I don’t follow the perfect diet. I follow the one that actually fits my life...and spoiler? *I'm still stable* Almost a decade after being diagnosed with Relapsing Remitting Multiple Sclerosis. Listen, I tried the whole “do it exactly right” thing: 🥦 Every checklist 🥕 Every MS Diet rule 🥬 Every supplement you could spell without vowels And every time I slipped up? I told myself I didn’t have what it takes. But here’s the truth I wish someone told me sooner: 💥 You don’t need a flawless protoc
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FacebookAlene Brennan
I don’t follow the perfect diet. I follow the one that actually fits my life...and spoiler? *I'm still stable* Almost a decade after being diagnosed with Relapsing Remitting Multiple Sclerosis.
Alene Brennan. . I don’t follow the perfect diet. I follow the one that actually fits my life...and spoiler? *I'm still stable* Almost a decade after being diagnosed with Relapsing Remitting Multiple Sclerosis. Listen, I tried the whole “do it exactly right” thing: 🥦 Every checklist 🥕 Every MS Diet rule 🥬 Every supplement you ...
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Happy Halloween! 🎃 Phoebe was diagnosed with relapsing remitting MS (RRMS) in 2020. She got crafty and shared with us her ‘Haunted House of MS’. 👻 In Phoebe’s house, she’s visited by symptoms like fatigue, spasms and double vision. Whether your MS has given you a trick or a treat today, we’ll be there to support you. 🧡 Find support for your MS symptoms on our website: https://mssoc.uk/3UQiJA1 | MS Society UK
Happy Halloween! 🎃 Phoebe was diagnosed with relapsing remitting MS (RRMS) in 2020. She got crafty and shared with us her ‘Haunted House of MS’. 👻 In Phoebe’s house, she’s visited by symptoms like fatigue, spasms and double vision. Whether your MS has given you a trick or a treat today, we’ll be there to support you. 🧡 Find support for your MS symptoms on our website: https://mssoc.uk/3UQiJA1 | MS Society UK
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mstrust.org.ukFeb 15, 2024
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Relapsing remitting MS
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mstrust.org.uk
Mar 1, 2022
@darlingitsdani who lives with relapsing remitting multiple sclerosis (RRMS) talks about a time of self-advocacy when insurance denied doctor recommended treatment. Watch the full video for more insights from Dani on navigating the MS journey here:https://bit.ly/4aIUFEZ | MyMSTeam
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@darlingitsdani who lives with relapsing remitting multiple sclerosis (RRMS) talks about a time of self-advocacy when insurance denied doctor recommended treatment. Watch the full video for more insights from Dani on navigating the MS journey here:https://bit.ly/4aIUFEZ | MyMSTeam
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Niti was diagnosed with relapsing remitting MS (RRMS) while on maternity leave with her 6-month-old son. 🍼 "It felt like it wasn’t just me who got the diagnosis, but my husband and son too.” Niti shares her most memorable #MSConversation about her diagnosis. She realised that MS didn’t define her, so it shouldn’t define her family either. Read more about Niti’s story: 🔗 https://mssoc.uk/4jCRsMe | MS Society UK
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📢Up to 60,000 people with relapsing-remitting multiple sclerosis (MS) could benefit from ublituximab - a new treatment option we've recommended for adults with the condition. Learn more: https://www.nice.org.uk/guidance/ta1025?utm_medium=organic&utm_source=facebook&utm_campaign=ublituximab&utm_content=finalvideo | National Institute for Health and Care Excellence
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📢Up to 60,000 people with relapsing-remitting multiple sclerosis (MS) could benefit from ublituximab - a new treatment option we've recommended for adults with the condition. Learn more: https://www.nice.org.uk/guidance/ta1025?utm_medium=organic&utm_source=facebook&utm_campaign=ublituximab&utm_content=finalvideo | National Institute for Health and Care Excellence
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Relapsing remitting MS
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@darlingitsdani who lives with relapsing remitting multiple sclerosis (RRMS) talks about a time of self-advocacy when insurance denied doctor recommended treatment. Watch the full video for more insights from Dani on navigating the MS journey here:https://bit.ly/4aIUFEZ | MyMSTeam
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@darlingitsdani who lives with relapsing remitting multiple sclero…
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Niti was diagnosed with relapsing remitting MS (RRMS) while on maternity leave with her 6-month-old son. 🍼 "It felt like it wasn’t just me who got the diagnosis, but my husband and son too.” Niti shares her most memorable #MSConversation about her diagnosis. She realised that MS didn’t define her, so it shouldn’t define her family either. Read more about Niti’s story: 🔗 https://mssoc.uk/4jCRsMe | MS Society UK
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The changes from relapsing-remitting MS to secondary progressive MS are often challenging to recognize. In this week's Wisdom Wednesdays, Aaron Boster MD explains how one can potentially tell when there is a transition. | Multiple Sclerosis Foundation
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Happy Halloween! 🎃 Phoebe was diagnosed with relapsing remitting MS (RRMS) in 2020. She got crafty and shared with us her ‘Haunted House of MS’. 👻 In Phoebe’s house, she’s visited by symptoms like fatigue, spasms and double vision. Whether your MS has given you a trick or a treat today, we’ll be there to support you. 🧡 Find support for your MS symptoms on our website: https://mssoc.uk/3UQiJA1 | MS Society UK
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90% of people with relapsing-remitting multiple sclerosis will begin to experience fewer relapses after 40 years of age. They will notice gradually worsening fatigue, anxiety, depression, foot drop, stumbles, more bowel and bladder accidents. The disease modifying treatments (DMTs) do a terrific job of reducing new relapses/ lesions but do not restore lost functions. But there are professions, treatments and technologies that have been shown to help achieve meaningful improvements in function. I
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Niti’s MS Letter 💌 Niti was diagnosed with relapsing remitting MS (RRMS) while on maternity leave with her 6-month-old son. 🍼 Niti shares how her MS diagnosis has impacted family life. And how, at first, she felt worried about being a mum to her son while living with MS. “Being a mum isn’t about hiding your struggles. It’s about showing how you keep going, no matter what.” She realised, over time, that MS didn’t define her, so it shouldn’t define her family either. 🧡 | MS Society UK
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