Thank you to everyone who has participated in our research collaboration studies!
Thank you to everyone who has participated in our research collaboration studies this year. ‘Supporting Transitions to Adulthood Resources (STAR) Project’ and ‘The Lived Experience of Health-Related Quality of Life for Adults with Muscular Dystrophy’ have closed. We will publish reports on our website once the results have been analysed.
Civil Service WAM Placements - Applications Now Open!
Applications are currently open to graduates with disabilities for ten month, paid, mentored work placements in the Civil Service based nationwide at Executive Officer level. WAM are seeking graduates from ALL disciplines.
This week we would love to highlight the family of Abbie Byrne
The family went all out to arrange a celebration that Abbie would have loved, and their friends and family came together to raise an incredible €6,035.00 for MDI. We were blown away by this generosity.
7 September is World Duchenne Awareness Day
On 7 September the World Duchenne Organisation will launch a documentary that portrays the lives of people living with Duchenne muscular dystrophy across the globe, it will share their journeys, challenges and successes, and captures the resilience and determination of the Duchenne community. People are encouraged to share it with their wider communities.
MDI is a partner in Rare Diseases Irelands campaign ‘Get Rare Aware’.
This campaign is calling on the Government to urgently double the number of conditions screened for in Ireland’s newborn bloodspot screening (NBS) programme also known as the ‘heel prick test’ to the European average of 18.
Check out our fun and interactive online youth activities over the coming months!
The MDI Youth Team would like to welcome its young & young adult members to join us for some fun and interactive online youth activities over the coming months. These events will be run in conjunction with "Celeb Entertainment".
September is Muscular Dystrophy Awareness Month!
MDI is excited for Muscular Dystrophy Awareness month and looking forward to sharing many family stories, engaging with our members and the online community, and launching our ’30 Days of Strength’ campaign on social media #30daysOfStrength,” This September go green in support of raising awareness for Muscular Dystrophy!
Highlights from the SMA event hosted by MDI and SMA Ireland
MDI in collaboration with SMA Ireland held an event for people with SMA and their families in Mullingar Park Hotel on Tuesday 20 August. This event was kindly supported by an independent grant from Roche, who had no editorial influence over the content.
The legendary Forde sisters raise €6,320 for Muscular Dystrophy Ireland this year!
A big shout to Caoimhe & Aisling – the legendary Forde sisters who have spent the summer fundraising in memory of their brother Ciarán, who passed away 10 years ago this year. The girls took on the mighty Cork City Marathon in June and thanks to their incredible family & friends raised €4,820! They then hosted a fundraising collection in Kanturk in August which raised an incredible €1,500 – bringing their total fundraising for the year to €6,320.00!
Spotlight on members of our community living with neuromuscular conditions: Annette Marie Murphy
As part of our members’ stories series, Annette Marie Murphy is delighted to share her story about her career.
A HUGE thank you “Team MDI” who took part in the VHI Women’s Mini Marathon 2024
Together, they raised €3,898 to support our services this year and raise awareness of MDI through the event. We hope to build our team even further next year so watch this space!
We are excited to announce the launch of our 8-week Adapted Pilates series.
Classes are commencing Wednesday 4th September at 2.30pm and will continue for 8 consecutive weeks. Based on feedback, we know many of your teens have half days from school on Wednesdays, making this an ideal time to join in. This programme is a fantastic way to stay active, connect with others, and support the Muscular Dystrophy community.
Spotlight on members of our community living with neuromuscular conditions: Cormac O’Callaghan
As part of our members’ stories series, Cormac O’Callaghan is delighted to share his story about his involvement in cycling. I compete in paracycling at national and international levels. It helps me push myself and feel accomplished. I get to meet and compete with other great athletes from Ireland and around the world.
Last chance to book your place – SMA Community Gathering.
A wee reminder of the closing dates to book your place for our summer Spinal Muscular Atrophy (SMA) Community Gathering which takes place on Tuesday 20 August at the Mullingar Park Hotel: Monday 5 August is the final day for young people to book a place Tuesday 13 August is the final day for adults to book a place( Bookings for under 5s are now closed).
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.
My Neuro Survey 2024-2025
Are you getting the care and support you need for your neurological condition? Everyone deserves access to the right care, treatment and support at the right time, no matter who you are or where you live. Unfortunately, too often this isn’t the case. We are asking you to share your experiences and help improve neurological services for everyone affected by neurological conditions throughout Ireland.
The Kevin Gannon Memorial Cup will be taking place on Saturday 20th July in IT Blanchardstown
The Kevin Gannon Memorial Cup will be taking place on Saturday 20th July in IT Blanchardstown
Muscular Dystrophy Ireland supports Changing Places Awareness Day 2024!
It is a day dedicated to making a noise about what Changing Places toilets are and why they are so important. At the heart of the campaign is the call for Changing Places toilets to be installed in all big public spaces so that people can access their community.
The Ollie Hickey Fund: Supporting Mollie’s Horse Riding Journey
We are delighted to share how the Ollie Hickey Fund has positively impacted the life of one of our young members, Mollie. With the support of the fund, Mollie has been able to start horse riding lessons. Her grandad proudly shares that Mollie finds ‘tremendous enjoyment’ riding her horse, Scoobie. This experience not only enriches Mollie's life but also helps her develop new skills and build her confidence.
Spotlight on members of our community living with neuromuscular conditions: David Kennedy
As part of our members’ stories series, we are delighted to share David Kennedy story about the benefits he gains from keeping active through swimming.