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@saali 

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saali

Multiple sclerosis feel very depressed lately

Hi everyone, Today I am not sleeping I feel very depressed and moody swing feel very sad, as if the whole world against me, As if no one cares about me, as if nothing can cheers me up, I had only yesterday I had so much courage and confidence but today all day i feel so bad very very annoyed and ...

@Leeb 

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Leeb

Ticklish?

I'm not ticklish, never have been. When it recently came up in conversation, I wondered if that was common in pwMS, possibly even an early sign? So, are you ticklish, and what type of MS are you battling?

@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 

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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.

@pichardo 

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pichardo

Me quiero ir a mi Pueblo natal

Hola buenas tardes saludos soy d Jalisco Mexico y tengo ppms, mi vida matrimonial, ya no existe estoy aqui por mi ocrevus q ya va aser cada 9 meses, me toca en Enero y me quiero ir a Mexico y tratar algo en Mexico ya no estoy bien aqui tengo 59 años 8 en ocrevus saludos

@Beans9985 

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Beans9985

420 friendly

Dose anyone in use thc to realx?

@AVFCotterill 

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AVFCotterill

Any MS’rs run?

Hi all, I was diagnosed in 2015, hit rock bottom in 2022 and couldn’t walk more than 100m. Ocrevus changed my life and I ran my first 10k yesterday. Any other MS’rs run? Looking for inspiration to do a half marathon and to spread a bit of positivity that if I can do it, anyone can! I’m not fixed bu...

@sophiemg 

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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...

So excited

I decided to write down some of my thoughts about living with MS. It turns out I had loads to say. It turned into a book. I published it today! I just wanted to gush. I’m sure you understand lol 😎✊👨‍🦽

@StacyJG 

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StacyJG

New medication

I just got put on Zeposia and amantadine. Amantadine is supposed to help with fatigue, brain fog, tremors and muscle spasticity. It’s also prescribed for Parkinson’s and for ulcerative colitis. Anybody have any thoughts or experiences with either of these medication’s?