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.

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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I make my own decisions

I make my own decisions

The World vs.MS

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Blog

14-01-2019

6 minutos, 51 segundos

“I’ll just do that for you!”, or “you can’t do that, you shouldn’t be doing that!”. It’s something that happens to all of us who live with MS from time to time, other people relishing in making our decisions for...

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How Fabienne helped Charlotte Demand More from life with MS

How Fabienne helped Charlotte Demand More from life with MS

The World vs.MS

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Blog

24-08-2018

6 minutos, 9 segundos

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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Is it time for your MS performance review?

Is it time for your MS performance review?

The World vs.MS

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Demand more

16-08-2018

3 minutos, 17 segundos

Anybody living with MS will know that living with the disease is a marathon, not a sprint. With a variety of individual symptoms that can fluctuate and change over a lifetime,1 it can be easy to let MS creep in and take control. Small lifestyle changes can be made on a daily basis without you...

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