Hi everybody sorry to bother you I have been a Brighton supporter since my dad took me along to the Goldstone on the 10th of march 1984 to see the Albion against Man City (TV cameras were there and everything well a gantry in the east stand )
But my point is on Sat 10.30am 8/5/2010 . Me and the Family are doing a walk for my 3 year old niece Eloise from the Palace pier to the west pier in Brighton and back . Well i say we but what we mean is Eloise is . Hopefully it will be achievable with the help of her walker and (buggy just incase)We have called it a 'walk' but that means walk, toddle or push! .
This is to raise money for and awareness of the Charity UNIQUE . Even if you are not in a position to donate (below at Virgin money) . please spend a little time reading about this Unique rare chromosone disorder at Unique - The Rare Chromosome Disorder Support Group - www.RareChromo.org .or on the Virgin money page . All the best and thanks for taking some time to read this Steve Doswell AKA Galebs
Virgin Money Giving | Fundraising | Eloise's walk for rare chromosome disorders
uk.virginmoneygiving.com
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But my point is on Sat 10.30am 8/5/2010 . Me and the Family are doing a walk for my 3 year old niece Eloise from the Palace pier to the west pier in Brighton and back . Well i say we but what we mean is Eloise is . Hopefully it will be achievable with the help of her walker and (buggy just incase)We have called it a 'walk' but that means walk, toddle or push! .
This is to raise money for and awareness of the Charity UNIQUE . Even if you are not in a position to donate (below at Virgin money) . please spend a little time reading about this Unique rare chromosone disorder at Unique - The Rare Chromosome Disorder Support Group - www.RareChromo.org .or on the Virgin money page . All the best and thanks for taking some time to read this Steve Doswell AKA Galebs
Virgin Money Giving | Fundraising | Eloise's walk for rare chromosome disorders
uk.virginmoneygiving.com
content
My page: Virgin Money Giving - Service unavailable
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. If you get another chance please give it a go if not thanks for trying and hopefully you are one more person that knows a little more about Unique and rare chromosone disorders .