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I have been staying at the MDI Home from Home apartment since 2015. I live Dublin and I’m from Enniskillen County Fermanagh. I was confined to bed for 12 years and a wheelchair user for a decade – MDI has been brilliant to be able to go somewhere that I know everything I need a there.
The Disability Federation of Ireland are working alongside European partners on the IN-HABIT project. DFI is a federation of member organisations working with people with disabilities to implement the UN CRPD and ensure their equal participation in society. MDI aswell as other charities that provide advice and support to people with disabilities are member organsation are a part of DFI. The goal of the IN-HABIT project is to foster inclusive housing solutions by strengthening the capacity of housing professionals, service providers, and local authorities to support people with disabilities. The target groups of this partnership are Housing professionals, Service providers for people with disabilities, Local authority professionals and People with disabilities & their circle of support members.
This Expression of Interest Form invites interest from those who are interested in the future of rare disease services in Ireland through contributing to the work of the IOG, and who have experience accessing these services, live with or care for someone with a rare disease, or are interested in contributing in a tangible way to the development and implementation of more trusted, and more efficient, relevant rare disease services and research in Ireland.
Muscular Dystrophy Ireland (MDI), the national charity supporting people living with neuromuscular conditions, celebrated the arrival of six Football Power Chairs, funded by the UEFA Children’s Foundation, and Lord’s Taverners Ireland/RevUp and in partnership with the Football Association of Ireland (FAI).
Book your stay now at www.mdi.ie or call our National nformation Line on +353 01 6236414
This vehicle will be available to service users in the Southern region for short-term loan spells, subject to terms and conditions. The aim is to support access to medical, clinical, and other essential journeys where possible.
At Muscular Dystrophy Ireland (MDI), we are always striving to improve the mobility, independence, and daily experiences of our members. This month, we are delighted to announce two fantastic additions to our Transport and Equipment Service — both acquired with our service users’ needs in mind. Whether you are looking for temporary mobility support or require specialist equipment for safe travel, these new options are here to help.
Muscular Dystrophy Ireland (MDI) is pleased to announce that a Size 3 OMBRELO™ special-needs stroller is now available for use through the MDI Transport Service. This equipment will be used exclusively in MDI vehicles, providing enhanced comfort, postural support, and safe, reliable travel for service users who require additional assistance during journeys.
The launch at the National Sports Campus was attended by Minister for Sport Patrick O’Donovan and FAI CEO David Courell, underlining strong leadership support for disability inclusion in sport. Funded by the UEFA Children’s Foundation and Lord’s Taverners Ireland / RevUp, in partnership with the FAI
This very special weekend offers families living with neuromuscular conditions the opportunity to come together in a safe, inclusive and supportive environment, with a programme of fun activities, shared experiences and much-needed time to connect.
Thank you so much to all who attended the 2025 National Connection Conference this year. We are so grateful we got to meet so many members, experts and supporters on the day. We are incredibly grateful to our sponsors, who make days like these possible: Biogen Roche Novartis
Proposed Cost Of Disability Payment: Everything you need to know. Over the last few weeks, there has been a lot of talk about a proposed cost of disability payment, so let's break down all the details we know so far.
It is unclear what the payment will consist of, but according to an Indecon report in 2021, additional Costs of Disability averaged between €9,482 - 11,734 per year.
As we approach the Christmas season, we are mindful of those in our community who are remembering loved ones who have passed and for whom this time of year can bring many mixed emotions. We extend our sympathy and hope the season goes gently for you. Please remember that Muscular Dystrophy Ireland (MDI) is here for you should you wish to avail of support.
The pathway outlines recommendations for the key specialists and services involved in DMD care, supporting coordinated and consistent care for children, young people and adults living with DMD.
Muscular Dystrophy Ireland (MDI) held its national conference today at Croke Park, with Minister for Health Jennifer MacNeill officially speaking at the event. The conference brought together people living with muscular dystrophy and related neuromuscular conditions, along with their families, clinicians, researchers, and disability advocates from across the country.
MDI provide a written submission to the Joint Committee on Health on issues relating to rare diseases, including access to and reimbursement for medicines.
Planning to join us at our conference on 7 December? We want to ensure all our attendees have a smooth and accessible experience! Check out this helpful video on how to access the CHANGING PLACES TOILET at the Cusack Suite, Croke Park
Planning to join us at our conference on 7 December? We want to ensure all our attendees have a smooth and accessible experience! Check out this helpful video on how to access the car park and Cusack Suite, Croke Park:
Buying MDI Christmas cards directly supports Muscular Dystrophy Ireland and helps to fund our support services for people with neuromuscular conditions across Ireland and their families..
Join us at Croke Park on Saturday, 7 December, for a fantastic day filled with connection, fun, and learning. Don’t miss this amazing opportunity for: Youth Programme – ages 8–17 and Children’s Programme – ages 5–7.
A review is under way to decide if Givinostat for Duchenne muscular dystrophy will be reimbursed in Ireland. Your experience of living with Duchenne can help inform this decision - share your story in the survey link.
Secure your spot now and be part of a powerful day of coming together as a community to share and learn together. Find out more about our exciting programmes and book your place
Be part an unforgettable experience as we come together as a community, fostering meaningful connections, sharing knowledge, and supporting one another. Our conference is a warm and inclusive space for adults and young people living with muscular dystrophy and related neuromuscular conditions, as well as their families, healthcare professionals, and other stakeholders. We look forward to warmly welcoming you and sharing an enriching experience together.
The Disability Federation of Ireland has said that while it welcomes the €619m increase in funding for disability services, the Budget overall represents a devastating setback for disabled people unable to work.
We are delighted to invite you to our FSHD community gathering on Saturday 11 October. Please note this event will now take place online only. It will be opportunity for people living with FSHD and their families to connect as a community and learn together. We have lined up an exciting programme of speakers and topics that we hope you will find informative and empowering.
Researchers at DCU are examining the supportive care needs of people with pre-existing physical disabilities who are diagnosed with cancer.
As part of Muscular Dystrophy Awareness month, we wish to let you know that 23 September is OPMD Awareness Day, when the OPMD Community comes together to raise awareness of Oculopharyngeal Muscular Dystrophy and to celebrate all members of the OPMD community.
Myositis is an inflammatory autoimmune condition that can cause muscles to become weak and painful. Idiopathic inflammatory myopathies are an umbrella term for the different types of myositis. These autoimmune conditions mean the body attacks its own muscles, connective tissue, blood vessels, skin, lungs, and other organs. This often occurs together with other symptoms, such as muscle swelling, pain, fatigue, difficulty moving limbs or lifting arms, increased falls, trouble swallowing, and others.
Paddy Hickey called in to MDI today and the team were delighted to wave him off as he embarks on the third edition of Walk4Ollie on Monday and the road to €100,000 for the Ollie Hickey Fund! We will be following his progress all next week, so watch this space!
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