Stepping With Sophie: Photos

Me in my supportive chair

Fun at the beach

Fun in the sun

My fav...sand play

A leisurely stroll

A stroll with my siblings

How I shouldn't stand...

I stand so much nicer and 'flat footed' with my frame

My fav at the park...the swings

I may not be able to get up...but i can come down alright

My monthly donkey rides at The Donkey Sanctuary to help my gait in my legs

Concentrating on riding

Having a ride on Billy the Donkey

Off on a stroll with Billy the Donkey

Always wearing a smile

Snuggle time

Practicing some walking with my frame

I walk with a smile

'Yay! I'm doing it!'

My twin by my side...every step of the way

Me at the park

Ballpool fun

Box play

A helping hand from Mummy to walk through a tunnel

Water play

Always finding something to laugh about

'I get by with a little help from my friend!'...my twin friend

My twin stepping with me on my journey

Trying to catch up with my twin

Watching the rabbits together

'I'm coming Heidi!'

I look after my twin just as much as she looks after me

I love my twin sister

Getting ready to go out toegther

I love getting messy

or as i like to call it 'sensory play'

Me with my family...my Mummy, baby brother Barrett, big sister Lily, twin sister Heidi and my Daddy

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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