Parents in Sport week is an annual campaign, taking place this year from 7th- 13th October 2019.
Cerebral Palsy Sport are sharing some of the feedback received from parents at our events through #CPVoices as well as getting sharing awareness about the annual campaign.
The Parents in Sport Week campaign looks to increase positive parental involvement in youth sport and, by doing so, improve the experiences of young people across the UK.
This year’s aim by the NSPCC is to get parents to make theSports Parents Promise to encourage their child’s safe enjoyment of sport.
Cerebral Palsy Sport have been encouraging the parents of it’s participants to make the promise.
The Promise outlines what makes a great sports parent and allows parents to acknowledge the contribution they make to their child’s enjoyment of sport, and allows clubs, coaches and other sports organisations to really get parents on board and take an interest in their child’s sporting life.
The promise is supported by important and helpful information parents need to help keep their child safe in sport and support them in the best way they can.
For further information please visit the NSPCC website here
“To make a real difference to lives of disabled children,
the Government must make them a priority, including by appointing a Minister
for Disabled Children; by clarifying and reviewing the rights and
responsibilities within the system; and by ensuring there is sufficient funding
for services for disabled children and their families.
These are the demands of the Disabled Children’s Partnership (DCP) of which Cerebral Palsy Sport are members. The DCP have identified three pillars to underpin and ensure improved support for disabled children and their families. Stephen Kingdom, DCP Campaign Manager has written a blog setting out the way to build better support for children and families, and you can read it below.
To make a real difference to lives of disabled children, the Government must make them a priority, including by appointing a Minister for Disabled Children; clarifying and reviewing the rights and responsibilities within the system; and ensuring there is sufficient funding for services for disabled children and their families.
It’s been a turbulent few months in the country, with the Brexit deadline approaching and a possible election looming into view. It is easy to forget that, therefore, that there are other things going on. For the DCP, that means continuing to campaign for better support for disabled children and their families. In this blog, DCP campaign manager Stephen Kingdom, sets out three pillars on which to build better support for children and families.
In the midst of the recent political drama, there have also been some important developments and announcements for disabled children and their families over the summer. In June, the DCP launched our new Give It Back campaign with The Sun, calling on the government to put back the £434 million missing from budgets for social care for disabled children. In July, the Commons Education Committee published a report on school funding which described the funding for special educational needs and disability as ‘completely inadequate’; and this was followed this month by a damning National Audit Office report which concluded that ‘The system for supporting pupils with SEND is not, on current trends, financially sustainable’. At the same time, the Local Government Association reported a £1.4 billion – and growing – funding gap for children’s services.
The Government has responded with additional funding for schools and for social care; and with the announcement of a review of the SEND system. These are, of course to be welcomed. But that welcome needs to be heavily caveated. The additional funding for schools includes £700 million for ‘high needs’, but this is less that the projected shortfall and only guaranteed for one year. As for the social care, the increased funding needs to meet the well-documented pressures on adult social care; as well as child protection and children in care. It is doubtful that much, if any, of the increased funding will reach disabled children and their families. And whilst we are pleased to see the government has recognised the need to review how the system is working, it is action we need to address the crisis in support for disabled children and their families.
To this end, we have identified three pillars to underpin and ensure improved support for disabled children and their families. These will form our main campaigning calls for the next year:
Make disabled children a priority
Disabled children to be made a priority across government, at both national and local level and the Government to appoint a Minister for Disabled Children
At both national and local level, responsibility for the support that disabled children and their families need sits with a range of organisations. All too often, the needs of disabled children and their families are not the priority within those services; and no-one sees it as their responsibility to ensure that services join-up and meet the needs of families. This needs to change: the government should appoint a Minister for Disabled Children with clear responsibility, accountability and power across departments to make sure that the right support from health, social care, education and other services is in place for families. This arrangement should also be mirrored in local areas.
Clarify rights and review the law
The government to work with parents to clarify the existing rights and entitlements; and to undertake a review of the legal framework to strengthen and simplify it.
The existing law related to disabled children and their families stems from over 10 different Acts of Parliament, regulations and guidance which have developed over the past 50 years. It is difficult for parents to navigate; and it leads to different services and agencies shifting responsibility between themselves, and with families falling between the gaps. The government must work with parents to improve guidance on the current system – so that it is easier for them to know their rights – and introduce reforms to make the system simpler, and rights and responsibilities clearer.
Address funding shortfalls and create a dedicated fund
The government to increase funding for health and social care for disabled children to meet the current funding gap; and to introduce a new innovation fund to support joined-up working and early intervention.
There is currently a £1.5 billion funding gap across health and social care support for disabled children and their families. The government must fill this funding gap as a matter of urgency.
To support longer term sustainability, we are also calling on the government to set up an Early Intervention and Family Resilience Innovation Fund. This would support projects that transform disabled children’s health and social care by fixing problems at the earliest point of identified need and by focusing on the family as a whole. The Fund would initially support a vanguard of innovative service providers but with the infrastructure to upscale successful projects, leading to cashable savings, as well as long-term economic and social return. Projects would be robustly evaluated and learning would be shared to ensure that what works is promoted and has a sustained impact on the lives of disabled children and their families.