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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...

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

Finally started treatment I thought it was going to be alot worse than it has been so I'm grateful for that. Or they given me placebo. February is always a though month for me it's the last month I got to speak to my mum. She had MS. Died 2018 it feels like longer. It's still strange to me. Anyw...

I felt really good today, i didn't do much just played some video games but by 6pm i was exhausted. i lay down for a nap but i woke up exhausted, dizzy and it felt like my heart beat was in my head i could hear and feel it. it this common and caused by MS?

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...

Hi everyone, I know that it just isn't possible to stay positive all the time in the face of MS, and we shouldn't be expected to, sometimes it's tough and we just need to let ourselves feel how we do in that moment. BUT I would really love it if from time to time we could all share something that w...

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...

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...

Hi friends. It's been a while since I posted so I'll give you a quick run down. I went off all ms meds in sept of last year due to having a 1 in 100 chance of contracting PML. Then in december I had a flair up that had me in bed until march. It was horrific to say the least. So in march I started my...