It has been almost ten years since the Tánaiste made a promise to children with scoliosis and spina bifida that they would not have to wait longer than four months for treatment. As he will be aware, many parents see that as a broken promise and they do not want any more broken promises, which is why they are concerned about the Remy Farrell report, which was published a few days ago, and its recommendations.
The starting point for everyone in the House is that we need to get this right, that we need to have an inquiry that is fit for purpose and has the confidence of advocacy groups and parents. I think the Tánaiste said today on the floor of the Dáil that the start date of 1 January 2019 is too rigid. I have been saying that. It has to go beyond that. I understand that the Scoliosis Advocacy Network and Spina Bifida Hydrocephalus Ireland have written to the Tánaiste seeking a meeting. My understanding is that they have not received a response. I urge him to meet them and others to ensure he hears their concerns. Let us ensure we have an inquiry that is fit for purpose, that can answer the questions, that there is no hiding place-----