Stepping With Sophie: Ways to Donate

Online
Click on the link below to make your donations online via JustGiving
www.justgiving.com/stepping-with-sophie

Text
Or you can text SJOY55 followed by a space and either of the following amounts £1 £2 £3 £4 £5 or £10 to 70070

Cheque
Alternatively you can send a cheque made payable to 'Tree of Hope Children's Charity (Stepping with Sophie...in her wish to walk) to
The Tree of Hope Children’s Charity
23 St Leonards Road
Bexhill On Sea
Eastbourne
East Sussex
TN40 1HH

Please ensure you mention Sophie Case on anything that you send to the charity, as this will ensure the money is credited to Sophie's pot rather than the general one...and don't forget to ask me for a Gift Aid form to fill in and send along with your cheque also.

Online when you shop
If you shop online, then there is an easy and free way to help us raise funds.
We’ve teamed up with easyfundraising who provide a shopping directory listing some of your favourite online stores. Hundreds of popular retailers are participating including Argos, Next, Debenhams, John Lewis, Toys R Us, M&S and over 2000 others.

At no extra cost to you, the retailer will give us up to 15% of every purchase you make – it’s that simple!
It’s completely FREE to register and you won’t pay a penny more for your shopping when you use the easyfundraising site. In fact you can even SAVE MONEY as many retailers offer discounts, special offers and even 'e-vouchers' exclusive to easyfundraising.
If you shop online anyway then why not raise valuable extra funds for us by using this fantastic scheme by following these 3 easy steps...

Before shopping online go to our easyfundraising website by clicking here
Follow the simple steps to sign up.
Each time you shop online do it through our easyfundraising link on our homepage (or alternatively going to https://www.easyfundraising.org.uk/support-a-good-cause/ and typing in Stepping With Sophie as your good cause to support) See if the site you are using to shop is registered with easyfundraising.org.uk. If it is, click the link and shop as normal. A percentage of what you spend will be donated automatically to our fund.

Please encourage your friends and family to sign up too and raise even more money for Stepping with Sophie.

Thank you

Online when you search

Are you one of the millions of people that use a search engine every day?

Switch your searching to easysearch and raise money!

Every time you search the web using http://steppingwithsophie.easysearch.org.uk instead of Google or any other search engine, half a penny is raised for Stepping With Sophie. Search just 15 times a day and you can raise around £25 a year.

Thank you so much for your support! :-)

About me

My name is Sophie Joy, I am almost 3 years old and I have Spastic Diplegia Cerebral Palsy (although as we like to say 'I may have Cerebral Palsy, but Cerebral Palsy doesn't have me!') I was born on the 6th December 2009 with my identical twin sister...although I haven't been able to come first with most things due to my disability, I can always say I was the first to enter the world, a whole minute before my sister!! We were born 8 weeks early after Mummy went into premature labour; we weighed just 4lb 2oz and 4lb 3oz and the first month of our life we spent in the Neonatal Unit at our local hospital, where we also stayed for Christmas!...luckily Father Christmas knew we were there! :-) The first few months of life at home after NNU were great, we were both doing really well for being born prematurely...feeding well, sleeping well, crying well! It wasn't until my twin started to do things a lot sooner than me that my family noticed I was a little delayed with my mobility, however this at the time was just put down to developmental delay due to being born prematurely! Ironically for us however, Nana has been a teacher for children with CP for years so was able to see the signs of CP in me and my Mummy and Daddy finally pushed for a diagnoses to get me the support I needed! To date, I have had just over a year of physiotherapy to help not only with the tight muscles (spasticity) in my legs, but to install the correct messages to the part of my brain which doesn't work properly...the part that isn't telling my legs to do what they should be doing and climb, walk and run like other children my age do all of the time! My Mummy and Daddy have to work hard to keep my physio up at home and I have had to work tremendously hard just to do simple things such as crawl, kneel up and climb small obstacles. Although I have come on remarkably really, from only being able to commando crawl when I first started physio at around 1 1/2 years old to now at 2 3/4 years being able to walk using my Kaye Walker (albeit with the difficulties with come with spasticity of the legs of course) and my family are all extremely proud of the things I have achieved...I still have a long way to go and physiotherapy will be on going for the rest of my life to 'manage' my CP...It will never cure it! Despite this, I am a happy little girl and my family say I always have a smile on my face!...I love to play with my friends at nursery, being creative, looking at books, getting messy, being outdoors, everything else any other nearly 3 year old loves to do! I love the little bit of independence that walking with my frame brings, but the one thing I long to do however is play in the park properly with my twin sister Heidi, my big sister Lily and my baby brother Barrett! This is why my Mummy and my Daddy have set up this page, to get me the key to the brighter future I deserve! That key is an operation called Selective Dorsal Rhizotomy (SDR), which I am very fortunate Mummy came across and researched tirelessly for me...this operation would mean the Dr’s could take the tightness in my muscles away and without that horrid tightness which restricts me from doing so many things I want to be doing, I could hopefully learn to walk independently and maybe one day be running in the park with my brother and sisters!

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