6.1K views · 129 reactions | I don’t follow the perfect diet. I...
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6.1K views · 129 reactions | I don’t follow the perfect diet. I...
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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Relapsing remitting MS
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2.7K views · 21 reactions | @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 | Facebook
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2.7K views · 21 reactions | @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 | Facebook
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9.9K views · 120 reactions | 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 | Facebook
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Relapsing–remitting MS Treatment
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2.7K views · 21 reactions | @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 | Facebook
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9.9K views · 120 reactions | 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 | Facebook
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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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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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