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Why the MS Register is so important to u

I have a conflict of interest to declare: I am on the UK MS Register committee. - The MS Register here struggles to get more sign-ups. Everything you share is to further the cause of MS research. Your data is secured properly and never ever shared, outside of the anonymised research data. - The Fre...

@EllieSmith 

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EllieSmith

Tic disorder from MS?

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...

@Aiga_Akmentina 

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Aiga_Akmentina

What`s your well-being story

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...

@Francine@ 

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Francine@

Hi I am Francine

I was diagnosed with MS Nov 97 so nearly 23 years. I have been on various treatments . I am now on Ocrevus 6 monthly infusion. But because of COVID-19 my treatment has been delayed my last dose was the 26th September 2019 I was supposed to have my next dose In March . I just wanted to know if anyo...

@dvtrv 

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dvtrv

Friend request from Lamine_Sene

From Barbados, doesn’t have MS but apparently knows someone who does and Ocrevus is mentioned. I’m assuming it’s fake to declined offer

@kbuda 

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kbuda

Friends

New here and not sure how to find friends. Is this like FB for MS?

@PPE_ForTheMind 

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PPE_ForTheMind

PPE for the Mind - live session today

If you’ve missed it, we’ve been releasing a video a week as part of a course to help build mental resilience called 'PPE for the Mind'. This week we’re doing things a little differently - join Neuropsychologist Jo and MSer Gemma for a live zoom session, 4pm BST, today (Friday 26th June). Places ar...

@angieH 

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angieH

RRMS to SPMS?

I have read that rrms always eventually becomes spms. Is this so? I have a neuro who says that usually by my age (53 and diagnosed at 29), ms has established the pattern it is going to be. One sounds promising and one not so much. What would clue me in that it’s becoming spms? I have more difficu...

alone

I am victim of domestic abuse due to having ms it sucksseems I cannot post this here

alone

I am victim of domestic abuse due to having ms it sucks