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Look out for Lexi! Hello my name is Lexi. I was born on 31st December 2007. I have a rare Chromosome Disorder, which means I may never walk or talk, it is called 1p36 deletion Syndrome. http://www.treeofhope.org.uk/look-out-for-lexi/

Look out for Lexi! Hello my name is Lexi. I was born on 31st December 2007. I have a rare Chromosome Disorder, which means I may never walk or talk, it is called 1p36 deletion Syndrome. http://www.treeofhope.org.uk/look-out-for-lexi/

Happiest little girl  My name is Jessica I am 2 years and 9 months old. Everyone tells me I am the happiest little girl they know! I was born with a rare brain condition called dysgenesis of the corpus callosum. This means that the central part of my brain hasn't formed correctly. This part of the brain is used to send signals from one side of the brain to the other - this is how we learn.  http://www.treeofhope.org.uk/happiest-little-girl/

Happiest little girl My name is Jessica I am 2 years and 9 months old. Everyone tells me I am the happiest little girl they know! I was born with a rare brain condition called dysgenesis of the corpus callosum. This means that the central part of my brain hasn't formed correctly. This part of the brain is used to send signals from one side of the brain to the other - this is how we learn. http://www.treeofhope.org.uk/happiest-little-girl/

As I walk on my toes  Hi, my name is Haydn Jones and I am 4 years old from Sutton. I was born at 29 weeks and weighed 3lbs 2oz.  I spent the first 6 weeks in hospital and when I weighed 5lbs I was allowed home with my Mum and Dad. When I left hospital Mum and Dad were told I had had a bleed on the left side of my brain, but at that point they didn’t know what that meant, and what it would mean for my future. http://www.treeofhope.org.uk/as-i-walk-on-my-toes/

As I walk on my toes Hi, my name is Haydn Jones and I am 4 years old from Sutton. I was born at 29 weeks and weighed 3lbs 2oz. I spent the first 6 weeks in hospital and when I weighed 5lbs I was allowed home with my Mum and Dad. When I left hospital Mum and Dad were told I had had a bleed on the left side of my brain, but at that point they didn’t know what that meant, and what it would mean for my future. http://www.treeofhope.org.uk/as-i-walk-on-my-toes/

Help Alexia walk  Alexia Rose from Weeley in Essex was born at 28 weeks and 2 days weighing 2lb 15oz. We spent 2 months in the special care baby unit where she did really well. When we took her home Alexia had a lot of episodes where she stopped breathing or choked and as she grew we realised she wasn't hitting any milestones and was extremely stiff.  http://www.treeofhope.org.uk/help-alexia-walk/

Help Alexia walk Alexia Rose from Weeley in Essex was born at 28 weeks and 2 days weighing 2lb 15oz. We spent 2 months in the special care baby unit where she did really well. When we took her home Alexia had a lot of episodes where she stopped breathing or choked and as she grew we realised she wasn't hitting any milestones and was extremely stiff. http://www.treeofhope.org.uk/help-alexia-walk/

Cody’s wish to talk  Cody was a normal little boy. He reached his all of his milestone as a toddler learning to crawl, walk and to say a few words. At age of 18 months his words disappeared however. He went back to babbling again and had very little eye contact. That's when he was diagnosed and my world fell apart. http://www.treeofhope.org.uk/codys-wish-to-talk/

Cody’s wish to talk Cody was a normal little boy. He reached his all of his milestone as a toddler learning to crawl, walk and to say a few words. At age of 18 months his words disappeared however. He went back to babbling again and had very little eye contact. That's when he was diagnosed and my world fell apart. http://www.treeofhope.org.uk/codys-wish-to-talk/

Charlotte loves to dance  My name is Charlotte from Wilmslow in Cheshire and I am 2 years old and have a twin brother called Daniel. We were born 8 weeks prematurely and unfortunately, although Daniel has no problems, it was discovered that I had a bleed on the brain which has resulted in me having quadriplegic cerebral palsy. http://www.treeofhope.org.uk/charlotte-loves-to-dance/

Charlotte loves to dance My name is Charlotte from Wilmslow in Cheshire and I am 2 years old and have a twin brother called Daniel. We were born 8 weeks prematurely and unfortunately, although Daniel has no problems, it was discovered that I had a bleed on the brain which has resulted in me having quadriplegic cerebral palsy. http://www.treeofhope.org.uk/charlotte-loves-to-dance/

Step by step  My name is Ollie. I have Spastic Diplegia which is a form of Cerebral Palsy.  It means the muscles in my legs are always tight which is very painful and means I am unable to walk without my walker.   http://www.treeofhope.org.uk/step-by-step/

Step by step My name is Ollie. I have Spastic Diplegia which is a form of Cerebral Palsy. It means the muscles in my legs are always tight which is very painful and means I am unable to walk without my walker. http://www.treeofhope.org.uk/step-by-step/

Kayden’s Story – Kayden’s wish to walk  Hello, my name is Kayden and I am 3 years old from Thurso in the Higlands. I was diagnosed with Spastic Diplegic Cerebral Palsy when I was 15 months old. This means that the muscles in my legs are so tight I'm unable to straighten them making it difficult for me to do simple things like sitting on the floor with my legs out front of me, standing or walking on my own. http://www.treeofhope.org.uk/kaydens-story-kaydens-wish-to-walk/

Kayden’s Story – Kayden’s wish to walk Hello, my name is Kayden and I am 3 years old from Thurso in the Higlands. I was diagnosed with Spastic Diplegic Cerebral Palsy when I was 15 months old. This means that the muscles in my legs are so tight I'm unable to straighten them making it difficult for me to do simple things like sitting on the floor with my legs out front of me, standing or walking on my own. http://www.treeofhope.org.uk/kaydens-story-kaydens-wish-to-walk/

Leo’s dream to walk Leo is 2 years old from Manchester who has spastic diaplagia cerebral palsy. He needs a surgery called Selective Dorsal Rhizotomy (SDR).  http://www.treeofhope.org.uk/leos-dream-to-walk/

Leo’s dream to walk Leo is 2 years old from Manchester who has spastic diaplagia cerebral palsy. He needs a surgery called Selective Dorsal Rhizotomy (SDR). http://www.treeofhope.org.uk/leos-dream-to-walk/

Felix’s wheelchair  Felix was born with a rare life limiting genetic condition of mitochondrial disease. He is unable to sit unaided or crawl and walk. We try to focus on the things he can do well rather than his disabilities.   http://www.treeofhope.org.uk/felixs-wheelchair/

Felix’s wheelchair Felix was born with a rare life limiting genetic condition of mitochondrial disease. He is unable to sit unaided or crawl and walk. We try to focus on the things he can do well rather than his disabilities. http://www.treeofhope.org.uk/felixs-wheelchair/

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