You know it will definitely gather income. Good for you. Rehashing unresearched claims that have yet to be clinically trialled is not OK. It is even less OK when it’s done on the backs of people who day in day out, live in hope because they want to get on with life instead of having to go on living with critical illnesses. It is a hideous way of earning some bucks.Read More
In ever memory of physical betrayal and every second of dislike of my illness, I am still intrigued by its complexities and continue to care for all its nuts and bolts.Read More
As you move on in life, you will find that perhaps your diagnosis was something that needed to happen to see what is really important in life.
It is not an expensive new car, clothes, jewelry.
It’s health and acceptance, though flawed the best of times.
Despite having my inner dialogue running into philosophical mayhem, parameters on what I perceived to be acceptable have been reset, and my inner dialogue needs a fix as an intuitively sharp anguish took over my mindset last week.Read More
Let me count… Roughly speaking, I was diagnosed with MS about 5000 days ago. That’s one fair bit of experience under my hood, right? But… When talking to people, new or otherwise, it can be difficult telling them you’re living with an incurable neurodegenerative illness. Sometimes it feels like being in an uninterrupted car crash, minus the […]Read More
🎀 3443 Needles 🎀 2018 Best Blog Post @ Ireland Blog Awards Ashville Media Group October 26th, 2018 This is my favourite pose. Stretched out, in an apparent hug with what could be the floor or a bed. But, do not be confused, for I am not that hung up about yoga. I wasn’t on […]Read More
“What’s wrong with my brain?” doesn’t automatically mean, “Is my mind, my soul therefore broken as well?”Read More
In the UK, it takes over 12 years to develop a new medicine to the standards of quality, efficacy and safety laid down by legislation. It typically costs £1.15 billion to do all the research and development necessary before a new medicine can be licensed for use. The majority of medicines under development never […]Read More
“Instead of going into the possibility of ending their life in a wheelchair, I refer to the opposite side of the scale. When they say “But 25% of people with MS will end up in a wheelchair!” I say “Perhaps, but that means that 75% of people with MS will not end up in one at all!”Read More
1960s During the 1960s, scientific research into the cause of MS came to focus on two main lines of inquiry that are still being explored today. The first emerged from analysis of the immune system. White blood cells that react against myelin, specifically against a component called myelin basic protein, were discovered in both EAE […]Read More
19th century Until the early years of the 19th century, physicians relied on superstition, hearsay, and “the wisdom of the ancients” to care for the sick. Medical ideas were not scientifically tested. Even so, physicians were often good observers and we can look back today and identify people who undoubtedly had MS from descriptions written […]Read More
20th century In the 19th century, scientists first learned that bacteria cause many diseases. As the 20th century began, they discovered even smaller organisms, viruses, and developed techniques for growing and studying bacteria and viruses in the laboratory. This later led to research on viral causes of MS. In 1906, the Nobel Prize for Medicine […]Read More
Oops… We can’t find the page you’re looking for. Maybe this page might help? MS Societies around the World (2018) Or, why not travel around IMSM with me by visiting these pages? A powerful letter to my MS Do I have stupid written on my forehead? MS anxiety I’m an ex and I’m loving it! You […]Read More
Children and multiple sclerosis? Although life was good in my last relationship, I secretly decided that having children would probably not be on my list of things to do. Not because of the lack of love, but because I didn’t want to pass on my illness to my future son or daughter. When we eventually […]Read More
Note: I am not a medical professional nor do I intend to provide any medical advice to anyone. Please see your family doctor or neurologist if you have any health care concerns. My intention is to provide accurate information from the perspective of an informed patient. Note: As an MS patient you can experience several […]Read More
Please consult with your neurologist, MS nurse or GP if you feel your medication is not working as well as you had hoped. I am not a medical professional nor do I intend to provide any medical advice to anyone. Please see your family doctor or neurologist if you have any health care concerns. My […]Read More
This is something totally off-topic but it’s something that is becoming more and more a regular news story. It’s making me afraid, short of not freaking out because Ask.fm is the reason why. You might have heard of this website if you’re living in Ireland because it has been linked to several cases of vicious […]Read More
© Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me, 2011-2012. Unauthorised use and/or duplication of this material without express and written permission from this blog’s author and/or owner is strictly prohibited.Read More