Looking for
something specific?

Hi everyone, So we used to meet up every month at a gorgeous pub in Victoria, and whilst this has not been possible we have been connecting over Zoom. It's been great to reconnect with old friends who couldn't make the drinks and to meet new people too, including little ones too <3. So, if a...

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...

During the lockdown I've been binge watching House. They mention MS as a possible diagnosis every other episode, but I'm half way through season 5 and I still haven't seen an actual case... I feel discriminated!

Hello everyone, I've headache which last for a long time. Painkillers can not do anything with it. I really suffer much sometimes like now I do. Does anyone have the same problem and what do you do for coping with it?

I signed a contract for conducting clinical trials of the drug. My relatives did not approve of my decision and each time they scared me with scary stories and the fact that I would be an experimental mouse🤷. In Ukraine, MS treatment is very expensive, and I think that for me this is a chance to ge...

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...

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...

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...

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...

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