Hi all I’m just looking for any information on flu jab entitlement My gps have said ms doesn’t make me entitled to a flu jab is this correct ? Thanks all Liz

Good evening all. Having recently been diagnosed with MS having had two relapses in 6 months. This is all very new and alien to me. Consultant now talking medication. Want to get opinions tablets or injection? Any advice and help greatly appreciated.

Hi everyone, it has been a long time since I have been on here. I was wondering if anyone could help me please. So I went to see a consultant about my options for meds, at present I only qualify for the injectables. I will be having an up to date scan to access this and make a decision. In my exa…

If I were on my own being assessed for help with my disabilities and had sat on my arse all my life on my own before I was struck down and crippled by MS, assistance would be granted hand over over fist. But if you’re married, what has my problems got to do with my wife? Am I any different to…

Hi folks first time posting and was just wondering, does anyone else get a strange sensation as if your skin covered in creepy crawleys. Sounds silly i know but it drive’s me bonkers

I lived alone for a long time. I was doing myself any things I need for a long time. But now things goes worse: I hardly can move out of the bed to a wheelchair. My disease progressing, there is nothing can I do. Now I’ve got a wife and we have a baby. He is a clever boy 9 months old. I’…

Hey guys! It’s my first time posting a comment, I’m just hoping for some advice really 😊 I’m having serious trouble sleeping. It takes me so long to fall asleep, then I’m waking up (pretty wide awake) every couple of hours or so. Then I’m ready to get up really earl…

What do you think about MSers getting the shingles vaccine? Good or bad idea? My GP says I’m too young but I thought that getting shingles if you have MS is bad. I had chicken pox as a child. Not sure whether to insist I have it.

Hello everyone, I’ve got SPms, diagnosed out of the blue 3 years ago, my symptoms/mobility is getting slowly worse, walking with a limp, pins and needles in left hand/ loss of dexterity blah blah blah, you know how it is. My issue is, I’ve been a self employed carpenter for the last 30 …

Hey all. Hope everyone is doing well. Seen my Neurologist last week and he has decided to change plans after seeing my latest MRI. So I was suppose to be going on to Ocruvus but that plan is not happening now. He has decided to take me off Copaxon completely and not replace it with anything at th…