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I am arranging a Midland get together Sunday 30th August 11.00 start but relaxed, it is a big hotel so those that want to distance its good, free WiFi so if you need to bring family there is TV and comfortable seating. I will be posting on Facebook and Twitter too so make a note, all MSers welcome, ...

www.wholesorts.com Bi Monthly blog, makes a decent read as to how an MS er copes with the difficult times and is a good one to share with those that have no idea what MS is www.wholesorts.com

Hi all, I started on copaxone 4 weeks ago. The first two weeks went really well & I had no side effects. Since then every time I have injected I’ve come out in a hot red swollen rash, which has then turned into a hard lump, like a marble (sometimes bigger) in the injection site. Has anyone e...

I’m struggling at the moment. As we went into lockdown, my partner of 11 years decided to tell me he effing hates living with me and dumped me, the same week as I had to have my 19 year old dog put to sleep. He knew from the outset of the relationship that I had ms and it is a degenerative disease...

There's a guy I know, you may know him too, who is taking on a bit of a monumental challenge to raise money to be split three ways between Shift.MS, the MS Trust and MS Society:- http://bit.ly/MS3SDW So please consider a small donation and/or share the challenge around your social network. Thanks...

Here's somebody aiming to raise megabucks for MS through shift, the MS Society and the MS Trust. His efforts look really impressive (check out the link bit.ly/MS3SDW) I think he deserves all the support we can give him...

It touches home as I am a 45 years old female with very aggressive Multiple Sclerosis that does stand up comedy. Ms has negatively impacted my life in so many ways, but I gotta say that it has made me stronger and a better person in a lot of ways. I feel so happy and excited to see myself recover fr...

@dominics is going above and beyond for 3 MS charidees so all you pop pickers follow the link https://www.justgiving.com/fundraising/djs3charitysplit and dig as deep as you can then share the bejesus out of that link

My doctor told me that I have dormant multiple sclerosis meaning that I have the gray areas in my head and most of the symptoms but not the bands in my spine. My question is : is it normal to have symptoms for years before a real diagnosis? My dr told me that dormant ms isn’t a real diagnosis. So as...

I’d love to hear about everyone’s hobbies and interests- whether it’s something you were into pre-diagnosis that you’ve adapted to work around your MS symptoms, or if it’s something completely new to you that you wouldn’t have discovered without your MS. You never know when someone might need an u...