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Ruby's Fund
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Ruby's Story
Ruby was born on 8th July 2007. She was a healthy weight of 8lb 11oz. Initially everything appeared to be fine with no significant problems. Ruby was our second child. The first thing we noticed about Ruby was she never really smiled. At about 6 months of age we noticed that Ruby was not reaching certain milestones. We just put this down to her being a late starter. Ruby then began making "odd movements” where she would drop her head and raise her arms. This repeated movement would go on for up to 60 minutes, and at its worst occurring 30+ times a day. We recorded this movement and took the film to show the GP. From there we were referred to Macclesfield District General Hospital to see the Paediatrician. Luckily Ruby started doing the head dropping, arm raising movements whilst the doctor was assessing her. From there we went straight to Pendlebury Childrens Hospital where Ruby under went 4 months of intensive investigations. We now know that the head dropping, arm raising movements where Infantile Spasms- a form of epilepsy. After genetic testing Ruby was diagnosed with a very rare condition called Isodicentric_15 or IDIC 15 syndrome. It means she was born with a partial duplication on chromosome 15. This isn't inherited, it just happened. It occurs randomly during the formation of cells and there is NO cure for IDIC 15. They say no two children with the condition are exactly alike.
Some of the symptoms Ruby has are: seizures, hypotonia, fine and gross motor delays, cognitive difficulties, sensory and processing disorder, behavioral issues, speech/language delays, and living independently in the future is almost impossible. We believe that there are less than 100 families in the UK affected by this disorder.
Ruby attends Manchester Childrens Hospital and Macclesfield District General Hospital to see the doctors. She has a geneticist, neurologist, cardiologist, ophthalmologist, and a paediatrician.
Ruby's general development is significantly delayed as... show more a result of her condition.
Ruby has cardiac rhabdomyomas (benign heart tumours). She frequently has seizures. It is unknown how her future development will be affected.
Ruby likes to play with both her brothers. She and her family use sensory play equipment as much as possible in order to enhance her development.
Above all, Ruby is a happy little girl with an infectious smile and is full of cuddles! show more
Ruby was born on 8th July 2007. She was a healthy weight of 8lb 11oz. Initially everything appeared to be fine with no significant problems. Ruby was our second child. The first thing we noticed about Ruby was she never really smiled. At about 6 months of age we noticed that Ruby was not reaching certain milestones. We just put this down to her being a late starter. Ruby then began making "odd movements” where she would drop her head and raise her arms. This repeated movement would go on for up to 60 minutes, and at its worst occurring 30+ times a day. We recorded this movement and took the film to show the GP. From there we were referred to Macclesfield District General Hospital to see the Paediatrician. Luckily Ruby started doing the head dropping, arm raising movements whilst the doctor was assessing her. From there we went straight to Pendlebury Childrens Hospital where Ruby under went 4 months of intensive investigations. We now know that the head dropping, arm raising movements where Infantile Spasms- a form of epilepsy. After genetic testing Ruby was diagnosed with a very rare condition called Isodicentric_15 or IDIC 15 syndrome. It means she was born with a partial duplication on chromosome 15. This isn't inherited, it just happened. It occurs randomly during the formation of cells and there is NO cure for IDIC 15. They say no two children with the condition are exactly alike.
Some of the symptoms Ruby has are: seizures, hypotonia, fine and gross motor delays, cognitive difficulties, sensory and processing disorder, behavioral issues, speech/language delays, and living independently in the future is almost impossible. We believe that there are less than 100 families in the UK affected by this disorder.
Ruby attends Manchester Childrens Hospital and Macclesfield District General Hospital to see the doctors. She has a geneticist, neurologist, cardiologist, ophthalmologist, and a paediatrician.
Ruby's general development is significantly delayed as... show more a result of her condition.
Ruby has cardiac rhabdomyomas (benign heart tumours). She frequently has seizures. It is unknown how her future development will be affected.
Ruby likes to play with both her brothers. She and her family use sensory play equipment as much as possible in order to enhance her development.
Above all, Ruby is a happy little girl with an infectious smile and is full of cuddles! show more
Hours of operation
Monday9:30AM - 4:00PMTuesday9:30AM - 4:00PMWednesday9:30AM - 4:00PMThursday9:30AM - 4:00PMFriday9:30AM - 4:00PMSat, SunClosed
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4 recommendations and reviews from 3 people
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Referral from
April 27, 2016
Danielle W. asked:Does any one know any baby classes for a 3 month old in sandbach or surrounding areas please xJade G. replied:Check out https://m.facebook.com/rubysfundsensorycentre/
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Referral from
March 29, 2015
Jennie M. asked:Hi. Where can I find the timetable for this week please?Ruby's F. replied:www.rubysfund.co.uk
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Referral from
October 13, 2015
Bob P. asked:does anyone know any good hallloween events to take kids too?Anita-Lee W. replied:https://www.facebook.com/rubysfundsensorycentre the Halloween party is the first advert. it's lovely fun!Anita-Lee W. replied:Ruby's fund Congleton (they are on Facebook)
Recommendations from Anita-Lee W.
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