We are back from our holidays greeted by the best news ever, my friend Chantelle got her double lung transplant on Monday after only been on the list for about 8 weeks! This is how it should be for everyone and I’m so happy for her. She has a little boy and husband and I am so thrilled that once she recovers she can be the mum and wife she has longed to be. Please pray she recovers well and will be home in no time!

So yes we are back from our holidays and we had a great time!
We stayed on Pete’s parents boat, it’s a different one from last time we went, this one is bigger and abit more luxurious, hurrah! We sailed around the Ionian Islands in Greece. At first the weather wasn't too great, I was sea sick on the first day and vomited up a load of sputum into a bucket, nice! On Wednesday (I think) there was a storm including thunder and lightening and then the weather was great afterwards. One day dolphins swam by the side of the boat which was fantastic; sadly I didn't manage to get a picture!
I'm glad we only went for a week though as I find it a very tiring holiday, living on a boat is hard work and although I didn't actually help with much of the sailing what I did do, tired me out! When I say its hard work its just little things like flushing the toilet is hard as it’s a pump, and getting in and out of bed as the bed is really high up or going below and top of deck as you are constantly going up and down some steps. Then staying on top of my physio was hard work as my stuff was packed away everywhere (you cant leave thing loose on a boat as it goes everywhere when you sail if you do!) and the cabin was warm to do my physio in, plus my nebulisers took longer as they seemed to get clogged up even though I rinsed them with boiled water or bottled water.
So although it’s a fun holiday, it tires you out and after a week I ready to come home! It took a day and a half to get rid of my land sickness; this is where when you go on land you feel like the room is rocking because you are so used to being on a boat!
Just so people can get an idea of how much medication people with CF take, this is a photo of everything I had to take on holiday with me for one week. This photo doesn't include my food tablets though.
I had a problem at the airport for the first time ever with my medication. I always take all my medication in my hand luggage because if my suitcase got lost or delayed I'd be in trouble. Therefore I take all my nebuliser stuff in my bag which is liquid. I put them in a plastic bag like required, well two plastic bags as one wasn't enough and I wanted to keep them separate and the woman got funny with me saying they weren't labelled as medication and in future I needed to bring the labels for all my medication. I told her they came in big boxes and there wouldn't be room so she told me to cut the sticker off every box that the pharmacist sticks on. Have you heard anything so silly?! She then put them through a vapouriser I assume to check they weren't dangerous and insisted putting them all in one bag when I'd separated my tobi and pulmozyme from my nebusal as they needed to go back in the cool bag. As if I could keep all my medication in their original packaging, I'd need a bloody sack to carry it all! I have a letter from my doctor which she never even asked for, I know they have a job to do but its so frustrating when they are talking about something they don't know about.
If you remember I complained last year that I had some problems with suncream, well I tried banana boat and Hawaii tropic this time and they were lot better combined with my salty sweat so thanks for those suggestions!
Here is a video of photos we took. Warning! The song has ALOT of swearing in it, so if you are easily offended turn your sound down! I had to have this song though to accompany the video!