Saturday, 15 October 2011

Catch up time!! Sun, Sea, Wine and Weddings n I end up in Hospital!

The point when you know you need to rest, but life goes on and your not ready to sit around and just watch it!!

To say this last week has been difficult is an understatement.  I had an amazing holiday in Cyprus and really didn't over do it, but it just seemed to take its tole, then work was very stressy for the first 3 days of been home and so when thursday last week came and i finished my shift at work my body just gave in!!  I had planned to go with my friend for my first gym experience, because it's a little scary going alone, but there was no way my body was gonna let me.  I came home and sat on the sofa, n that's where i stayed all night.  I knew IV's were on the card, i'd already upped my steroids to 20mg and put myself on Cipro, Dr Jo (me) is very good really at prescribing, but you know sometimes it's just not gonna be enough.  I should of rang friday morning to book my IV's but wanted to rest and just give the Cipro n Steroids a chance.

I was looking forward too my weekend, Friday I was going out for a curry with Steve and his friends for his birthday, so I spent all day in bed, just a little trip out to get my nails done, needed a little TLC! :) I got ready and actually cause i'd had a lot of rest felt ok for the night, i drank a whole bottle of wine, prob not the best idea, but sometimes i think CF is enough to turn ya to drink n hey think of the calories i packed away! Curry and a bottle of Wine!! hee hee, i can justify everything.


Shame I couldn't justify it in the morning, till about 2pm i stayed in bed, resting, n when the hangover wore off, i still felt crappy with my silly lungs.  Steve was pretty hungover too, so we had afternoon on sofa watching Flubber of all things, you really know you feel rubbish when you watch them kind of films.

Sat night was Gem and Gaz's Wedding Reception at home, it was for their wedding that I went to Cyprus, which was amazing day in Cyprus.

 

I went on holiday with Steph my best friend, we had a lovely time and staying in a lovely hotel with breakfast to die for, i'm still missing the pancakes every morning now, its just way too much effort over here to make them for breakfast.  I ate really well on holiday, put nearly a kg on, normally i loose weight on holiday cause i'm not doing my feed.


So Sat was the wedding reception at home and eventually i found the energy to get ready, was a little late, but least i made it, it was a struggle, i knew my lungs were been pretty naughty.  On the night, i decided to drive, a few cokes n i had some energy, i do like the dance floor, but i had to just dance to songs i really liked, i had created a new dance, the chest pain move, one hand holding my lung n the other doing some crazy move! Had a good night though, even though it was hard work.


Sunday i had planned not to do or go anywhere, my phone vibrated and then started to ring, but i ignored it, then i rolled over just to check who it was, it was 10am so it wasn't that early but i was still tired.  It was a message and missed call from Gem and a message.  The message that read "Nat has passed away".  I sat bolt upright and hit the call button! We all knew Nat was really poorly and we all know how cruel CF can be, but i guess deep down inside you hope for that miracle.  It was kind of an expected shock, the whole time i'd been in Cyprus, i'd been checking facebook and sending texts.  When i got back life distracted me a little from been so on edge which i think it's why it was such a huge shock.

Me and Nat had a strange friendship, i guess you'd say we were CF friends, not really talking about other parts of our lives, more about the IVs, lung function, feeds and just the general crap that goes on at the hospital, she was a very private girl, not like me i broadcast my CF way too much sometimes.  Why i can't just answer the question people constantly ask with a "Yes i do have a bad cold/cough" I don't know, instead i'm like "Oh I have Cystic Fibrosis".  I wouldn't say i'm looking for sympathy, cuz i don't like that one bit, it's just i've never hidden it.  People tend to know me for an hour n they know i have CF, i've normally coughed n they comment or its just come up in conversation! I find for me it makes life easier, i know not everyone is so open about it! I think it's just the way i've been bought up, at school all the kids knew i had CF made it easier when i had to scoff all me treats, drink that horrible orange juice with maxijul in and stay in at dinner time till i'd eaten all my dinner, god dinner ladies r crueler than kids!

So this week has been a struggle, i knew i needed IV's so tuesday i started Ceftaz n Col at home, my lung function was an all time low again of 27% which kinda scares me, i'm not ready for my lung function to be that low to be honest! Its was 37 before i went Cyprus, so the 10% drop quite a lot n quite fast!  My lungs were filling fast with crap n mornings getting out of bed in the morning to go work was a real struggle, i was coughing my guts up just making it to the kettle to get my much needed cuppa tea, then puffing n panting back up the stairs with it to do my ivs, nebs n get ready! I was nakered by time i was ready!!

I've even had a trip to walk in centre as i thought i'd got a UTI, i went loo 3 or 4 times at work n was a reddish ting to me wee, they tests my wee n said it was clear, no infection, bit protein but no blood but it looked like blood shud be present.  I had kidney pain too in left kidney, so yesterday i my day off i dragged my little ass up to the hospital to get checked out, my wee still a mystery, still same results! Turns out though after a little brain wave from the SHO that i've actually been eating too much beetroot!! Yes beetroot makes ya wee red, it's a no brainer really!! Quite funny, but quite relieved it was just the beetroot! lol! It's my nan's fault getting me addicted to Cheese Spread on Toast n Beetroot Salad on top!! Weird yes i know, but don't knock it till u tried it, i been eating it every day for breakie! I find breakfast the hardest meal to eat, i tend to have fads on something, eat it constantly everyday for a month then i don't know what have when i'm bored of it, so i'll have a week or too eating bickies for breakie before i find something knew to fad on!!

The docs decided i needed come in especially after i told i really was struggling at home, i've not been in here for a year! But here I am, i've been on drip for 18hours so far, peeing like a trooper, so annoying when u attached n need a wee!! I think i really needed to come in, i've cleared loads with physio today, not had percussion for years i swear i'm gonna wake up battered n bruised tomorrow, she really pummeled me!! But guess it's worth if if can sort these lungs of mine out!

I've had so many iv courses this year at home, n i'm so tired of them not working properly or me only feeling better for a few weeks!! I hope this time i really do sort myself out, or they sort me out, at home it's so hard sometimes cuz it's all on you to make urself better!! So i'm gonna rest, let someone else pump drugs in n let physios treat me n be a good girl for a change, just hope it works!! :) xxx


Sunday, 9 October 2011

A Very Special Young Lady, Today is her day!!

This week i've started writing my blog entry so many times but it just didn't seem to flow, i had show much to tell n so much to say!

Today none of that matters it can all wait, Today i wanna tell you about my beautiful friend who in the early hours of this morning lost her fight to this life threatening disease that I and so many of my friends fight every single day just to keep going.  

Early i'm stood washing my dishing, such a mundane and ordinary task, a task to which I got out of breathe doing a coughed quite a lot, a task which most of us hate but take for granted every day cause it's just so simple to do!  I had a few days worth to do this afternoon, it's something that's not felt important, today it was kinda therapeutic as I stood looking out my window thinking about my amazing friend.  


Natalie was so brave when I met her, she was about 17, she was 22 and on Halloween this year would of been 23.  Nat has been using an NIV every night for last 6 years, it was only 5 weeks ago after her holiday to Tenerife it was the first time i can honestly say I was scared for her, she struggled on so bravely every single day, yeah it was tough, we all know how tough some days can be.  Nat had IV's booked in every 6 weeks and she has battled on everyday year after year fighting to be here with them lungs she was born with.  I remember so many times she'd say i was born with these lungs, they're gonna get me through.  

She never wanted a transplant, just before her 18th Birthday she was told without one she'd be lucky to see her 21.  Well she say that and celebrated in style and every day since has battled hard, she wasn't ready for this, she wanted so much more and three weeks after reading Kirstie Tannock's Story in a magazine she had decided she thought she was ready for a Transplant, something she had never wanted before.  I was so happy when she told, i filled up with tears, 

Nat wanted to live so much, but unfortunately things just kept getting worse for her this last few weeks and the best they could do was make her as comfortable as possible.  My nurse said it was peaceful and perfect for her and she looked absolutely beautiful.  Which is kind of a relief, now she is free from pain and probably up there in Heaven with all our friends we have lost over last few years having an amazing party, catch up and all sitting looking down on us wondering why we are all crying.
Preventing Cross Infection!!! xxx :) xx
Gem's Hen Do

I'm been teary all day, it's just so tough knowing another friend looses her fight, but Nat my lovely you were a true inspiration of a girl who fought everyday and i will never forget that, time was against you, it just ran out way too fast for you.  


I will never forget you, i'm gonna miss you. 

All my love, breathe easy and rest in peace sweetie!! :) xxx

Sunday, 11 September 2011

Intraconazole finally started, IV's again but i'm doing good for a change i think!!

It's now 2 and half weeks since i started my Intraconazole! When I started my lung function was a crappy 32%, my orals finished a day later and my steroids down to the normal 10mg, so i had 2 weeks where it was only the intraconazole that i was on different.  My liver behaved and after the second week my dose was increased from 100mg once a day to 100mg twice a day.  I was quite chesty when i first started and a bit tired from coming home from my holiday and really not wanting to be back at work or even be in the UK, you could of put me on a one way plane back to Turkey and I would of been a very happy girl.  I started the intraconazole on the tuesday and had to work wed, thurs, sat, sun and monday.  Couple of days were over time, wed and thurs were a struggle and i really wasn't looking forward to three days in a row, but sat i went to work and it didn't seem to much of a struggle, neither did sun and mon to be honest.  I actually felt quite good at work, normally even when i'm well i struggle to do clear rail (which is putting on clothes that people have tried on back in the right place), i struggle cuz the weight of the clothes and the walking round the shop alot, i normally struggle with delivery too, but i felt good.  I had been doing my nebs in the morning, thats something now i think i have to give in too that it's something i need to do most mornings just to clear my lungs  from the night time filling up.  But i actually feel good.

After two weeks my lung function had increased by 3% to 35%, they say with intraconazole an increase of 5% is really really good so i was happy with my 3% so far.  I'm now on IV's though so its gonna be difficult to work out what's doing what, i'm on iv's before my holiday to Cyprus on 24th Sept.  I would never go on holiday without a course of IV's first and its really tough having them when i don't really need them but hey ho be worth it for my holiday.  I'm on Tazocin IV not had for a while, now nearly had a week and i'm nearly on 3 weeks for my Intraconazole, i'm in clinic tomorrow which is monday so we'll see how doing.

When i last had intraconazole i noticed my morning coughing fit calm down and on some mornings not even happen, i'm now on day 3 of no morning coughing fit as i walk down the stairs, normally i make it down the stairs fill the kettle and while the kettle is boiling have a huge coughing fit.  I hope this is the intraconazole but its difficult with the IV's too, not had Tazocin for about 3 years, and i'm so remembering the reason's why i dodged it, bowels well they are mega dodgy, silly me went n had a curry last night so it's not gonna be good later on today, hee hee!! N the taste in me mouth, u just can't shake it, horrible.  So can't wait for these two weeks to end, i really hope with the IV's n Intraconazole before Cyprus i can hit 40% lung function again, it would be ace to prove to Dr Lim that it really is helping.  i'm keeping a little diary for him this time to prove things.  He only said initially i can have it for 4-6 weeks.  So fingers crossed.

Anyway really should get my ass moving, we moving my nan today to her new flat.  Need to find lots of energy for this afternoon, yesterday was brill, i'm so designing her new flat and before i went to work we went to all the home shops, next, bhs, argos, and a furniture shop.  We bought so much stuff, new wardrobes, sofa, table n chairs, dinner set, cushions, bedding, towels, my dream job!! Grandma do u like this, ooo yes i'll have that!! Her bathroom has a pink theme, bedroom turquoise and lime green and living room red with poppy dinner set.  So cute.  I love all stuff we picked!! Was ace picking it all out and not paying.  Dad must of gone to checkout bout 4 times in bhs cuz we kept filling trolley's.  So today i get to start making the place pretty!!

So excited for my nan moving, she going to be so much happier, this new build flats is an extra care center and now she 93 she needs bit more help.  It's so modern though, i would live there myself.  I'll get photos!!

Sophie is doing really well and i'm so proud of her everyday, yesterday with lots of help she did a little walking!! She's such a brave little star.

Right i'm off to pack n unpack!!

Speak soon!

Love me xxx