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@LaurKay 

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LaurKay

Does anyone have shoe recommendations?

Since my diagnosis I've fallen 3 times, breaking my ankle, tearing tendons and ligaments in my leg and shattering my humerus. Does anyone have any shoe recommendations for stability when walking around in everyday life? Does anyone find things like splints or AFOs are helpful?

@rooneyleoni 

Last reply

rooneyleoni

Checking in on my fellow chronic illness warriors tonight.

How is your body feeling as we wind down? Drop a emoji in the comments that matches your current vibe, whether it's 🛋️, 🔋, or 🌧️. No pressure to be okay.

@SherryCLE01 

Last reply

SherryCLE01

One little thing

What’s one little thing you do for yourself to find a bit of joy while managing MS? For me, it’s watching a funny movie or comedy special — laughing always lifts my spirits. I’d love to hear about your little joys.
South Euclid, United States

@abrhym1 

Last reply

abrhym1

🥀 أشتاق إلى نفسي | I Miss Myself

🇬🇧 English I miss the version of me who didn't have to think twice before doing the simplest things. I miss the freedom of living without constantly checking in with my body. Sometimes, the hardest part of illness is realizing how much of your old life you quietly grieve. 🇸🇦 العربية أشتاق إلى...

@sophiemg 

Last reply

sophiemg

Kesimpta & Immune System

Hi guys, I’m looking at my options for medication and drawn to Kesimpta and trying my best to do the research! However, I work with children and it’s not uncommon for me to catch a cough/cold across the academic year! My question is, do you think it’s wise for me to take Kesimpta as I’m likely t...

Fitness 🧡

Went to my normal Pilates class this morning saw my older Pilates friends 🥰. As the hotel is shut today 😢. How is everyone?
Braunton, United Kingdom

🥀 Simplest wishes / 🥀 أبسط الأمنيات

🇸🇦 العربية: هناك من يحلم بالنجاح والثروة والسفر، وهناك من كل ما يتمناه أن يستيقظ يومًا واحدًا دون ألم، وأن يعيش ساعات قليلة دون أن يضطر إلى التفكير في جسده. 🇬🇧 English: Some people dream of success, wealth, and travel. Others dream of something far simpler: waking up one day without pain and ...

@Trevor 

EditedLast reply

Trevor

Be your own advocate !!

I had HSCT for Multiple Sclerosis here in the UK. I was discharged from Hospital 11 years ago this Christmas. I have been in remission ever since, despite the MS Society UK telling me among others ‘not to do it, because the treatment was dangerous.’ Their actual words to me were ‘Don’t do it, it’s d...