A teenage girl with cerebral palsy who had to wait for five years for spinal fusion surgery for scoliosis saw her spinal curvature deteriorate from 30 to over 135 degrees in that time. An investigation into Ivy\u2019s* (17) case was published today (Thursday, 29th June) by the Ombudsman for Children\u2019s Office (OCO). Ivy and her family told the OCO about the enormous toll that the uncertainty surrounding her surgery had taken on Ivy\u2019s life, both physically and mentally. She told us that she could not meet her friends, go to school or even breathe at times as the curvature worsened. When Ivy eventually had her surgery in 2021 her pain was significantly reduced and her quality of life improved.<\/p>\n
In its findings, the OCO determined that the administrative actions of Children\u2019s Health Ireland (CHI) had a negative impact on Ivy\u2019s life and made seven recommendations to address those concerns. These include that CHI carry out an audit of the waiting list for children\u2019s scoliosis care and to allow for the patient or their family\/ caregiver or GP to initiate a review of their own care.<\/p>\n
Commenting on the report into Ivy\u2019s case, OCO Director of Investigations, Nuala Ward said:<\/p>\n
\u201cIvy\u2019s story shows the devastating consequences that waiting for this life-changing surgery can have on a child. When Ivy and her family came to us, after previously raising their concerns a number of times with their GP, consultant and Children\u2019s Health Ireland, it was clear that the whole family had suffered significant distress and anguish at Ivy\u2019s deteriorating condition in the five years she had to wait for surgery.<\/p>\n
\u201cOur investigation found a number of administrative failures in how Ivy\u2019s case was dealt with by CHI, including poor communication with her and her family about her care. We\u2019ve made several recommendations to address our concerns to try and prevent a repeat of these mistakes. A key issue we raised is that professionals must pay attention to parents, children and indeed, GPs, when they contact a hospital to say a child\u2019s condition is deteriorating. This is vital information that should be considered when reviewing a case and must never be ignored.<\/p>\n
\u201cHowever, this case is not just about Ivy. We are publishing this case on behalf of the 309 children and their families who, as of May 2023, were waiting for scoliosis treatment in Ireland. In 2017 we published Waiting for Scoliosis Treatment; A Children\u2019s Rights Issue about ongoing delays and the failure, by Government, to adequately address the issue of access to scoliosis treatment for children. We know there has some been improvements with additional investment in 2022 but we believe that the government must honour the promise it made back in 2017; that no child will be waiting longer than four months for their scoliosis surgery in Ireland. This is a promise they made to these children and it has been repeatedly broken with devastating consequences. We must never forget, that these children are in significant pain and distress while they wait, their life suspended, their childhood passing them by. They need to believe that the government cares and will make right their promise to them.\u201d<\/p>\n","protected":false},"excerpt":{"rendered":"