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Il blog di The World vs. MS

The World vs. MS mette al centro le persone, rivolgendosi a tutti coloro che convivono con la sclerosi multipla (SM) o a chiunque voglia dare il proprio contributo per sconfiggere la malattia.

Ecco le loro storie, e i nostri ultimi aggiornamenti.

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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Blogs

24-08-2018

6 minuti, 9 secondi

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 minuti, 17 secondi

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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How does your personality impact your life with MS?

How does your personality impact your life with MS?

The World vs.MS

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Demand more

16-08-2018

6 minuti, 16 secondi

Some personality traits might make you less likely to step outside your comfort zone and to put up with things, such as MS symptoms or side effects from its treatment. But understanding how you approach things can help you to do them a bit differently. We’ve put together some questions to help you understand your...

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How Telma’s husband helped her Demand More from life with MS

How Telma’s husband helped her Demand More from life with MS

The World vs.MS

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Blogs

08-08-2018

4 minuti, 25 secondi

Not long ago, I was chatting to a friend and I said to her: “Sometimes, people think that a miracle happened to me to be as I am, but that’s not what happened.” Dilma knowingly replied, “People see your smile, but they didn’t see your tears and what they want is to smile when they...

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Birgit Bauer: Quality of life and MS

Birgit Bauer: Quality of life and MS

The World vs.MS

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Blogs

30-05-2018

5 minuti, 40 secondi

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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Mar Mendibe : Quality of life and MS

Mar Mendibe : Quality of life and MS

The World vs.MS

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Blogs

30-05-2018

6 minuti, 46 secondi

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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My inner strength revealed

My inner strength revealed

The World vs.MS

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Blogs

14-05-2018

7 minuti, 26 secondi

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.

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Joanne’s parenting tips

Joanne’s parenting tips

The World vs.MS

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Blogs

14-05-2018

4 minuti, 10 secondi

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 to look after myself and a little one at the same time. I am no expert on mummy or MS stuff, but this is what I have learnt so far on coping:

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Paula’s family planning and pregnancy tips

Paula’s family planning and pregnancy tips

The World vs.MS

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Blogs

30-04-2018

8 minuti, 8 secondi

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 sclerosis.

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