🌱 The Power of a Happy Gut in #MS! 🌟 Consistent bowel movement isn't just comfort—it's key! 🌀 An off-balance gut can amplify neuro symptoms in MS. But remember, what stirs one's gut may not stir another's. Find YOUR gut groove! 🕺💃 Seeking more lifestyle tips? Dive into

Lucky I wasn’t going for a #swim yesterday. There was an #invasion of #jellyfish

These look amazing and I wonder would they work for people living with #multiplesclerosis. Shift Robotics youtube.com/shorts/PTjVdTn…

Serena Carberry from University Of Limerick, is researching couples experience of MS - questions about your relationship, your experience of MS, and how you cope. More details in the link below⬇️ 20031912.wixsite.com/information-sh…… #msresearch #MS

This is valuable research and I have already shared my samples. Please share #MultipleSclerosis #MS #Ireland

#Connemara a nice day out touring.

In the volatile NHS world, remember that ‘patient leaders’ - those who’ve been through stuff, who know stuff, who want to change stuff…. can help. We are not there just to challenge, but to support. We have insights, wisdom and (com)passion. Turn to us, not away from us.

A key element of this should be that all patients who use the health service should be included. However, those on Invalidity Pension cannot without risking losing their support. Those in receipt of Carers Allowance similarly take a risk. This must change!!

If @DonnellyStephen wants to give patients, like me, a voice, why is he blocking our comments. The value of comments is you will get positive and negative viewpoints. All are valuable in developing a #patient centred system which is safe for all.

If you have MS, live in the UK, and would be interested in taking part in some research interviews about your journey from diagnosis to managing your condition (with vouchers as a thank you for your time), send me a DM and I’ll tell you how to get involved.

In today’s Irish Examiner there is an article about medicinal #cannabis. I was interviewed for this article. theMSguide.com 🧠 MS Ireland MS Society NI HSE Research & Development Shift.ms/Lauren MS Society UK #multiplesclerosis #spacticity #pain irishexaminer.com/lifestyle/heal…

I was a collaborator in this paper, trying to set a strategic neurological research agenda for Europe. European Academy of Neurology PPI Ignite Network Ireland MS Ireland theMSguide.com 🧠 PPI Ignite Network @ University of Galway NUI Galway Medicine IPPOSI EUPATI European Patients' Forum Made WITH Patients onlinelibrary.wiley.com/doi/10.1111/en…

The long-awaited Disability Action Plan, the Government’s response to years of underfunding of the disability sector, will be published today. The launch will be live streamed from 1pm at this link youtube.com/merrionstreet #DisabilityActionPlan

Don't forget tonight 7:30p🎧📻 RTÉ One radio we highlight how ♿accessibility is still an afterthought with new tourism projects in Ireland using the example of The Emigrant Park in New Ross which cost €1million & won an urban planning award. #LastOneOnTheTrain #Ableism

Magdalen Rogers, Neurological Alliance of Ireland speaks of the vital need for neurology nurses. Posts already funded are not in post due to HSE moratorium Department of Health HSE Ireland #patientsdeservebetter

A fantastic idea.

It was great to speak on this podcast about my experiences as a patient researcher Embedding Patient Perspectives into Clinical Research┃Robert Joyce youtu.be/5rqeTc4WSjk?si…