Children’s Services

Kate Green Excerpts

Wednesday 30th January 2013 Westminster Hall

[Angela Smith]

I empathise and agree with the point my hon. Friend makes. I will refer to that issue later in my speech. It is about not only distance, but cost, which in the case of low-income families can be an incredibly difficult burden to bear.

More than six in 10 parents of disabled children say that they cannot get the services they and their child need in their local area. A measly one in 10 parents told Scope that the process of getting local services was simple. Families with disabled children and children with SEN want to use the services that many families simply take for granted: child care, so that parents can work; short breaks, which enable families to rest and a disabled child to enjoy a leisure activity; therapeutic services, to support development such as speech and language; and, of course, the right educational setting, so a child can learn and reach their potential.

A lack of local, accessible services can have a devastating impact on a family’s quality of life. Recent research by Scope found that 80% of the families with disabled children who cannot access the services they need locally report feeling anxious and stressed, and more than half said that as a consequence they missed out on doing family activities together, such as days out or celebrating birthdays.

As my hon. Friend pointed out, families with disabled children travel on average more than 4,300 miles a year —84 miles a week—to access the services they need. The logistics and complicated arrangements necessary to get them to appointments, school and activities on time are vast. Travelling long distances is extremely demanding, particularly for children who tire easily or become distressed if they are contained for long periods. For disabled children and children with SEN, such journeys can be even more stressful. As one mother of a disabled child put it:

“Not being able to access the fun things for my child has left us isolated and almost housebound for most of the month. It is difficult to access things as we don’t drive and no thought is put in to the placement of services for disabled families who need to use public transport. It is always assumed we drive. Therefore public transport costs a fortune and takes at least twice as long. Services are a distance away, so if you don’t drive it means you just don’t go to services at all, which means being housebound and being further isolated.”

In some cases, the immense financial burden placed on families can literally tear them apart, which is the important point my hon. Friend made earlier.

[Kate Green (Stretford and Urmston) (Lab)]

My hon. Friend describes a situation with which we are all familiar in our constituencies. One concern that parents in my constituency report is that funding for home-to-school transport has been reduced significantly due to pressure on councils’ budgets. Does she agree that it is extremely important to ensure that families can manage the day-to-day journey to school readily and affordably and that it ought to be given priority in any local offer?

[Angela Smith]

Transport is extremely important, as my hon. Friend points out, but so is the consistency of the service. Having the same driver, routine and route to school is often incredibly important for children, particularly those with autism, for example. There are issues with consistency of service and central Government funding for local government to ensure that such services are consistent and of a high quality.