Tell MS It Ends With Us — #MSEndsWithUs
3,727 views 6 months ago
People affected by multiple sclerosis tell MS how it’s changed their lives, for the good and the bad. Learn about MS, watch more videos and join the conversation at https://ntlms.org/JoinUs. #multiplesclerosis #MSEndsWithUs

Shorts

Stories of life with multiple sclerosis are told through the everyday moments people with MS experience. The National MS Society amplifies the stories of people living with MS to raise awareness — until the moment we find a cure. http://nationalmssociety.org/msawareness
"Multiple sclerosis may be a part of who you are, but it doesn't define you." Every day, people do whatever it takes to move their lives forward despite MS.

Tracey’s Story

National MS Society
5.5K views4 years ago

Lydia's Story

National MS Society
4.9K views4 years ago

Tyler’s Story

National MS Society
3.6K views4 years ago

Chloe's Story

National MS Society
7.3K views7 years ago

Jim's Story

National MS Society
5.8K views7 years ago
Videos about what the Society does for people with MS and their friends and families.
The Ask an MS Expert weekly webinar series is an opportunity to learn more about multiple sclerosis from top MS experts. Each week’s edition will focus on a topic related to the MS community and feature a presentation followed by the opportunity to ask the expert your questions live.
National MS Society
• 5 months ago
We are BEYOND grateful to everyone who came together for #MarchTogether! From the incredible streamers to the generous donors, we are so glad to have you as a part of the #StreamToEndMS family. 🧡
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National MS Society
• 5 months ago
From Times Square to Milwaukee, people all over the U.S. are showing their support for people living with MS! 🧡 Times Square - New York City, New York City and County Building - Denver, Colorado Hoan Bridge - Milwaukee, Wisconsin Charlotte, North Carolina Murray Baker Bridge - Peoria, Illinois
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National MS Society
• 7 months ago
"Love works in strange ways and fate (or bicycles) brings people together for a reason. Thanks to visiting a friend’s wife in the hospital while wearing a cycling shirt, I met my future wife. Jenny’s father lives with MS and was the reason she started a team. The next thing I know I am doing my first Bike MS ride in 2007. After bumping into each other at numerous rides, and a random team meeting, we started talking to each other and going on rides together One thing led to another, and in 2013 we were married on the bike path at the gazebo where we would meet up. Shortly after we were married, Jenny was diagnosed with MS: making our connection to MS part of our relationship. 2025 will mark 18 Bike MS rides we have completed together. And after all that: we still live happily ever after." -Jerry S.
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National MS Society
• 7 months ago
📣CALLING ALL STREAMERS 📣 You can help us achieve our vision of a world free of MS, one stream at a time. Learn how you can #StreamToEndMS at ntlms.org/Stream25.
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National MS Society
• 8 months ago
"My best advice for anyone living with MS or their caregivers is to be open about their MS, symptoms and treatment plans to those around them. The more people that can understand what you’re going through in the best way that they can will make you feel less alone." -Larkin, #ThisIsMS
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National MS Society
• 8 months ago
Thanks for sharing your Bike MS 2024 memories! They’ve already got us feeling nostalgic. 😍 We can’t wait to see what 2025 brings!
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