Young MSers Keeping Dreams Alive

Ed Tobias avatar

by Ed Tobias |

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This will be my final column for this year because of the Christmas and New Year holidays.

Rather than ending 2017 with another 500 or so fascinating words from me, I’d like to leave you, instead, with this video. It was produced by a group of young Europeans who have MS. It was shown in November at a “Young People’s Festival for MSers” in Prague. It’s called “My Dream is Alive.”

As we head into a new year let’s, all follow the lead of these young people. Let’s do all we can to keep our dreams alive.

Happy holidays to all.



Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to multiple sclerosis.


LAURIE avatar


I've lived with MS for 32 years. Since I was diagnosed, each day has been a slow, painful, agonizing torture. It started with a limp, then a cane, a walker, then a wheelchair.
I've tried every MS related drug and procedure. All have not helped and most have caused crippling side effects.
I'm just tired of fighting a losing battle.

Michael Ledman avatar

Michael Ledman

Rich people with this disease live poor people die ???


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