Looking for
something specific?

Hey guys, I've been diagnosed with Ms since I was 13 and had lots of scarring before then, had nearly 10 years of treatment. However, my Ms keeps becoming active. The next and only drug they are suggesting is cladribine /mavenclad. So taking it for the short amount of time over two years. I'd lik...

Hi All, I am new to this site and wanted to introduce myself. I was unofficially diagnosed with MS whilst living in the US but due to limited understanding and MRI facilities in the UK, not officially diagnosed until 2008. Currently medically retired and enjoying life. I have spent the lockdown peri...

A few years ago before leaving the country I wanted to create a "breakfast club" in London for people with ms to meet up for a cup of coffee and a chat. Now that I'm back I want to continue from where I left. Covid permitting. Raise your hand if you might be interested!

Well after a few weeks of rest at home I'm now back to work, and so thankfully to be. My son's would like to see me take off more time, but as I have told them I have always liked working and I will continue to for as many more years as I'm able. I'm a stubborn women, I guess but I will not give in...

Hello everyone! I was recently diagnosed with optic neuritis (and what apparently has been MS for several years now) and after long consideration I finally decided to opt for steroid pulse therapy (5 x 1000 mg methylprednisolone). The first few days were fine, I didn't experience any euphoria, slee...

I would appreciate if someone could discuss with me privately about MS and share own thoughts. If you have been diagnosed recently it is abaolutely fine.

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

https://www.youtube.com/watch?v=mzaidLfVgSY&feature=youtu.be The world 🌍 of health is adapting to an entirely new way of operating, including switching to digital delivery of care and telemedicine. But what does this mean practically for people with MS? 🤔💭 In episode 1 of this miniseries, we’re ...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...