Columns The MS Wire - A Column by Ed Tobias Young MSers Keeping Dreams Alive Young MSers Keeping Dreams Alive by Ed Tobias | December 22, 2017 Share this article: Share article via email Copy article link 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. Ed *** 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. Print This Page About the Author Ed Tobias People say to write what you know and Ed Tobias knows about MS. He's lived with the illness since 1980, when he was 32 years old. Ed's a retired, award-winning broadcast journalist and his column combines his four decades of MS experiences with news and comments about the latest in the MS community. In addition to writing his column, Ed is one of the patient moderators on the MS News Today Facebook, Twitter, and Instagram sites. He’s also the author of “The Multiple Sclerosis Toolbox: Hints and Tips for Living with M.S.” Ed and his wife split their time between the Washington, D.C. suburbs and Florida’s Gulf Coast, trying to follow the sun. Tags new year Comments LAURIE 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. Reply Michael Ledman Rich people with this disease live poor people die ??? Reply Leave a comment Fill in the required fields to post. Your email address will not be published. Your Name Your Email Your Comment Post Comment
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