Pain in My MS: Hurdles, Help, and Hacks
Are you willing to approach your MS pain management with renewed optimism? Let these real-life strategies from other community members inspire you: https://bit.ly/3G1G51q
#ThisIsMS #MSLife #MSCommunity #MSSupport
Worth the talk: MS treatment options and optimization�
Our new Worth the Talk video series tackles all your treatment-related questions and concerns, offering the facts you need and the guidance you deserve. Tune in to the first video here: https://bit.ly/3DV7uBz
#MS #MultipleSclerosis #ThisIsMS #MSCommunity #MSTreatment
MS Community Spotlight stories
If you haven’t caught up on the first MS Community Spotlight stories, you’re missing out! Stay tuned for others coming your way the rest of the month as we highlight the diverse voices in our community. https://bit.ly/3DjacjR
#MSSpotlight #MSAwareness #ThisIsMS #MSLife #MSCommunity
MS and fatigue: Why do my batteries always need to be recharged?
Does it feel like your batteries always need to be recharged? On the first episode of our new series, “Get Tough on MS,” doctors and patients alike offer advice and personal life hacks to help you address fatigue and its relentless impact. Watch here: https://bit.ly/4bhWc6H
#MS #MultipleSclerosis #MSSupport #MSSymptoms #GetToughOnMS
Stay tuned for our Get Tough on MS series!
Looking to take full control of your MS this year? Our upcoming physician-led video series will help you do just that — through practical guidance, inspiration, and more. Let’s get tough together! https://bit.ly/4hUDLXN
#ThisIsMS #MSLife #MSCommunity #MSSupport
Community Perspectives: Meet one of our MS Advocates
Meet Desirée Lama, diagnosed with RRMS at age 17. She knows how tough life with the disease can be in such a superficial, overcritical world. Here’s how she hopes to help.
#ThisIsMS #MSLife #MSCommunity #MSSupport #MSFighter
Desiree Lama: Building trust and a plan with an MS team
Not yet sure about your MS team — and maybe even its treatment recommendations? One patient shares how to build trust and a plan that you feel comfortable with: https://bit.ly/40JnuxV
#MSTreatment #ThisIsMS #MSLife #MSCommunity #MSSupport
If you could ask one question to a therapist specializing in rare disease, what would it be?
On Rare Disease Day, Feb. 28, we're passing the mic to YOU! This is your chance to seek guidance on the unique challenges of living with rare. Simply click on the link below to learn more or drop your question on this post. It might just get answered on video!
https://bionews.com/keepin-it-rare/
#RareDiseaseDay2025 #RareDiseaseDay #RareDiseaseAwareness
Rochelle Roberts: Responding to MS treatment uncertainty
Hesitant to begin a new MS treatment? Rochelle Roberts, who lives with RRMS, offers her advice on this big decision: https://bit.ly/3CybiYD
#ThisIsMS #MSLife #MSSupport #MSFighter #MSTreatment
Want to share your story as part of our annual #MSCommunitySpotlight? Send your submissions with a written story and pictures, or any questions to [email protected] or message MS News Today on Instagram or Facebook.
#MSAwareness #ThisIsMS #MSLife #MSCommunity #MSSupport
Call for submissions- 2025 MS Community Spotlight
Want to share your story as part of our annual #MSCommunitySpotlight? Send your submissions with a written story and pictures, or any questions to [email protected] or message MS News Today on Instagram or Facebook.
#MSAwareness #ThisIsMS #MSLife #MSCommunity #MSSupport
Top News Stories and Patient Perspectives
Our top news stories and patient perspectives made quite the impact this year! Which one was your favorite? https://bit.ly/4fsFXUM
#MS #MultipleSclerosis #ThisIsMS #MSLife #MSCommunity