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Niamh McCarron says people with chronic illnesses and disabilities have been asking for remote working for years, often getting told that it can’t be supported, for a whole list of reasons
The CE Scheme in the Care Centre was run by the Multiple Sclerosis CEP Co. Ltd. The CE Scheme is now being run by MS Ireland.
Enter the MS Ireland Summer Raffle 2021 and grab your chance to win €1,000
Enter the MS Ireland Summer Raffle 2021 and grab your chance to win €1,000
Dear Member,
Please see below the Notice of the Multiple Sclerosis Society of Ireland’s Annual General Meeting ('AGM'). All documentation including the Notice and the AGM Information Pack is available on our website ms-society.ie. The following link will bring you to the AGM Notice and Information Pack (which includes the financial statements for the year ended 31st December 2020 and the Candidates’ Profiles) AGM and Information Pack
Votes for the AGM may be registered virtually at the AGM or by proxy. Here is the link to the Proxy Form.
The National Transport Authority (NTA) is conducting research with the aim of gaining a better understanding of the accessibility requirements and experience of users of small public service vehicle (SPSV), for example taxis and hackneys.
I have been diagnosed with Relapsing Remitting Multiple Sclerosis for 10 years now. That’s one MRI per year- plus the clinical trial related ones. Let’s say that I have been in a giant, buzzing magnet over 20 times.
Dear Member,
Please see below the Notice of the Multiple Sclerosis Society of Ireland’s Annual General Meeting ('AGM'). All documentation including the Notice and the AGM Information Pack is available on our website ms-society.ie. The following link will bring you to the AGM Notice and Information Pack (which includes the financial statements for the year ended 31st December 2020 and the Candidates’ Profiles).
Votes for the AGM may be registered virtually at the AGM or by proxy. Here is the link to the Proxy Form.
This week we thought we’d take a different look at Life with MS. The MS and Me bloggers are in touch with each other a lot. We share updates on how our MS is faring and ask questions about treatments and symptoms. It is fair to say however, that a significant percentage of our WhatsApp messages involve pictures and stories about the furrier members of our families.
Anyone who has a pet will understand the joy they bring, but a quick poll of our bloggers suggests that having a dog or cat is beneficial to our well-being and how we live well with MS. Our pets are our companions, confidantes and always agree with us! This week Ciara, Rosie and Niamh share their pet stories.