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@solomon 

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solomon

Can we have a completely unserious conversation today? 😂

What's one tiny thing that can ruin your mood faster than it has any right to? Bad Wi-Fi? Someone chewing too loudly? A phone battery on 2% when you need it most? 😭 Let's give our brains a break from serious conversations for a minute. What's yours?

@sleepyalex 

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sleepyalex

Struggling to adjust to diagnosis

Is anyone else struggling to adjust (or did struggle) to their diagnosis? I was diagnosed with RRMS back in March of this year and I’m feeling low about it all, especially now I’m having to start to use a stick and my right leg is getting worse. I’m having to think of things like grab rails around...

@SmoothJoes 

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SmoothJoes

Up all night every night peeing

I stop drinking by 4 pm go to sleep by 10, wakes up every 2 hours sometimes every hour to go. Anybody else experience this?

@rooneyleoni 

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rooneyleoni

We need to normalize celebrating tiny wins.

Today, my win was actually making a hot, proper meal instead of eating snacks over the kitchen counter. What is your micro-win for today, no matter how small it looks to anyone else? Let's hype each other up! 🎉

@culver 

Last reply

culver

Venting

Am s tired of ppl call me about their problems like am not sick myself.. Am trying to clean my house , wash clothes and do my dishes which takes me a few days to complete. O can’t help everyone when I need help myself but no one understands..

@Dabbi 

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Dabbi

Spms

How common is it to transition from rrms to spms even though you are on medication like rituximab?

@Dnorwood 

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Dnorwood

Lifestyle changes

I feel like since being diagnosed I’ve been experiencing my biggest lifestyle changes. I really feel like it has caused me to rely a lot on others. Whether it be the performance of simple everyday tasks or money management. You never really knew how much it is that you took on till you can’t anymore...

@Treesa52 

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Treesa52

Humble

Yesterday I took a walk with my daughter, because of my balance I used my cane for the first time. What a humbling experience. Is using a walking aid embarrassing for any of you?

@Yasminae 

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Yasminae

Teachers with MS? How are we impacted?

Hey guys, I’ve recently started my PGCE and have already caught my first flu at a primary school 🫠 I was wondering how teachers get on while being on ocrevus or any other immunosuppressant for MS. Any advice would be greatly appreciated 🙏🏽