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This is Zoë's story. 🎥 “By the time you’re 40, it will feel as though you’re in a body that isn’t yours.” Zoë lives with primary progressive MS (PPMS). Thanks to MS research, Zoë will begin to take Ocrevus. And she hasn't developed any new lesions since starting the infusions. Zoë’s #MSLetter reminds us that life with MS can be unpredictable. But there is hope. We must continue to fund research to find treatments to slow or stop MS progression, for everyone. 🔬 Every MS Letter tells a story. He
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This is Caroline’s story. 🎥 Caroline lives with secondary progressive MS (SPMS), after being diagnosed nearly 40 years ago. Caroline’s MS Letter is a story of resilience. She talks about the highs and the lows of life with MS. And she reminds her younger self: “You have MS. It doesn’t have you.” Read Caroline’s MS Letter: https://mssoc.uk/3MGvo7K | MS Society UK
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Jasmine lives with secondary progressive MS (SPMS) at just 24. This is her story. "Having advanced MS affects everything... It’s made me feel absolutely alone at times. This is why I want to put my story out there." 💬 Jasmine tells us about her experience with assisted living, personal care and maintaining independence. Read more about Jasmine’s experience ➡️ https://mssoc.uk/3WfQYlC [Note: We know that everyone is affected by MS differently and we want everyone’s stories to be heard. If you li
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