Advocating for people living with neuromuscular conditions and their families:MDI and our umbrella organisations – Budget 2025 asks and general election manifestos.
We provide an overview of key issues identified by MDI as important for our community and a flavour of how some of these umbrella organisations are championing these causes in their pre-budget 2025 submissions and election manifestos. We are members of Care Alliance Ireland, Disability Federation of Ireland, Health Research Charities Ireland (HRCI),The Irish Platform for Patient Organisations, Science & Industry (IPPOSI), Neurological Alliance of Ireland (NAI), Rare Diseases Ireland (RDI) and The Wheel. You can read their specific submissions/manifestos by clicking on each of the organisations’ names above.
PUBLIC CONSULTATION: Contribute to development of the new National Rare Disease Strategy
This consultation looks at what areas are important to the many stakeholders across the rare disease community, healthcare providers, the public and others. We aim to make sure that the new National Rare Disease Strategy responds to their needs.
Newborn babies to be tested for Spinal Muscular Atrophy from next year – a victory for our community!
We are really pleased to share the good news that Spinal Muscular Atrophy (SMA) has been approved for inclusion in Ireland's National Newborn Bloodspot Screening Programme, commonly known as the heel prick test. Approval of SMA is a massive milestone for the community and overall progress of newborn screening in Ireland. It is particularly valuable because new treatments have become available for SMA in recent years with the potential to significantly improve outcomes through earlier diagnosis and treatment.