cheap sensory toys


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Families who have children and young people with special needs very often deal with similar life styles. We have all had concerns ranging from education,acess to services,respite and other issues directly related to their childrens needs. Parents of disabled children bring families together for friendship, to share information and to support one another.

The forum was created by parents who have children with special needs and is run by parents so we are all in this together. With us you will realise you are not alone

Parents of disabled children launched in October 2009 and we are growing day by day and are fastly becoming a major support resource for all




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cheapsensorytoys
I just had a quick look and it says -
Quote:During the official campaign period for the General Election the e-Petitions system will be closed to new submissions and signatures.

So you can't vote till next week after all the election stuff is finished. x
[/quote]

Thanks Smile

Heart Lizzie Heart

Mummy to a lovely boy called Jack who is 4.
Jack has Cerebral Palsy, Auditory Neuropathy, Cerebral Visual Impairment and Nystagmus.
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#26 05-06-2010, 05:40 PM
Think it's a joke you have to wait so long. Matt got high rate care DLA just before his 2nd birthday but we had to wait a year before we could claim mobility. It was a real struggle trying to explain that he stops breathing anywhere (several times at Tesco's whilst shopping). the probs we had was proving he was different to any normal 3 yr old. He can't be left alone for even a sec as he stops breathing freq xx
Think it's a joke you have to wait so long. Matt got high rate care DLA just before his 2nd birthday but we had to wait a year before we could claim mobility. It was a real struggle trying to explain that he stops breathing anywhere (several times at Tesco's whilst shopping). the probs we had was proving he was different to any normal 3 yr old. He can't be left alone for even a sec as he stops breathing freq xx
Think it's a joke you have to wait so long. Matt got high rate care DLA just before his 2nd birthday but we had to wait a year before we could claim mobility. It was a real struggle trying to explain that he stops breathing anywhere (several times at Tesco's whilst shopping). the probs we had was proving he was different to any normal 3 yr old. He can't be left alone for even a sec as he stops breathing freq xx
Think it's a joke you have to wait so long. Matt got high rate care DLA just before his 2nd birthday but we had to wait a year before we could claim mobility. It was a real struggle trying to explain that he stops breathing anywhere (several times at Tesco's whilst shopping). the probs we had was proving he was different to any normal 3 yr old. He can't be left alone for even a sec as he stops breathing freq xx
(This post was last modified: 07-06-2011 03:24 PM by Mel22.)

Heart Mum to Abigail 8 & Matthew 4. Children with disabilities are like butterflies with a broken wing. They are just as beautiful as all others, but they need help to spread their wings.
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#27 07-06-2011, 03:23 PM
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