Young MSers Keeping Dreams Alive

Young MSers Keeping Dreams Alive
0
(0)


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.

Ed Tobias is a retired broadcast journalist. Most of his 40+ year career was spent as a manager with the Associated Press in Washington, DC. Tobias was diagnosed with Multiple Sclerosis in 1980 but he continued to work, full-time, meeting interesting people and traveling to interesting places, until retiring at the end of 2012.
×
Ed Tobias is a retired broadcast journalist. Most of his 40+ year career was spent as a manager with the Associated Press in Washington, DC. Tobias was diagnosed with Multiple Sclerosis in 1980 but he continued to work, full-time, meeting interesting people and traveling to interesting places, until retiring at the end of 2012.

How useful was this post?

Click on a star to rate it!

Average rating 0 / 5. Vote count: 0

No votes so far! Be the first to rate this post.

As you found this post useful...

Follow us on social media!

We are sorry that this post was not useful for you!

Let us improve this post!

Tell us how we can improve this post?

2 comments

  1. LAURIE says:

    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.

Leave a Comment

Your email address will not be published. Required fields are marked *