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Multiple sclerosis (MS) is a neurological disease of the central nervous system and can be life-altering. This MS Awareness Month, we’re highlighting stories of strength, resilience, and progress of those living with MS. Karen Jacoby joins us to share her journey, from diagnosis to hope, and how the MS community is making a real difference. Watch her story and learn how you can help move research and support forward. (Sponsored) | The Morning Show
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Multiple sclerosis (MS) is a neurological disease of the central nervous system and can be life-altering. This MS Awareness Month, we’re highlighting stories of strength, resilience, and progress of those living with MS. Karen Jacoby joins us to share her journey, from diagnosis to hope, and how the MS community is making a real difference. Watch her story and learn how you can help move research and support forward. (Sponsored) | The Morning Show
69.3K viewsMay 5, 2025
FacebookThe Morning Show
How will YOU challenge MS this MS Awareness Month? Will you run a marathon? Stream a video game? Host a virtual trivia night? Join the Marianetti family and turn your ordinary hobbies into extraordinary actions! Whether you choose to create, stream, write, game, craft, bake, walk, cycle, run – however you decide to challenge MS, know that this May, #WeChallengeMS together. Visit https://bit.ly/2KCHwDt today to choose how you’ll join the movement and support those affected by MS. | MS Canada
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How will YOU challenge MS this MS Awareness Month? Will you run a marathon? Stream a video game? Host a virtual trivia night? Join the Marianetti family and turn your ordinary hobbies into extraordinary actions! Whether you choose to create, stream, write, game, craft, bake, walk, cycle, run – however you decide to challenge MS, know that this May, #WeChallengeMS together. Visit https://bit.ly/2KCHwDt today to choose how you’ll join the movement and support those affected by MS. | MS Canada
1.9K viewsApr 27, 2020
FacebookMS Canada
It’s World MS Day! Join us as we celebrate the global MS movement and build community. One way people stay connected is through self-help groups, bringing together people with common life experiences. While we can’t meet in person, many groups have gone virtual. Groups like the MS Youngsters, a group of teens living with MS. How are you staying connected to the MS community during this time? | National Multiple Sclerosis Society
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It’s World MS Day! Join us as we celebrate the global MS movement and build community. One way people stay connected is through self-help groups, bringing together people with common life experiences. While we can’t meet in person, many groups have gone virtual. Groups like the MS Youngsters, a group of teens living with MS. How are you staying connected to the MS community during this time? | National Multiple Sclerosis Society
38.1K viewsMay 30, 2020
FacebookNational Multiple Sclerosis Society
“I don’t feel tired. I feel like I have the flu.” Talking about MS isn’t easy. MS community members speak out. | MS Society UK
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“I don’t feel tired. I feel like I have the flu.” Talking about MS isn’t easy. MS community members speak out. | MS Society UK
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FacebookMS Society UK
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Life with MS is like a box of chocolates. 🍫 You never know what you're gonna get. Many MS symptoms can be unpredictable, and fatigue is one of them. Everyone's MS is different, and no two people will experience MS the same way. Read 10 ways to manage your MS fatigue: https://mssoc.uk/45IJo6e | MS Society UK
63.5K views8 months ago
FacebookMS Society UK
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It’s World Multiple Sclerosis (MS) Day! With your help, we’re shining a light on what it’s like to live with MS. From diagnosis to lived experience, each story is as varied and unique as the people living it, and people from all over shared their stories with us. Your diagnosis story not only helps illuminate life with MS, but reminds us that we’re in this together. | National Multiple Sclerosis Society
6.8K viewsMay 30, 2024
FacebookNational Multiple Sclerosis Society
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This MS Awareness Week, YOU have the power to make a difference. 🧡 Host a cook-off, organize a cornhole tournament, or create your own unique event! Your passion will fuel hope for those living with MS. Together, we can create a world free of MS! | National Multiple Sclerosis Society
34.1K viewsJan 15, 2025
FacebookNational Multiple Sclerosis Society
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🧡 A chance to win £10,000 🧡 Definite support for people with MS It's a win win! Enter our weekly lottery today for as little as £1 a week. 18 , GB Only, T&C's apply begambleaware.org | MS Society UK
12K viewsNov 1, 2023
FacebookMS Society UK
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March is MS Awareness Month, but for those living with multiple sclerosis, it's a daily reality. In this interview, Julie, who was diagnosed with MS in 2007, shares insights into the invisible struggles, the unique journeys, and the incredible community that defines life with MS. To learn more about Julie’s story with MS, listen to the "MS warriors Talk Bladder and Bowel" podcast episode: https://bit.ly/4id1hjj🧡 #MultipleSclerosisAwareness #MultipleSclerosis #MSwarrior #ChronicIllness #MSEndsWi
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🎀 P R E E🎗 on Instagram: "🎥 🐝 Check out the 1hr recorded LIVE stream on my YT Channel for #vsmsfest @mscanadaofficial 🧡 (It’s under the live section)! #multiplesclerosis #mscanada #vsmsfest #msawareness #multiplesclerosisawarenss #autoimmunedisease #thisisms #lifewithms #mswarrior #msstrong"
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Gina, MS, & Roxanne, RN, BSN on Instagram: "“Morning” sickness?? More like all day, every day sickness. Rude. Let’s rally to change morning sickness to all day sickness 🤣🤣🤣 That persistent nausea doesn’t care if it’s 8am or 2pm. I don’t get super nauseous all the time, but when I do? Of course it’s right after I eat something I love. Farewell to that chocolate bar or scone😭 Why does this happen?! Blame the hormones! In early pregnancy, your body’s going through ma
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