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@Gortz

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Gortz

Celebs with MS

It's been interesting to watch people in the limelight afflicted with MS. When Christina Applegate got her DX it was just before mine and a lot of my symptoms started adding up to make sense. The treatments she talks about remind me how it is different for us all. I've recently watched a few inte...

@Gortz

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Gortz

What does fatigue feel like for YOU?

As we all experience MS a little differently and as our symptoms remit or evolve i'm curious as to what the most common affliction fatigue feels like to you? At the start i would have an hour or two of dense brain fog (usually in the early afternoon) which i combated by shifting my working hours ar...
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@Robert1960

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Robert1960

I just found this site. My first post. Im here in case someone needs t

I'm open to talk to if you are having issues with your MS or just need someone to listen. I have Primary progressive MS for 12 years. I have some tricks for dealing with PP.

@DonnaSPC

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DonnaSPC

👋🏻 Hi

Just joining the group! Diagnosed in 1997. Hope to learn some new tricks or advice!
Peoria, United States

@DonnaSPC

DonnaSPC

👋🏻 Hi

Just joining the group! Diagnosed in 1997. Hope to learn some new tricks or advice!
Peoria, United States

@Punitor

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Punitor

MS help

I was diagnosed with MS two years ago, I feel so alone and feel like my life's drifting away, are there any positive stories on how to beat this disease, first time posting

@Laura106

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Laura106

New to Ms, any tips?

Hi all, hope you are doing well? I was diagnosed Feb after suffering numbness and dizziness since October. They have said that I had optic neuritis and I am still struggling with it to be honest. It is affecting my work which is computer based. Has anyone got any advice to help me with my eyes o...

@billyshift

billyshift

Are video appointments a good thing?

In 2021 we surveyed over 2,000 MSers to capture their thoughts on how things like remote appointments are impacting our access to healthcare. • 51% of MSers found it challenging to attend face-to-face appointments with their MS healthcare team. • 42% of MSers were dissatisfied with the level of acc...

@Emsy129

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Emsy129

jc Virus

Hi new to this site and newly diagnosed just 3 months ago. Today I saw my neurologist, (I have had 3 treatments of tysabri) and found out my JC virus was very high positive. I will have 3 more tysabri treatments and then cross over to kesimpta. Is anyone on kesimpta or had to swap treatments because...

@EmEve9

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EmEve9

New here

Just had a preliminary diagnosis of primary progressive MS, second MRI due August to confirm. Here to find out more information and what to expect? I read someone's description that your legs feel like you're wading in water when you walk and that's soon accurate!