Help Baby Grace Ava Williams who was born 23.11.12 and has the life limiting condition 'Edwards Syndrome'. Please help support Baby Grace.

Berkshire, UK
Joined December 2012
@MarishPrimary Thank you so much for all the money you raised from the sponsored walk for Baby Grace. #EdwardsSyndrome #Trisomy18
Great Ormond Street have said no to operating on Grace! Please help her find another way to get op. #EdwardsSyndrome
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@bmwalker89 Thank you so much, please see paypal link is below; paypal.com/cgi-bin/webscr?cm…
Sponsored Walk to raise money for Baby Grace, from Langley Village Park to Windsor on Sunday, 31 March at 12:00, £10/person. Please join us
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Today is National Trisomy 18 Awareness Day. It occurs on the 18 day (18 chromosome) of the 3 month (3 copies of the chromosome) of the year.
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Secretary of State has told us that nobody can be denied an op unless they have clinical justification, which they don't. #EdwardsSyndrome
They've arranged an ethics mtg about Grace next week.They're saying its not worth operating as she'lll "be disabled anyway" #EdwardsSyndrome
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Does anyone know a child with EdwardsSyndrome?Pls contact us. Are there any known Edwards babies who survived heart op?Did it prolong life?
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Laura has found published literature from US that stated cardiac intervention prolongs their lives #EdwardsSyndrome #Trisomy18
After mtg with a cardiologist from Great Ormond St they won't operate on Graces heart as the "text book" says not to operate on T18 babies!
Grace made front page news last week!
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Unfortunately the blood flow through Grace's lungs has increased so she has begun new medication, accompanied with a short stay in hospital.
Grace posing for the camera on her first photoshoot, with the very talented @lauzphotography #edwardssyndrome
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Cosy Grace all ready for a day out
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Gorgeous Grace and her proud Daddy
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