Monday, June 18, 2012

We miss you

Hard to believe that it is coming up to three years since you left us, you are always in our thoughts and prayers.  I know we have own angel who has supported us whenever we need that extra help, but it is hard.  You were a brilliant daughter, sister, granddaughter, cousin and friend and we all miss you so terribly much.

Wednesday, September 2, 2009

Naoise Book

Hi All,
We are working on a project to convert Naoise blog into a book which we hope will celebrate her life as well as raise a few bob for Temple Street Hospital. Our intention is that the main body of the book would have her blog entries accompanied by the messages that people have left for her.
I want to check if anybody had any objections to their name or message appearing in the book. If somebody wishes to remove any item could they please send me an email at mcgderek@gmail.com and I will ensure that the relevant message or name is removed.
We hope to have the book ready for Christmas.
Thanks to everybody for their continued support and best wishes.
Derek

Monday, July 27, 2009

Naoise's Months Mind

Hello Everyone, We would like to express our deepest thanks for all the support, cards and letters we have received during this difficult time.

We also wanted to let you know that Naoise's months mind will be held at 10.00 am on Sunday August 2nd in St. Anthony's Church, Clontarf. Hope to see you there.

Michelle & Derek

Tuesday, June 30, 2009

Day +138

Naoise, our beautiful daughter, left us at 2:10 this morning. Her passing was peaceful. Ar dheis Dé go raibh sí

Sunday, June 28, 2009

Day +137

We wanted to let you know that Naoise’s battle for life is coming to an end. The medical team here on Bone Marrow Transplant Ward 23 in Newcastle have done their very best throughout the last five months. However, they have now confirmed that this is likely to be Naoise’s last week. Naoise has gone through so much in the last few months and even now she is showing her amazing spirit in her final moments. We are so proud of our daughter and the effect she has had on everyone she has met. She has made her mark in her short life and we believe she is now going to a better place. We thank you so much for your support, gifts, cards, wishes and prayers for Naoise. We ask that she continues to be in your thoughts and prayers for the week ahead.
Naoise’s Mum & Dad

Friday, June 19, 2009

Day +126


Hi All, I’m very sorry for not keeping you all up to date but as you’ll see it was a very hectic week. I won’t go through day by day update instead I’ll just talk about the big things. You know I had a biopsy last Friday, well it seems that every time I have a biopsy something dramatic happens and this case was no different. I thought I got over the biopsy quite quickly and I had a reasonable ok day on Monday and Tuesday with ok nights (only up about 3 to 5 times per night). But what was happening was my weight was gradually going up and up. I came in at around 32kg and three weeks ago I was 35kg but by Tuesday night I was heading towards 41kg. Everything here is measured, checked and weighed, so when my weight started going up and up the doctors started to get worried. It turned out that my kidney was not working quite as well as it should and so I was taking on more fluid than I could get rid of. The docs here were quite worried and kept looking at all the fluids that was going into me. They decided to change a lot of my meds from transfusions (which require the medicine to be diluted with water) to direct feeds into my tubes. They also said I had to limit my drinking to 150mls per day, which was nearly impossible. Dad went home on Wednesday morning and he was only home a couple of hours when he got a call to come back to help out. My mums dad (gaga Christy) was over for another visit and at the start wasn’t allowed into my room. So dad came back on Thursday morning and he brought Nana Ruth and gaga Michael, so now I had a small crowd and surprise surprise on Thursday afternoon the doctors decided that my grand parents could come in. It was great to be able to spend some time with them. Also by this stage I still hadn’t wee that much so the doctors changed my medicines and put me on a huge amount diuretics. Everybody seemed a little concerned and we sat tight and weighted. Late on Thursday night all changed again and I started to wee for Ireland, in fact I kept on going all today. Now the next issue is this. As you know I’ve been pooing loads for the past couple of months, well now I seemed to have stopped, or as Prof Cant say’s ‘I’m on a go slow’. Speaking of Prof Cant, he came in this afternoon and said that he was very pleased that my kidneys were back working and that the biopsy results from last week showed some improvements so he was a little happier, but still concerned about the lack of poo. So as you can see it’s been a very busy couple of days with lots going on, as usual.
Oh, the last big piece of news is that I got a personal letter from Brian Cowen on official government paper. Everybody over hear was very impressed that our Taoiseach took time to send me a letter. So that’s all for now, lets hope that everything returns back to normal real soon. Thanks to Marie for my bag, you are right a lady can never have too many ! and thanks to Ross for my cool dvd – I love it.

Saturday, June 13, 2009

Day +121

Hi all, well last night was as we had expected kinda tough and today was a total right off as I have just spent the day asleep and going to the toilet. It is always the same when I come back from a biopsy. I suppose it is the antistatic taking its effect. I also had loads of drugs to take today which the nurses just worked away while I slept and slept. I was supposed to have a shower, but I just couldn’t bring myself to take one and you know how much I love my showers. The only thing I did was to play with Amanda but that was only for a half an hour. So short note tonight. I hope tomorrow is a little bit more active and I’m feeling a little better. Nite Nite, Love Naoise.