The World vs.MS is all about making a real difference to the lives of those living with multiple sclerosis (MS) and the people who support them. We’re working to encourage them to always Demand More from their life with the condition through awareness, education and understanding.
Our mission is to help more people living with MS to live the best life they possibly can.
Whether it was the boy who laughed when you fell, or the lady in the restaurant who kept staring at you, we’d love to hear who or what made you Demand More from life with MS. And don’t forget, all the stories we recieve will be submitted for the chance to be brought to life in their very own film
This year, we’re asking people to Demand More from life with MS. By sharing moments of when others have changed their life with MS for the better, we hope to inspire more to stop and think about all the compromises they’ve had to make since their diagnosis, to break out of the routine and Demand More.
Shortlisting of the final stories will take place towards the end of this year, so be sure to submit yours in plenty of time if you want to be in with a chance. Creation of the films will begin in January 2018.
Having taken medical retirement in 2012, Patrick now devotes much of his time to sharing advice for how to live with the ups and downs of MS on his website, Aid4Disabled.
You may have heard of Barbara’s book and blog ‘Stumbling in Flats’. Her honesty and sense of humour within her stories has helped her to win fans across the globe.
Joao took part in The World vs.MS Round 1 last year and won! Having lived with MS for years, Joao is always trying to find innovative ways to improve life with the condition.
Shana was diagnosed with MS in 2008. Since then she has campaigned heavily for the MS Society to improve the lives of those living with MS, just like her.
Charlotte was diagnosed with MS 20 years ago. She has always loved to write and now puts her skills to exceptionally good use giving advice and interviewing others with the condition on her blog, Sep-ensemble.
"I hope that The World vs.MS will engage the global community into thinking about life from the point of view of someone with MS or any other condition that may result in someone facing similar issues."
Trishna Bharadia Living with MS
Jacobo is a lawyer and has been living with MS since 2007. Having worked as a youth representative for his local MS organisation in Spain for five years, he has now joined the EMSP Young People’s Network.
“I want people who have MS to look forward and not look back. If The World vs.MS can help achieve this, then this is a positive.”
Living with MS
Sanofi Genzyme help people with debilitating and complex conditions that are often difficult to diagnose and treat.
Driven by their commitment to people living with these conditions, they strive to develop strong relationships with them to truly understand their needs.
“This is the moment we’ve been waiting for – the chance to help members of the MS community stop accepting less and start expecting more. Because there’s still so much more that can be done”
Suzanna van Straaten, Commercial Director MS, EMEA