Charity sky dive

Hi everybody
AS you will all be aware i have been working hard with my physio and have improved so much. Mummy has said i am like a different little girl. I think i just like to prove doctors wrong to think eighteen months ago the doctors tried to get my family to sign a do not resusitate on me as they thought i had no quality of life. well i have definately showed them what a happy little girl i am. i have had a very busy week with my cousins who came to visit and have been swimming and ice skating. Mummy got a bit tearful at ice skating as she thought that was something she would never get to do but with the help of a specially adapted board that fixed to my wheelchair i did, it was the best fun ever.

Obviously my family are keen for me to continue to progress but its expensive paying for therapy even in this country it is nearlly one thousand pounds a month which my family dont have. It would obviously greatly increase if they took me back to America. Any way a very kind man (and extremely talented photographer) called adam is doing a charity abseil for me.  all support would be appreciated as he is extremely scared of heights ( sorry adam i am probably not making you sound very macho) but people need to know how much you care and what you are doing for us. Any one wishing to donate can do it either on paypal on my blog or through adams site which has the bank details on. His web address is adamalexphotography.com and scroll down and click on the link one of them has the bank details on.
All support would be appreciated

Lots of love isabella and family

one year on

Well its now been over a year since we returned from America and what a year it has been. I have moved to bicknacre with mummy and tony and we are in the middle of trying to sort out building work so that the house can be adapted for me but as with everything else with the council it all takes time and a long time at that. Daddy and amanda have had a baby so i have a little sisiter called darcy who gives me lots of kisses and cuddles.

 I did really well in America and mummy has been very busy this year trying to find therapy in this country that i can continue to do so that i continue to improve. I have a lovely lady called Adyta who i see she is very nice but she works me very very hard. i see her every friday and once a month i have a week of intensive therapy, my family have to pay for this privately and it costs nearlly one thousand pounds every month. Mummy has said that they are soon going to start more fundraising so that i dont have to stop my treatment as i am doing so well. I play with my toys on my own now and can move things in between my hands, i have started rolling onto my stomach although i cant always get off my stomach and need some help. i am getting stringer all the time and my balance is getting better. I still cant sit on my own but i am much closer and opnly need a bit of help now as i am still a bit wobbly but can correct myself a lot more if i starte going to one side. I have also started to put some weight through my legs but they are not strong enough to take all my weight yet. Before i went to America i had a standing frame but could only manage a couple of minutes before i got too distressed were as now i go in for one hour every day and really enjoy it. I have even been known to complain if i get taken out to early.
well i hope everyone is great and hope to see you all soon at a fundraising event. details of future events will be posted soon along with dates, times and prices