Multiple Sclerosis

Neurology (Research)

Hands holding human brain

Journal of Neurology & Neurosurgery – JNNP’s ambition is to publish the most ground-breaking and cutting-edge research from around the world, encompassing the entire genre of neurological sciences

Journal Watch Neurology – Its mission is to help clinicians efficiently understand medical developments to improve patient care and foster professional development

NetmedNeurology – Your First Place To Look™ for authoritative, in-depth articles covering the full spectrum of neurology

Neuroscience Ireland – The aim of the Society is to advance research and education in the neurosciences in Ireland, and to represent Irish neuroscience researchers both nationally and internationally

Updated: March 18th, 2019 (update ongoing)

Signature

2018 Winner Best Blog Post with ‘3443 Needles’, Blog Awards Ireland, Ashville Media Group, Dublin, Ireland

Everyday Health: Top 10 MS Blogs to Follow in 2020
Feedspot: Top 50 MS Blogs to follow in 2020, 2019, 2018, 2017
MyTherapy: Multiple Sclerosis Blogs: 10 of the Best in 2019
Everyday Health: Top 10 MS Blog of 2018
MyTherapy: Best MS Blog for Simplicity 2018
Ireland Blog Awards: Finalist 2014, 2015, 2017


© Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me, 2019. Unauthorized use and/or duplication of this material without express and written permission from this site’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to Willeke Van Eeckhoutte and irelandms.com with appropriate and specific direction to the original content.

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      • Martha Kennedy

        I wish my dad were alive to see these pictures. He was a scientist and, besides having MS, was interested in the disease itself. Although back then they knew how MS works there were no pictures of it, not like these. Thank you!

        • Billie

          So sorry to hear your dad is not here anymore, Martha. I’m glad, however that you saw the image as it sometimes makes it clearer to people what MS is really like. Being an invisible illness, people don’t always equate a damaged brain to MS, which is sad of course.

          • Martha Kennedy

            I remember my dad giving people what amounted to an anatomy lesson about the circuits in the brain/spine and explaining that what was happening to him was something like a broken electrical wire or extra insulation in a circuit that blocked the flow of electricity. It was difficult for people to see the mind as giant circuit breaker or to understand that the reason my dad could not walk well was not because he was physically damaged in the sense people understand but because messages were not traveling clearly. Pictures such as these would have made it much easier. Honestly, sometimes reading your blog is difficult for me because there are always so many things I wish I could tell him. I wish I could tell him what people have learned in the meantime (though still not enough, maybe). He would be fascinated by it. Well, anyway, over the years I’ve also learned there are innumerable sad stories, not just his and mine. And some of the saddest stories I’ve seen are of people who lived beyond themselves, their minds, their physical abilities and their sense of who they are. This experience has put my whole little story in perspective. <3

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