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The World vs.MS Blog

O The World vs.MS fala sobre pessoas. Fala de qualquer pessoa que viva com esclerose múltipla (EM) ou de qualquer pessoa que se sinta inspirada para ajudar a vencer a EM.

Descubra as suas histórias e as nossas últimas novidades.

How to throw the stumbling seriousness of life overboard!

How to throw the stumbling seriousness of life overboard!

The World vs.MS

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Blog

29-03-2019

5 minutos, 47 segundos

Splash. It hits the water, the seriousness of life. Without a life vest, it drowns beneath the surface as I ride all the way to the beach on a wave of smiles. While all that seriousness did its best to...

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I am the expert in my MS!

I am the expert in my MS!

The World vs.MS

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Blog

21-03-2019

9 minutos, 16 segundos

A background to my story Growing up, I was a bit of a stroppy teenager (I’m sure if my mum was reading this she would be saying “a bit” really sarcastically right about now!) thing is, I’m glad that I...

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Patient Focused Priorities: Birgit’s perspective

Patient Focused Priorities: Birgit’s perspective

The World vs.MS

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Blog

25-02-2019

5 minutos, 30 segundos

MS is life changing. Nothing new there. Whether it’s about your first diagnosis or new symptoms and episodes occurring, we’re forever facing new challenges. It’s a never-ending cycle. Before you even know it, you can find yourself trapped in the...

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Prioridades Focadas no Paciente: a perspectiva de João

Prioridades Focadas no Paciente: a perspectiva de João

The World vs.MS

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Blog

07-02-2019

7 minutos, 25 segundos

O que sentiu quando foi diagnosticado com EM? Quando o diagnóstico é confirmado somos apanhados de surpresa, não só porque não sabemos o que está errado, mas porque sabemos que ainda não há cura para esta doença. Felizmente, no meu...

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Patient Focused Priorities: Jacobo’s perspective

Patient Focused Priorities: Jacobo’s perspective

The World vs.MS

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Blog

31-01-2019

5 minutos, 46 segundos

  How have your priorities changed since being diagnosed with MS? Considering I have been living with Multiple Sclerosis for over ten years since I was diagnosed, my objectives have changed hugely. When I was first diagnosed with MS, I...

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Patient Focused Priorities: Barbara’s perspective

Patient Focused Priorities: Barbara’s perspective

The World vs.MS

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Blog

31-01-2019

6 minutos, 49 segundos

  What feelings did you have when you were first diagnosed with MS? MS has never been known for its great timing. In 2011, I was in the middle of changing career direction, my son was about to start high...

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How digital solutions can help people living with MS

How digital solutions can help people living with MS

The World vs.MS

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Blog

14-01-2019

8 minutos, 5 segundos

New digital technologies are taking hold in our lives apace. Everywhere you look, you see new ‘digital tools’ and other gadgets making the move from analogue to digital. Data, bills and all the other documents that were once on paper...

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MS, self-reflection and compromise

MS, self-reflection and compromise

The World vs.MS

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Blog

14-01-2019

8 minutos, 13 segundos

Soon after my diagnosis of MS, I realised that life was now all about give and take. I was giving up everything, MS was taking. Not only that, I was navigating a whole new world without a map – there...

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Telling people at work about your MS

Telling people at work about your MS

The World vs.MS

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Blog

14-01-2019

9 minutos, 58 segundos

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...

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