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What do you expect next? I had to put my love one and a nursing home. She is on a feeding tube now and can’t walk

I have MS and I am new to this group.

I was wondering whether anybody had tried the Alinker, I bought this a short while ago and thought I would start using it now the warm weather is on its way. apparently, there is one in my area (Southend) and is bright yellow, so I am sure I would’ve seen it somewhere, but not seen it. if you have s...

I'm Marta and I live in Lisbon, Portugal. I have my diagnosis since 2007 when I was 21 years old. I'm a midwife and have two great kids. I'm currently on occrevus

New here so thought I'd introduce myself. Call me Elz. Diagnosed Oct 22. Currently on Copaxone. Main symptoms: Vertigo, numbness in feet and nerve pain in arm.

Hi I have many symptoms and have been referred to a Neurologist in May this year. I just wondered people's experiences, like, what does the Neurologist do? Do they do tests or just look at symptoms? I'm trying to jot down the symptoms in a diary so I don't forget them. I've read a little about the ...

Hey everyone I’ve just been diagnosed with MS I’m looking in to treatments there’s either brabio or plegridy any one else been on these what are the side effects??? Thanks to u all xxx 😊

Im new on here and wanted to ask your opinions and advise for travelling. Im going to Australia next month and I'm traveling alone with my 6 year old son to met my husband out there. Im fine with planes but I am a terrible sleeper and wanted to ask if anyone ha staken rescue remedy before to help t...

My name is Tina. I’m new to the site. Currently on a short leave from work due to a flare up. I thought it could be nice to meet a bunch of people who understand what I’m dealing with.

Hi just joined today so be gentle with me lol

Hi, my name is Tima. I was diagnosed in 2020 with RRMS, the beginning was hard and scary because it's something I didn't know or was aware of. I've gotten used to some things, but there are some things that are still hard to get used to. There are times when I feel out of place with things, but I do...

Hi! I just wanted to jump on here since I follow the shift.ms Instagram page and enjoy the content and engagement. I'm fairly new to MS. Symptoms started Christmas day 2021 whilst on shift at work. Initial thoughts were I'd slipped a disc in my spine. Fast forward to an mri showing a delightful lesi...

Thank you for welcoming me to the group 🥰

I’m new My name is kim I’m from Pennsylvania

Hi there thanks for your message Nice to be sharing my thoughts with ms With people who understand

Im really sad with my ms as an amazing part of you i was died like dancing and being active now i have to think twice before walking

Hello everybody. I'm new here.

hi all I'm carl I've just joined I a single man of 49 I do a lot for MS charity

I diagnosed with MS 12 june , im not bad i see with left eye 80 % , i use betaferon every second day Btw im muslim but for all christian people merry christmas , wish u a the besst 🥰

Is the new medicine you’re taking working for you have do you feel any different?