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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Tell us about your childs diagnosis
cheapsensorytoys
Hi lm Jean and my daugher LIsa has Autism and cerebral palsy although she is not a child anymore she is 23 l use the trem not a child anymore lightly as she is really not a lot of real speech just says yes and no in right places or whatever she thinks you want her to say if she is asked a negative question she will give a negative answer and the same goes for positive questions her she is now she also has hirchsprungs disease in her bowel and is now being tested for crohns l thought the new symptoms was to do with her hirchsprungs but specialist says no now so have to wait for her to have gastroscopy that will be fun on the whole she is a happy wee soul tantrums are fading slow but sure but she doesnt like clothes on she rips them up l have good suport from my family which is a god send
enough about me and mine hope everyone else is well and coping
take care
Katiebubbles
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#11 12-02-2009, 06:13 PM
Nice to see members getting into the post and introducing themselves on this post.
Hopefully more members will be along shortly to say hello.

[Image: smalldis2.png]
From sensory toys to a brand new range of special needs bibs:
www.cheapdisabilityaids.co.uk
Our Irish members can also use our new website for Ireland which is

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#12 12-03-2009, 10:23 AM
My name is Donna and my freinds call me Dolly since school and it kind of stuck,im 24 years old and from Kent.
I have an 2 year old boy who is my only child.
He has GDD and struggling to find out why.
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#13 12-03-2009, 10:33 AM
cheapsensorytoys
Hi im Donna,i have a daughter Dallas 9 yrs and she has Aicardi Syndrome which is a rare neurological disorder,which includes agenesis of corpus collosum,severe seizures and retinal luancea.

Problems which arise from this syndrome is sight problems ,though she sees fine,seizures daily and non mobile.

Dallas is our angel,she is a happy little girl who always smiles.Though she has lots of problems she is healthy and loves her food.

I have cared for Dallas for the last 8yrs while my husband has worked,though last year we decided for my husband to help me at home and give up work after she a scoliosis surgey plus we have little support from our families.

Its hard hard work but she is our baby and we will keep fighting for her no matter what.
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#14 12-03-2009, 02:43 PM
its true, no matter what age theyre still our babies Big Grin i never used to get it when my mom told me off when i was 18 and would say 'your still my baby' but now having 3 of my own i totally agree. Euan too is a food lover, albeit certain foods hehe they told us children with cystinosis didnt really eat but then they met euan who could probably eat all day bless him!

xx
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#15 12-04-2009, 08:00 PM
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