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Blog de The World vs.MS

The World vs.MS se centra en las personas. El objetivo es que las personas con esclerosis múltiple o cualquiera que sienta la motivación se unan en la lucha contra la enfermedad.

Aquí están sus historias y nuestras últimas actualizaciones.

Mar Mendibe : Calidad de vida

Mar Mendibe

Blogs

30.05.18

La Dra. Mar Mendibe es una neuróloga con más de 18 años de experiencia. Su experiencia en todos los aspectos de la EM es de particular interés en medicina y cirugía. Mar actualmente trabaja en el Hospital Universitario Cruces y es también profesor del Departamento de Neurociencia de la Universidad del País Vasco.

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Birgit Bauer: Quality of life and MS

Birgit Bauer

Blogs

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

Blogs

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

Blogs

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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Paula’s family planning and pregnancy tips

Paula Bornachea

Blogs

30.04.18

Getting to know you Can you tell us more about yourself? My name is Paula, I am 33 years old, I am a computer teacher, I’m married and I have two children. I also have relapsing-remitting multiple sclerosis for almost 10 years. In addition, for six years I have been blogging my stories with multiple…

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How to feel like you are winning, when you’re a parent with MS

Jenny Clarkson

Blogs

30.04.18

Being a parent is hard.  When children are tiny, there are night feeds, lack of sleep, tantrums, weaning and potty training to contend with.  As they get older, there is homework, friends, hobbies and emotions to juggle.  Now that my kids are 8 and 10, I can safely say that things do not necessarily get…

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Mark’s affair with his MStress

TWvsMS | Mark

Blogs

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

Blogs

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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An initiative to educate, empower and unite the MS community

The World vs.MS

Blogs

21.12.17

The global vs.MS survey was carried out by Sanofi Genzyme to shed light on the realities of MS, paving the way for The World vs.MS initiative. We asked people living with relapsing MS (RMS) and RMS care partners about the physical and emotional impact of the disease. Here’s what they said:

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Cuanto más sabemos, más podemos hacer. Visita nuestras páginas educativas sobre el control de la EM.

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