Sort 43 results by

Page 3

Is my MS progressing?

https://www.youtube.com/watch?v=MM-6kNE4YYw&list=PLVUOB-ZqvZOGuy6t95B67vi5A6nQTY0BS Progression is often the elephant in the room, serving to build fear and trepidation for people who are living with MS. Through investigative conversations that unpick the human side of the topic, ‘Is my MS progres...

@minnie 

Last reply

minnie

Soursop - MS people

Hi there, Ive had MS (relapse and remittance) for 15 year now. I was just wondering whether anyone has heard of 'Soursop' or have tried the herbs/ drink. If so, How did you find it? The reason why I am asking is because I have heard from a number of people (people who don't know each other) that ...

@DominicS 

Last reply

DominicS

Long term Cladribine results

Are you taking Cladribine for your MS. Turns out it is pretty decent stuff! - Another example of why we need everyone with MS to sign up to the UK MS Register. - https://ukmsregister.org/ - "Over half of MS patients analysed did not relapse or experience disability progression during 60 months of f...

Coronvairus /Ocrelizumab vaccine trial

Hi all, - If you take ocrelizumab (Ocrevus) , as I do, and want to participate in a vaccine trial then have a read of this post on the Barts MS blog and get in touch with them via the blog. - https://multiple-sclerosis-research.org/2020/06/mscovid19-covax-or-coronavirus-ocrelizumab-vaccination-study...

Call out for a counsellor

Hello MS team! I am an actor writing a play which includes my experiences as an MS warrior. I wanted to know if anyone here has MS counselling experience or can recommend? I would love to have a chat with them by way of researching other perspectives of MS, rather than just my own. I'd also be ...

@angieH 

Last reply

angieH

MS In menopause

Hi. I have been searching for information on how MS looks in menopause. I mean for anyone who has/is with experience of this stage of life, can I just say it is difficult. I am finding it hard to pull apart what is symptom of MS vs menopause. I mean cog fog, fatigue, moods, joint pain, dizzines...

@Aiga_Akmentina 

Last reply

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...

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...