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@Irene_Kostyk 

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Irene_Kostyk

M.S. Warrior

<p>I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.</p>

@Isabel 

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Isabel

Tysabri

Can anyone tell me if Tysabri infusions are free I have been recently been diagnosed with RR MS and will be starting this infusion soon. Are they free if you only have private health insurance 😊

@Safra_Iqbal 

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Safra_Iqbal

Can women with ms get pregnant

I was told women with ms can get pregnant and their is no difference of it. But what are the chances of a woman living with ms former than 11 years being conceived is she has her ms completely under control? When I was diagnosed at a young age and learnt about the sickness my only wish was to have ...

Daily Briefing Covid-19 [Apr 20th &#039;20]

<p>Afternoon all,<br> –<br> Not sure when I ought to drop the Covid-19 tag from the headline. I think it should last as long the lockdown lasts. We see the conversation subtly changing now to more of the looking ahead. You can’t panic forever.<br> ——<br> MS Stuff<br> R...</p>

@JoyceG. 

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JoyceG.

No DMT at the moment...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

Cognitive deficits advice

I’ve realised since my diagnosis my cognitive ability has decreased drastically! Does anyone have any techniques or exercises they do that help ?

@lukezni 

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lukezni

Stormy weather

Seems like a bit of a weird question but does stormy weather effect your ms? There is currently a storm hitting here (the first since I've been diagnosed with ms) and my head feels like what could only be described as stuffy/heavy? My ears have a constant feel to them as if they are about to pop

Experiences of Ocrevus

Before I start, I want to say, I know it's early days... I was diagnosed in Aug 2019 with RRMS after 18months with a CIS diagnosis. My initial scan showed lesions but they couldn't tell how old or if active. 6 months later a second scan was stable. 6 months later my third scan showed new lesions wh...

@mser79 

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mser79

3rd infusion of lemtrada?

Hi I am 10 years in with RR MS, and had 2 very successful doses of alemtuzumab, in January 2016 and January 2017. I responded very well to the alemtuzumab neurologically (despite being highly prone to any virus, cold or infection going in the 1st year) and in 2018 was in extremely good neurologica...

Mavenclad

Hi i was diagnosed with RRMS in 2012 when i was 26. Now 33 I've tried Copaxone, Gylenya and am on my second year of Mavenclad. With Copaxone i had a relapse and never felt any relief. Also i have permanent divots in my legs and arm because of it. Gylenya I was happy with but still finding symptoms w...