The report acknowledges that the law around meeting needs of Disabled children is muddled and confusing, and that protections sitting across different pieces of legislation makes it harder for everyone to understand what rights children and families have. It recommends the creation of a new legal framework, accompanied by clear statutory guidance – so everyone knows what support Disabled children can expect.
It also recommends the introduction of a national eligibility criteria, and using the definition of Disability from section 6 of the Equality Act 2010 when considering eligibility for Social Care – this could make it easier for families to get support without a diagnosis in place.
The report also talks about supporting social care workers to better understand the difference between providing the support needed to meet Disabled children’s individual needs (including carers support so their families can continue to care safely) and safeguarding. Separating these two duties could have a real impact on family’s experience of parent blame.
We think these are good ideas – and we welcome them.
If implemented, the proposals have the potential to significantly improve the lives of PDA children and their families.
We urge the government to accept these proposals in full and move quickly to reform the law.
If you want to use your voice to encourage this change, you might want to email your MP and ask them to support these changes.
You can find your MP’s email address here.