Can you remember who first suggested you needed a Needs Assessment? Who where they? Why did they make this suggestion?
Are you willing to share your answers to EHCP section H1? If yes, please make sure you remove personal data, such as names.
Have you been through the EHCP process? What advice would you share with families who have a newly diagnosed child?
Are there key transition moments when taking legal advice is advisable, during the process of getting or maintaining an EHCP?
Have any charities helped in your EHCP process? If yes, who are they and how did they help?
Is the EHCP a legal document? If yes, does my child have a legal right to support?