I sit around doing nothing. Earlier he said to me about something (cant remember what!) that 'it would give me something to do' and I had a go at him saying just because I dont work I don't need him finding things for me to do.
Anyway last night I ended up crying when we got home and just had a moan about my cf, I mean thats allowed once in a while isn't it? I explained I felt useless, that I was an intelligent person and had the potential to do great things with my career (seriously I think I could have been a great lawyer!) but because of my stupid cf I couldn't, I couldn't even handle doing a job that wasn't that demanding. I just moaned about everything, down to the fact all my bras are now too tight for me because my chest has gotten so much wider from I dunno, coughing and stuff, and they all now dig into me. I feel useless because we are skint because I have no wage now and don't even qualify for benefits for 6 months. When we were having tea Petes parents asked me what was happening job wise, I explained I had felt better since giving up work and didn't plan to go back. They said 'well we would all feel better if we didn't work', in a jokey way and i'm sure they were just joking around and didn't mean anything by it but I dont feel like people understand how I feel about giving up work, about giving up having a possible career. It is not something I want to do but I know its for the best. I just feel like I have no purpose at the moment, i've always had a goal to work towards and now I feel like there is just... nothing. Im so ungrateful because there are people with cf worse off than me but I cant help how negative i'm feeling at the moment. I feel like i'm getting left behind, my friends are all doing great stuff, Pete has a great job and i'm just doing nothing......!
So anyway today I bought a load of new bras, I got 36's. So I wont have that problem anymore, I also walked the dogs around town as I needed to pay a cheque in and post a letter. I also went food shopping which I find extremely hard work as we live on the bottom floor and you have to walk down stairs to get to our flat so back up them to get the next lot of bags and its hard work....! Ive got a new book to read called the constant princess, its about Catherine of Aragon (yes my Tudors obsession continues), its by the woman who wrote the other Boleyn girl and that was a really good book. I got this book off ebay for £1.20, bargain! So going to read that now, then kill myself later ... No i'm just kidding :o)
Sunday, 7 September 2008
feeling abit down
I have also been thinking bout having children, I always assumed I would be able to. But I was reading that cf booklet the hospital gave me and it says they recommend your lung function is above 60%, well mine is 41%..... So now im thinking I wont be able to have children and if I do my health will get even worse and I will die. I know thats very dramatic but thats what happens eventually if your health keeps going downhill! Surprisingly I dont really want to die, i've always accepted I will die before the average person but even when you accept that, it doesn't mean you dont mind dying in your 20's or 30's. People don't like talking to me about me dying, they say im different etc. erm no i'm not, i'm not invincible. So now I dont even know if i'm going to be able to have a baby, I mean i'm not planning to get get pregnant tomorrow but it was always something I planned to do. The idea of not has really upset me because it's like the most important thing a woman can do in my eyes, so I would feel like a failure. And its so annoying when there are people just popping kids out all the time that they don't really want, they don't realise how lucky they are that they can just do that!
Alongside all these 'great' thoughts i've been having, my chest has been feeling rubbish. I keep getting pains in my chest and my chest feels like its too big for my body so I cant breathe properly. Im getting out of breath easily and coughing all the time, i'm also coughing up little really hard, kind of rubbery bits of sputum (nice ey?). Also my body is achy but i'm not sure if this is from falling down the hole the other day, i've got a lovely black bruise on my leg from that by the way, its about the size of my hand!
I went to see The Duchess last night at the cinema, which is a great film by the way and I was coughing in the queue for the tickets, the queue for the popcorn (yum!) and eventually went to the toilet and coughed loads of stuff up in there, luckily the toilets were empty. I eventually stopped coughing, its so embarrassing, people were looking at me and im sure a woman moved away from me. If I hadn't have stopped coughing I dont think I would have been able to stay, I cant stand it! Ive got one of those cea cards now, so I paid for my cinema ticket and Pete got his for free as my carer, so that was good!
On a positive note, I saw a dress I liked for my bridesmaids on the internet. So grabbed my friend and we went for her to try it on, it was lovely. So I have bought it and going to order the others. I know its abit early but I really liked it and they won't sell it forever, I dont like many bridesmaid dresses so to find one I like is a miracle and I had to get it! It was nice to get out of the flat and see my friend too!
Thursday, 4 September 2008
bad start to the day
So now we are all sat watching ER and my leg is killing, im annoyed, not a good start to the day!
I've joined the gym, but they have to wait until a doctor has seen my evidence or something like that. So I don't know how long that is going to take, I wish they'd hurry up so I could get started!
My appetitie is abit poor at the moment, I hardly ate any tea last night (cos it was horrible) and i've not been having lunch, although I did yesterday because Pete took me out for lunch. Anyway Pete went and got me some hagen daz icecream last night, so dont think ill be losing any weight in a hurry.
I might take the dogs for a walk later, although when I took them on tuesday it didn't go well. Alfie kept trying to hump Murphy all the time and their leads got all tangled up when they were barking at another dog and I dropped Alfies lead. So I looked abit stupid running after him... coughing, infront of people. So we will see how today goes.....