georgies needs
Donation protected
Hi There
Georgie is now 12 years old and doing really well, sadly he is not able to walk or stand unaided and uses his power chair full time.
We are currently trying to raise as much funds as possible to enable us to give him the best life with all he needs to keep that gorgeous smile on his face.
We are asking people to have a SORT OUT for us of the following items:
Clothes Shoes Handbags Bedding Towels CD Xbox Games Un-Wanted Gifts Brass wear and teddies.
I will do all the hard work and sort it and sell it for him and it wont cost you a penny.
We also support Little Havens hospice for children Farleighs hospice Essex Air Ambulance Duchenne Uk Muscular Dystrophy Uk to name a few.
Please keep Georgie in your minds and help me give him a live worth living.
All my thanks
TJ xxxx
Latest update.
Our brown eyed baby is now 9 years old and is still smiling and is very cheeky, he lives life to the full the best way he can living with Duchenne Muscular Dystrophy.
We are constantly coming across hurdles to overcome and sometimes need to ask for help to achieve them.
We work very hard indeed to make sure Georgie has a wonderful life along side is beautiful twin sister Lili Jane.
we support lots of other charitys linked to Georgie in the hope of helping others too.
Please donate no matter how small to give Georgie a life worth living and not a horrid duchenne life !
Thank you so very much always for your love and support.
GeorgIE is now pretty much a full time wheel chair user and is soon to get his first electric chair.
We are so proud of how he embraces his journey and try to have as much fun as possible he now plays power chair football
and boccia.
We are trying so hard to give him the best life possible in every way
Our building work is now complete but we are now installing hoists etc so it's really never ending.
Please help us keep his pot growing
All our love x
Please help us raise the last few thousand to start our build to adapt our home for Georgie.
Sadly Georgie had Duchenne Muscular Dystrophy a rare muscle wasteing conditon that is life limiting and just awful to say the least, he will get weaker and weaker as he grows and this includes his heart and lungs.
Please help us give him a home he can get around in nicely once wheelchair bound.
We are also fund raising for the research to into this condition, we will give Georgie the best chance thats one thing for sure.
Thank you all so much
All out love
Tj Baz Lili Jane & Georgie Nye xxx
Georgie is now 12 years old and doing really well, sadly he is not able to walk or stand unaided and uses his power chair full time.
We are currently trying to raise as much funds as possible to enable us to give him the best life with all he needs to keep that gorgeous smile on his face.
We are asking people to have a SORT OUT for us of the following items:
Clothes Shoes Handbags Bedding Towels CD Xbox Games Un-Wanted Gifts Brass wear and teddies.
I will do all the hard work and sort it and sell it for him and it wont cost you a penny.
We also support Little Havens hospice for children Farleighs hospice Essex Air Ambulance Duchenne Uk Muscular Dystrophy Uk to name a few.
Please keep Georgie in your minds and help me give him a live worth living.
All my thanks
TJ xxxx
Latest update.
Our brown eyed baby is now 9 years old and is still smiling and is very cheeky, he lives life to the full the best way he can living with Duchenne Muscular Dystrophy.
We are constantly coming across hurdles to overcome and sometimes need to ask for help to achieve them.
We work very hard indeed to make sure Georgie has a wonderful life along side is beautiful twin sister Lili Jane.
we support lots of other charitys linked to Georgie in the hope of helping others too.
Please donate no matter how small to give Georgie a life worth living and not a horrid duchenne life !
Thank you so very much always for your love and support.
GeorgIE is now pretty much a full time wheel chair user and is soon to get his first electric chair.
We are so proud of how he embraces his journey and try to have as much fun as possible he now plays power chair football
and boccia.
We are trying so hard to give him the best life possible in every way
Our building work is now complete but we are now installing hoists etc so it's really never ending.
Please help us keep his pot growing
All our love x
Please help us raise the last few thousand to start our build to adapt our home for Georgie.
Sadly Georgie had Duchenne Muscular Dystrophy a rare muscle wasteing conditon that is life limiting and just awful to say the least, he will get weaker and weaker as he grows and this includes his heart and lungs.
Please help us give him a home he can get around in nicely once wheelchair bound.
We are also fund raising for the research to into this condition, we will give Georgie the best chance thats one thing for sure.
Thank you all so much
All out love
Tj Baz Lili Jane & Georgie Nye xxx
Organizer
Tina-Jane Nye
Organizer