Walk4Ollie 2024 is live!
This year the Walk4 Ollie event takes place from 16th – 20th July, and the route follows the amazing Waterford Greenway from Dungarvan, through Waterford City, Graiguenamanagh, Carlow Town, Monasterevin and finishing up in their hometown of Enfield. Paddy & Claire Hickey will be joined by friends, family and MDI members along the 200km route
The MDI-Dr John Roche Education Bursary, totalling €2,000 annually is now open for applications.
We are excited to announce that the Muscular Dystrophy Ireland-Dr John Roche Education Bursary, totalling €2,000 annually, is now open for applications. MDI hopes to support two of our members with €1,000 each towards their education costs this Autumn. The deadline for applications is Friday 26 July 2024.
MDI wishes the Republic of Ireland Powerchair Football Squad the best of luck in Inverclyde Scotland this weekend
We would like to wish the Republic of Ireland Powerchair Football Squad the best of luck as players, coaches Paul Gorman and Conal Fagan, and support staff take to the waters, roads, and skies tomorrow to travel to Inverclyde Scotland for this weekend’s tournament with hosts Scotland, England, and Northen Ireland. Great matches ahead, renewing old rivalries and catching up with old friends.
New Study on Biomarkers for Charcot-Marie-Tooth Type 1
This study is a continuation of prior research that has shown promising results in understanding CMT1A more deeply. Participation requires a single visit to Tallaght University Hospital for a standard blood draw and clinical assessment, which is conducted in one day to minimise inconvenience to participants. Full details about this study are available here.
European Commission Returns Translarna™ Opinion to CHMP For Re-evaluation
We are pleased to announce that the European Commission (EC) has decided not to adopt the Committee for Medicinal Products for Human Use's (CHMP) negative opinion on the renewal of the conditional marketing authorization of Translarna™ (ataluren).
Notice of AGM 2024
I am writing to inform you that Muscular Dystrophy of Ireland Company Limited by Guarantee (MDI) will hold its 2024 Annual General Meeting (“AGM”) on Saturday, 8th June 2024 at 12.30 pm at the registered office of the Company at 75 Lucan Road, Chapelizod, Dublin 20, D20 DR77 and, for members using Zoom facility, at the member’s home address as recorded in the register of members of the Company.
Watch: MDI Duchenne Muscular Dystrophy Community Gathering (Dublin, 18.11.2023)
We are happy to share our recording of our Duchenne muscular dystrophy community gathering which took place online and at MDI in Dublin on 18 November 2023. This is part of our series of condition specific community gatherings that aims to facilitate people living with specific conditions and their families to get together as a community and learn together.
Letter from Chairperson Mr. Patrick Cassidy: Nomination process for potential election to our board of directors is now open
Ppaid-up members of Muscular Dystrophy Ireland CLG as of 31st March 2024, we are pleased to let you know that, as of 1 May 2024, the nomination process for potential election to our board is now open.
Muscular Dystrophy Ireland proud to be welcomed on board as a partner for Carers Week 2024
Carers Week 2024 is set to take place from the 10th to the 16th of June this year with preparations already underway for what we hope will be a great week for all involved. This year will see a mixture of both online and in-person events being offered to promote an inclusive week for everyone.
Expansion of heel prick test could save or improve the lives of 200 babies born each year in Ireland.
MDI joined with other members of Rare Diseases Ireland outside the Dáil to launch a new Get Rare Aware campaign calling for the number of conditions newborn babies are screened for under the HSE National Newborn Bloodspot Screening Programme, more commonly known as the heel prick test, to be expanded from the current nine to the European average of 18 minimum. Support the campaign by contacting your Oireachtas representatives and ask them to demand that Ireland is above average when it comes to newborn screening.
![[Watch]: The tech helping teen with Duchenne muscular dystrophy live his musical dream | BBC News](https://images.squarespace-cdn.com/content/v1/63c138561d3afd3c27c17d5d/1712761630243-244S5THUMRQ8OL9UCWTV/Screenshot+2024-04-10+160654.png)
[Watch]: The tech helping teen with Duchenne muscular dystrophy live his musical dream | BBC News
An assistive technology has now given the 16-year-old the potential to keep playing music longer. And he has been given the chance to perform at America’s music, tech and film festival.
Lights, Camera, Action - Vlog Your Irish Adventure- It’s On Us!
Are you ready to be the star of your own adventure? At Muscular Dystrophy Ireland we're on a mission to spotlight accessible locations, attractions, and thrilling experiences across Ireland, and we need your help to make it happen. Whether you're exploring solo, with a friend, a partner, or with the family, we invite you to be a part of this exciting initiative.
Save The Date: Muscular Dystrophy Ireland’s national conference 2024
We are delighted to announce that Muscular Dystrophy Ireland’s national conference will take place in person on Sunday, 10 November 2024, in Croke Park. There will be two programmes, one for adults and another for under-18-year-olds. Details of the programmes and booking form will be released at a later date. Stay tuned for updates!
Pathways: Navigating third level education for students with neuromuscular conditions
MDI’s latest report emphasises the urgent need for improved accessibility in Irish third level institutions. Inclusive Pathways: Navigating third level education for students with neuromuscular conditions highlights the challenges faced by students with neuromuscular conditions in accessing higher education.
Today we visited the Friends in Need Pop-Up shop in Long Walk Shopping Centre, Dundalk
All proceeds from the shop and the raffle will be donated to MDI to support youth services in the Northeast. If you are in the area, please drop in to pick up a bargain or buy a ticket for the raffle, some amazing prizes to be won between now and Saturday.
The Neurological Alliance of Ireland is calling for a dedicated Consultant Neurologist for Bantry hospital
On Tuesday March 26th at 1pm NAI will be holding an online event to enable TDs and counsellors to hear from local patients, patient organisations and clinicians on the need for a dedicated Neurology Service for Bantry hospital. Bantry hospital currently provides some clinics for neurological patients and there is an urgent need to secure and develop a dedicated neurology outpatient service in Bantry for patients throughout West Cork and Kerry.
Take action now for local neurology services: #patientsdeservebetter
The Neurological Alliance of Ireland, the national umbrella for neurological charities, together with 23 of its member organisations is asking people to take action for local neurology services. The Patient Deserve Better campaign is a joint initiative brought to you by NAI and Roche Products (Ireland) Ltd.
Reminder: MDI Membership renewal deadline is March 31st 2024.
If you’ve encountered any challenges renewing your membership, please don’t hesitate to reach out to us through our information line at +353 01 6236414. One of our decicated team will be happy to assist you.
Irish Wheelchair Association’s ability programme inviting jobseekers
Providing holistic, person-centred Coaching to enable a person to become an independent jobseeker or employee. Funded by the Dormant Accounts Fund and administered through Pobal, Ability is an employability and job-seeking skills programme for people aged 18 and over with a physical disability who want to get closer to work and progress on their career journey.
New Campaign for Neurology Services Launching March 12th
We’re one of 23 organisations joining the Neurological Alliance of Ireland’s Patients Deserve Better campaign which is calling for regional neurology services in 5 hospitals across the country.