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I have a nine year old daughter who has SMA Type II.
She received her Electric Wheelchair when she was 4 years old and at this time it covered some of her needs, it would take her from A to B.
Now she is older she need something to get her more independence, the trouble with Wiltshire Wheelchair services is that they just fob you off.
I have asked for a new assessment of my child due to the fact she has grown, she needs more independence and more movement for a Wheelchair but they say she does not need one.
Other parents with children who have Electric Wheelchairs have a lot more functions than my daughters, it seem the louder you are the more they do something but I feel all children should be treated the same and not that some can have better than others.
I am unsure where to go to next as this is making me very sad and angry