You are visitor number

20 September 2011

Dresses!

I am still looking for a dress to wear for the awards in a couple of weeks. I would laugh if I had other things to wear, but I've lost a lot of weight since I last went anywhere and they're all huge on me. I've also got loads of scars everywhere and I want to hide them. Oh and my legs aren't great either! I'm hoping that my wig will be ready before the awards, so I should at least have some hair. And I want to get it done in London on the day of the awards, because it's made of real hair and you can do anything with it.

On Saturday, I got to go to the Lantern Procession in Ulverston for the first time in 4 years and it was amazing.  My Mabel lantern was still wet at about 2pm and so mum had to use the hairdryer on it.  Loads of our friends had made lanterns as well, some from my bucket list and lots supporting Anthony Nolan and Bone Marrow Awareness.

Me with my Mabel lantern
The Bucket List Lantern
Today, I went to Apollo Cinemas in Barrow to watch 'I don't know how she does it'.  The Apollo have given our family an honorary lifetime membership and we laugh because when I go in, they just say 'Hi Alice, just go on through'! The film was really funny and if you get the chance to see it, go.  

Mum and me have been busy planning something very special.  I can't say what yet, but I will do soon.  But it will be amazing and it will help lots and lots of other people and I hope people will support us doing it!

I've had lots of lovely things sent to me and it's really difficult to write back to everyone but I want to say thank you so much for thinking of me. I love the bandanas, especially the ones from other countries and today I had Australia on my head!  I also got a cute Angry Birds T-shirt from Tracy in America, thank you.  A few schools have written to me, I got some really cute pictures drawn from Kenya and I'm enjoying a whole stack of letters and things from the International School in Alicante. 

The last thing but the most important is that mum found out that two more people who signed up through my recruitment clinics are going to donate their cells very soon.  I can't explain how happy it makes me to know that they've got a chance. I keep thinking about all the people that will be able to have a life because of the people like you who have listened. So thank you :)

Oh and you can still vote for me and Milly in the awards by clicking on the link at the top of this screen!

Updated video ...

A few months ago, Abigail Breslin and Cassidy Reiff wrote and recorded a song for me with their band 'CABB' ... it now has an updated video which shows some of my bucket list wishes coming true.  I love this song, just figuring out how to save it to play on my iPod

Raymond & Sebo sing for me!

"2 The Universe" with their song dedicated to Alice




15 September 2011

VOTE HERE

Thank you for all of your emails helping me do this ...

VOTE FOR ALICE & MILLY HERE x

Sarna, wigs and lanterns

I eventually escaped from Alder Hey on Friday and I was really pleased to be back home as I had a Mabel lantern to make. I started off well but then didn't do any more until late last night, but it's nearly done now. I'm in Liverpool again now but I'll finish the legs on Friday (it has only got 2 legs so far)! Every year, our town Ulverston, has a lantern procession through the cobbled streets and loads of people make lanterns from willow and once it's dark we light them and do the walk. This year the theme is Vikings but we're ignoring that and doing a mix of bone marrow awareness lanterns and bucket list lanterns. We have cinema ticket lanterns, sharks, a big camera, my Emma Bridgewater mug and of course Mabel. They are all things from my bucket list! I can't wait because I've always been in hospital and I've missed the last 3 years. I will put some photos on here next week. We had Merseyside Police in the hospital today telling us all how to be safe. We can remember someone from the dog unit sent us a message saying that I could go and see them training and meet some of the dogs. But then we couldn't find the email and Mum said we'd look stupid just randomly phoning police stations so I never got to go. Anyway, because they were there today, they gave us all the details again and now I'm hoping to go one day. I also went to the Andrew Collinge salon in Liverpool which was amazing. Not for my own hair, I'm getting a real hair wig! I had a really nice time and I picked a nice long style in quite a warm reddish brown. I can't wait for it to come cos then I get to go back and they will cut and style it on my head! I think that mum is going to try and book an appointment at the same time. My skin has been really horrid for years because ive had so much treatment. After i started my blog, an American company called ISClinical sent me a box of creams and things. The serum is making my scars fade and get softer and I love the body complex as well, ive decided that it smells happy!. One of the things you get with Hodgkin's is itching and it's not as bad as it used to be but it does still annoy me. Well we've found something for that as well and it works. It's called Sarna and my mums American friend gave it to me try and now I'm in love with it. It makes it all cold and tingly! I have a Lush bath and then I put Sarna on and it feels really nice. A few people have been busy nominating me for an award thing and they let us know that I've been shortlisted and we get to go to London for the night, as long as I'm well enough. What is really nice, is that Milly has been nominated too, for all her fundraising and charity things. But it is all down to the votes we get. So if you would like to vote for me and Milly, please do. I'm looking forward to the night but it feels a bit like school was when they picked two teams and you were terrified of been the last one picked. The link is www.inspirationawards.co.uk but I still don't know how to put a proper link on here. Will ask mum tomorrow. I'm in the second category and Milly is in the last one. I had three tweets today from people who have just signed up to be a BM donor. Hearing that makes me really happy, thank you and keep spreading the word and posting on Twitter and Facebook for me. I'll put pictures up when I'm home on my proper computer. I don't think I can do it on this.