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Il blog di The World vs.MS

The World vs.MS è un’iniziativa fortemente incentrata sulle persone. Riguarda tutti coloro che convivono con la SM,

o chiunque voglia unirsi alla lotta per sconfiggere la malattia. Ecco le loro storie, e i nostri ultimissimi aggiornamenti.

Telling people at work about your MS

Carla King

Blog

19.11.18

So, you’ve been diagnosed with Multiple Sclerosis and, along with all of the emotional turmoil that comes with being diagnosed with a life-long condition, you’re also worried about work. The majority of MS diagnoses happen when people are in their twenties and thirties; a time when you are likely to be at an exciting point…

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How Fabienne helped Charlotte Demand More from life with MS

Charlotte Tourmente

Blog

24.08.18

From my perspective On the morning of 5 December 2010, I fell to the floor when getting out of bed. The right side of my body no longer responded; I was paralysed on one side. I nevertheless had enough strength (the paralysis would worsen over the upcoming days) to drag myself into the living room…

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Mar Mendibe : Quality of life and MS

Mar Mendibe

Blog

30.05.18

Dr Mar Mendibe is a neurologist with over 18 years’ experience. Her experience spans all aspects of MS but her particular interest is in medicine and surgery. Mar currently works at the Cruces University Hospital and is also a Professor of the Department of Neurosciences at the University of the Basque Country.

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Birgit Bauer: Quality of life and MS

Birgit Bauer

Blog

30.05.18

Quality of life is the phrase on everyone’s lips. Everyone strives for it. Generally speaking, it’s everything coming together that means people can lead a good life. Being happy and satisfied. Things like eating right, having a nice home, money for everything that’s good for you. Everyone has their own priorities, but there’s one factor that’s important for everyone: health.

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My inner strength revealed

Paul Kerr

Blog

14.05.18

I was first diagnosed with MS in 2005, and my son Zander was born in 2006, while I was still adjusting to my illness. I can only view this timing as miraculous, as it had such an impact on me. I’m sure every new parent finds that having a baby completely re-orientates your concerns and…

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Joanne’s parenting tips

Joanne Chapman

Blog

14.05.18

I was diagnosed a year before falling pregnant with my little man, who is now a pre-schooler. When he was born, I was told to “savour every moment as they grow up so fast”. The similarity of being a Mother and having MS is to be prepared. To do this, I wanted to understand how…

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Mark’s affair with his MStress

TWvsMS | Mark

Blog

25.04.18

An image of wires bared back at the ends is often used as a visual image to illustrate the clinical process of Multiple Sclerosis. It shows how the nerves might appear under a microscope with their damaged myelin coating. Faulty electrics can be fixed, rewired, replaced. Electricians, engineer’s even DIY enthusiasts can make the necessary…

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Bringing together the MS community across the Nordic and Baltic countries.

The World vs.MS

Blog

10.04.18

On Tuesday 8th May, The World vs.MS goes live across the Nordic and Baltic countries. Many great things happen when people get together and unite around a shared goal. The World vs.MS is going live with a unique event that can inspire the 55,150 people living with MS in the Nordic and Baltic countries to…

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Mission Summit: Kiki’s story

TWvsMS | Kiki

Blog

01.12.17

One of the most powerful reasons to share MS stories is to inspire others. Not only do they touch the lives of those living with MS and those around them, they can even motivate people with no links to MS to take action. Kiki is one of those people. A chance encounter with the mountain…

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