Sort 453 results by

Page 32

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...

@Dawson.McWatch 

Last reply

Dawson.McWatch

Post for men

I'm wondering if any men have experienced fertility issues? I'm on Ocrevus and wondering if the drug (or MS in general) can affect my sperm count/motility. Was it harder to conceive or were you even able to get your girlfriends/wives pregnant at all?

@Sonnnsonnn 

Last reply

Sonnnsonnn

Mental health and Lockdown

Hey, I have been in lockdown with my family since 17th March and as of recent (the past week or so), I have really struggled with my mental health. I suffer from depression which is believed to be due to MS, so I take 50mg Sertraline a day. As I have been extremely down the past few days my partne...

@angieH 

Last reply

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...

@kbuda 

Last reply

kbuda

Friends

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

@Alex1723 

Last reply

Alex1723

Paramedicine with MS

Hi guys, I have always wanted to be a paramedic (am currently an RN) but have recently been tentatively diagnosed with MS. I am wondering if anyone has successfully gained employment as a paramedic with a known diagnosis of MS or whether I need to put this dream to bed. Thank you :)

@.Bryony. 

Last reply

.Bryony.

Tysabri Eligibility

Hi all, I wondered if anyone could help answer some questions/give their experience.... I was diagnosed in May this year with rapid RRMS following loss of sensation/power in right leg/Side in December 19 and then optic neuritis in April 20. First MRI was in March 20. I was originally told I would r...

@PPE_ForTheMind 

Last reply

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...

@AMD7L 

Last reply

AMD7L

my story

my age is 25. i have MS since 12 years. now i'm adapted with it but it kills everything inside of me. i feel like a zombie. no feelings, no desires, no hops, and no wishes. what i've to do now. help me i wanna be a human again .

@Vixen 

Last reply

Vixen

SPMS rejection

Time to get campaigning again folks; NICE have rejected Siponimod for SPMS in the UK https://www.mstrust.org.uk/news/siponimod-active-secondary-progressive-ms-rejected-nice Might have to get my battle hat on again.....