If you would like to make a donation, our preferred method is for you to visit your local NATIONWIDE Building Society and make a donation by either postal order or cheque quoting the details below: PLEASE MAKE DONATIONS PAYABLE TO AMY JARRETT
Sort Code-070093 Account No-33333334 Ref No-0226/126 355 688
Thank You!
We have a PO BOX address if you would prefer to send a cheque/postal order to us personally made payable to AMY JARRETT
M Russell PO Box 5918 Southend on Sea SS1 9HJ You can also donate using the donation button below - although please be aware we are charged a commission as it is a Paypal site
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| ***WE HAVE REACHED OUR TARGET*** Thank you to all who made this possible
Hello my name is Amy Hana Chelsey Jarrett I am 8 yrs old and live in Southend on Sea
I am a very special little girl because I was born with a rare brain disorder called SEPTO OPTIC DYSPLASIA in March 2001
Because of my condition I am totally blind as my optic nerves didn’t grow and in addition have multiple hormone deficiency due to a mid-line brain defect…which also affects my sleeping habits and more
I am also on the autistic spectrum, which means I can be a challenge and a little pickle for my family!!!
I have behavioural problems and am developmentally delayed in many areas and I need help and support at all times
My mummy and daddy have found a hospital in China that offers umbilical stem cell treatment that could give me sight, plus improve other problems I have
Children like me have had this procedure and life has improved for them all. Some can now see well enough that they can see their family and friends for the first time!
WE NEED TO ASK YOU FOR YOUR HELP TO MAKE THIS HAPPEN FOR ME TOO…
This treatment is not available anywhere else in the world. It costs a lot of money,so we need to ask for your support to help us cover the costs of the treatment and the flights...
PLEASE HELP US TO RAISE £35,000
PARENTS NOTE
... Although this is the beginning of our journey, we hope that every penny will add up to giving us the opportunity to help our daughter This is our first glimmer of hope to be able to help Amy since she was born
We cannot let this chance go by… can we?
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