Anthony Byrne MP today met with wonderful mums Wendi and Tracey and their sons Reef & Harrison to celebrate the Federal Government’s decision that will continue funding of $250 per month for the Inborn Error of Metabolism (IEM) Programme.
Over the past few months parents across Australia like Wendi & Tracey have led a successful community campaign to ensure they maintained their $250 per month IEM Grant to financially support them in continuing to purchase strict low protein products for their children who suffer from the Inborn Error of Metabolism disorder.
In the Budget 2015 the Abbott Government decided to finish the IEM Programme on 31 December 2015, as a $11.7 million budget saving measure but it would have increased the cost of living pressures on families with children suffering from IEM.
“I am so proud of the local community campaign led by Wendi Emmerson and Tracey Scott who as parents continue to go above and beyond in looking after their children Reef and Harrison but who need financial support to purchase the strict low protein products for their children. I welcome Minister Sussan Ley’s decision to continue the IEM Programme but I wish to point out that it should not have been cut in the first place. Children like Reef and Harrison have a unique condition, which should automatically result in Government support. I will continue to campaign to ensure this IEM Grant remains a permanent feature in the Federal Health Budget in the years ahead,” said Mr Byrne.
Media Enquires: Daniel White (03) 9796 7533.